Benzonitrile (PhCN) [C7H5N] by Asch

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Reaxys ID 506893 View in Reaxys

1/1 CAS Registry Number: 100-47-0 Chemical Name: benzonitrile; phenyl cyanide; PhCN Linear Structure Formula: C6H5NC Molecular Formula: C7H5N Molecular Weight: 103.123 Type of Substance: isocyclic InChI Key: JFDZBHWFFUWGJE-UHFFFAOYSA-N Note:

Substance Label (301) Label References 4f

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2-1

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2g; 2k

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(BN)2

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T3D

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1; 3

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2(23)

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12b

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17a

Polyak, Maria; Varga, Gergely; Szilagyi, Bence; Juhasz, Laszlo; Docsa, Tibor; Gergely, Pal; Begum, Jaida; Hayes, Joseph M.; Somsak, Laszlo; Bioorganic and Medicinal Chemistry; vol. 21; nb. 18; (2013); p. 5738 - 5747, View in Reaxys; Guan, Qi; Feng, Dongjie; Bai, Zhaoshi; Cui, Yuanhang; Zuo, Daiying; Zhai, Min'An; Jiang, Xuewei; Zhou, Wenbo; Bao, Kai; Wu, Yingliang; Zhang, Weige; MedChemComm; vol. 6; nb. 8; (2015); p. 1484 - 1493, View in Reaxys

Tsuchiya, Daisuke; Kawagoe, Yuhsuke; Moriyama, Katsuhiko; Togo, Hideo; Organic Letters; vol. 15; nb. 16; (2013); p. 4194 - 4197, View in Reaxys; He, Haitao; Qi, Chaorong; Hu, Xiaohan; Lu, Ouyang; Xiong, Wenfang; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 80; nb. 10; (2015); p. 4957 - 4965, View in Reaxys; Liu, Lixin; Dong, Jianyu; Zhang, Yaxing; Zhou, Yongbo; Yin, Shuang-Feng; Organic and Biomolecular Chemistry; vol. 13; nb. 39; (2015); p. 9948 - 9952, View in Reaxys

Noe, Marco; Perosa, Alvise; Selva, Maurizio; Green Chemistry; vol. 15; nb. 8; (2013); p. 2252 - 2260, View in Reaxys; Li, Long-Bo; Dan, Wen-Jia; Tan, Fang-Fang; Cui, Li-Hui; Yuan, Zhi-Peng; Wu, Wen-Jun; Zhang, Ji-Wen; Chemical and Pharmaceutical Bulletin; vol. 63; nb. 1; (2015); p. 33 - 37, View in Reaxys

16a

Kivrak, Arif; Zora, Metin; Tetrahedron; vol. 70; nb. 4; (2014); p. 817 - 831, View in Reaxys; Flesch, Daniel; Gabler, Matthias; Lill, Andreas; Gomez, Roberto Carrasco; Steri, Ramona; Schneider, Gisbert; Stark, Holger; SchubertZsilavecz, Manfred; Merk, Daniel; Bioorganic and Medicinal Chemistry; vol. 23; nb. 13; (2015); p. 3490 - 3498; Art.No: 12247, View in Reaxys

Chatterjee, Tanmay; Dey, Raju; Ranu, Brindaban C.; Journal of Organic Chemistry; vol. 79; nb. 12; (2014); p. 5875 - 5879, View in Reaxys; Choi, Jong-Hoo; Prechtl, Martin H. G.; ChemCatChem; vol. 7; nb. 6; (2015); p. 1023 - 1028, View in Reaxys

2a; 4a; 4h; 4i; 4j; 4k; 6a

Azarifar, Davood; Najminejad, Zohreh; Journal of the Iranian Chemical Society; vol. 12; nb. 1; (2015); p. 107 - 111, View in Reaxys

Iosub, Andrei V.; Stahl, Shannon S.; Journal of the American Chemical Society; vol. 137; nb. 10; (2015); p. 3454 3457, View in Reaxys

20/225

2018-05-24 12:11:44

3f'

Yang, Chu-Ting; Han, Jun; Liu, Jun; Gu, Mei; Li, Yi; Wen, Jun; Yu, Hai-Zhu; Hu, Sheng; Wang, Xiaolin; Organic and Biomolecular Chemistry; vol. 13; nb. 9; (2015); p. 2541 - 2545, View in Reaxys

1a; 1n; 1o; 1p; 1q

Zhang, Ji-Shu; Chen, Tieqiao; Yang, Jia; Han, Li-Biao; Chemical Communications; vol. 51; nb. 35; (2015); p. 7540 7542, View in Reaxys

2-7

Geng, Hui; Huang, Pei-Qiang; Tetrahedron; vol. 71; nb. 23; (2015); p. 3795 - 3801, View in Reaxys

Table 3, Entry 1; Table 3, Entry 10

Xu, Zhicheng; Xiao, Yunqing; Ding, Hong; Cao, Changsheng; Li, Haitao; Pang, Guangsheng; Shi, Yanhui; Synthesis (Germany); vol. 47; nb. 11; (2015); p. 1560 - 1566; Art.No: SS-2014-F0771-OP, View in Reaxys

Lin, Hong-Yan; Li, Zi-Kang; Bai, Li-Fei; Baloch, Shahla Karim; Wang, Fang; Qiu, Han-Yue; Wang, Xue; Qi, Jin-Liang; Yang, Raong-Wu; Wang, Xiao-Ming; Yang, Yong-Hua; Biochemical Pharmacology; vol. 96; nb. 2; (2015); p. 93 - 106, View in Reaxys

10e

Rassadin, Valentin A.; Boyarskiy, Vadim P.; Kukushkin; Organic Letters; vol. 17; nb. 14; (2015); p. 3502 - 3505, View in Reaxys

Zhu, Yamin; Li, Linyi; Shen, Zengming; Chemistry - A European Journal; vol. 21; nb. 38; (2015); p. 13246 - 13252, View in Reaxys

10h

Škoch, Karel; Císařová, Ivana; Štěpnička, Petr; Chemistry - A European Journal; vol. 21; nb. 45; (2015); p. 15998 16004, View in Reaxys

IIc

Glushkov; Ausheva; Anikina; Vikharev; Safin; Shklyaev; Pharmaceutical Chemistry Journal; vol. 35; nb. 7; (2001); p. 358 - 363, View in Reaxys; Perevoshchikova; Gorbunov; Rozhkova; Slepukhin; Shklyaev; Russian Journal of Organic Chemistry; vol. 50; nb. 4; (2014); p. 513 - 517; Zh. Org. Khim.; vol. 50; nb. 4; (2014); p. 525 - 528,4, View in Reaxys

Zhu, Hua-Jie; Lu, Kai-Tao; Sun, Guang-Ri; He, Jin-Bao; Li, Hai-Qing; Pittman Jr., Charles U.; New Journal of Chemistry; vol. 27; nb. 2; (2003); p. 409 - 413, View in Reaxys; De Luca, Lidia; Giacomelli, Giampaolo; Synlett; nb. 12; (2004); p. 2180 - 2184, View in Reaxys; Byrne, Cillian; Houlihan, Kate M.; Devi, Prarthana; Jensen, Paul; Rutledge, Peter J.; Molecules; vol. 19; nb. 12; (2014); p. 20751 - 20767, View in Reaxys

Dolliver, Debra D.; Bhattarai, Bijay T.; Pandey, Arjun; Lanier, Megan L.; Bordelon, Amber S.; Adhikari, Sarju; Dinser, Jordan A.; Flowers, Patrick F.; Wills, Veronica S.; Schneider, Caroline L.; Shaughnessy, Kevin H.; Moore, Jane N.; Raders, Steven M.; Snowden, Timothy S.; McKim, Artie S.; Fronczek, Frank R.; Journal of Organic Chemistry; vol. 78; nb. 8; (2013); p. 3676 - 3687, View in Reaxys; Sanchez, Ana I.; Meneses, Ricardo; Minguez, Jose M.; Nunez, Araceli; Castillo, Rafael R.; Filace, Fabiana; Burgos, Carolina; Vaquero, Juan J.; Alvarez-Builla, Julio; Cortes-Cabrera, Alvaro; Gago, Federico; Terricabras, Emma; Segarra, Victor; Organic and Biomolecular Chemistry; vol. 12; nb. 24; (2014); p. 4233 - 4242, View in Reaxys

1a, 2a

Damodara, Dandu; Arundhathi, Racha; Likhar, Pravin R.; Advanced Synthesis and Catalysis; vol. 356; nb. 1; (2014); p. 189 - 198, View in Reaxys

Veedu, Rakesh N.; Kvaskoff, David; Wentrup, Curt; Australian Journal of Chemistry; vol. 67; nb. 3; (2014); p. 457 468, View in Reaxys

Conole, Daniel; Beck, Thorsten M.; Jay-Smith, Morgan; Tingle, Malcolm D.; Eason, Charles T.; Brimble, Margaret A.; Rennison, David; Bioorganic and Medicinal Chemistry; vol. 22; nb. 7; (2014); p. 2220 - 2235, View in Reaxys; Pepino; Pelez; Faillace; Ceballos; Moyano; Argüello; RSC Advances; vol. 4; nb. 104; (2014); p. 60092 - 60101, View in Reaxys

Louvel, Julien; Guo, Dong; Agliardi, Marta; Mocking, Tamara A. M.; Kars, Roland; Pham, Tan Phát; Xia, Lizi; De Vries, Henk; Brussee, Johannes; Heitman, Laura H.; Ijzerman, Adriaan P.; Journal of Medicinal Chemistry; vol. 57; nb. 8; (2014); p. 3213 - 3222, View in Reaxys

16e

Draghici, Bogdan; Vullo, Daniela; Akocak, Suleyman; Walker, Ellen A.; Supuran, Claudiu T.; Ilies, Marc A.; Chemical Communications; vol. 50; nb. 45; (2014); p. 5980 - 5983, View in Reaxys

Wang, Li-Ya; Tsai, Henry J.; Lin, Hui-Yi; Kaneko, Kimiyoshi; Cheng, Fen-Ying; Shih, Hsin-Siao; Wong, Fung Fuh; Huang, Jiann-Jyh; RSC Advances; vol. 4; nb. 27; (2014); p. 14215 - 14220, View in Reaxys

5a; PhCN

Tang, Hai-Tao; Zhou, Yun-Bing; Zhu, Yu; Sun, Hong-Chao; Lin, Min; Zhan, Zhuang-Ping; Chemistry - An Asian Journal; vol. 9; nb. 5; (2014); p. 1278 - 1281, View in Reaxys

Golubev, Pavel R.; Pankova, Alena S.; Kuznetsov, Mikhail A.; European Journal of Organic Chemistry; vol. 2014; nb. 17; (2014); p. 3614 - 3621, View in Reaxys

Vorona, Svetlana; Artamonova, Tatiana; Zevatskii, Yuri; Myznikov, Leonid; Synthesis (Germany); vol. 46; nb. 6; (2014); p. 781 - 786; Art.No: SS-2013-Z0723-OP, View in Reaxys

Yin, Wenzhu; Liu, Rui; He, Guangke; Lv, Wangjie; Zhu, Hongjun; RSC Advances; vol. 4; nb. 71; (2014); p. 37773 37778, View in Reaxys

21/225

2018-05-24 12:11:44

1a; Ph-CN

Kim, Ju Hyun; Choi, Suh Young; Bouffard, Jean; Lee, Sang-Gi; Journal of Organic Chemistry; vol. 79; nb. 19; (2014); p. 9253 - 9261, View in Reaxys

Ueno, Ryota; Shirakawa, Eiji; Organic and Biomolecular Chemistry; vol. 12; nb. 38; (2014); p. 7469 - 7473, View in Reaxys

8c; PhCN

Jones, Alison S.; Paliga, James F.; Greenhalgh, Mark D.; Quibell, Jacob M.; Steven, Alan; Thomas, Stephen P.; Organic Letters; vol. 16; nb. 22; (2014); p. 5964 - 5967, View in Reaxys

1a; BN

Vörös, Attila; Mucsi, Zoltn; Ban, Zoltn; Timri, Gza; Hermecz, Istvn; Mizsey, Pter; Finta, Zoltn; Organic and Biomolecular Chemistry; vol. 12; nb. 40; (2014); p. 8036 - 8047, View in Reaxys

2; 5

Das, Tuluma; Chakraborty, Amarnath; Sarkar, Amitabha; Tetrahedron Letters; vol. 55; nb. 52; (2014); p. 7198 7202, View in Reaxys

2a; PhCN

Chen, Mengmeng; Zhang, Min; Xiong, Biao; Tan, Zhenda; Lv, Wan; Jiang, Huanfeng; Organic Letters; vol. 16; nb. 22; (2014); p. 6028 - 6031, View in Reaxys

1a; 1j; 1k; 1l

Cheng, Xu; Pei, Shuchen; Xue, Chenchen; Cao, Kaifei; Hai, Li; Wu, Yong; RSC Advances; vol. 4; nb. 109; (2014); p. 63897 - 63900, View in Reaxys

Salfetnikova; Vasil'ev; Rudenko; Russian Journal of Organic Chemistry; vol. 34; nb. 6; (1998); p. 838 - 844, View in Reaxys; Vaganova; Shteingarts; Russian Journal of Organic Chemistry; vol. 40; nb. 5; (2004); p. 747 - 750, View in Reaxys; Kovacs, Dora; Woelfling, Janos; Szabo, Nikoletta; Szecsi, Mihaly; Kovacs, Ida; Zupko, Istvan; Frank, Eva; European Journal of Medicinal Chemistry; vol. 70; (2013); p. 649 - 660, View in Reaxys

Foster, Jennifer; Pincock, Alexandra L.; Pincock, James A.; Thompson, Kim A.; Journal of the American Chemical Society; vol. 120; nb. 51; (1998); p. 13354 - 13361, View in Reaxys; Kusurkar, Radhika; Goswami, Shailesh; Vyas, Sandhya; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 42; nb. 12; (2003); p. 3148 3151, View in Reaxys; Xia, Guangxin; You, Xiaodi; Liu, Lin; Liu, Haiyan; Wang, Jianfa; Shi, Yufang; Li, Ping; Xiong, Bing; Liu, Xuejun; Shen, Jingkang; European Journal of Medicinal Chemistry; vol. 62; (2013); p. 1 - 10, View in Reaxys

11a

Nanni, Daniele; Pareschi, Patrizia; Walton, John C.; Journal of the Chemical Society, Perkin Transactions 2; nb. 6; (2002); p. 1098 - 1104, View in Reaxys; Weidauer, Maik; Irran, Elisabeth; Someya, Chika I.; Haberberger, Michael; Enthaler, Stephan; Journal of Organometallic Chemistry; vol. 729; (2013); p. 53 - 59, View in Reaxys

Murata, Miki; Sambommatsu, Tomoko; Watanabe, Shinji; Masuda, Yuzuru; Synlett; nb. 12; (2006); p. 1867 1870, View in Reaxys; Murayama, Koichi; Sawada, Yayoi; Noguchi, Keiichi; Tanaka, Ken; Journal of Organic Chemistry; vol. 78; nb. 12; (2013); p. 6202 - 6210, View in Reaxys

PhCN; 1a

Ramadhar, Timothy R.; Bansagi, Jazmin; Batey, Robert A.; Journal of Organic Chemistry; vol. 78; nb. 3; (2013); p. 1216 - 1221, View in Reaxys

Reddy, Mallu Chenna; Manikandan, Rajendran; Jeganmohan, Masilamani; Chemical Communications; vol. 49; nb. 54; (2013); p. 6060 - 6062, View in Reaxys

Knapp, Spring Melody M.; Sherbow, Tobias J.; Yelle, Robert B.; Juliette, J. Jerrick; Tyler, David R.; Organometallics; vol. 32; nb. 13; (2013); p. 3744 - 3752, View in Reaxys

2a; BnCN

Satoh, Yasushi; Obora, Yasushi; Journal of Organic Chemistry; vol. 78; nb. 15; (2013); p. 7771 - 7776, View in Reaxys

Kang, Byungjoon; Fu, Zhenqian; Hong, Soon Hyeok; Journal of the American Chemical Society; vol. 135; nb. 32; (2013); p. 11704 - 11707, View in Reaxys

IId

Rozhkova, Yu. S.; Galata; Vshivkova; Shklyaev, Yu. V.; Russian Journal of Organic Chemistry; vol. 49; nb. 7; (2013); p. 1055 - 1061; Zh. Org. Khim.; vol. 49; nb. 7; (2013); p. 1070 - 1076,7, View in Reaxys

Itagaki, Shintaro; Sunaba, Hanako; Kamata, Keigo; Yamaguchi, Kazuya; Mizuno, Noritaka; Chemistry Letters; vol. 42; nb. 9; (2013); p. 980 - 982, View in Reaxys

21a

Enthaler, Stephan; Weidauer, Maik; Irran, Elisabeth; Epping, Jan Dirk; Kretschmer, Robert; Someya, Chika I.; Journal of Organometallic Chemistry; vol. 745-746; (2013); p. 262 - 274, View in Reaxys

Vernekar, Amit A.; Patil, Sagar; Bhat, Chinmay; Tilve, Santosh G.; RSC Advances; vol. 3; nb. 32; (2013); p. 13243 - 13250, View in Reaxys

Shu, Zhibin; Ye, Yuxuan; Deng, Yifan; Zhang, Yan; Wang, Jianbo; Angewandte Chemie - International Edition; vol. 52; nb. 40; (2013); p. 10573 - 10576; Angew. Chem.; vol. 125; nb. 40; (2013); p. 10767 - 10770,4, View in Reaxys

13a

Sutter, Marc; Pehlivan, Leyla; Lafon, Romain; Dayoub, Wissam; Raoul, Yann; Metay, Estelle; Lemaire, Marc; Green Chemistry; vol. 15; nb. 11; (2013); p. 3020 - 3026, View in Reaxys

Fazullina; Ryapisova; Kashevarova; Fridland; Russian Journal of General Chemistry; vol. 83; nb. 11; (2013); p. 2119 - 2121; Zh. Obshch. Khim.; vol. 83-11; nb. 0044-460X; (2013); p. 1929 - 1931,3, View in Reaxys

22/225

2018-05-24 12:11:44

124.1

Patent; Portola Pharmaceuticals, Inc.; US2012/108566; (2012); (A1) English, View in Reaxys

Sokolov; Aksinenko; Martynov; Russian Journal of General Chemistry; vol. 82; nb. 6; (2012); p. 1180 - 1182, View in Reaxys

S35

Modak, Arindam; Mondal, John; Bhaumik, Asim; Green Chemistry; vol. 14; nb. 10; (2012); p. 2840 - 2855, View in Reaxys

1a; 4a

Chun, Yu Sung; Kim, Ju Hyun; Choi, Suh Young; Ko, Young Ok; Lee, Sang-Gi; Organic Letters; vol. 14; nb. 24; (2012); p. 6358 - 6361, View in Reaxys

compound 21; 21

Patent; GREEN GROSS CORPORATION; LEE, Jinhwa; SEO, Hee Jeong; KANG, Suk Youn; PARK, EunJung; KIM, Min Ju; LEE, Suk Ho; KIM, Jong Yup; KIM, Jeongmin; JUNG, Myung Eun; KIM, Hyun Jung; KIM, Mi-Soon; HAN, Ho Kyun; AHN, Kwang Woo; LEE, Min Woo; LEE, Ki-Nam; PAE, Ae Nim; PARK, WooKyu; WO2011/5052; (2011); (A2) English, View in Reaxys

4.35

Patent; BOEHRINGER INGELHEIM INTERNATIONAL GMBH; HOFFMANN, Matthias; DAHMANN, Georg; FIEGEN, Dennis; HANDSCHUH, Sandra; KLICIC, Jasna; LINZ, Guenter; SCHAENZLE, Gerhard; SCHNAPP, Andreas; EAST, Stephen P.; MAZANETZ, Michael Philip; SCOTT, John; WALKER, Edward; WO2011/92128; (2011); (A1) English, View in Reaxys

A-10a

Patent; FIBROGEN, INC.; WO2009/89547; (2009); (A1) English, View in Reaxys

Table 1. Nitrile 1-7

Polshettiwar, Vivek; Varma, Rajender S.; Tetrahedron Letters; vol. 49; nb. 16; (2008); p. 2661 - 2664, View in Reaxys

7, R2=Ph

Morgan, Ian R.; Yazici, Arife; Pyne, Stephen G.; Skelton, Brian W.; Journal of Organic Chemistry; vol. 73; nb. 7; (2008); p. 2943 - 2946, View in Reaxys

4, Ar = Ph

Adib, Mehdi; Mohammadi, Bagher; Bijanzadeh, Hamid Reza; Synlett; nb. 2; (2008); p. 177 - 180, View in Reaxys

nitrile T. 2, E. a

Sabitha, Gowravaram; Bhikshapathi; Nayak, Sambit; Yadav; Ravi; Kunwar; Tetrahedron Letters; vol. 49; nb. 40; (2008); p. 5727 - 5731, View in Reaxys

T2, E1, Nitrile

Sardarian; Shahsavari-Fard; Shahsavari; Ebrahimi; Tetrahedron Letters; vol. 48; nb. 14; (2007); p. 2639 - 2643, View in Reaxys

12d

Wiglenda, Thomas; Gust, Ronald; Journal of Medicinal Chemistry; vol. 50; nb. 7; (2007); p. 1475 - 1484, View in Reaxys

product, Tab.2.run 1

Schareina, Thomas; Zapf, Alexander; Maegerlein, Wolfgang; Mueller, Nikolaus; Beller, Matthias; Tetrahedron Letters; vol. 48; nb. 7; (2007); p. 1087 - 1090, View in Reaxys

Murata, Miki; Yamasaki, Hiyoruki; Ueta, Tsukasa; Nagata, Masayuki; Ishikura, Masanori; Watanabe, Shinji; Masuda, Yuzuru; Tetrahedron; vol. 63; nb. 19; (2007); p. 4087 - 4094, View in Reaxys

starting to 6

Charton, Julie; Cousaert, Nicolas; Bochu, Christophe; Willand, Nicolas; Deprez, Benoit; Deprez-Poulain, Rebecca; Tetrahedron Letters; vol. 48; nb. 8; (2007); p. 1479 - 1483, View in Reaxys

Langer, Peter; Anders, Joachim T.; European Journal of Organic Chemistry; nb. 4; (2002); p. 686 - 691, View in Reaxys; Murahashi, Shun-Ichi; Okano, Yuriko; Sato, Hideomi; Nakae, Takahiro; Komiya, Naruyoshi; Synlett; nb. 11; (2007); p. 1675 - 1678, View in Reaxys

Naguib; Iltzsch; El Kouni; Panzica; Biochemical Pharmacology; vol. 50; nb. 10; (1995); p. 1685 - 1693, View in Reaxys; Tsai, Kuo-Pei; Chen, Chung-Yuan; Environmental Toxicology and Chemistry; vol. 26; nb. 9; (2007); p. 1931 - 1939, View in Reaxys

72: R=Ph

Fish, Paul V.; Allan, Gillian A.; Bailey, Simon; Blagg, Julian; Butt, Richard; Collis, Michael G.; Greiling, Doris; James, Kim; Kendall, Jackie; McElroy, Andrew; McCleverty, Dawn; Reed, Charlotte; Webster, Robert; Whitlock, Gavin A.; Journal of Medicinal Chemistry; vol. 50; nb. 15; (2007); p. 3442 - 3456, View in Reaxys

table 1, entry 4

Supsana, Paraskevi; Liaskopoulos, Theodoras; Tsoungas, Petros G.; Varvounis, George; Synlett; nb. 17; (2007); p. 2671 - 2674, View in Reaxys

tab1, 3, entry13

Salama, Tarek A.; Elmorsy, Saad S.; Khalil, Abdel-Galel M.; Ismail, Mohamed A.; Tetrahedron Letters; vol. 48; nb. 35; (2007); p. 6199 - 6203, View in Reaxys

educt to 1f, 1v

Zhang, Guolin; Hu, Yongzhou; Journal of Heterocyclic Chemistry; vol. 44; nb. 4; (2007); p. 919 - 922, View in Reaxys

Tomashenko; Sokolov; Tomashevskii; Potekhin; De Meijere; Russian Journal of Organic Chemistry; vol. 43; nb. 10; (2007); p. 1421 - 1426, View in Reaxys

Wan, Shuangyi; Green, Michael E.; Park, Jung-Hyun; Floreancig, Paul E.; Organic Letters; vol. 9; nb. 26; (2007); p. 5385 - 5388, View in Reaxys

Shishkin, V. E.; Mednikov, E. V.; Anishchenko, O. V.; No, B. I.; Russian Journal of General Chemistry; vol. 69; nb. 10; (1999); p. 1673 - 1673; Zhurnal Obshchei Khimii; vol. 69; nb. 10; (1999); p. 1748 - 1748, View in Reaxys; Kartashov; Malkova; Arkhipova; Sokolova; Russian Journal of Organic Chemistry; vol. 42; nb. 7; (2006); p. 966 - 968, View in Reaxys

23/225

2018-05-24 12:11:44

benzonitrile

Elzein, Elfatih; Kalla, Rao; Li, Xiaofen; Perry, Thao; Parkhill, Eric; Palle, Venkata; Varkhedkar, Vaibahv; Gimbel, Art; Zeng, Dewan; Lustig, David; Leung, Kwan; Zablocki, Jeff; Bioorganic and Medicinal Chemistry Letters; vol. 16; nb. 2; (2006); p. 302 - 306, View in Reaxys

1 (Ar1 = Ph)

Kiselyov, Alexander S.; Smith II, Leon; Tetrahedron Letters; vol. 47; nb. 15; (2006); p. 2611 - 2614, View in Reaxys

3 (Ar=Ph)

Adib, Mehdi; Jahromi, Amin Haghighat; Tavoosi, Narjes; Mahdavi, Mohammad; Bijanzadeh, Hamid Reza; Tetrahedron Letters; vol. 47; nb. 17; (2006); p. 2965 - 2967, View in Reaxys

ArH; Table 3, Entry Schmidt, Luciana C.; Rey, Valentina; Penenory, Alicia B.; European Journal of Organic Chemistry; nb. 9; (2006); p. 7 2210 - 2214, View in Reaxys Tab. 1, entry 4

Crestani, Marco G.; Arevalo, Alma; Garcia, Juventino J.; Advanced Synthesis and Catalysis; vol. 348; nb. 6; (2006); p. 732 - 742, View in Reaxys

1h, Ar-CN, R=H

Nakao, Yoshiaki; Oda, Shinichi; Yada, Akira; Hiyama, Tamejiro; Tetrahedron; vol. 62; nb. 32; (2006); p. 7567 7576, View in Reaxys

R2CN, R2=C6H5

Rao, K. Srinivasa; Reddy, D. Srinivasa; Pal, Manojit; Mukkanti; Iqbal, Javed; Tetrahedron Letters; vol. 47; nb. 26; (2006); p. 4385 - 4388, View in Reaxys

Table 2, Entry 1, subs.

Kaboudin, Babak; Elhamifar, Dawood; Synthesis; nb. 2; (2006); p. 224 - 226; Art.No: Z14505SS, View in Reaxys

agent to 3c

Hogan, Anne-Marie L.; O'Shea, Donal F.; Journal of the American Chemical Society; vol. 128; nb. 32; (2006); p. 10360 - 10361, View in Reaxys

IIa

Volkova; Albanov; Russian Journal of Organic Chemistry; vol. 42; nb. 11; (2006); p. 1730 - 1731, View in Reaxys

Table 3. Ent.9-12, R-CN

Takahashi, Tatsuya; Sugimoto, Osamu; Koshio, Jiro; Tanji, Ken-ichi; Heterocycles; vol. 68; nb. 9; (2006); p. 1973 1979, View in Reaxys

tab. 1, entry 1

Mukherjee, Chandrani; Zhu, Dunming; Biehl, Edward R.; Hua, Ling; European Journal of Organic Chemistry; nb. 23; (2006); p. 5238 - 5242, View in Reaxys

3, ent. a,f,k,l,n,p,q

Adib, Mehdi; Mahmoodi, Niusha; Mahdavi, Mohammad; Bijanzadeh, Hamid Reza; Tetrahedron Letters; vol. 47; nb. 52; (2006); p. 9365 - 9368, View in Reaxys

Ph-CN

Lee, Yong Rok; Suk, Jung Yup; Tetrahedron Letters; vol. 41; nb. 24; (2000); p. 4795 - 4799, View in Reaxys; Stavber; Kralj; Zupan; Synlett; nb. 7; (2001); p. 1152 - 1154, View in Reaxys; Dejaegher; Mangelinckx; De Kimpe; Synlett; nb. 1; (2002); p. 113 - 115, View in Reaxys; Kiselyov, Alexander S.; Tetrahedron Letters; vol. 47; nb. 17; (2006); p. 2941 - 2944, View in Reaxys; Britovsek, George J. P.; Ugolotti, Juri; Hunt, Patricia; White, Andrew J. P.; Chemical Communications; nb. 12; (2006); p. 1295 - 1297, View in Reaxys; Sorokoumov; Morozkina; Balova; Chemistry of Heterocyclic Compounds; vol. 42; nb. 5; (2006); p. 615 - 624, View in Reaxys

Senaiar, Ramesh S.; Young, Douglas D.; Deiters, Alexander; Chemical Communications; nb. 12; (2006); p. 1313 1315, View in Reaxys

1, Ar = C6H5

Adib, Mehdi; Mahdavi, Mohammad; Mahmoodi, Niusha; Pirelahi, Hooshang; Bijanzadeh, Hamid Reza; Synlett; nb. 11; (2006); p. 1765 - 1767, View in Reaxys

sub., Tab.1, entry 1

Kobayashi, Kazuhiro; Hayashi, Kazutaka; Miyamoto, Kazuna; Morikawa, Osamu; Konishi, Hisatoshi; Synthesis; nb. 17; (2006); p. 2934 - 2938, View in Reaxys

BZN

Melandri, Sonia; Consalvo, Daniela; Caminati, Walther; Favero, Paolo G.; Journal of Chemical Physics; vol. 111; nb. 9; (1999); p. 3874 - 3879, View in Reaxys; Del Carmen Grande, Maria; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1324 - 1327, View in Reaxys

BzCN

Chiesa, M. Vittoria; Schmidt, Richard R.; European Journal of Organic Chemistry; nb. 21; (2000); p. 3541 - 3554, View in Reaxys; Sherman, Andrei A.; Yudina, Olga N.; Shashkov, Alexander S.; Menshov, Vladimir M.; Nifant'ev, Nikolay E.; Carbohydrate Research; vol. 330; nb. 4; (2001); p. 445 - 458, View in Reaxys; De Paz, Jose-Luis; Ojeda, Rafael; Reichardt, Niels; Martin-Lomas, Manuel; European Journal of Organic Chemistry; nb. 17; (2003); p. 3308 3324, View in Reaxys; De Paz, Jose Luis; Martin-Lomas, Manuel; European Journal of Organic Chemistry; nb. 9; (2005); p. 1849 - 1858, View in Reaxys

Aitken; Farrell; Kirton; Chemistry of Heterocyclic Compounds; vol. 37; nb. 12; (2001); p. 1526 - 1531, View in Reaxys; Mlinaric-Majerski, Kata; Margeta, Renato; Veljkovic, Jelena; Synlett; nb. 13; (2005); p. 2089 2091; Art.No: G13705ST, View in Reaxys

Table 2. Entry 1. Prod.

Li, Dongmei; Shi, Feng; Guo, Shu; Deng, Youquan; Tetrahedron Letters; vol. 46; nb. 4; (2005); p. 671 - 674, View in Reaxys

tab1, 1, entry a

Kiselyov, Alexander S.; Tetrahedron Letters; vol. 46; nb. 10; (2005); p. 1663 - 1665, View in Reaxys

substrate, tab 4/5

Yadav, Veejendra K.; Babu, K. Ganesh; European Journal of Organic Chemistry; nb. 2; (2005); p. 452 - 456, View in Reaxys

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2018-05-24 12:11:44

educt to 16

Scliroeder, Kerstin; Sander; European Journal of Organic Chemistry; nb. 3; (2005); p. 496 - 504, View in Reaxys

educt to 1a,1f

Kaboudin, Babak; Saadati, Fariba; Journal of Heterocyclic Chemistry; vol. 42; nb. 4; (2005); p. 699 - 701, View in Reaxys

2, R%3& = C6H5

Su, Weike; Yang, Dianwen; Li, Jianjun; Synthetic Communications; vol. 35; nb. 11; (2005); p. 1435 - 1440, View in Reaxys

prod.,Tab.2,entry 1

Sarvari, Mona Hosseini; Synthesis; nb. 5; (2005); p. 787 - 790; Art.No: Z18204SS, View in Reaxys

educt to 4a

Heravi, Majid M.; Montazeri, Naser; Rahimizadeh, Mohammad; Bakavoli, Mehdi; Ghassemzadeh, Mitra; Journal of Heterocyclic Chemistry; vol. 42; nb. 5; (2005); p. 1021 - 1025, View in Reaxys

Tab.3.run6

Biondini, Daniele; Brinchi, Lucia; Germani, Raimondo; Goracci, Laura; Savelli, Gianfranco; European Journal of Organic Chemistry; nb. 14; (2005); p. 3060 - 3063, View in Reaxys

15a

Ramachandran, P. Veeraraghavan; Burghardt, Thomas E.; Bland-Berry, Layla; Journal of Organic Chemistry; vol. 70; nb. 20; (2005); p. 7911 - 7918, View in Reaxys

VII

Britsun; Esipenko; Kudryavtsev; Lozinskii; Russian Journal of Organic Chemistry; vol. 41; nb. 9; (2005); p. 1333 1336, View in Reaxys

R2CN, R2=Ph

Concellon, Jose M.; Suarez, Jose Ramon; Del Solar, Virginia; Journal of Organic Chemistry; vol. 70; nb. 18; (2005); p. 7447 - 7450, View in Reaxys

Table 2, entry 5

Choudary, Boyapati M.; Kantam, Mannepalli L.; Ranganath, Kalluri V. S.; Rao, Kottapalli K.; Angewandte Chemie - International Edition; vol. 44; nb. 2; (2005); p. 322 - 325, View in Reaxys

BNTL

Zhu, Dongqiang; Pignatello, Joseph J.; Environmental Science and Technology; vol. 39; nb. 7; (2005); p. 2033 - 2041, View in Reaxys

C6H5CN

Sun, Xue-Long; Kai, Toshitsugu; Takayanagi, Hiroaki; Furuhata, Kimio; Synlett; nb. 9; (1999); p. 1399 - 1400, View in Reaxys; Sun, Xue-Long; Sato, Noriko; Kai, Toshitsugu; Furuhata, Kimio; Carbohydrate Research; vol. 323; nb. 1-4; (1999); p. 1 - 6, View in Reaxys; Walczynski; Timmerman; Zuiderveld; Zhang; Glinka; Farmaco; vol. 54; nb. 8; (1999); p. 533 - 541, View in Reaxys; Petrova; Platonov; Kolesnikova; Ribalova; Bagryanskaya; Gatilov; Journal of Fluorine Chemistry; vol. 103; nb. 1; (2000); p. 63 - 73, View in Reaxys; Siglow, Klaus; Neusser, Hans Juergen; Journal of Physical Chemistry A; vol. 105; nb. 33; (2001); p. 7823 - 7827, View in Reaxys; Al-Awadi, Nouria; Ibrahim, Yehia; Kaul, Kamini; Dib, Hicham; Journal of Physical Organic Chemistry; vol. 14; nb. 8; (2001); p. 521 525, View in Reaxys; Xu, Xiaoliang; Zhang, Yongmin; Journal of the Chemical Society. Perkin Transactions 1; nb. 21; (2001); p. 2836 - 2839, View in Reaxys; Prasad, Mailavaram Raghu; Rao, Akkinepalli Raghu Ram; Rao, Pamulaparthi Shanthan; Rajan, Kombu Subramanian; Synthesis; nb. 14; (2001); p. 2119 - 2123, View in Reaxys; Nair, Vijay; Rajan, Roshini; Balagopal, Lakshmi; Thomas, Siji; Narasimlu; Tetrahedron Letters; vol. 43; nb. 49; (2002); p. 8971 - 8974, View in Reaxys; Ercoli, Marcella; Mina, Lorenzo; Boido, Caterina Canu; Boido, Vito; Sparatore, Fabio; Armani, Ugo; Piana, Antonietta; Farmaco; vol. 59; nb. 2; (2004); p. 101 - 109, View in Reaxys; Ferge; Maguhn; Hafner; Muehlberger; Davidovic; Warnecke; Zimmermann; Environmental Science and Technology; vol. 39; nb. 6; (2005); p. 1393 - 1402, View in Reaxys

Eisch, John J.; Gitua, John N.; European Journal of Inorganic Chemistry; nb. 12; (2002); p. 3091 - 3096, View in Reaxys; Ockey, Denise A.; Gadek, Thomas R.; Bioorganic and Medicinal Chemistry Letters; vol. 14; nb. 2; (2004); p. 389 - 391, View in Reaxys

6, R=Phenyl

Ambhaikar, Narendra B.; Herold, Marike; Liotta, Dennis C.; Heterocycles; vol. 62; (2004); p. 217 - 222, View in Reaxys

byprod. of 1a, 2a

Al-Etaibi, Alya; Abdallah, Mariam; Al-Awadi, Nouria; Ibrahim, Yehia; Hasan, Mohammad; Journal of Physical Organic Chemistry; vol. 17; nb. 1; (2004); p. 49 - 55, View in Reaxys

Tab. 3; entry 7

Paul, Himadri; Basu, Susmit; Bhaduri, Sumit; Lahiri, Goutam Kumar; Journal of Organometallic Chemistry; vol. 689; nb. 2; (2004); p. 309 - 316, View in Reaxys

tab.2, entry 4, prod.

Rieke, Reuben D.; Lee, Jun-Sik; Kye, Young-Sik; Harbison, Gerard S.; Journal of Organometallic Chemistry; vol. 689; nb. 21; (2004); p. 3421 - 3425, View in Reaxys

Figure 5

Nishiura, Katsutoshi; Urawa, Yoshio; Soda, Shigeru; Advanced Synthesis and Catalysis; vol. 346; nb. 13-15; (2004); p. 1679 - 1684, View in Reaxys

2 for 3a

Gong, Denghuang; Zhang, Ling; Yuan, Chengye; Synthetic Communications; vol. 34; nb. 18; (2004); p. 3259 - 3264, View in Reaxys

Nakao, Yoshiaki; Oda, Shinichi; Hiyama, Tamejiro; Journal of the American Chemical Society; vol. 126; nb. 43; (2004); p. 13904 - 13905, View in Reaxys

substr. Tab. 2, entry 5

Shin, Hyunik; Choi, Bo Seung; Lee, Ki Kon; Choi, Hyeong-Wook; Chang, Jay Hyok; Lee, Kyu Woong; Nam, Do Hyun; Kim, No-Soo; Synthesis; nb. 16; (2004); p. 2629 - 2632, View in Reaxys

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2018-05-24 12:11:44

Tab.2.run1

Beletskaya, Irina P.; Sigeev, Alexander S.; Peregudov, Alexander S.; Petrovskii, Pavel V.; Journal of Organometallic Chemistry; vol. 689; nb. 23; (2004); p. 3810 - 3812, View in Reaxys

Table 2. product

Schareina, Thomas; Zapf, Alexander; Beller, Matthias; Journal of Organometallic Chemistry; vol. 689; nb. 24 SPEC. ISS.; (2004); p. 4576 - 4583, View in Reaxys

Perosa, Alvise; Tundo, Pietro; Selva, Maurizio; Zinovyev, Sergei; Testa, Alberto; Organic and Biomolecular Chemistry; vol. 2; nb. 15; (2004); p. 2249 - 2252, View in Reaxys

R-CN, R=Ph

Prasad, B. A. Bhanu; Bisai, Alakesh; Singh, Vinod K.; Organic Letters; vol. 6; nb. 26; (2004); p. 4829 - 4831, View in Reaxys

PhCB

Polson, Matthew I. J.; Medlycott, Elaine A.; Hanan, Garry S.; Mikelsons, Larisa; Taylor, Nick J.; Watanabe, Masashi; Tanaka, Yasutaka; Loiseau, Frederique; Passalacqua, Rosalba; Campagna, Sebastiano; Chemistry - A European Journal; vol. 10; nb. 15; (2004); p. 3640 - 3648, View in Reaxys

starting to 1*

Budesinsky, Milos; Kulhanek, Jiri; Boehm, Stanislav; Cigler, Petr; Exner, Otto; Magnetic Resonance in Chemistry; vol. 42; nb. 10; (2004); p. 844 - 851, View in Reaxys

PhCN, entry 4,5

Hashemi, Mohammed M.; Akhbari, Maryam; Synthetic Communications; vol. 34; nb. 15; (2004); p. 2783 - 2787, View in Reaxys

RCN, R = Ph

Garcia Ruano, Jose L.; Aleman, Jose; Teresa Aranda; Angeles Fernandez-Ibaez; Mercedes Rodriguez-Fernandez; Carmen Maestro; Tetrahedron; vol. 60; nb. 44; (2004); p. 10067 - 10075, View in Reaxys

Tab. 2, entry 11

Venkat Narsaiah; Nagaiah; Advanced Synthesis and Catalysis; vol. 346; nb. 11; (2004); p. 1271 - 1274, View in Reaxys

ArCN (Tab. run 1-4)

Penney, Jonathan M.; Miller, Joseph A.; Tetrahedron Letters; vol. 45; nb. 25; (2004); p. 4989 - 4992, View in Reaxys

Tab.1. prod., entry 1

Sharghi, Hashem; Sarvari, Mona Hosseini; Synthesis; nb. 2; (2003); p. 243 - 246, View in Reaxys

5, R2 = H

Pan, Kevin; Scott, Malcolm K.; Lee, Daniel H. S.; Fitzpatrick, Louis J.; Crooke, Jeffery J.; Rivero, Ralph A.; Rosenthal, Daniel I.; Vaidya, Anil H.; Zhao, Boyu; Reitz, Allen B.; Bioorganic and Medicinal Chemistry; vol. 11; nb. 2; (2003); p. 185 - 192, View in Reaxys

9 (R1=H)

Curtis, Neil R; Diggle, Helen J; Kulagowski, Janusz J; London, Clare; Grimwood, Sarah; Hutson, Peter H; Murray, Fraser; Richards, Pawel; Macaulay, Alison; Wafford, Keith A; Bioorganic and medicinal chemistry letters; vol. 13; nb. 4; (2003); p. 693 - 696, View in Reaxys

educt to benzyl amine

Maki, Shojiro; Okawa, Makiko; Makii, Toshimichi; Hirano, Takashi; Niwa, Haruki; Tetrahedron Letters; vol. 44; nb. 18; (2003); p. 3717 - 3721, View in Reaxys

II, R7=Ph

Cywin, Charles L.; Zhao, Bao-Ping; McNeil, Daniel W.; Hrapchak, Matt; Prokopowicz III, Anthony S.; Goldberg, Daniel R.; Morwick, Tina M.; Gao, Amy; Jakes, Scott; Kashem, Mohammed; Magolda, Ronald L.; Soll, Richard M.; Player, Mark R.; Bobko, Mark A.; Rinker, James; DesJarlais, Renee L.; Winters, Michael P.; Bioorganic and Medicinal Chemistry Letters; vol. 13; nb. 8; (2003); p. 1415 - 1418, View in Reaxys

2 (Ar2=C6H5)

Xu, Xiaoliang; Zhang, Yongmin; Journal of Chemical Research, Synopses; nb. 2; (2003); p. 84 - 86, View in Reaxys

Ar1CN, Tab. 1, entry 6

Miller, Joseph A.; Dankwardt, John W.; Penney, Jonathan M.; Synthesis; nb. 11; (2003); p. 1643 - 1648, View in Reaxys

Meshram; Ganesh; Madhavi; Eshwaraiah; Yadav; Gunasekar; Synthetic Communications; vol. 33; nb. 14; (2003); p. 2497 - 2503, View in Reaxys

Tab.2.run8

Sundermeier, Mark; Mutyala, Sateesh; Zapf, Alexander; Spannenberg, Anke; Beller, Matthias; Journal of Organometallic Chemistry; vol. 684; nb. 1-2; (2003); p. 50 - 55, View in Reaxys

Table 1. product 1

Srinivas; Mahender; Das, Biswanath; Chemistry Letters; vol. 32; nb. 8; (2003); p. 738 - 739, View in Reaxys

2 (R2=H)

Cho, Won-Jea; Min, Sun Young; Le, Thanh Nguyen; Kim, Tae Sung; Bioorganic and Medicinal Chemistry Letters; vol. 13; nb. 24; (2003); p. 4451 - 4454, View in Reaxys

educt to 1a

Kaboudin, Babak; Navaee, Kian; Heterocycles; vol. 60; nb. 10; (2003); p. 2287 - 2292, View in Reaxys

arene (table 3, entry8)

Cellier, Pascal P.; Spindler, Jean-Francis; Taillefer, Marc; Cristau, Henri-Jean; Tetrahedron Letters; vol. 44; nb. 38; (2003); p. 7191 - 7195, View in Reaxys

4, R1=Ph

Zhao, Hua-Rong; Zhao, Xin-Jian; Huang, Xian; Synthetic Communications; vol. 32; nb. 21; (2002); p. 3383 - 3387, View in Reaxys; Vugts, Danielle J.; Jansen, Helen; Schmitz, Rob F.; De Kanter, Frans J. J.; Orru, Romano V. A.; Chemical Communications; nb. 20; (2003); p. 2594 - 2595, View in Reaxys

15, R4=Ph

Palacios, Francisco; Alonso, Concepcion; Pagalday, Jaione; Ochoa de Retana, Ana Maria; Rubiales, Gloria; Organic and Biomolecular Chemistry; vol. 1; nb. 7; (2003); p. 1112 - 1118, View in Reaxys

26/225

2018-05-24 12:11:44

C6H5-CN

Laskin, Alexander; Lifshitz, Assa; Journal of Physical Chemistry A; vol. 102; nb. 6; (1998); p. 928 - 946, View in Reaxys; Das, Biswanath; Madhusudhan; Venkataiah; Synlett; nb. 10; (1999); p. 1569 - 1570, View in Reaxys; Srinivas; Reddy, E. Bolla; Das, Biswanath; Synlett; nb. 4; (2002); p. 625 - 627, View in Reaxys; Sundermeier, Mark; Zapf, Alexander; Mutyala, Sateesh; Baumann, Wolfgang; Sans, Juergen; Weiss, Stefan; Beller, Matthias; Chemistry - A European Journal; vol. 9; nb. 8; (2003); p. 1828 - 1836, View in Reaxys

Tab., nitrile, entry 1 Baxendale, Ian R.; Ley, Steven V.; Sneddon, Helen F.; Synlett; nb. 5; (2002); p. 775 - 777, View in Reaxys t.2, pr., entry 3

Iranpoor; Firouzabadi; Aghapour; Synthetic Communications; vol. 32; nb. 16; (2002); p. 2535 - 2541, View in Reaxys

18d

Batsila, Christina; Kostakis, George; Hadjiarapoglou, Lazaros P; Tetrahedron Letters; vol. 43; nb. 34; (2002); p. 5997 - 6000, View in Reaxys

2, R3=C6H5

Herrera, Antonio; Martinez-Alvarez, Roberto; Chioua, Mourad; Chioua, Rachid; Sanchez, Angel; Tetrahedron; vol. 58; nb. 50; (2002); p. 10053 - 10058, View in Reaxys

Table 1, entry 1; PhCN

Saikia, Pramod; Ilias; Prajapati, Dipak; Sandhu, Jagir S.; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 41; nb. 10; (2002); p. 2109 - 2111, View in Reaxys

1k/7

Ishino, Yoshio; Mihara, Masatoshi; Kageyama, Manabu; Tetrahedron Letters; vol. 43; nb. 37; (2002); p. 6601 - 6604, View in Reaxys

Lebedeva; Mikhailovskii; V'yugin; Davydova; Russian Journal of Physical Chemistry A; vol. 76; nb. 6; (2002); p. 1028 - 1030, View in Reaxys

1b (nitrile)

De Lijser, H. J. Peter; Fardoun, Fadia H.; Sawyer, Jody R.; Quant, Michelle; Organic Letters; vol. 4; nb. 14; (2002); p. 2325 - 2328, View in Reaxys

Chen, Jinglong; Song, Qiuling; Wang, Congyang; Xi, Zhenfeng; Journal of the American Chemical Society; vol. 124; nb. 22; (2002); p. 6238 - 6239, View in Reaxys

nitril, amidoxime 1

Poulain, Rebecca F.; Tartar, Andre L.; Deprez, Benot P.; Tetrahedron Letters; vol. 42; nb. 8; (2001); p. 1495 - 1498, View in Reaxys

2, Tab.1., run 1.

Patrick, Timothy B.; Juehne, Thomas; Reeb, Elmer; Hennessy, Daniel; Tetrahedron Letters; vol. 42; nb. 21; (2001); p. 3553 - 3554, View in Reaxys

RCN to 3a, k-q

Gangloff, Anthony R.; Litvak, Joane; Shelton, Emma J.; Sperandio, David; Wang, Vivian R.; Rice, Kenneth D.; Tetrahedron Letters; vol. 42; nb. 8; (2001); p. 1441 - 1443, View in Reaxys

2, R2: Ph

Su; Li; Zhang; Journal of Chemical Research - Part S; nb. 1; (2001); p. 32 - 33, View in Reaxys

1, R=Ph

Kaminski; Glass; Skowronska; Synthesis; nb. 9; (2001); p. 1308 - 1310, View in Reaxys

XIIIa

Tselinskii; Mel'nikova; Romanova; Russian Journal of Organic Chemistry; vol. 37; nb. 3; (2001); p. 430 - 436, View in Reaxys

ArCN, Ar=Ph

Gao, Yang; Wang, Hui; Xu, Minghua; Lian, Hongzhen; Pan, Yi; Shi, Yaozeng; Organic Preparations and Procedures International; vol. 33; nb. 4; (2001); p. 351 - 356, View in Reaxys

Sub., Table, run 6

Takamizawa; Wakasa; Fuchikami; Synlett; nb. 10; (2001); p. 1623 - 1625, View in Reaxys

Prodt.,Tab.1,run 1,R=CN

Lipshutz, Bruce H.; Tomioka, Takashi; Pfeiffer, Steven S.; Tetrahedron Letters; vol. 42; nb. 44; (2001); p. 7737 7740, View in Reaxys

entry 5, table 2

Sundermeier, Mark; Zapf, Alexander; Beller, Matthias; Sans, Juergen; Tetrahedron Letters; vol. 42; nb. 38; (2001); p. 6707 - 6710, View in Reaxys

Ar%1&CN T. 1, e. 7

Miller, Joseph A.; Tetrahedron Letters; vol. 42; nb. 40; (2001); p. 6991 - 6993, View in Reaxys

2d; PhCN

Ausheva; Glushkov; Shurov; Shklyaev; Russian Chemical Bulletin; vol. 50; nb. 9; (2001); p. 1648 - 1656, View in Reaxys

nitrile for 12

Welniak; Polish Journal of Chemistry; vol. 75; nb. 1; (2001); p. 55 - 62, View in Reaxys

2 R=C6H5

Zhong; Zhang; Chen; Journal of the Indian Chemical Society; vol. 78; nb. 6; (2001); p. 316 - 318, View in Reaxys

Table 1, entry 1

Yang, Soon Ha; Chang, Sukbok; Organic Letters; vol. 3; nb. 26; (2001); p. 4209 - 4211, View in Reaxys

Chatani; Tatamidani; Ie; Kakiuchi; Murai; Journal of the American Chemical Society; vol. 123; nb. 20; (2001); p. 4849 - 4850, View in Reaxys

Tab.4, prod., entry 1

Ley, Steven V.; Leach, Andrew G.; Storer, R.Ian; Journal of the Chemical Society. Perkin Transactions 1; nb. 4; (2001); p. 358 - 361, View in Reaxys

T. 1-1

Pawlas; Vedso; Jakobsen; Huusfeldt; Begtrup; Journal of Organic Chemistry; vol. 66; nb. 12; (2001); p. 4214 - 4219, View in Reaxys

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2018-05-24 12:11:44

2, R2=Ph

Zhou, Longhu; Zhang, Yongmin; Shi, Daqing; Synthesis; nb. 1; (2000); p. 91 - 98, View in Reaxys; Ducept, Pascal C.; Marsden, Stephen P.; Synlett; nb. 5; (2000); p. 692 - 294, View in Reaxys

2(entry 1)

Ali, Sayyed Iliyas; Nikalje, Milind D.; Dewkar, Gajanan K.; Paraskar, Abhimanyu S.; Jagtap; Sudalai; Journal of Chemical Research - Part S; nb. 1; (2000); p. 30 - 31, View in Reaxys

Tab1, prod, run1, methA

Kashiwagi, Yoshitomo; Kurashima, Futoshi; Kikuchi, Chikara; Anzai, Jun-Ichi; Tetsuo, Osa; Heterocycles; vol. 53; nb. 7; (2000); p. 1583 - 1587, View in Reaxys

Table 1, RCN, rows Merchant, Kevin J.; Tetrahedron Letters; vol. 41; nb. 19; (2000); p. 3747 - 3749, View in Reaxys 1-4 2, Ar'=Ph

Quadrelli; Campari; Mella; Caramella; Tetrahedron Letters; vol. 41; nb. 12; (2000); p. 2019 - 2022, View in Reaxys

2, R = Ph

Zhou, Longhu; Zhang, Yongmin; Tetrahedron; vol. 56; nb. 19; (2000); p. 2953 - 2960, View in Reaxys

Bel'skii; Russian Chemical Bulletin; vol. 49; nb. 2; (2000); p. 251 - 255, View in Reaxys

educt to 7b

Robin, Sylvie; Rousseau, Gerard; European Journal of Organic Chemistry; nb. 17; (2000); p. 3007 - 3011, View in Reaxys

Table 8, No. 7

Le Questel, Jean-Yves; Berthelot, Michel; Laurence, Christian; Journal of Physical Organic Chemistry; vol. 13; nb. 6; (2000); p. 347 - 358, View in Reaxys

Subst.,Tab.1/2, run 7/5

Lee; Lin; Tetrahedron Letters; vol. 41; nb. 45; (2000); p. 8803 - 8806, View in Reaxys

educt to 2, 3

Maeda, Yutaka; Sato, Ryu; Wakahara, Takatsugu; Okamura, Mutsuo; Akasaka, Takeshi; Fujitsuka, Mamoru; Ito, Osamu; Kobayashi, Kaoru; Nagase, Shigeru; Kako, Masahiro; Nakadaira, Yasuhiro; Horn, Ernst; Journal of Organometallic Chemistry; vol. 611; nb. 1-2; (2000); p. 414 - 419, View in Reaxys

2 (R = Ph)

Barman, Dhiren C.; Thakur, Ashim J.; Prajapati, Dipak; Sandhu, Jagir S.; Chemistry Letters; nb. 10; (2000); p. 1196 - 1197, View in Reaxys

ArCN, Ar=C6H5

McCarroll, Andrew J.; Walton, John C.; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2000); p. 1868 - 1875, View in Reaxys

1, X=CN

Smith, Keith; Gibbins, Tracy; Millar, Ross W.; Claridge, Robert P.; Journal of the Chemical Society, Perkin Transactions 1; nb. 16; (2000); p. 2753 - 2758, View in Reaxys

sch.1,interm.

Alterman; Hallberg; Journal of Organic Chemistry; vol. 65; nb. 23; (2000); p. 7984 - 7989, View in Reaxys

1, R1=H

Tan, Cheng-Quan; Zheng, Xianmou; Ma, Zhaolan; Gu, Yijian; Synthetic Communications; vol. 29; nb. 1; (1999); p. 123 - 127, View in Reaxys

educt to 54

Raap, Jan; Nieuwenhuis, Saskia; Creemers, Alain; Hexspoor, Sander; Kragl, Udo; Lugtenburg, Johan; European Journal of Organic Chemistry; nb. 10; (1999); p. 2609 - 2621, View in Reaxys

entry 1

Iranpoor; Zeynizadeh; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2747 - 2752, View in Reaxys

Table 2, col 2, entry Maligres, Peter E.; Waters, Marjorie S.; Fleitz, Fred; Askin, David; Tetrahedron Letters; vol. 40; nb. 47; (1999); p. 2 8193 - 8195, View in Reaxys substrate (entry 1)

Mansour Lakouraj; Bahrami; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 38; nb. 8; (1999); p. 974 - 975, View in Reaxys

Vleggaar, Robert; Zeevaart, Jacob G.; Tetrahedron Letters; vol. 40; nb. 52; (1999); p. 9301 - 9303, View in Reaxys

elimin. fragment, 1

Al-Awadi, Nouria A.; Elnagdi, Mohamed H.; Kaul, Kamini; Ilingovan, Swaminathan; El-Dusouqui, Osman M. E.; Journal of Physical Organic Chemistry; vol. 12; nb. 8; (1999); p. 654 - 658, View in Reaxys

12a

Leite, Lucia Fernanda C.C.; Ramos, Mozart N.; Da Silva, Joao Bosco P.; Miranda, Ana L.P.; Fraga, Carlos A.M.; Barreiro, Eliezer J.; Farmaco; vol. 54; nb. 11-12; (1999); p. 747 - 757, View in Reaxys

subs., Tab. 1, entry 11

Varma, Rajender S.; Naicker, Kannan P.; Organic Letters; vol. 1; nb. 2; (1999); p. 189 - 191, View in Reaxys

RCN (run 1, 13)

Luo, Fen-Tair; Jeevanandam, Arumugasamy; Tetrahedron Letters; vol. 39; nb. 51; (1998); p. 9455 - 9456, View in Reaxys

RCN R=C6H5

Ishihara, Hideharu; Yosimura, Katsuhiro; Kouketsu, Mamoru; Chemistry Letters; nb. 12; (1998); p. 1287 - 1288, View in Reaxys

11 (R2=H)

Cho, Won-Jea; Kim, Eui-Ki; Park, Myun-Ji; Choi, Sang-Un; Lee, Chong-Ock; Cheon, Seung Hoon; Choi, BoGil; Chung, Byung-Ho; Bioorganic and Medicinal Chemistry; vol. 6; nb. 12; (1998); p. 2449 - 2458, View in Reaxys

4, Table 2, Entry 9

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Patent-Specific Data (61) Prophetic ComLocation in Patent pound

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Druglikeness (1) 1 of 1

LogP

1.745

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

23.79

Lipinski Number

Veber Number

Derivative (65) Comment (Derivative)

References

Komplex mit CyRossarie et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 63,71, View in Reaxys clohexanol in CCl4: ΔH,ΔG,ΔS Komplex mit Phenol: Dipolmoment

Gramstad; Tjessem; Journal of Molecular Structure; vol. 41; (1977); p. 231,233, 235, 236, View in Reaxys

Komplex mit SO2: Bodrikov et al.; Doklady Chemistry; vol. 227; (1976); p. 253; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 227; (1976); p. Komplexbildung863, View in Reaxys skonst.; ΔH; ΔS; IR Donor-AkzeptorKomplex m. AsBr3 (1:1): K in Cyclohexan (aus 1HNMR)

Vakhrin; Grechishkin; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 187; ; p. 314, View in Reaxys

L*Cl2 35Cl-,14NNQR

Dresvyankin et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 114; ; p. 2584, View in Reaxys

L*CHCl3 35Cl-,14N-NQR

Dresvyankin et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 144; ; p. 2584, View in Reaxys

L*2CHCl3 35Cl-,14N-NQR

Dresvyankin et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 144; ; p. 2584, View in Reaxys

2L*Cl2 α/α 35Cl-,14N-NQR

Dresvyankin et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 114; ; p. 2584, View in Reaxys

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Komplex mit 1 oder Dresvyankin; Journal of Structural Chemistry; vol. 16; (1975); p. 444; ; p. 478, View in Reaxys 1/2 Cl2: 14N-NMR, 35Cl-NMR Komplex mit H2As3(CO)10: gelb, 1H NMR, IR (Tab.1)

Deeming; Hasso; Journal of Organometallic Chemistry; vol. 88; (1975); p. C21, View in Reaxys

Additionsverb. mit Co2+-, Ni2+-, Cu2+Montmorillonit (IR)

de la Calle et al.; Anales de Quimica (1968-1979); vol. 71; (1975); p. 243, View in Reaxys

H-Brueckenkomplex m. Phenol: K (in CCl4, 25, 55grad); ΔH (aus IR-α(OH))

Lutskii et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 812; ; p. 1374, View in Reaxys

(C7H5N)*(CH4O): Bildungskonst. (Tab.2)

Kupletskaya et al.; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 2594,2610, View in Reaxys

(C7H5N)*(C6H6O) Kupletskaya et al.; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 2594,2610, View in Reaxys : Bildungskonst. (Tab.2) Komplex mit CHCl3 (1:1, 1:2) 14N-NQR, 35ClNQR (77 K) -> Evidenz fuer ClTeilnahme

Grechishkin et al.; Russian Journal of Physical Chemistry; vol. 48; (1974); p. 931; ; p. 1580, View in Reaxys

Addukt mit Thionylchlorid: F: -72grad

Tolopko et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 39; nb. 4; (1973); p. 395,94, View in Reaxys

Komplex mit Burnett et al.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. TBMN: Gleich69; (1973); p. 864, View in Reaxys gew.-konst. (Tab. 2) Cs-Salz: Photoemission

Kawamura; Inokuchi; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 710,712, View in Reaxys

Na-Salz: Photoemission

Kawamura; Inokuchi; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 710,712, View in Reaxys

Rb-Salz: Photoemission

Kawamura; Inokuchi; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 710,712, View in Reaxys

BF3-Addukt: 11B-, 19F-NMR

Fluck; Steck; Phosphorus and Sulfur and the Related Elements; vol. 1; (1972); p. 283, View in Reaxys

Komplex-B. mit 5Fluorindol: K(f)

Mitsky et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 3442,3443, View in Reaxys

Anion-Radikal<K>+: IR, CNBande

Juchnovski; Binev; Journal of Molecular Structure; vol. 7; (1971); p. 490,491,493, View in Reaxys

Addukt NbCl5*C7H5N: Rel.Stab.-konst.

Merbach; Baenzli; Chimia; vol. 25; (1971); p. 222, View in Reaxys

Komplex mit DTBNO, ESR, Komplexbildungskonstante

Murata; Mataga; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 354,355-360, View in Reaxys

PhCN- Li+: K(Deuteriumaustausch); Aktivierungsenergie (in THF)

Ichikawa; Tamaru; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1451, View in Reaxys

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2018-05-24 12:11:44

PhCN- Na+: K(Deuteriumaustausch); Aktivierungsenergie (in THF)

Ichikawa; Tamaru; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1451, View in Reaxys

PhCN- Rb+: K(Deuteriumaustausch); Aktivierungsenergie (in THF)

Ichikawa; Tamaru; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1451, View in Reaxys

PhCN- K+: K(Deu- Ichikawa; Tamaru; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1451, View in Reaxys teriumaustausch); Aktivierungsenergie (jeweils in THF, Monoethylenglykol, Diethylenglykoldimethylether, PhCN) K-Komplex: Anionenradikal: rot; UV

Panayotov; Tsvetanov; Monatshefte fuer Chemie; vol. 101; (1970); p. 1672,1676, 1679, View in Reaxys

Rb-salt: photoelectric response <quantum yield>

Kawamura et al.; Chemical Physics Letters; vol. 5; (1970); p. 80, View in Reaxys

Komplex mit Phenol: Kass, ΔGgrad, ΔHgrad, ΔSgrad

Martin et al.; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 797,799, View in Reaxys

Hetero-Excimere m. Aminen: Fluoreszenz-Sp., Bindungszustand

Rehm; Weller; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 69; (1970); p. 183,193,196, View in Reaxys

Hetero-Excimere m. aromat. KW: Fluoreszenz-Sp., Bindungszustand

Rehm; Weller; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 69; (1970); p. 183,193,196, View in Reaxys

EDA-Komplex mit Diethylanilin: Emissionsdaten; μ

Beens; Weller; Acta Physica Polonica; vol. 34; (1968); p. 593,595, 596, View in Reaxys

Clathrat: C7H5N * Diamin ( C18H20O2) : Dielektrizitaetskonst. bei 1.) -185grad / 8.56 Hz und bei 2.) + 20grad / 160 KHz u. 8.56 Hz; dielektrischer Verlust bei -185grad u. +20grad / 8.56 Hz

Davies; Williams; Transactions of the Faraday Society; vol. 64; (1968); p. 529,543, View in Reaxys

Komplex m. ICl: Raman; IR

Klaboe et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 3667,3670, 3674, View in Reaxys

Komplex m. Jod: Raman; IR

Klaboe et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 3667,3670, 3674, View in Reaxys

Komplex m. Brom: Raman; IR

Klaboe et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 3667,3670, 3674, View in Reaxys

Na-Komplex, Rk. Ichikawa et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 1015, View in Reaxys m. D2, 80grad (Aktivierungsenergie) Vb. mit Pyrrol: Dipolmoment in Cyclohexan: 4.05 D,

Bertin; Lumbroso; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 263; (1966); p. 181, View in Reaxys

33/225

2018-05-24 12:11:44

bezogen auf Konz. 0: 4.61 D Dimethyl-diethylphosphoniumiodidKomplex

Issleib; Bleck; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 336; (1965); p. 234,242, View in Reaxys

Verb. mit Iod: IRAbsorption in Cyclohexan

Lorenzelli; Gazzetta Chimica Italiana; vol. 95; (1965); p. 218,220, View in Reaxys

<C14H28P>I*<C6 H5CN>2 mit Dimethyl-dicyclohexylphosphoniumiodid

Issleib; Bleck; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 336; (1965); p. 234,242, View in Reaxys

Additionsverb. m. 2 Janz; Ahmad; Venkatasetty; Journal of Physical Chemistry; vol. 68; (1964); p. 889,891, View in Reaxys Mol HCl C7H5N*2HCl: unbestaendig Elektronen-Donator-Acceptor-Komplex mit Tetracyanoaethylen: Charge-transferSp.; Charge-transfer-Energie

Voigt; Reid; Journal of the American Chemical Society; vol. 86; (1964); p. 3930,3932, View in Reaxys

Forts.: wss. Schwe- Caronna; Marino; Gazzetta Chimica Italiana; vol. 94; (1964); p. 31,33, 34, View in Reaxys felsaeure (0grad) mit dem NatriumSalz der Stickstoffwasserstoffsaeure (zuletzt 1/2h Raumtemp.) erhalten; F: 237grad (Bzl.) Additionsverb. m. HCl C7H5N*HCl, F: 62-65grad (nach Sintern bei 57grad; geschl. Kapillare), in Me. u. Acn. l; in Bzl., CCl4 u. Ae. unloesl., IR-Abs.

Janz; Ahmad; Venkatasetty; Journal of Physical Chemistry; vol. 68; (1964); p. 889,891, View in Reaxys

Verb. C28H21NO3: Caronna; Marino; Gazzetta Chimica Italiana; vol. 94; (1964); p. 31,33, 34, View in Reaxys Die von Japp, Tressider , B. 16 <1883> 2652; Japp, Klingemann, Soc.57 <1890> 708, (aus Benzonitril, Benzil in konz. H2SO4) erhaltene Verb. wurde neben Benzoesaeure u. N'Phenyl-N-benzoylharnstoff auch aus Benzil in konz. Na-Verb.: ESR

Greber; Egle; Makromolekulare Chemie; vol. 59; (1963); p. 174,176, View in Reaxys

Komplexbildung m. Augdahl; Klaboe; Spectrochimica Acta; vol. 19; (1963); p. 1665,1669, View in Reaxys ICl System Benzonitril- Amaya; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 1067, View in Reaxys Cyclohexan: Ber. des elektrostatischen Teils der van Laar'schen Gleichung, Vergleich

34/225

2018-05-24 12:11:44

mit experimentellen Werten Komplex mit Br2, Klaboe; Journal of the American Chemical Society; vol. 84; (1962); p. 3458, View in Reaxys B. u. absorptionsspektroskop. Nachweis des DonatorAcceptor-Komplexes in CCl4-Lsg.: KomplexbildungsKonst. K(c): 0.2 Mol-1 Komplex mit ICl, B. u. absorptionsspektroskop. Nachweis des 1:1 Donator-Acceptor-Komplexes in CCl4Lsg.: Komplexbildungs-Konst. K(c): 8.1 Mol-1

Klaboe; Journal of the American Chemical Society; vol. 84; (1962); p. 3458, View in Reaxys

Komplex mit IBr, B. u. absorptionsspektroskop. Nachweis des 1:1 Donator-Acceptor-Komplexes in CCl4Lsg.: Komplexbildungs-Konst. K(c): 2.05 Mol-1

Klaboe; Journal of the American Chemical Society; vol. 84; (1962); p. 3458, View in Reaxys

Komplex mit I2, B. Klaboe; Journal of the American Chemical Society; vol. 84; (1962); p. 3458, View in Reaxys u. absorptionsspektroskop. Nachweis des Donator-Acceptor-Komplexes in CCl4-Lsg.: KomplexbildungsKonst. K(c)20grad: 0.8 Mol-1 System mit Bernsteinsaeuredinitril: Thermische Analyse

Naveau,J.; Bulletin des Societes Chimiques Belges; vol. 70; (1961); p. 662 - 689, View in Reaxys

AssoziationskonInami et al.; Journal of the American Chemical Society; vol. 83; (1961); p. 4745,4748, View in Reaxys stante u. Grenzwert fuer die Aequivalentleitfaehigkeit v. geloestem Tetra-butyl-ammonium-perchlorat, Vgl. mit anderen Lsgm. AssoziationskonInami et al.; Journal of the American Chemical Society; vol. 83; (1961); p. 4745,4748, View in Reaxys stante u. Grenzwert fuer die Aequivalentleitfaehigkeit v. geloestem Tetra-butyl-ammonium-pikrat, Vergleich m. anderen Lsgm. compound with Meerwein et al.; Archiv der Pharmazie (Weinheim, Germany); vol. 291; (1958); p. 541,553, View in Reaxys copper (I)-tetrafluoroborate (mp: 70 degree ); Further Data see Handbook (Preparation)

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<hexakis-benzoni- Hieber; Wiesboeck; Chemische Berichte; vol. 91; (1958); p. 1156,1160, View in Reaxys; Vohler; Chemische Berichte; trile cobalt (II)>vol. 91; (1958); p. 1161,1164, View in Reaxys bis-<tetracarbonylcobaltate >; Further Data see Handbook (Preparation, IR Bands, Electrical data) compound with sil- Meerwein et al.; Archiv der Pharmazie (Weinheim, Germany); vol. 291; (1958); p. 541,553, View in Reaxys ver-tetrafluoroborate (mp: 99-101 degree , hygroscopic); Further Data see Handbook

N-phenyl-N'-benzyl-thiourea (mp: 147 degree )

Cutter; Taras; Industrial and Engineering Chemistry, Analytical Edition; vol. 13; (1941); p. 830, View in Reaxys

benzimidoylmerCondo et al.; Journal of the American Chemical Society; vol. 59; (1937); p. 231, View in Reaxys capto-acetic acidhydrochloride (decomp. by/at 125 degree )

cis-dichloro-bisJensen; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 231; (1937); p. 365,368, View in Reaxys benzonitrile platinum (mp: 219 degree ); Further Data see Handbook (Dipole moment) Purification (1) References Markgraf et al.; Journal of Organic Chemistry; vol. 29; (1964); p. 2629, View in Reaxys Melting Point (9) 1 of 9

Melting Point [°C]

188 - 191

Kokare, Nagnnath D.; Shinde, Devanand B.; Monatshefte fur Chemie; vol. 140; nb. 2; (2009); p. 185 - 188, View in Reaxys 2 of 9

Melting Point [°C]

-12.82

Lebedev, B. V.; Bykova, T. A.; Kiparisova, E. G.; Pankratov, V. A.; Mitina, L. M.; Korshak, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 6; (1984); p. 1352 - 1358,1209 - 1214, View in Reaxys 3 of 9

Comment (Melting Point)

Schmelzpunkt bei 1 at (-13.8grad) bis 5030 at (+80grad).

Timmermans; Kasanin; Bulletin des Societes Chimiques Belges; vol. 68; (1959); p. 527,537, View in Reaxys 4 of 9

Melting Point [°C]

-12.75

Witschonke; Analytical Chemistry; vol. 26; (1954); p. 562, View in Reaxys 5 of 9

Melting Point [°C]

-13.8

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys 6 of 9

Melting Point [°C]

-12.1

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys 7 of 9

Melting Point [°C]

-13.2

Menschutkin; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 44; (1912); p. 1940; Chem. Zentralbl.; vol. 84; nb. I; (1913); p. 805, View in Reaxys 8 of 9

Melting Point [°C]

-13.1

Timmermans; Chem. Zentralbl.; vol. 82; nb. II; (1911); p. 1015, View in Reaxys 9 of 9

Melting Point [°C]

-12.9

v. Schneider; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 19; (1896); p. 157; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 22; (1897); p. 232, View in Reaxys

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Boiling Point (165) Boiling Point [°C] Pressure (Boiling Point) [Torr]

Comment (Boiling Point)

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100

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78 - 79

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0.05

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81 - 83

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62.5

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100

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85 - 86

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760

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77.85 - 78.85

48 - 49

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72 - 73

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760

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15 - 16

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72 - 75

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3.5

Olah, George A.; Narang, Subhash C.; Fung, Alexander P.; Gupta, B.G.Balaram; Synthesis; nb. 8; (1980); p. 657 - 658, View in Reaxys

72 - 75

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69 - 70

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70 - 71

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40 - 41

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760

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760

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96 - 98

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185 - 195 35 - 38

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190.7

68 - 70

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189 - 190 188 - 191

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73 - 75

Krause; Shaikh; Synthesis; (1975); p. 502, View in Reaxys

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68 - 70

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104 - 106

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80 - 82

Ege,G.; Beisiegel,E.; Synthesis; (1974); p. 22 - 23, View in Reaxys

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190.5 126 - 128

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189 - 191

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85 - 87

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81 - 83

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75 - 76

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66.5 - 67

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70 - 73

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87 - 88

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70 - 72

Appel et al.; Chemische Berichte; vol. 104; (1971); p. 1030,1031 - 1033, View in Reaxys

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192 - 193

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0.2

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

0.2

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

0.3

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

38 - 40

0.2

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

40 - 42

0.2

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

105

115

Kanaoka et al.; Chemical and Pharmaceutical Bulletin; vol. 18; (1970); p. 397,398, View in Reaxys

59 - 63

Dennis; Journal of Organic Chemistry; vol. 35; (1970); p. 3253, View in Reaxys

191.5 - 198

690

Chekmareva et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 6; (1970); p. 735; Khimiya Geterotsiklicheskikh Soedinenii; vol. 6; (1970); p. 794, View in Reaxys

65 - 70

Yamato; Sugasawa; Tetrahedron Letters; (1970); p. 4383, View in Reaxys

40 - 55

0.2

Grigg; Jackson; Journal of the Chemical Society [Section] C: Organic; (1970); p. 552,555, View in Reaxys

180.7

Suzuki et al.; Kogyo Kagaku Zasshi; vol. 72; (1969); p. 720; Chem.Abstr.; vol. 72; nb. 33224; (1970), View in Reaxys

66 - 67

Smirnow et al.; Zhurnal Organicheskoi Khimii; vol. 5; (1969); p. 1392,1359, View in Reaxys

66 - 66.5

Smirnow et al.; Zhurnal Organicheskoi Khimii; vol. 5; (1969); p. 1355,1324, View in Reaxys

72 - 73

Troszkiewicz et al.; Roczniki Chemii; vol. 43; (1969); p. 1151,1153, View in Reaxys

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75 - 76

Troszkiewicz et al.; Roczniki Chemii; vol. 43; (1969); p. 1151,1153, View in Reaxys

Streeter; Bartulin; Revista de la Real Academia de Ciencias Exactas, Fisicas y Naturales de Madrid; vol. 62; (1968); p. 2-497,498-507; Chem.Abstr.; vol. 70; nb. 11312z; (1969), View in Reaxys

46 - 46.5

Yamakawa et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 1046,1047,1050, View in Reaxys

161

Becker et al.; Tetrahedron; vol. 24; (1968); p. 1031, View in Reaxys

Gutmann; Scherhaufer; Monatshefte fuer Chemie; vol. 99; (1968); p. 335, View in Reaxys

Balachandran et al.; Journal of Organic Chemistry; vol. 33; nb. 10; (1968); p. 3891, View in Reaxys

75 - 77

Kresze; Wucherpfennig; Chemische Berichte; vol. 101; (1968); p. 365, View in Reaxys

92 - 94

Kanaoka et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 280,283,284, View in Reaxys

78 - 79

Misono et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 2875,2884, View in Reaxys

68 - 70

Kaiser et al.; Journal of Organic Chemistry; vol. 32; (1967); p. 3640,3643, View in Reaxys

186

Koehler et al.; Chemische Berichte; vol. 100; nb. 4; (1967); p. 1073, View in Reaxys

87 - 89

Sonobe; Kogyo Kagaku Zasshi; vol. 70; (1967); p. 2305,2307, View in Reaxys

85.8

24.5

Ogata; Sakanishi; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 2294,2296,2297, View in Reaxys

Misono et al.; Bulletin of the Chemical Society of Japan; vol. 39; (1966); p. 854, View in Reaxys

77 - 81

Smith et al.; Journal of Organic Chemistry; vol. 31; (1966); p. 4100, View in Reaxys

0.2

George,T.A. et al.; Journal of the Chemical Society; (1965); p. 2157 - 2165, View in Reaxys

188 - 192

Svetkin,Yu.V.; Minlibaeva,A.N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 35; (1965); p. 836 - 838,840 - 841, View in Reaxys

190 - 193

Martin,D.; Chemische Berichte; vol. 98; (1965); p. 3286 - 3296, View in Reaxys

93 - 94

Gruenanger; Langella; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. 36; nb. 3; (1964); p. 387,388-390; Chem.Abstr.; vol. 62; nb. 3973g; (1965), View in Reaxys

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186 - 188

76 - 76.3

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1.5

Overberger; Sarlo; Journal of the American Chemical Society; vol. 85; (1963); p. 2446, View in Reaxys

189 - 191

754

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2018-05-24 12:11:44

185 - 188

Trippett; Walker; Journal of the Chemical Society; (1960); p. 2976, View in Reaxys; Patent; Shell Intrenationale Research Maatschappij N.V.; NL105424; (1959); Chem.Abstr.; vol. 60; nb. 5403h; (1964), View in Reaxys; Patent; Shell; GB920987; (1963); Chem.Abstr.; vol. 61; nb. 620; (1964), View in Reaxys

55.3

Prokof'ewa et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 1318,1294, View in Reaxys

123

Engelsma; Kooyman; Recueil des Travaux Chimiques des Pays-Bas; vol. 80; (1961); p. 537,544, View in Reaxys

Mukaiyama,T. et al.; Journal of Organic Chemistry; vol. 26; (1961); p. 2202 - 2206, View in Reaxys

Vekemans-Segers,J.; Normant,H.; Bulletin de la Societe Chimique de France; (1961); p. 2355 - 2360, View in Reaxys

190.9

760

Wright; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 454, View in Reaxys; Wright; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 784,786, View in Reaxys

95 - 96

Mukaiyama,T. et al.; Journal of Organic Chemistry; vol. 26; (1961); p. 2202 - 2206, View in Reaxys

53 - 54

Payne,G.B. et al.; Journal of Organic Chemistry; vol. 26; (1961); p. 659 663, View in Reaxys

191

766

Cumper; Vogel; Journal of the Chemical Society; (1960); p. 4723,4725, View in Reaxys

Ferris,A.F.; Journal of Organic Chemistry; vol. 25; (1960); p. 12 - 18, View in Reaxys

188

735

Larson; Iwamoto; Journal of the American Chemical Society; vol. 82; (1960); p. 3239, View in Reaxys

81.5 - 82.5

Ferris et al.; Journal of Organic Chemistry; vol. 25; (1960); p. 1813, View in Reaxys

63 - 65

Trippett; Walker; Journal of the Chemical Society; (1960); p. 2976, View in Reaxys

174 - 190

Akanuma et al.; Nippon Kagaku Zasshi; vol. 81; (1960); p. 333; Chem.Abstr.; vol. 56; nb. 406; (1962), View in Reaxys

Patent; CIBA; DE1009619; (1955), View in Reaxys

Brown; Johannesen; Journal of the American Chemical Society; vol. 72; (1950); p. 2934,2936, View in Reaxys

189

758

Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys

94 - 95

Swain; Journal of the American Chemical Society; vol. 69; (1947); p. 2306,2307, View in Reaxys

191.1

760

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

Houben; Fischer; Chemische Berichte; vol. 66; (1933); p. 339,344, View in Reaxys

Naumann; Chemische Berichte; vol. 47; (1914); p. 1369, View in Reaxys

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 575, View in Reaxys

191.3

760

Timmermans; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 442, View in Reaxys

190.6

760

Wuyts; Bulletin de la Societe Chimique de France; vol. <4> 5; (1909); p. 409, View in Reaxys; Kahlbaum; v. Wirkner; Chemische Berichte; vol. 27; (1894); p. 1897; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys

43/225

2018-05-24 12:11:44

187.6

721

Guye; Mallet; Chem. Zentralbl.; vol. 73; nb. I; (1902); p. 1315, View in Reaxys

190.7

760

Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1249, View in Reaxys

189.7 - 190.2

747.6

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

69.1

Kahlbaum; v. Wirkner; Chemische Berichte; vol. 27; (1894); p. 1897; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys

103.9

Kahlbaum; v. Wirkner; Chemische Berichte; vol. 27; (1894); p. 1897; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys

121.3

100

Kahlbaum; v. Wirkner; Chemische Berichte; vol. 27; (1894); p. 1897; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys

174.4

500

Kahlbaum; v. Wirkner; Chemische Berichte; vol. 27; (1894); p. 1897; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys

38.4

Fluessigkeit.

Refractive Index (83) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

Kahlbaum; v. Wirkner; Chemische Berichte; vol. 27; (1894); p. 1897; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys References

1.5191 - 1.5246

632.8

21.462 - 32.755

Wang, Nong; Mao, Chunfeng; Peng, Xuhong; An, Xueqin; Shen, Weiguo; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 732 738, View in Reaxys

1.5252

589

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys

1.529

589

Prokof'ewa et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 1318,1294, View in Reaxys; Viswanathan; Anand Rao; Prasad; Venkateshwara Rao; Journal of Chemical and Engineering Data; vol. 41; nb. 2; (1996); p. 173 - 174, View in Reaxys

1.5272

589

Belen'kii, L. I.; Poddubnyi, I. S.; Krayushkin, M. M.; Russian Chemical Bulletin; vol. 42; nb. 11; (1993); p. 1844 - 1848; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 11; (1993); p. 1928 - 1931, View in Reaxys

1.5289

589

Sheludyakov,V.D. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 2259 - 2266,2061 - 2067, View in Reaxys; Smirnow et al.; Zhurnal Organicheskoi Khimii; vol. 5; (1969); p. 1355,1324, View in Reaxys; Sohar, P.; Koevesdi, I.; Szabo, J.; Katocs, A; Fodor, L.; et al.; Magnetic Resonance in Chemistry; vol. 27; nb. 8; (1989); p. 760 - 766, View in Reaxys

1.527

589

Badr, M.Z.A.; Aly, M.M.; Mahgoub, S.A.; Fahmy, A.M.; Atallah, A.A.; Bulletin of the Chemical Society of Japan; vol. 61; (1988); p. 1779 - 1784, View in Reaxys

1.5279

589

Sakakibara, Yasumasa; Okuda, Fumio; Shimobayashi, Akira; Kirini, Kunihiko; Sakai, Mutsuji; et al.; Bulletin of the Chemical Society of Japan; vol. 61; (1988); p. 1985 - 1990, View in Reaxys

1.5305

589

Mitrasov, Yu. N.; Mikhailova, O. N.; Yal'tseva, N. S.; Nikiforov, N. G.; Kormachev, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 6; (1987); p. 1417 - 1418,1268, View in Reaxys

1.5284

589

Grandberg et al.; Doklady Chemistry; vol. 149; (1963); p. 278; Doklady Akademii Nauk SSSR; vol. 149; (1963); p. 838, View in Reaxys; Schroth, W.; Kluge, H.; Frach, R.; Hodek, W.; Schaedler, H. D.; Journal fuer Praktische Chemie (Leipzig); vol. 325; nb. 5; (1983); p. 787 - 802, View in Reaxys

44/225

2018-05-24 12:11:44

1.5285

589

Chawla, B.; Mehta, S. K.; Jasra, R. V.; Suri, S. K.; Canadian Journal of Chemistry; vol. 61; (1983); p. 2147 - 2150, View in Reaxys

1.5288

589

Sheludyakov,V.D. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 42; nb. 8; (1972); p. 1870 - 1871,1859 - 1860, View in Reaxys; Feldhues, U.; Schaefer, H. J.; Synthesis; nb. 2; (1982); p. 145 - 146, View in Reaxys

1.5275

589

Sosnovsky et al.; Synthesis; (1979); p. 722, View in Reaxys

1.528

589

Exner; Bocek; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 50,53, View in Reaxys; Patent; Syrow et al.; SU679576; (1979); Ref. Zh., Khim.; vol. 9; nb. N74P; (1980), View in Reaxys Cumper; Vogel; Journal of the Chemical Society; (1960); p. 4723,4725, View in Reaxys; Sosnovsky; Krogh; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 34; (1979); p. 511,512, View in Reaxys

1.5276

589

Sosnovsky; Krogh; Synthesis; (1978); p. 703, View in Reaxys

1.5278

589

Mauret et al.; Bulletin de la Societe Chimique de France; (1976); p. 429, View in Reaxys

1.5282

589

Semenii,V.Ya. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; nb. 6; (1974); p. 1251 - 1255,1229 - 1232, View in Reaxys; Engelsma; Kooyman; Recueil des Travaux Chimiques des Pays-Bas; vol. 80; (1961); p. 537,544, View in Reaxys

1.5277

589

Vowinkel,E.; Bartel,J.; Chemische Berichte; vol. 107; (1974); p. 1221 1227, View in Reaxys

1.526

589

25.5

Tachikawa; Bard; Chemical Physics Letters; vol. 26; (1974); p. 246,250, View in Reaxys

1.527

589

Buzykin et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 1202,1197, View in Reaxys

1.534

589

Kukhar',V.P. et al.; Zhurnal Organicheskoi Khimii; vol. 9; (1973); p. 43 45,41 - 43, View in Reaxys

1.5278

589

Payne,G.B. et al.; Journal of Organic Chemistry; vol. 26; (1961); p. 659 663, View in Reaxys; Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 5-6; (1973); p. 36; Chem.Abstr.; vol. 82; nb. 30686; (1975), View in Reaxys

1.5281

589

Urano et al.; Yuki Gosei Kagaku Kyokaishi; vol. 30; (1972); p. 154,158,159, View in Reaxys

1.5269

589

Radau; Hartke; Archiv der Pharmazie; vol. 305; nb. 9; (1972); p. 702 707, View in Reaxys

1.5225

589

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

1.525

589

Razvodovskaya,L.V. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 1446 - 1451,1452 - 1456, View in Reaxys

1.523

589

Gillis; Dain; Journal of Organic Chemistry; vol. 36; (1971); p. 518, View in Reaxys

1.529

Fowler et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 460, View in Reaxys

1.5306

589

Chekmareva et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 6; (1970); p. 735; Khimiya Geterotsiklicheskikh Soedinenii; vol. 6; (1970); p. 794, View in Reaxys

1.5281

589

Ismailow et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 3; (1969); p. 9,11; Chem.Abstr.; vol. 72; nb. 43071; (1970), View in Reaxys

1.5285

589

Nuridzhanyan,K.A. et al.; Zhurnal Organicheskoi Khimii; vol. 5; nb. 5; (1969); p. 869 - 874,856 - 860, View in Reaxys

1.5261

589

Troszkiewicz et al.; Roczniki Chemii; vol. 43; (1969); p. 1151,1153, View in Reaxys

1.5287

589

Becker et al.; Tetrahedron; vol. 24; (1968); p. 1031, View in Reaxys

45/225

2018-05-24 12:11:44

1.532

Misono et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 2875,2884, View in Reaxys

Ogata; Sakanishi; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 2294,2296,2297, View in Reaxys

1.5283

589

1.5272

589

1.5291

589

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys

1.526

589

George,T.A. et al.; Journal of the Chemical Society; (1965); p. 2157 - 2165, View in Reaxys; Misono et al.; Bulletin of the Chemical Society of Japan; vol. 39; (1966); p. 854, View in Reaxys

1.5266

589

Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 2; (1965); p. 18; Chem.Abstr.; vol. 63; nb. 13111; (1965), View in Reaxys; Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 4; (1965); p. 70,71; Chem.Abstr.; vol. 64; nb. 10539; (1966), View in Reaxys

1.5258

589

Svetkin,Yu.V.; Minlibaeva,A.N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 35; (1965); p. 836 - 838,840 - 841, View in Reaxys

1.5273

589

1.5242

589

Sil'berman et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2713,2734, View in Reaxys

1.5292

589

Grandberg; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 569,570, View in Reaxys

1.5272

589

Guye; Mallet; Chem. Zentralbl.; vol. 73; nb. I; (1902); p. 1315, View in Reaxys; Overberger; Sarlo; Journal of the American Chemical Society; vol. 85; (1963); p. 2446, View in Reaxys

1.527

589

Michel; Gueibe; Bulletin des Societes Chimiques Belges; vol. 70; (1961); p. 330, View in Reaxys

1.0228

Wright; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 454, View in Reaxys

1.5252

589

Wright; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 454, View in Reaxys; Wright; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 784,786, View in Reaxys

1.5257

589

Ferris et al.; Journal of Organic Chemistry; vol. 25; (1960); p. 1813, View in Reaxys

1.5207

589

Ferris,A.F.; Journal of Organic Chemistry; vol. 25; (1960); p. 12 - 18, View in Reaxys

1.52283

656.3

Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys

1.52823

589

Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys

1.54208

486.1

Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys

1.55346

434

Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys

1.5235

589

Patent; Am. Cyanamid Co.; US2459128; (1946), View in Reaxys

1.52444

667.8

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

1.52526

656.3

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

Mataga et al.; Bulletin of the Chemical Society of Japan; vol. 39; (1966); p. 2562, View in Reaxys

46/225

2018-05-24 12:11:44

1.53056

589

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

1.53082

587.6

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

1.5418

501.6

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

1.54461

486.1

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

1.55326

447.1

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

1.52665

589

Kao; Yen; Chien; Journal of the Chinese Chemical Society (Peking); vol. 2; (1934); p. 240, View in Reaxys

1.52876

589

Kao; Yen; Chien; Journal of the Chinese Chemical Society (Peking); vol. 2; (1934); p. 240, View in Reaxys

1.52096

656.3

Martin; Collie; Journal of the Chemical Society; (1932); p. 2658,2662, View in Reaxys

1.5269

656.3

11.6

v.Auwers; Chemische Berichte; vol. 61; (1928); p. 1048, View in Reaxys

1.5326

587.6

11.6

v.Auwers; Chemische Berichte; vol. 61; (1928); p. 1048, View in Reaxys

1.5464

486.1

11.6

v.Auwers; Chemische Berichte; vol. 61; (1928); p. 1048, View in Reaxys

1.5587

434

11.6

v.Auwers; Chemische Berichte; vol. 61; (1928); p. 1048, View in Reaxys

1.527

656.3

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.5323

589

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.5551

486.1

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.5244

656.3

Kahlenberg; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 657, View in Reaxys; Berliner; Dissertation <Breslau 1886>, S. 34, View in Reaxys

1.52892

589

Kahlenberg; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 657, View in Reaxys; Berliner; Dissertation <Breslau 1886>, S. 34, View in Reaxys

1.55688

434

Kahlenberg; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 657, View in Reaxys; Berliner; Dissertation <Breslau 1886>, S. 34, View in Reaxys

1.52035

656.3

25.5

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.5257

589

25.5

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.55144

434

25.5

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.52135

656.3

24.8

Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys

1.54033

486.1

24.8

Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys

47/225

2018-05-24 12:11:44

1.52555

656.3

16.2

Costa; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1891); p. 336, View in Reaxys

1.54495

486.1

16.2

Costa; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1891); p. 336, View in Reaxys

1.55721

434

16.2

Costa; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1891); p. 336, View in Reaxys

1.5306

589

Gladstone; Journal of the Chemical Society; vol. 45; (1884); p. 246, View in Reaxys

Density (68) 1 of 68

Density [g·cm-3]

1.00955

Measurement Temperature 14.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 2 of 68

Density [g·cm-3]

1.00512

Measurement Temperature 19.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 3 of 68

Density [g·cm-3]

1.00069

Measurement Temperature 24.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 4 of 68

Density [g·cm-3]

0.99626

Measurement Temperature 29.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 5 of 68

Density [g·cm-3]

0.99183

Measurement Temperature 34.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 6 of 68

Density [g·cm-3]

0.9874

Measurement Temperature 39.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 7 of 68

Density [g·cm-3]

1.98296

Measurement Temperature 9.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 8 of 68

Density [g·cm-3]

0.98296

Measurement Temperature 45.34 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 9 of 68

Density [g·cm-3]

1.01399

48/225

2018-05-24 12:11:44

Density [g·cm-3]

1.01221

Measurement Temperature 11.99 [°C] Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys 11 of 68

Density [g·cm-3]

0.99092 - 0.99544

Measurement Temperature 30 - 35 [°C] Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 12 of 68

Density [g·cm-3]

0.98311 - 1.00034

Measurement Temperature 25 - 45 [°C] Gill, Dip Singh; Singh, Parvinder; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 5; (1999); p. 478 - 481, View in Reaxys 13 of 68

Density [g·cm-3]

0.9999

Measurement Temperature 25 [°C] Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 14 of 68

Density [g·cm-3]

0.99106

Measurement Temperature 35 [°C] Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 15 of 68

Density [g·cm-3]

0.98213

Measurement Temperature 45 [°C] Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 16 of 68

Density [g·cm-3]

0.9965

Measurement Temperature 30 [°C] Viswanathan; Anand Rao; Prasad; Venkateshwara Rao; Journal of Chemical and Engineering Data; vol. 41; nb. 2; (1996); p. 173 - 174, View in Reaxys 17 of 68

Density [g·cm-3]

0.97352

Measurement Temperature 55 [°C] Goralski; Tkaczyk; Piekarski; Journal of Solution Chemistry; vol. 25; nb. 12; (1996); p. 1227 - 1240, View in Reaxys 18 of 68

Density [g·cm-3]

0.98268

Measurement Temperature 45 [°C] Goralski; Tkaczyk; Piekarski; Journal of Solution Chemistry; vol. 25; nb. 12; (1996); p. 1227 - 1240, View in Reaxys 19 of 68

Density [g·cm-3]

0.99177

Measurement Temperature 35 [°C]

49/225

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Goralski; Tkaczyk; Piekarski; Journal of Solution Chemistry; vol. 25; nb. 12; (1996); p. 1227 - 1240, View in Reaxys 20 of 68

Density [g·cm-3]

1.00065

Measurement Temperature 25 [°C] Goralski; Tkaczyk; Piekarski; Journal of Solution Chemistry; vol. 25; nb. 12; (1996); p. 1227 - 1240, View in Reaxys 21 of 68

Density [g·cm-3]

0.98301 - 1.00034

Measurement Temperature 24.9 - 44.9 [°C] Gill, Dip Singh; Singh, Parvinder; Singh, Jasbir; Singh, Pritam; Senanayake, Gamini; Hefter, Glenn T.; Journal of the Chemical Society, Faraday Transactions; vol. 91; nb. 17; (1995); p. 2789 - 2796, View in Reaxys 22 of 68

Density [g·cm-3]

1.00034

Measurement Temperature 298 [°C] Gill, Dip Singh; Singh, Rajinder; Ali, Vazid; Singh, Jasbir; Rehani, Sharwan Kumar; Journal of the Chemical Society, Faraday Transactions; vol. 90; nb. 4; (1994); p. 583 - 586, View in Reaxys 23 of 68

Density [g·cm-3]

1.0089

Reference Temperature [°C]

Measurement Temperature 20 [°C] Mitrasov, Yu. N.; Mikhailova, O. N.; Yal'tseva, N. S.; Nikiforov, N. G.; Kormachev, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 6; (1987); p. 1417 - 1418,1268, View in Reaxys 24 of 68

Density [g·cm-3]

1.0051

Measurement Temperature 25 [°C] Tarasova, G. V.; Khashchina, M. V.; Tyurin, S. A.; Bulgarevich, S. B.; Bogdan, I. G.; Russian Journal of Physical Chemistry; vol. 60; nb. 8; (1986); p. 1235 - 1237; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 2058 - 2061, View in Reaxys 25 of 68

Density [g·cm-3]

0.9918

Measurement Temperature 35 [°C] Rajkumar, X. Rosario; Raman, K. V.; Arulraj, S. J.; Journal of the Indian Chemical Society; vol. 62; nb. 7; (1985); p. 516 518, View in Reaxys 26 of 68

Density [g·cm-3]

1.00064

Measurement Temperature 25 [°C] Chawla, B.; Mehta, S. K.; Jasra, R. V.; Suri, S. K.; Canadian Journal of Chemistry; vol. 61; (1983); p. 2147 - 2150, View in Reaxys 27 of 68

Density [g·cm-3]

0.7717 - 0.7666

Measurement Temperature 30 - 35 [°C] Oswal et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 17; (1979); p. 605, View in Reaxys 28 of 68

Density [g·cm-3]

1.002

Reference Temperature [°C]

Measurement Temperature 25 [°C] Mauret et al.; Bulletin de la Societe Chimique de France; (1976); p. 429, View in Reaxys 29 of 68

Density [g·cm-3]

1.00071

50/225

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Measurement Temperature 25 [°C] Miller et al.; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 417,418, 419, View in Reaxys 30 of 68

Miller et al.; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 417,418, 419, View in Reaxys

31 of 68

Akhmetkarimov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 458,460, View in Reaxys

32 of 68

Density [g·cm-3]

1.004

Reference Temperature [°C]

Measurement Temperature 20 [°C] Akhmetkarimov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 458,460, View in Reaxys 33 of 68

Density [g·cm-3]

1.0076

Reference Temperature [°C]

Measurement Temperature 20 [°C] Ismailow et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 3; (1969); p. 9,11; Chem.Abstr.; vol. 72; nb. 43071; (1970), View in Reaxys; Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 5-6; (1973); p. 36; Chem.Abstr.; vol. 82; nb. 30686; (1975), View in Reaxys 34 of 68

Density [g·cm-3]

1.0097

Reference Temperature [°C]

Measurement Temperature 20 [°C] Chekmareva et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 6; (1970); p. 735; Khimiya Geterotsiklicheskikh Soedinenii; vol. 6; (1970); p. 794, View in Reaxys 35 of 68

Density [g·cm-3]

1.007

Reference Temperature [°C]

Measurement Temperature 20 [°C] Smirnow et al.; Zhurnal Organicheskoi Khimii; vol. 5; (1969); p. 1355,1324, View in Reaxys 36 of 68

Density [g·cm-3]

1.0043

Reference Temperature [°C]

Measurement Temperature 20 [°C] Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 2; (1965); p. 18; Chem.Abstr.; vol. 63; nb. 13111; (1965), View in Reaxys; Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 4; (1965); p. 70,71; Chem.Abstr.; vol. 64; nb. 10539; (1966), View in Reaxys 37 of 68

Density [g·cm-3]

1.0051

Reference Temperature [°C]

Measurement Temperature 20 [°C] Turner; Merry; Journal of the Chemical Society; vol. 97; (1910); p. 2076, View in Reaxys; Prokof'ewa et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 1318,1294, View in Reaxys 38 of 68

Density [g·cm-3]

1.0228

Reference Temperature [°C]

51/225

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Measurement Temperature 0 [°C] Wright; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 784,786, View in Reaxys 39 of 68

Density [g·cm-3]

0.9483 - 1.0064

Reference Temperature [°C]

Measurement Temperature 19.3 - 87 [°C] Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys 40 of 68

Density [g·cm-3]

0.859 - 1.0065

Reference Temperature [°C]

Measurement Temperature 19.7 - 180.7 [°C] Friend; Hargreaves; Phil. Mag.; vol. <7> 35; (1944); p. 619,628, View in Reaxys 41 of 68

Density [g·cm-3]

0.96 - 1.023

Reference Temperature [°C]

Measurement Temperature 0 - 70 [°C] Boettcher; Physica; vol. 6; (1939); p. 59,67, View in Reaxys 42 of 68

Density [g·cm-3]

0.99628

Reference Temperature [°C]

Measurement Temperature 30 [°C] Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys 43 of 68

Density [g·cm-3]

1.00948

Reference Temperature [°C]

Measurement Temperature 15 [°C] Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys 44 of 68

Density [g·cm-3]

1.02275

Reference Temperature [°C]

Measurement Temperature 0 [°C] Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys 45 of 68

Density [g·cm-3]

1.0012

Reference Temperature [°C]

Measurement Temperature 25 [°C] Kao; Yen; Chien; Journal of the Chinese Chemical Society (Peking); vol. 2; (1934); p. 240, View in Reaxys 46 of 68

Density [g·cm-3]

1.0052

52/225

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Reference Temperature [°C]

Measurement Temperature 20 [°C] Kao; Yen; Chien; Journal of the Chinese Chemical Society (Peking); vol. 2; (1934); p. 240, View in Reaxys 47 of 68

Density [g·cm-3]

1.0006

Reference Temperature [°C]

Measurement Temperature 25 [°C] Sugden; Journal of the Chemical Society; (1933); p. 768,773, View in Reaxys 48 of 68

Density [g·cm-3]

0.96 - 1.006

Reference Temperature [°C]

Measurement Temperature 20 - 75 [°C] Azim; Bhatnagar; Mathur; Phil. Mag.; vol. <7> 16; (1933); p. 580,583, View in Reaxys 49 of 68

Density [g·cm-3]

1.00105

Reference Temperature [°C]

Measurement Temperature 25 [°C] Martin; Collie; Journal of the Chemical Society; (1932); p. 2658,2662, View in Reaxys 50 of 68

Density [g·cm-3]

1.0109

Reference Temperature [°C]

Measurement Temperature 11.6 [°C] v.Auwers; Chemische Berichte; vol. 61; (1928); p. 1048, View in Reaxys 51 of 68

Density [g·cm-3]

0.96 - 1.0222

Reference Temperature [°C]

Measurement Temperature 0 - 70 [°C] Martin; Journal of the Chemical Society; (1928); p. 3277, View in Reaxys 52 of 68

Density [g·cm-3]

0.9319 - 1.0209

Reference Temperature [°C]

Measurement Temperature 0 - 100 [°C] Bingham; van Klooster; Kleinspehn; Journal of Physical Chemistry; vol. 24; (1920); p. 10, View in Reaxys 53 of 68

Density [g·cm-3]

1.003

Reference Temperature [°C]

Measurement Temperature 25 [°C] Dunstan; Hilditch; Thole; Journal of the Chemical Society; vol. 103; (1913); p. 140, View in Reaxys 54 of 68

Density [g·cm-3]

0.9692

53/225

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Reference Temperature [°C]

Measurement Temperature 60 [°C] Turner; Merry; Journal of the Chemical Society; vol. 97; (1910); p. 2076, View in Reaxys 55 of 68

Density [g·cm-3]

0.9831

Reference Temperature [°C]

Measurement Temperature 45 [°C] Turner; Merry; Journal of the Chemical Society; vol. 97; (1910); p. 2076, View in Reaxys 56 of 68

Density [g·cm-3]

0.9974

Reference Temperature [°C]

Measurement Temperature 30 [°C] Turner; Merry; Journal of the Chemical Society; vol. 97; (1910); p. 2076, View in Reaxys 57 of 68

Density [g·cm-3]

1.02279

Reference Temperature [°C]

Measurement Temperature 0 [°C] Timmermans; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 442, View in Reaxys 58 of 68

Density [g·cm-3]

1.001

Reference Temperature [°C]

Measurement Temperature 25 [°C] Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys 59 of 68

Density [g·cm-3]

1.0227

Reference Temperature [°C]

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys 60 of 68

Density [g·cm-3]

1.0227

Reference Temperature [°C]

Measurement Temperature 0 [°C] Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys 61 of 68

Density [g·cm-3]

1.0035

Measurement Temperature 20.9 [°C] Guye; Mallet; Chem. Zentralbl.; vol. 73; nb. I; (1902); p. 1315, View in Reaxys 62 of 68

Density [g·cm-3]

1.0036

Reference Temperature [°C]

54/225

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Measurement Temperature 25 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 63 of 68

Density [g·cm-3]

1.0102

Reference Temperature [°C]

Measurement Temperature 15 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 64 of 68

Density [g·cm-3]

1.0191

Reference Temperature [°C]

Measurement Temperature 4 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 65 of 68

Density [g·cm-3]

1.0003

Reference Temperature [°C]

Measurement Temperature 25.5 [°C] Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys 66 of 68

Density [g·cm-3]

1.0005

Reference Temperature [°C]

Measurement Temperature 24.8 [°C] Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys 67 of 68

Density [g·cm-3]

1.0052

Measurement Temperature 18 [°C] Gladstone; Journal of the Chemical Society; vol. 45; (1884); p. 246, View in Reaxys 68 of 68

Density [g·cm-3]

1.0084

Reference Temperature [°C]

16.8

Measurement Temperature 16.8 [°C] Kopp; Justus Liebigs Annalen der Chemie; vol. 98; (1856); p. 375, View in Reaxys Adsorption (MCS) (57) 1 of 57

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

15 - 25

Partner (Adsorption (MCS))

quartz sand

Arp, Hans Peter H.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Toxicology and Chemistry; vol. 25; nb. 1; (2006); p. 45 - 51, View in Reaxys

55/225

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2 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

hexane

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

zeolite Y

Dias, Silvia Claudia Loureiro; Lemos De Macedo, Julio; Dias, Jose Alves; Physical Chemistry Chemical Physics; vol. 5; nb. 24; (2003); p. 5574 - 5579, View in Reaxys 3 of 57

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

-163.15 - 26.85

Partner (Adsorption (MCS))

Si(100)

Tao, Feng; Wang, Zhong Hai; Xu, Guo Qin; Journal of Physical Chemistry B; vol. 106; nb. 14; (2002); p. 3557 - 3563, View in Reaxys 4 of 57

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

ambient temperature

Partner (Adsorption (MCS))

fluorine-containing aluminium borate

Brichka; Brei; Polish Journal of Chemistry; vol. 75; nb. 5; (2001); p. 719 - 732, View in Reaxys 5 of 57

Description (Adsorption (MCS))

Chemisorption

Comment (Adsorption (MCS))

ambient temperature

Partner (Adsorption (MCS))

fluorine-containing aluminium borate

Brichka; Brei; Polish Journal of Chemistry; vol. 75; nb. 5; (2001); p. 719 - 732, View in Reaxys 6 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Comment (Adsorption (MCS))

ambient temperature

Partner (Adsorption (MCS))

fluorine-containing aluminium borate

Brichka; Brei; Polish Journal of Chemistry; vol. 75; nb. 5; (2001); p. 719 - 732, View in Reaxys 7 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

aq. HClO4

Partner (Adsorption (MCS))

Cu, Ag, Au, Rh, Ir, Pd, Pt

Mrozek; Wasileski; Weaver; Journal of the American Chemical Society; vol. 123; nb. 51; (2001); p. 12817 - 12825, View in Reaxys 8 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetonitrile; H2O

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Temperature (Adsorption (MCS)) [°C]

30 - 130

Comment (Adsorption (MCS))

Ratio of solvents: 40/60 MeCN/water

Partner (Adsorption (MCS))

C-ZrO2

Mao, Yun; Carr, Peter W.; Analytical Chemistry; vol. 72; nb. 1; (2000); p. 110 - 118, View in Reaxys 9 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetonitrile; H2O

Temperature (Adsorption (MCS)) [°C]

Comment (Adsorption (MCS))

Ratio of solvents: 40/60 MeCN/water

Partner (Adsorption (MCS))

PBD-ZrO2

Mao, Yun; Carr, Peter W.; Analytical Chemistry; vol. 72; nb. 1; (2000); p. 110 - 118, View in Reaxys 10 of 57

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

graphitized carbon black Sterling MT 3100degD4

Davydov; Kalashnikova; Karnatsevich; Lopatin; Russian Journal of Physical Chemistry A; vol. 74; nb. 4; (2000); p. 619 624, View in Reaxys 11 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

graphitized carbon black Sterling MT 3100degD4

Davydov; Kalashnikova; Karnatsevich; Lopatin; Russian Journal of Physical Chemistry A; vol. 74; nb. 4; (2000); p. 619 624, View in Reaxys 12 of 57

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

C60

Davydov; Kalashnikova; Karnatsevich; Lopatin; Russian Journal of Physical Chemistry A; vol. 74; nb. 4; (2000); p. 619 624, View in Reaxys 13 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

C60

Davydov; Kalashnikova; Karnatsevich; Lopatin; Russian Journal of Physical Chemistry A; vol. 74; nb. 4; (2000); p. 619 624, View in Reaxys 14 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetonitrile; H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

PS-ZrO2

Zhao, Jianhong; Carr, Peter W .; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3619 - 3628, View in Reaxys

57/225

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15 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetonitrile; H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

Ph-SiO2

Zhao, Jianhong; Carr, Peter W .; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3619 - 3628, View in Reaxys 16 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetonitrile; H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

PRP-1

Zhao, Jianhong; Carr, Peter W .; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3619 - 3628, View in Reaxys 17 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetonitrile; H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

PBD-ZrO2

Zhao, Jianhong; Carr, Peter W .; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3619 - 3628, View in Reaxys 18 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

aq. H2SO4

Partner (Adsorption (MCS))

Zou, Shouzhong; Williams, Christopher T.; Chen, Eddy K.-Y.; Weaver, Michael J.; Journal of Physical Chemistry B; vol. 102; nb. 45; (1998); p. 9039 - 9049, View in Reaxys 19 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

aq. HClO4

Partner (Adsorption (MCS))

Zou, Shouzhong; Williams, Christopher T.; Chen, Eddy K.-Y.; Weaver, Michael J.; Journal of Physical Chemistry B; vol. 102; nb. 45; (1998); p. 9039 - 9049, View in Reaxys 20 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

aq. HClO4

Partner (Adsorption (MCS))

Zou, Shouzhong; Williams, Christopher T.; Chen, Eddy K.-Y.; Weaver, Michael J.; Journal of Physical Chemistry B; vol. 102; nb. 45; (1998); p. 9039 - 9049, View in Reaxys

58/225

2018-05-24 12:11:44

21 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

MnCO3

Nikolenko; Kuprin; Kovalenko; Plaksienko; Dovban'; Russian Journal of Physical Chemistry A; vol. 71; nb. 10; (1997); p. 1657 - 1662, View in Reaxys 22 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

CaCO3

Nikolenko; Kuprin; Kovalenko; Plaksienko; Dovban'; Russian Journal of Physical Chemistry A; vol. 71; nb. 10; (1997); p. 1657 - 1662, View in Reaxys 23 of 57

Description (Adsorption (MCS))

Chemisorption

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

cholic acid

Caira; Nassimbeni; Scott; Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals; vol. 276-277; nb. pt 1-2; (1996); p. 113 - 120, View in Reaxys 24 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

perdeuterated tetradecyltrimethylammonium bromide; gold hydrophobized by perdeuterated octadecanethiol

Duffy, David C.; Davies, Paul B.; Bain, Colin D.; Journal of Physical Chemistry; vol. 99; nb. 41; (1995); p. 15241 - 15246, View in Reaxys 25 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

hydrated ZrO2

Nikolenko, N. V.; Vereshchak, V. G.; Parkhomenko, N. V.; Russian Journal of Physical Chemistry; vol. 68; nb. 2; (1994); p. 267 - 270; Zhurnal Fizicheskoi Khimii; vol. 68; nb. 2; (1994); p. 301 - 304, View in Reaxys 26 of 57

Description (Adsorption (MCS))

Desorption

Partner (Adsorption (MCS))

poly(vinylphenol-co-ethylstyrene-co-divinylbenzene)

Tan, Lay Choo; Carr, Peter W.; Frechet, Jean M. J.; Smigol, Vladimir; Analytical Chemistry; vol. 66; nb. 4; (1994); p. 450 457, View in Reaxys 27 of 57

Description (Adsorption (MCS))

Chemisorption

Partner (Adsorption (MCS))

poly(vinylphenol-co-ethylstyrene-co-divinylbenzene)

59/225

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Tan, Lay Choo; Carr, Peter W.; Frechet, Jean M. J.; Smigol, Vladimir; Analytical Chemistry; vol. 66; nb. 4; (1994); p. 450 457, View in Reaxys 28 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

KBr

Partner (Adsorption (MCS))

clayzic (zinc chloride on acid-treated montmorillonite)

Clark, James H.; Cullen, Stephen R.; Barlow, Simon J.; Bastock, Tony W.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 6; (1994); p. 1117 - 1130, View in Reaxys 29 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

KBr

Partner (Adsorption (MCS))

K10 (acid-treated montmorillonite)

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

K10 montmorillonite

Barlow; Bastock; Clark; Cullen; Tetrahedron Letters; vol. 34; nb. 20; (1993); p. 3339 - 3342, View in Reaxys 31 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

K10 montmorillonite supported zinc chloride

Barlow; Bastock; Clark; Cullen; Tetrahedron Letters; vol. 34; nb. 20; (1993); p. 3339 - 3342, View in Reaxys 32 of 57

Description (Adsorption (MCS))

Chemisorption

Temperature (Adsorption (MCS)) [°C]

99.9 - 249.9

Partner (Adsorption (MCS))

kaolinite (cation exchange form)

Taranukhina, L. D.; Paukshtis, E. A.; Goncharuk, V. V.; J. Appl. Chem. USSR (Engl. Transl.); vol. 65; nb. 6.1; (1992); p. 1287 - 1291,1067 - 1071, View in Reaxys 33 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

cyamelluric acid

Gavrilova, T. B.; Nikitin, Yu. S.; Rudnitskaya, T. A.; Finkel'shtein, A. I.; Russian Journal of Physical Chemistry; vol. 66; nb. 4; (1992); p. 570 - 572; Zhurnal Fizicheskoi Khimii; vol. 66; nb. 4; (1992); p. 1080 - 1083, View in Reaxys 34 of 57

Description (Adsorption (MCS))

Chemisorption

Solvent (Adsorption (MCS))

H2O; various solvent(s)

Partner (Adsorption (MCS))

Fe2O3/SiO2

Nikolenko, N. V.; Kholodkova, O. V.; Kuprin, V. P.; Davidenko, A. N.; Plaksienko, I. L.; J. Appl. Chem. USSR (Engl. Transl.); vol. 64; nb. 10.2; (1991); p. 2162 - 2165,2022 - 2024, View in Reaxys 35 of 57

Description (Adsorption (MCS))

Desorption

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Temperature (Adsorption (MCS)) [°C]

-173.1 - 226.9

Partner (Adsorption (MCS))

Au precovered with K

Solomun, T.; Baumgaertel, H.; Christmann, K.; Journal of Physical Chemistry; vol. 95; nb. 24; (1991); p. 10041 - 10049, View in Reaxys 36 of 57

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

-123.1 - 126.9

Partner (Adsorption (MCS))

Au-preadsorbed K

Solomun, T.; Baumgaertel, H.; Christmann, K.; Journal of Physical Chemistry; vol. 95; nb. 24; (1991); p. 10041 - 10049, View in Reaxys 37 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

-253.2

Partner (Adsorption (MCS))

on Au/ aq. 0.5 M H2SO4 with/without vacuum

Gao, Xiaoping; Davies, John P.; Weaver, Michael J.; Journal of Physical Chemistry; vol. 94; nb. 17; (1990); p. 6858 - 6864, View in Reaxys 38 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

naphthalene

Nechaev, E. A.; Nikolenko, N. V.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 155 - 157; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 276 - 278, View in Reaxys 39 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

benzamide

Nechaev, E. A.; Nikolenko, N. V.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 155 - 157; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 276 - 278, View in Reaxys 40 of 57

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

dibenzo-18-crown-6

Nechaev, E. A.; Nikolenko, N. V.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 155 - 157; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 276 - 278, View in Reaxys 41 of 57

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

-173.1

Partner (Adsorption (MCS))

Au(100)

61/225

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Solomun, T.; Christmann, K.; Baumgaertel, H.; Journal of Physical Chemistry; vol. 93; nb. 20; (1989); p. 7199 - 7208, View in Reaxys 42 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

carbopack F

Arnett, Edward M.; Hutchinson, Brenda J.; Healy, Marguerite H.; Journal of the American Chemical Society; vol. 110; nb. 16; (1988); p. 5255 - 5260, View in Reaxys 43 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

carbopack B

Arnett, Edward M.; Hutchinson, Brenda J.; Healy, Marguerite H.; Journal of the American Chemical Society; vol. 110; nb. 16; (1988); p. 5255 - 5260, View in Reaxys 44 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

graphite

Arnett, Edward M.; Hutchinson, Brenda J.; Healy, Marguerite H.; Journal of the American Chemical Society; vol. 110; nb. 16; (1988); p. 5255 - 5260, View in Reaxys 45 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

anthracite coal

Arnett, Edward M.; Hutchinson, Brenda J.; Healy, Marguerite H.; Journal of the American Chemical Society; vol. 110; nb. 16; (1988); p. 5255 - 5260, View in Reaxys 46 of 57

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

Cu2+-montmorrilonite

Soma, Y.; Soma, M.; Harada, I.; Journal of Physical Chemistry; vol. 89; nb. 5; (1985); p. 738 - 742, View in Reaxys 47 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

H2SO4; H2O

Temperature (Adsorption (MCS)) [°C]

22 - 24

Partner (Adsorption (MCS))

Gold

Gao, Ping; Weaver, Michael J.; Journal of Physical Chemistry; vol. 89; (1985); p. 5040 - 5046, View in Reaxys 48 of 57

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

120 - 375

Partner (Adsorption (MCS))

Ni(111)

Wexler, R. M.; Muetterties, E. L.; Journal of Physical Chemistry; vol. 88; nb. 18; (1984); p. 4037 - 4041, View in Reaxys 49 of 57

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

aq. NaOH

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Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

polystyrene XAD-4

Urano; Kano; Bulletin of the Chemical Society of Japan; vol. 57; nb. 8; (1984); p. 2051 - 2054, View in Reaxys 50 of 57

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

aq. NaOH

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

activated carbon Filtrasorb 400

Urano; Kano; Bulletin of the Chemical Society of Japan; vol. 57; nb. 8; (1984); p. 2051 - 2054, View in Reaxys 51 of 57

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

polystyrene XAD-4

Urano; Kano; Bulletin of the Chemical Society of Japan; vol. 57; nb. 8; (1984); p. 2051 - 2054, View in Reaxys 52 of 57

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

activated carbon Filtrasorb 400

Urano; Kano; Bulletin of the Chemical Society of Japan; vol. 57; nb. 8; (1984); p. 2051 - 2054, View in Reaxys 53 of 57

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

acetonitrile; various solvent(s)

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

mercury electrode

Wegert, H.; Baumgaertel, H.; Berichte der Bunsen-Gesellschaft; vol. 84; nb. 3; (1980); p. 274 - 277, View in Reaxys 54 of 57

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

acetonitrile; various solvent(s)

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

mercury electrode

Wegert, H.; Baumgaertel, H.; Berichte der Bunsen-Gesellschaft; vol. 84; nb. 3; (1980); p. 274 - 277, View in Reaxys

63/225

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55 of 57

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Paukshtis et al.; Kinetics and Catalysis; vol. 20; (1979); p. 162,164; ; p. 202, View in Reaxys; Koehler; Winde; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 9; (1969); p. 393, View in Reaxys 56 of 57

Description (Adsorption (MCS))

Adsorption

Tret'yakov et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 596,597,598; ; p. 1077, View in Reaxys; Baumer et al.; Berichte der Bunsen-Gesellschaft; vol. 82; (1978); p. 878,879-881, View in Reaxys; Snyder; Journal of Physical Chemistry; vol. 72; (1968); p. 489,491, View in Reaxys; Tul'bovich; Priimak; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 195; Zhurnal Fizicheskoi Khimii; p. 362, View in Reaxys 57 of 57

Description (Adsorption (MCS))

Chemisorption

Oranskaya et al.; Kinetics and Catalysis; vol. 16; (1975); p. 712, View in Reaxys Association (MCS) (131) 1 of 131

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

water-d2

Temperature (Association (MCS)) [°C]

24.84

Location

supporting information

Partner (Association (MCS))

hexakis((2S,2'S)-3,3'-((2,5-diiodo-1,4-phenylene)bis(oxy))bis(propane-1,2-diol)) iron complex

Bolliger, Jeanne L.; Belenguer, Ana M.; Nitschke, Jonathan R.; Angewandte Chemie - International Edition; vol. 52; nb. 31; (2013); p. 7958 - 7962; Angew. Chem.; vol. 125; nb. 31; (2013); p. 8116 - 8120, View in Reaxys 2 of 131

Description (Association (MCS))

Further physical properties of the complex

Comment (Association (MCS))

film

Partner (Association (MCS))

C112H124S12O4N4; gold

Kim, Wan-Sang; Shin, Dong-Myung; Chung, Gee-Won; Molecular Crystals and Liquid Crystals; vol. 464; nb. 1; (2007); p. 93 - 101, View in Reaxys 3 of 131

Description (Association (MCS))

Further physical properties of the complex

Comment (Association (MCS))

film

Partner (Association (MCS))

C92H92S12O4N4; gold

Kim, Wan-Sang; Shin, Dong-Myung; Chung, Gee-Won; Molecular Crystals and Liquid Crystals; vol. 464; nb. 1; (2007); p. 93 - 101, View in Reaxys 4 of 131

Description (Association (MCS))

Further physical properties of the complex

Comment (Association (MCS))

film

Partner (Association (MCS))

C160H132S12O4N4; gold

Kim, Wan-Sang; Shin, Dong-Myung; Chung, Gee-Won; Molecular Crystals and Liquid Crystals; vol. 464; nb. 1; (2007); p. 93 - 101, View in Reaxys 5 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gas

64/225

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Comment (Association (MCS))

excited state. Object(s) of Study: fluorescence

Partner (Association (MCS))

methanol

Borst, David R.; Pratt, David W.; Schaefer, Martin; Physical Chemistry Chemical Physics; vol. 9; nb. 32; (2007); p. 4563 4571, View in Reaxys 6 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gas

Comment (Association (MCS))

excited state. Object(s) of Study: fluorescence

Partner (Association (MCS))

acetonitrile

Borst, David R.; Pratt, David W.; Schaefer, Martin; Physical Chemistry Chemical Physics; vol. 9; nb. 32; (2007); p. 4563 4571, View in Reaxys 7 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gas

Comment (Association (MCS))

excited state. Object(s) of Study: fluorescence

Partner (Association (MCS))

NH3

Borst, David R.; Pratt, David W.; Schaefer, Martin; Physical Chemistry Chemical Physics; vol. 9; nb. 32; (2007); p. 4563 4571, View in Reaxys 8 of 131

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

phenol

Zecek, Petr; Dransfeld, Alk; Exner, Otto; Schraml, Jan; Magnetic Resonance in Chemistry; vol. 44; nb. 12; (2006); p. 1073 1080, View in Reaxys 9 of 131

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

nitrobenzene

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

Ni(Me4[12]aneN4)(ClO4)2

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

65/225

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Partner (Association (MCS))

pyrene

Zhu, Dongqiang; Pignatello, Joseph J.; Environmental Science and Technology; vol. 39; nb. 7; (2005); p. 2033 - 2041, View in Reaxys 11 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

CHCl3

Comment (Association (MCS))

ambient temperature

Partner (Association (MCS))

pyrene

Zhu, Dongqiang; Pignatello, Joseph J.; Environmental Science and Technology; vol. 39; nb. 7; (2005); p. 2033 - 2041, View in Reaxys 12 of 131

Description (Association (MCS))

Further physical properties of the complex

Comment (Association (MCS))

fluorescence

Partner (Association (MCS))

Meerts, W. Leo; Schmitt, Michael; Groenenboom, Gerrit C.; Canadian Journal of Chemistry; vol. 82; nb. 6; (2004); p. 804 819, View in Reaxys 13 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

methanol

Raghuvansh; Srivastava, Sunil K.; Singh, Ranjan K.; Asthana; Kiefer; Physical Chemistry Chemical Physics; vol. 6; nb. 3; (2004); p. 531 - 536, View in Reaxys 14 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

gaseous matrix

Comment (Association (MCS))

vibrational analysis

Partner (Association (MCS))

chloroform

Yamamoto; Ebata; Mikami; Journal of Chemical Physics; vol. 114; nb. 18; (2001); p. 7866 - 7876, View in Reaxys 15 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gaseous matrix

Comment (Association (MCS))

vibrational analysis

Partner (Association (MCS))

chloroform

Yamamoto; Ebata; Mikami; Journal of Chemical Physics; vol. 114; nb. 18; (2001); p. 7866 - 7876, View in Reaxys 16 of 131

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

phenol-d1

66/225

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Bagno, Alessandro; Menna, Enzo; Scorrano, Gianfranco; Zerbinati, Simonetta; Magnetic Resonance in Chemistry; vol. 39; nb. 12 SPEC. ISS.; (2001); p. S59-S66, View in Reaxys 17 of 131

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

C3H3(2)HF3NO

Bagno, Alessandro; Menna, Enzo; Scorrano, Gianfranco; Zerbinati, Simonetta; Magnetic Resonance in Chemistry; vol. 39; nb. 12 SPEC. ISS.; (2001); p. S59-S66, View in Reaxys 18 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Pressure (Association (MCS)) [Torr]

750.06

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

methanol

Letcher; Naicker; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1035 - 1047, View in Reaxys 19 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Pressure (Association (MCS)) [Torr]

750.06

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

ethanol

Letcher; Naicker; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1035 - 1047, View in Reaxys 20 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Pressure (Association (MCS)) [Torr]

750.06

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

propan-1-ol

Letcher; Naicker; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1035 - 1047, View in Reaxys 21 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

29.85 - 39.85

Partner (Association (MCS))

methanol

Abraham, Roshan; Abdulkhadar, M.; Asokan, C. V.; Journal of Chemical Thermodynamics; vol. 32; nb. 1; (2000); p. 1 - 16, View in Reaxys

67/225

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22 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

29.85 - 39.85

Partner (Association (MCS))

toluene

Abraham, Roshan; Abdulkhadar, M.; Asokan, C. V.; Journal of Chemical Thermodynamics; vol. 32; nb. 1; (2000); p. 1 - 16, View in Reaxys 23 of 131

Description (Association (MCS))

Enthalpy of association

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

4-Fluorophenol

Le Questel, Jean-Yves; Berthelot, Michel; Laurence, Christian; Journal of Physical Organic Chemistry; vol. 13; nb. 6; (2000); p. 347 - 358, View in Reaxys 24 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

diethyl ether

Partner (Association (MCS))

LiClO4

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gaseous matrix

Partner (Association (MCS))

methanol

Ishikawa, Seiichi; Ebata, Takayuki; Mikami, Naohiko; Journal of Chemical Physics; vol. 110; nb. 19; (1999); p. 9504 - 9515, View in Reaxys 26 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

gaseous matrix

Partner (Association (MCS))

methanol

Ishikawa, Seiichi; Ebata, Takayuki; Mikami, Naohiko; Journal of Chemical Physics; vol. 110; nb. 19; (1999); p. 9504 - 9515, View in Reaxys 27 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

various solvent(s)

Comment (Association (MCS))

rotational analysis. Object(s) of Study: in the presence of rare gases

Partner (Association (MCS))

H2O, D2O

Melandri, Sonia; Consalvo, Daniela; Caminati, Walther; Favero, Paolo G.; Journal of Chemical Physics; vol. 111; nb. 9; (1999); p. 3874 - 3879, View in Reaxys 28 of 131

Description (Association (MCS))

Further physical properties of the complex

68/225

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Solvent (Association (MCS))

gas

Partner (Association (MCS))

propen-2-ol

Trikoupis; Terlouw; Burgers; Journal of the American Chemical Society; vol. 120; nb. 46; (1998); p. 12131 - 12132, View in Reaxys 29 of 131

Description (Association (MCS))

Association with compound

Temperature (Association (MCS)) [°C]

20 - 30

Partner (Association (MCS))

toluene

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 30 of 131

Description (Association (MCS))

Association with compound

Temperature (Association (MCS)) [°C]

20 - 30

Partner (Association (MCS))

benzene

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 31 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

5,11,17,23-tert-butyl-lt;25,26,27,28-tetrakis-(2-pyridylmethyl)oxygt;-p-tert-butylcalix(4)arene

Danil De Namor, Angela F.; Piro, Oscar E.; Pulcha Salazar, Lupe E.; Aguilar-Cornejo, Adolfo F.; Al-Rawi, Nawar; Castellano, Eduardo E.; Sueros Velarde, Felix J.; Journal of the Chemical Society - Faraday Transactions; vol. 94; nb. 20; (1998); p. 3097 - 3104, View in Reaxys 32 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

5,11,17,23-tert-butyl-lt;25,26,27,28-tetrakis-(3-pyridylmethyl)oxygt;-p-tert-butylcalix(4)arene

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

5,11,17,23-tert-butyl-lt;25,26,27,28-tetrakis-(4-pyridylmethyl)oxygt;-p-tert-butylcalix(4)arene

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

benzene

69/225

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Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

diphenylphosphinic acid hydrazide

Yanchuk; Russian Journal of General Chemistry; vol. 67; nb. 2; (1997); p. 220 - 223, View in Reaxys 35 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

CaCO3

Nikolenko; Kuprin; Kovalenko; Plaksienko; Dovban'; Russian Journal of Physical Chemistry A; vol. 71; nb. 10; (1997); p. 1657 - 1662, View in Reaxys 36 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

SiO2

Nikolenko; Kuprin; Kovalenko; Plaksienko; Dovban'; Russian Journal of Physical Chemistry A; vol. 71; nb. 10; (1997); p. 1657 - 1662, View in Reaxys 37 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

methoxybenzene

Viswanathan; Anand Rao; Prasad; Venkateshwara Rao; Journal of Chemical and Engineering Data; vol. 41; nb. 2; (1996); p. 173 - 174, View in Reaxys 38 of 131

Description (Association (MCS))

Further physical properties of the complex

Pressure (Association (MCS)) [Torr]

684 - 1520

Partner (Association (MCS))

Araki, Mitsunori; Sato, Shin-Ichiro; Kimura, Katsumi; Journal of Physical Chemistry; vol. 100; nb. 25; (1996); p. 10542 10546, View in Reaxys 39 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

Ar2

Araki, Mitsunori; Sato, Shin-Ichiro; Kimura, Katsumi; Journal of Physical Chemistry; vol. 100; nb. 25; (1996); p. 10542 10546, View in Reaxys 40 of 131

Description (Association (MCS))

Spectrum of the complex

Solvent (Association (MCS))

D2O; acetone-d6

Temperature (Association (MCS)) [°C]

70/225

2018-05-24 12:11:44

Comment (Association (MCS))

NMR spectrum; Ratio of solvents: 1:1

Partner (Association (MCS))

<Pd(H2O)4>2+

Kaminskaia, Natalia V.; Kostic, Nenad M.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); nb. 18; (1996); p. 3677 - 3686, View in Reaxys 41 of 131

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CD3CN

Partner (Association (MCS))

N,N-dimethyl-1-naphthalenamine

Schaffner, Erik; Fischer, Hanns; Journal of Physical Chemistry; vol. 99; nb. 1; (1995); p. 102 - 104, View in Reaxys 42 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

4-cyano-N,N-dimethylaniline; 6-O-α-D-glucosyl-α-cyclodextrine

Nakamura, Asao; Sato, Shiro; Hamasaki, Keita; Ueno, Akihiko; Toda, Fujio; Journal of Physical Chemistry; vol. 99; nb. 27; (1995); p. 10952 - 10959, View in Reaxys 43 of 131

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

AgNO3

Alia, J. M.; Edwards, H. G. M.; Moore, J.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 12; (1995); p. 2039 - 2056, View in Reaxys 44 of 131

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

-196.1 - -73.1

Partner (Association (MCS))

antimony(V) fluoride

Hoti, Ramiz; Mihalic, Zlatko; Vancik, Hrvoj; Croatica Chemica Acta; vol. 68; nb. 2; (1995); p. 359 - 371, View in Reaxys 45 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

tetracationic cyclobis(paraquat-p-phenylene)

Smith, Eliot A.; Lilienthal, Ronald R.; Fonseca, Robert J.; Smith, Diane K.; Analytical Chemistry; vol. 66; nb. 19; (1994); p. 3013 - 3020, View in Reaxys 46 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

1,1'-dibenzyl-4,4'-bipyridinium

Smith, Eliot A.; Lilienthal, Ronald R.; Fonseca, Robert J.; Smith, Diane K.; Analytical Chemistry; vol. 66; nb. 19; (1994); p. 3013 - 3020, View in Reaxys 47 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

C30H30N4(4+)

Smith, Eliot A.; Lilienthal, Ronald R.; Fonseca, Robert J.; Smith, Diane K.; Analytical Chemistry; vol. 66; nb. 19; (1994); p. 3013 - 3020, View in Reaxys 48 of 131

Description (Association (MCS))

Further physical properties of the complex

71/225

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Partner (Association (MCS))

argon

Dahmen, U.; Stahl, W.; Dreizler, H.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 7; (1994); p. 970 - 974, View in Reaxys 49 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

dimethyl sulfoxide

Rzeszotarska, Jadwiga; Ranachowski, Przemyslaw; Kalinowski, Marek K.; Collection of Czechoslovak Chemical Communications; vol. 59; nb. 10; (1994); p. 2201 - 2208, View in Reaxys 50 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

hexane

Partner (Association (MCS))

lithium hexamethyldisilazane

Gebauer, Thorsten; Dehnicke, Kurt; Goesmann, Helmut; Fenske, Dieter; Zeitschrift fuer Naturforschung, B: Chemical Sciences; vol. 49; nb. 10; (1994); p. 1444 - 1447, View in Reaxys 51 of 131

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

benzene-d6

Partner (Association (MCS))

lithium hexamethyldisilazane

Eisen, Moris S.; Kapon, Moshe; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); nb. 23; (1994); p. 3507 - 3510, View in Reaxys 52 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

114.9 - 144.9

Partner (Association (MCS))

2,6,10,15,19,23-hexamethyltetracosane

Kawaki; Chemical and Pharmaceutical Bulletin; vol. 41; nb. 5; (1993); p. 797 - 803, View in Reaxys 53 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

114.9 - 144.9

Partner (Association (MCS))

dinonyl phthalate

Kawaki; Chemical and Pharmaceutical Bulletin; vol. 41; nb. 5; (1993); p. 797 - 803, View in Reaxys 54 of 131

Description (Association (MCS))

Enthalpy of association

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

20 - 50

Partner (Association (MCS))

phenol

Gramstad, Thor; Stangeland, Leiv Jonn; Acta Chemica Scandinavica; vol. 47; nb. 6; (1993); p. 605 - 609, View in Reaxys 55 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CCl4

72/225

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Temperature (Association (MCS)) [°C]

20 - 50

Partner (Association (MCS))

phenol

Gramstad, Thor; Stangeland, Leiv Jonn; Acta Chemica Scandinavica; vol. 47; nb. 6; (1993); p. 605 - 609, View in Reaxys 56 of 131

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

99.9 - 249.9

Partner (Association (MCS))

kaolinite (cation exchange form)

Taranukhina, L. D.; Paukshtis, E. A.; Goncharuk, V. V.; J. Appl. Chem. USSR (Engl. Transl.); vol. 65; nb. 6.1; (1992); p. 1287 - 1291,1067 - 1071, View in Reaxys 57 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

water

Abraham, Michael H.; Whiting, Gary S.; Fuchs, Richard; Chambers, Eric J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 2; (1990); p. 291 - 300, View in Reaxys 58 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

Hexadecane

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

dioxane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

lithium picrate

Tsvetanov, Ch. B.; Petrova, E. B.; Dimov, D. K.; Panayotov, I. M.; Smid, J.; Journal of Solution Chemistry; vol. 19; nb. 5; (1990); p. 425 - 436, View in Reaxys 60 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

xylene

Partner (Association (MCS))

acetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 61 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

xylene

Partner (Association (MCS))

acetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 62 of 131

Description (Association (MCS))

Stability constant of the complex with ...

73/225

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Solvent (Association (MCS))

various solvent(s)

Partner (Association (MCS))

chloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 63 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

various solvent(s)

Partner (Association (MCS))

chloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 64 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

benzene

Partner (Association (MCS))

chloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 65 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

benzene

Partner (Association (MCS))

chloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 66 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

xylene

Partner (Association (MCS))

chloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 67 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

xylene

Partner (Association (MCS))

chloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 68 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

various solvent(s)

Partner (Association (MCS))

trichloroacetic acid

74/225

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Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 69 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

various solvent(s)

Partner (Association (MCS))

trichloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 70 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

benzene

Partner (Association (MCS))

trichloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 71 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

benzene

Partner (Association (MCS))

trichloroacetic acid

Tsarevskaya, M. N.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 5.2; (1989); p. 1168 - 1172,1033 1036, View in Reaxys 72 of 131

Description (Association (MCS))

Association with compound

Temperature (Association (MCS)) [°C]

-173.1

Partner (Association (MCS))

Au(100)

Solomun, T.; Christmann, K.; Baumgaertel, H.; Journal of Physical Chemistry; vol. 93; nb. 20; (1989); p. 7199 - 7208, View in Reaxys 73 of 131

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

-173.1

Partner (Association (MCS))

Au(100)

Solomun, T.; Christmann, K.; Baumgaertel, H.; Journal of Physical Chemistry; vol. 93; nb. 20; (1989); p. 7199 - 7208, View in Reaxys 74 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

25 - 30

Pressure (Association (MCS)) [Torr]

750.06 - 750060

Partner (Association (MCS))

nitrobenzene

Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 20; nb. 7; (1988); p. 809 - 814, View in Reaxys

75/225

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75 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

cholic acid

Miyata, Mikiji; Shibakami, Motonari; Goonewardena, Wyjayanthi; Takemoto, Kiichi; Chemistry Letters; (1987); p. 605 608, View in Reaxys 76 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

4-oxo-2,2,6,6-tetramethylpiperidin-oxyl

Al-Bala'a, Imad; Bates, Richard D.; Journal of Magnetic Resonance (1969-1992); vol. 73; nb. 1; (1987); p. 78 - 89, View in Reaxys 77 of 131

Description (Association (MCS))

Enthalpy of association

Partner (Association (MCS))

phenylnitrenium ion

Meot-Ner (Mautner), Michael; El-Shall, M. Samy; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p. 4386 - 4390, View in Reaxys 78 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

phenylnitrenium ion

Meot-Ner (Mautner), Michael; El-Shall, M. Samy; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p. 4386 - 4390, View in Reaxys 79 of 131

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

acetone-d6

Partner (Association (MCS))

<α5-C9H7Fe(CO)2><BF4>

Hamund, Hassan H.; Moran, Grainne, M.; Journal of Organometallic Chemistry; vol. 307; (1986); p. 255 - 262, View in Reaxys 80 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

1.4-dibromobenzene

Nagaoka, Shin-ichi; Harrigan, Edward T.; Noda, Masayo; Hirota, Noboru; Higuchi, Jiro; Bulletin of the Chemical Society of Japan; vol. 59; nb. 2; (1986); p. 355 - 362, View in Reaxys 81 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CDCl3

Partner (Association (MCS))

trifluoroacetic acid

Schuster, Ingeborg I.; Journal of Organic Chemistry; vol. 50; nb. 10; (1985); p. 1656 - 1662, View in Reaxys 82 of 131

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

trifluoroacetic acid

76/225

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Schuster, Ingeborg I.; Journal of Organic Chemistry; vol. 50; nb. 10; (1985); p. 1656 - 1662, View in Reaxys 83 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-diphenyl-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 84 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-diphenyl-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 85 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-bis(4-methylphenyl)-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 86 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-bis(4-methylphenyl)-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 87 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-Bislt;4-(tert-butyl)phenylgt;-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 88 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

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Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-Bislt;4-(tert-butyl)phenylgt;-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 89 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-bis(2-methylphenyl)-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 90 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

2,6-bis(2-methylphenyl)-4-nitrophenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 91 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

4-nitro-2,6-bis(2',6'-dimethylphenyl)phenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 92 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

28.5

Partner (Association (MCS))

4-nitro-2,6-bis(2',6'-dimethylphenyl)phenol

Ueji, Shinichi; Journal of Organic Chemistry; vol. 50; nb. 15; (1985); p. 2711 - 2714, View in Reaxys 93 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

9H-carbazole

Kikuchi, Koichi; Hoshi, Masato; Kokubun, Hiroshi; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 146; (1985); p. 43 - 56, View in Reaxys

78/225

2018-05-24 12:11:44

94 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

-193.1 - 26.9

Partner (Association (MCS))

copper(II) phenylpropynoate

Muto, Yoneichiro; Sasaki, Ayako; Tokii, Tadashi; Nakashima, Michio; Bulletin of the Chemical Society of Japan; vol. 58; nb. 9; (1985); p. 2572 - 2576, View in Reaxys 95 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

nujol

Partner (Association (MCS))

copper(II) phenylpropynoate

Muto, Yoneichiro; Sasaki, Ayako; Tokii, Tadashi; Nakashima, Michio; Bulletin of the Chemical Society of Japan; vol. 58; nb. 9; (1985); p. 2572 - 2576, View in Reaxys 96 of 131

Description (Association (MCS))

Enthalpy of association

Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

boron trifluoride

Maria, Pierre-Charles; Gal, Jean-Francois; Journal of Physical Chemistry; vol. 89; nb. 7; (1985); p. 1296 - 1304, View in Reaxys 97 of 131

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

25 - 50

Partner (Association (MCS))

4-Fluorophenol

Austerheim, Asmund; Gramstad, Thor; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 39; nb. 7; (1985); p. 583 - 588, View in Reaxys 98 of 131

Description (Association (MCS))

Dipole moment of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

4-Fluorophenol

Austerheim, Asmund; Gramstad, Thor; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 39; nb. 7; (1985); p. 583 - 588, View in Reaxys 99 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

79/225

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Chmutova, G. A.; Kazymova, M. A.; Ermolaeva, L. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 2; (1985); p. 422 427,373 - 378, View in Reaxys 100 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

Chmutova, G. A.; Kazymova, M. A.; Ermolaeva, L. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 2; (1985); p. 422 427,373 - 378, View in Reaxys 101 of 131

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

para-chlorotoluene

Tsarevskaya, M. N.; Tsarevskii, N. A.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 5; (1985); p. 1155 - 1159,1029 - 1033, View in Reaxys 102 of 131

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

benzene

Tsarevskaya, M. N.; Tsarevskii, N. A.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 5; (1985); p. 1155 - 1159,1029 - 1033, View in Reaxys 103 of 131

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

para-xylene

Tsarevskaya, M. N.; Tsarevskii, N. A.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 5; (1985); p. 1155 - 1159,1029 - 1033, View in Reaxys 104 of 131

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

18.7 - 30.9

Partner (Association (MCS))

2,2,4-trimethylpentane

Miller, B. C.; Clerke, E. A.; Greer, S. C.; Journal of Physical Chemistry; vol. 87; nb. 3; (1983); p. 1063 - 1066, View in Reaxys 105 of 131

Description (Association (MCS))

Enthalpy of association

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

Cumene hydroperoxide

Morozov, O. S.; Mel'kin, V. I.; Vyshinskii, N. N.; Sokolov, N. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 6; (1983); p. 1380 - 1385,1240 - 1244, View in Reaxys 106 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

80/225

2018-05-24 12:11:44

Partner (Association (MCS))

Cumene hydroperoxide

Morozov, O. S.; Mel'kin, V. I.; Vyshinskii, N. N.; Sokolov, N. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 6; (1983); p. 1380 - 1385,1240 - 1244, View in Reaxys 107 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

Cumene hydroperoxide

Morozov, O. S.; Mel'kin, V. I.; Vyshinskii, N. N.; Sokolov, N. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 6; (1983); p. 1380 - 1385,1240 - 1244, View in Reaxys 108 of 131

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

34.1

Partner (Association (MCS))

N,N,N,N,N,N-hexamethylphosphoric triamide

Fujiwara, Hideaki; Takagi, Tatsuya; Yamazaki, Yutaka; Sasaki, Yoshio; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 78; (1982); p. 347 - 356, View in Reaxys 109 of 131

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

34.1

Partner (Association (MCS))

dibutyl sulfone

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

34.1

Partner (Association (MCS))

butyl sulfoxide

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

34.1

Partner (Association (MCS))

tetramethylurea

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Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

N,N,N,N,N,N-hexamethylphosphoric triamide

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

SbBr3

Kjuntsel, I. A.; Gordeev, A. D.; Journal of Molecular Structure; vol. 83; (1982); p. 357 - 360, View in Reaxys 114 of 131

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

SbCl3

Kjuntsel, I. A.; Gordeev, A. D.; Journal of Molecular Structure; vol. 83; (1982); p. 357 - 360, View in Reaxys 115 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

hexane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

triethylamine

Anunziata, J.; Singh, J.; Silber, J. J.; Canadian Journal of Chemistry; vol. 59; (1981); p. 1291 - 1296, View in Reaxys 116 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

hexane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

dibutylamine

Anunziata, J.; Singh, J.; Silber, J. J.; Canadian Journal of Chemistry; vol. 59; (1981); p. 1291 - 1296, View in Reaxys 117 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

hexane

Partner (Association (MCS))

N-butylamine

Anunziata, J.; Singh, J.; Silber, J. J.; Canadian Journal of Chemistry; vol. 59; (1981); p. 1291 - 1296, View in Reaxys 118 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

hexane

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Partner (Association (MCS))

diethylamine

Anunziata, J.; Singh, J.; Silber, J. J.; Canadian Journal of Chemistry; vol. 59; (1981); p. 1291 - 1296, View in Reaxys 119 of 131

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

hexane

Partner (Association (MCS))

tributyl-amine

Anunziata, J.; Singh, J.; Silber, J. J.; Canadian Journal of Chemistry; vol. 59; (1981); p. 1291 - 1296, View in Reaxys 120 of 131

Description (Association (MCS))

Enthalpy of association

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

1,3,5-trinitrobenzene

Tsvetkov, V. G.; Kupriyanov, V. F.; Vesnovskii, B. P.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 7; (1981); p. 1456 - 1459,1235 - 1238, View in Reaxys 121 of 131

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CHCl3

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

naphthalene

Kampar, V. E.; Gudele, I. Ya.; Kampare, R. B.; Valtere, S. P.; Neiland, O. Ya.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 11; (1981); p. 2553 - 2557,2201 - 2204, View in Reaxys 122 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Partner (Association (MCS))

α-cyclodextrin

Yamaguchi, Hiroyuki; Abe, Suemi; Journal of Physical Chemistry; vol. 85; nb. 12; (1981); p. 1640 - 1643, View in Reaxys 123 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

Eu(fod)3

Raber, Douglas J.; Johnston, Milton D.; Campbell, Catherine M.; Guida, Anne; Jackson, George F.; et al.; Monatshefte fuer Chemie; vol. 111; (1980); p. 43 - 52, View in Reaxys 124 of 131

Description (Association (MCS))

IR spectrum of the complex

Partner (Association (MCS))

hydrogen cyanide

Pacansky, J.; Coufal, H.; Journal of Physical Chemistry; vol. 84; nb. 24; (1980); p. 3238 - 3242, View in Reaxys 125 of 131

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

acetonitrile; various solvent(s)

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Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

mercury electrode

Wegert, H.; Baumgaertel, H.; Berichte der Bunsen-Gesellschaft; vol. 84; nb. 3; (1980); p. 274 - 277, View in Reaxys 126 of 131

Description (Association (MCS))

Association with compound

Aitken; Gilkerson; Journal of the American Chemical Society; vol. 95; (1973); p. 8551, View in Reaxys; Tran Ha-Phuong et al.; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 12; (1972); p. 234, View in Reaxys; Jawed; Bulletin of the Chemical Society of Japan; vol. 50; (1977); p. 2602, View in Reaxys; Bystrov; Nazarov; Doklady Physical Chemistry; vol. 148-153; (1963); p. 161; Doklady Akademii Nauk SSSR; vol. 148; (1963); p. 1335, View in Reaxys; Laurence; Wojtkowiak; Bulletin de la Societe Chimique de France; (1968); p. 2780, View in Reaxys; Persoons; Jungers; Bulletin de la Societe Chimique de France; (1968); p. 2729, View in Reaxys; Taylor; Kuntz Jun.; Journal of the American Chemical Society; vol. 91; (1969); p. 4006, View in Reaxys 127 of 131

Description (Association (MCS))

Stability constant of the complex with ...

Borisenko; Shchepkin; Optics and Spectroscopy; vol. 29; (1970); p. 24; ; p. 46, View in Reaxys; Gurka; Taft; Journal of the American Chemical Society; vol. 91; (1969); p. 4794,4797, 4798, View in Reaxys; Clark; Kolb; Journal of Organic Chemistry; vol. 42; (1977); p. 359,360, View in Reaxys; Jawed; Bulletin of the Chemical Society of Japan; vol. 50; (1977); p. 2602, View in Reaxys 128 of 131

Description (Association (MCS))

Enthalpy of association

Jawed; Bulletin of the Chemical Society of Japan; vol. 50; (1977); p. 2602, View in Reaxys; Rossarie et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 74; (1977); p. 188,189,195, View in Reaxys; Genkin et al.; Doklady Physical Chemistry; vol. 160-165; (1965); p. 732; Doklady Akademii Nauk SSSR; vol. 164; (1965); p. 1089, View in Reaxys 129 of 131

Description (Association (MCS))

Further physical properties of the complex

Kupletskaya et al.; Moscow University Chemistry Bulletin (English Translation); vol. 31; nb. 2; (1976); p. 72; ; p. 219, View in Reaxys 130 of 131

Description (Association (MCS))

Dipole moment of the complex

Baraton; Journal of Molecular Structure; vol. 10; (1971); p. 231,233, View in Reaxys 131 of 131

Description (Association (MCS))

Spectrum of the complex

Detoni et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 2851,2852, View in Reaxys; Hatton; Richards; Molecular Physics; vol. 5; (1962); p. 139; Chem.Abstr.; nb. 791; (1959), View in Reaxys Azeotropes (MCS) (23) 1 of 23

Lekhova; Belousova; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 1627; ; p. 2719, View in Reaxys

2 of 23

Azeotropes

cineol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 3 of 23

Azeotropes

phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 4 of 23

Azeotropes

iodobenzene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 5 of 23

Azeotropes

#m!-cresol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 6 of 23

Azeotropes

#o!-cresol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 7 of 23

Azeotropes

#p!-cresol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 8 of 23

Azeotropes

octanol-(1)

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Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 9 of 23

Azeotropes

dibutyl sulfide

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 10 of 23

Azeotropes

2-bromo-toluene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 11 of 23

Azeotropes

3-bromo-toluene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 12 of 23

Azeotropes

4-bromo-toluene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 13 of 23

Azeotropes

dipentyl ether

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 14 of 23

Azeotropes

(+-)-octanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 15 of 23

Azeotropes

diisopentyl ether

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 16 of 23

Azeotropes

ethyl-benzyl ether

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 17 of 23

Azeotropes

#O!-methyl-isoborneol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 18 of 23

Azeotropes

4-chloro-1-bromo-benzene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 19 of 23

Azeotropes

acetic acid phenyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 20 of 23

Azeotropes

carbamic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 21 of 23

Azeotropes

#O!-methyl-diethylene glycol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 22 of 23

Azeotropes

butyric acid isopentyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 23 of 23

Azeotropes

isovaleric acid isopentyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys Boundary Surface Phenomena (MCS) (1) 1 of 1

Description (Boundary Surface Phenomena (MCS))

Further surface properties

Partner (Boundary Surface Si(100) Phenomena (MCS)) Tao, Feng; Wang, Zhong Hai; Xu, Guo Qin; Journal of Physical Chemistry B; vol. 106; nb. 14; (2002); p. 3557 - 3563, View in Reaxys Chromatographic Data (4) Chromatographic Location data TLC (Thin layer chromatography)

References

supporting informa- Quinn, Dylan J.; Haun, Graham J.; Moura-Letts, Gustavo; Tetrahedron Letters; vol. 57; nb. tion 34; (2016); p. 3844 - 3847, View in Reaxys

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HPLC (High performance liquid chromatography)

supporting informa- Gao, Lingfeng; Tang, Haoming; Wang, Zhiyong; Chemical Communications; vol. 50; nb. 31; tion (2014); p. 4085 - 4088, View in Reaxys

GC (Gas chromatography)

Collins, Karl D.; Glorius, Frank; Tetrahedron; vol. 69; nb. 36; (2013); p. 7817 - 7825, View in Reaxys

HPLC (High performance liquid chromatography)

Voeroes, Attila; Baan, Zoltan; Mizsey, Peter; Finta, Zoltan; Organic Process Research and Development; vol. 16; nb. 11; (2012); p. 1717 - 1726, View in Reaxys

Circular Dichroism (1) References Saeva et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 7660,7662, View in Reaxys Compressibility (3) Description (Com- Comment (Compressibility) pressibility)

References

Isothermal compressibility

Uosaki, Yasuhiro; Matsumura, Hajime; Ogiyama, Hideki; Moriyoshi, Takashi; Journal of Chemical Thermodynamics; vol. 22; nb. 7; (1990); p. 797 - 801, View in Reaxys

Adiabatic compressibility

Lucas et al.; Molecular Physics; vol. 18; (1970); p. 505,511,513,515,519,520, View in Reaxys; Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys

Adiabatic compres- aus der SchallBhimasenachar; Venkateswarlu; Proceedings - Indian Academy of Sciences, Section A; nb. 11; sibility geschwindigkeit er- (1940); p. 28,29, View in Reaxys mittelt. Conformation (1) Object of Investiga- References tion Conformation

van Es; Journal of the Chemical Society; (1965); p. 3881, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1976); p. 429, View in Reaxys

Critical Temperature (1) Critical TemperaReferences ture [°C] 14.05 Crystal Phase (3) Description (Crystal Phase) Crystal structure determination

Baranowska-Majgier, Helena; Pyzuk, Wieslaw; Jeute, Wojciech; Ziolo, Jerzy; Journal of Chemical & Engineering Data; vol. 26; nb. 1; (1981); p. 51 - 53, View in Reaxys Comment (Crystal Phase)

References

.; Method of determination: Electron Diffraction

Portalone, Gustavo; Domenicano, Aldo; Schultz, Gyoergy; Hargittai, Istvan; Journal of Molecular Structure; vol. 160; (1987); p. 97 - 108, View in Reaxys

Crystal structure determination

Fauvet et al.; Acta Crystallographica, Section B: Structural Crystallography and Crystal Chemistry; vol. 34; (1978); p. 1376, View in Reaxys

Crystal habit

Veracini et al.; Molecular Physics; vol. 23; (1972); p. 59, View in Reaxys

Crystal Property Description (6) Colour & Other Location Properties

References

colourless

Patent; (18 pag.); CN107573259; (2018); (A) Chinese, View in Reaxys

Paragraph 0059

colourless

Song, Ren-Jie; Wu, Ji-Cheng; Liu, Yu; Deng, Guo-Bo; Wu, Cui-Yan; Wei, Wen-Ting; Li, Jin-Heng; Synlett; vol. 23; nb. 17; (2012); p. 2491 - 2496,6, View in Reaxys; Jasem, Yosef Al; Barkhad, Mohamed; Khazali, Mona Al; Butt, Hifsa Pervez; El-Khwass, Noha Ashraf; Azani, Mariam Al; Hindawi, Bassam Al; Thiemann, Thies; Journal of Chemical Research; vol. 38; nb. 2; (2014); p. 80 - 84, View in Reaxys

colourless

Saha, Debasree; Saha, Amit; Ranu, Brindaban C.; Tetrahedron Letters; vol. 50; nb. 44; (2009); p. 6088 - 6091, View in Reaxys; Telvekar, Vikas N.; Sasane, Kulbhushan A.; Synlett; nb. 18; (2010); p. 2778 - 2780, View in Reaxys; Rokade, Balaji V.; Prabhu, Kandikere Ramaiah; Journal of Organic Chemistry; vol. 77; nb. 12; (2012); p. 5364 - 5370, View in Reaxys

colourless

supporting informa- Zhu, Chenjie; Ji, Lei; Wei, Yunyang; Synthesis; nb. 18; (2010); p. 3121 - 3125, View in Reaxys; tion Zhu, Chenjie; Sun, Chengguo; Wei, Yunyang; Synthesis; nb. 24; (2010); p. 4235 - 4241; Art.No: F14610SS, View in Reaxys; Rokade, Balaji V.; Malekar, Sanjeev K.; Prabhu, Kandi-

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kere Ramaiah; Chemical Communications; vol. 48; nb. 44; (2012); p. 5506 - 5508, View in Reaxys colourless

supporting informa- Azath, Ismail Abulkalam; Suresh, Palaniswamy; Pitchumani, Kasi; New Journal of Chemistion try; vol. 36; nb. 11; (2012); p. 2334 - 2339, View in Reaxys

yellow

supporting informa- Allen, C. Liana; Burel, Celine; Williams, Jonathan M.J.; Tetrahedron Letters; vol. 51; nb. 20; tion (2010); p. 2724 - 2726, View in Reaxys

Decomposition (1) 1 of 1

Eland; Schulte; Journal of Chemical Physics; vol. 62; (1975); p. 3835, View in Reaxys

Dielectric Constant (8) Dielectric Constant Temperature (Dielectric Constant) [°C]

References

Schlossarczyk,H. et al.; Helvetica Chimica Acta; vol. 56; (1973); p. 875 - 944, View in Reaxys; Zaugg; Journal of the American Chemical Society; vol. 82; (1960); p. 2903,2905, View in Reaxys; Brown; Ives; Journal of the Chemical Society; (1962); p. 1608,1617, View in Reaxys; Boyer; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 262; (1966); p. 1449, View in Reaxys; Hartmann; Schmidt; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 62; (1968); p. 312, View in Reaxys; Hanson et al.; Journal of Applied Chemistry and Biotechnology; vol. 25; (1975); p. 727,728, View in Reaxys; Chastrette; Tetrahedron; vol. 35; (1979); p. 1441,1442, View in Reaxys; Mataga et al.; Bulletin of the Chemical Society of Japan; vol. 39; (1966); p. 2562, View in Reaxys; Gutmann; Chimia; vol. 31; (1977); p. 1,2, View in Reaxys; Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys; Decroocq; Jungers; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 252; (1961); p. 1454,1455, View in Reaxys; Tanaka; Ogata; Inorganic and Nuclear Chemistry Letters; vol. 10; (1974); p. 511,514, View in Reaxys; Eloranta; Kadaba; Transactions of the Faraday Society; vol. 66; (1970); p. 817,819, View in Reaxys; Weisbecker; Rouquie; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 68; (1971); p. 910, View in Reaxys; Tachikawa; Bard; Chemical Physics Letters; vol. 26; (1974); p. 246,250, View in Reaxys; Levin; Petrosyan; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 908; ; p. 1601, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys; Park; Bard; Journal of the American Chemical Society; vol. 97; (1975); p. 2978,2980, View in Reaxys; Jain; Soundararajan; Journal of Inorganic and Nuclear Chemistry; vol. 26; (1964); p. 1255,1257, View in Reaxys 25.58

Timmermans et al.; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 5,19, View in Reaxys

25.56 - 23.08

20 - 50

Fischer; Zeitschrift fuer Physik; vol. 127; (1950); p. 49,59, View in Reaxys

Le Fevre; Russell; Journal of the Chemical Society; (1936); p. 496,497, View in Reaxys; LeFevre; LeFevre; Journal of the Chemical Society; (1936); p. 487,490, View in Reaxys

Martin; Transactions of the Faraday Society; vol. 30; (1934); p. 759,761; Transactions of the Faraday Society; vol. 33; (1937); p. 191,192, 194, View in Reaxys

25.2

Sugden; Journal of the Chemical Society; (1933); p. 768,773, View in Reaxys

27.6 - 22.1

0 - 70

Ball; Journal of the Chemical Society; (1930); p. 570,596, View in Reaxys

26.3

Koch; Journal of the Chemical Society; (1928); p. 272, View in Reaxys

Dissociation Energy (1) Dissociation Ener- Bond Type gy [Jmol-1] 561031

Ph-CN

References Galli, Carlo; Gentili, Patrizia; Acta Chemica Scandinavica; vol. 52; nb. 1; (1998); p. 67 - 76, View in Reaxys

Dissociation Exponent (5) 1 of 5

Dissociation Exponent (pK)

Type (Dissociation Exponent)

a1/apparent

Vleggaar, Robert; Zeevaart, Jacob G.; Tetrahedron Letters; vol. 40; nb. 52; (1999); p. 9301 - 9303, View in Reaxys 2 of 5

Dissociation Exponent (pK)

1.06

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Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

1,1,1-trichloro-ethane

Type (Dissociation Exponent)

b1/apparent

Abraham, Michael H.; Duce, Philip P.; Prior, David V.; Barratt, Derek G.; Morris, Jeffrey J.; Taylor, Peter J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1989); p. 1355 - 1376, View in Reaxys 3 of 5

Dissociation Exponent (pK)

38.1

Dissociation Group

C-H

Temperature (Dissociation Exponent) [°C]

-78

Solvent (Dissociation Exponent)

tetrahydrofuran

Method (Dissociation Exponent)

spectrophotometric

Type (Dissociation Exponent)

a1/apparent

Fraser, Robert R.; Bresse, Monique; Mansour, Tarek S.; Journal of the American Chemical Society; vol. 105; nb. 26; (1983); p. 7790 - 7791, View in Reaxys 4 of 5

Comment (Dissociation Exponent)

(pk')pK(HB)

Martin et al.; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 797,799, View in Reaxys 5 of 5

Comment (Dissociation Exponent)

(pk')pK(A)H2O

Martin et al.; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 797,799, View in Reaxys Dynamic Viscosity (10) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

References

0.01063 - 0.01148

30 - 35

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys

0.00891 - 0.01196

24.9 - 44.9

Gill, Dip Singh; Singh, Parvinder; Singh, Jasbir; Singh, Pritam; Senanayake, Gamini; Hefter, Glenn T.; Journal of the Chemical Society, Faraday Transactions; vol. 91; nb. 17; (1995); p. 2789 - 2796, View in Reaxys

0.011958

24.9

Gill, Dip Singh; Singh, Rajinder; Ali, Vazid; Singh, Jasbir; Rehani, Sharwan Kumar; Journal of the Chemical Society, Faraday Transactions; vol. 90; nb. 4; (1994); p. 583 - 586, View in Reaxys

1.2E-05

Ho, Patience C.; Ramsey, J. B.; Journal of Chemical & Engineering Data; vol. 31; nb. 4; (1986); p. 430 - 434, View in Reaxys

0.003023 - 0.01471

19.7 - 180.7

Friend; Hargreaves; Phil. Mag.; vol. <7> 35; (1944); p. 619,628, View in Reaxys

0.01111

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

0.01447

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

0.00666 - 0.0194

0 - 70

Martin; Journal of the Chemical Society; (1928); p. 3277, View in Reaxys

0.005151 - 0.01957

0.3 - 100

Bingham; van Klooster; Kleinspehn; Journal of Physical Chemistry; vol. 24; (1920); p. 10, View in Reaxys

0.0125

Dunstan; Hilditch; Thole; Journal of the Chemical Society; vol. 103; (1913); p. 140, View in Reaxys

Electrical Data (28)

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2018-05-24 12:11:44

1 of 28

Description (Electrical Da- Dielectric loss ta) Boyer; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 262; (1966); p. 1449, View in Reaxys; Eloranta; Kadaba; Transactions of the Faraday Society; vol. 66; (1970); p. 817,819, View in Reaxys; Davies et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 75; (1979); p. 1428,1432, 1436, 1437, View in Reaxys; Levin; Petrosyan; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 908; ; p. 1601, View in Reaxys; Buchner; Barthel; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 101; nb. 10; (1997); p. 1509 - 1516, View in Reaxys; Barthel, Josef; Buchner, Richard; Hoelzl, Christian G.; Muensterer, Michael; Zeitschrift fur Physikalische Chemie; vol. 214; nb. 9; (2000); p. 1213 - 1231, View in Reaxys

2 of 28

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) temperature dependence Barthel, Josef; Buchner, Richard; Hoelzl, Christian G.; Muensterer, Michael; Zeitschrift fur Physikalische Chemie; vol. 214; nb. 9; (2000); p. 1213 - 1231, View in Reaxys

3 of 28

Description (Electrical Da- Dielectric relaxation time ta) Eloranta; Kadaba; Transactions of the Faraday Society; vol. 66; (1970); p. 817,819, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys; Fedotov, A. N.; Isaeva, E. S.; Gol'dshtein, I. P.; Russian Journal of Physical Chemistry; vol. 65; nb. 9; (1991); p. 1320 - 1324; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2501 - 2510, View in Reaxys; Buchner; Barthel; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 101; nb. 10; (1997); p. 1509 - 1516, View in Reaxys

4 of 28

Description (Electrical Da- Cole-Cole diagram ta) Poley; Appl. scient. Res.; vol. 4; (1955); p. 337,370, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys; Firman, P.; Marchetti, A.; Xu, M.; Eyring, Edward M.; Petrucci, S.; Journal of Physical Chemistry; vol. 95; nb. 18; (1991); p. 7055 - 7061, View in Reaxys

5 of 28

Description (Electrical Da- Dielectric anisotropy ta) Zboinski et al.; Chemical Physics; vol. 40; (1979); p. 77,83, View in Reaxys; Zboinski; Chemical Physics Letters; vol. 39; (1976); p. 336, View in Reaxys

6 of 28

Description (Electrical Da- Electrical properties ta) McIntyre; Hameka; Journal of Chemical Physics; vol. 70; (1979); p. 2215,2216, View in Reaxys

7 of 28

Description (Electrical Da- Relaxation frequency ta) Anderson; Ullman; Journal of Chemical Physics; vol. 55; (1971); p. 4406, View in Reaxys

8 of 28

Description (Electrical Da- Electrical conductivity ta) Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 46; (1903); p. 174; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 54; (1906); p. 163, View in Reaxys; Patten; Journ. Physical Chem.; vol. 6; p. 568, View in Reaxys; Walden; Birr; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 107,112, View in Reaxys; Wertyporoch; Altmann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 1,15, View in Reaxys; Lincoln; Journ. Physical Chem.; vol. 3; p. 469, View in Reaxys; Janz; Ahmad; Venkatasetty; Journal of Physical Chemistry; vol. 68; (1964); p. 889,891, View in Reaxys; Peach; Waddington; Journal of the Chemical Society; (1962); p. 600,601, View in Reaxys; Silberman et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2040,1908, View in Reaxys; Rybakow; Sil'berman; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 466,458; Chem.Abstr.; vol. 466, View in Reaxys

9 of 28

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von unverduenntem Benzonitril bei 21grad/0.80-3.99 cm. Poley; Appl. scient. Res.; vol. 4; (1955); p. 337,369, View in Reaxys

10 of 28

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) bei 21grad/1.25 cm, 3.20 cm und 3.99 cm. Poley; Appl. scient. Res.; vol. 4; (1955); p. 337,370, View in Reaxys

89/225

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11 of 28

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) in CCl4 bei 14grad. Le Fevre; Sullivan; Journal of the Chemical Society; (1954); p. 2873,2876, View in Reaxys

12 of 28

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) in CCl4 bei 25grad und 42/63 MHz. Fischer; Fessler; Zeitschrift fuer Naturforschung; vol. 8 a; (1953); p. 177,181, 182, View in Reaxys

13 of 28

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) in CCl4 bei 25grad und 42grad. Fischer; Fessler; Zeitschrift fuer Naturforschung; vol. 8 a; (1953); p. 177,181, 182, View in Reaxys

14 of 28

Description (Electrical Da- Photoelectricity (Becquerel effect) ta) Comment (Electrical Data) von in Aethanol geloestem Benzonitril. Levin et al.; Journal of Chemical Physics; vol. 21; (1953); p. 1654,1655, View in Reaxys

15 of 28

Description (Electrical Da- Electrical conductivity ta) Electric Conductivity [S/cm]

2.5E-06

Temperature of Electric Conductivity [°C]

vol. P: MVol.C; 1, page 432 - 450, View in Reaxys; Payne, D. S.; J. Chem. Soc.; (1953); p. 1052 - 1055 ; (from Gmelin), View in Reaxys 16 of 28

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von unverduenntem Benzonitril bei 20-50grad. Fischer; Zeitschrift fuer Physik; vol. 127; (1950); p. 49,59, View in Reaxys

17 of 28

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) in Benzol bei 23grad. Fischer; Zeitschrift fuer Naturforschung; vol. 4 a; (1949); p. 707,716; Naturwissenschaften; vol. 43; (1956); p. 153, View in Reaxys

18 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von binaeren Gemischen mit Siliciumchlorid, Zinn(IV)-chlorid und Titan(IV)-chlorid. Wertyporoch; Altmann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 1,15, View in Reaxys

19 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) mit Aluminiumbromid. Wertyporoch; Adamus; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 31,34, 35, 40, View in Reaxys

20 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Kaliumjodid, Natriumjodid, Lithiumjodid, Lithiumbromid und Silbernitrat in Benzonitril bei verschiedenen Temperaturen. Davies; Journal of the Chemical Society; (1933); p. 647, View in Reaxys; Martin; Journal of the Chemical Society; (1928); p. 3277, View in Reaxys

90/225

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21 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Silbernitrat in Benzonitril bei 25grad. Koch; Journal of the Chemical Society; (1928); p. 279,526, View in Reaxys; Mueller; Griengl; Mollang; Monatshefte fuer Chemie; vol. 47; (1926); p. 102, View in Reaxys

22 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) bei 25grad. Koch; Journal of the Chemical Society; (1928); p. 272, View in Reaxys; Mueller,R.; Griengl; Mollang; Monatshefte fuer Chemie; vol. 47; (1926); p. 87, View in Reaxys; Martin; Journal of the Chemical Society; (1928); p. 3277, View in Reaxys

23 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Trimethyl-p-tolyl-ammoniumjodid in Benzonitril bei 25grad. Creighton; Way; J. Franklin Inst.; vol. 186; (1918); p. 693; Chem. Zentralbl.; vol. 91; nb. III; (1920); p. 43, View in Reaxys

24 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Natriumjodid in Benzonitril bei 25grad. Kraus; Bray; Journal of the American Chemical Society; vol. 35; (1913); p. 1379, View in Reaxys

25 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) anorganischer Salze in Benzonitril. Shaw; Journal of Physical Chemistry; vol. 17; (1913); p. 170, View in Reaxys

26 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Piperidinpikrat in Benzonitril. Walden; Chem. Zentralbl.; vol. 84; nb. II; (1913); p. 331, View in Reaxys

27 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Tetrapropylammoniumjodid in Benzonitril. Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 274; Chem. Zentralbl.; vol. 84; nb. II; (1913); p. 209, View in Reaxys

28 of 28

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) einiger Polyjodide in Benzonitril. Dawson; Leslie; Journal of the Chemical Society; vol. 99; (1911); p. 1602, View in Reaxys

Electrical Moment (63) 1 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.42

Comment (Electrical Moment)

excited state

Kawski; Kuklinski; Bojarski; Chemical Physics Letters; vol. 419; nb. 4-6; (2006); p. 309 - 312, View in Reaxys 2 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.21

Borovikov; Makovetskii; Pivovarova; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 1; (1996); p. 33 - 38, View in Reaxys

91/225

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3 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

solvent dependence

Ivanov; Prezhdo; Tarasova; Kurskaya; Tyurin; Russian Journal of General Chemistry; vol. 66; nb. 5; (1996); p. 722 - 731, View in Reaxys 4 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.9

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

neat (no solvent)

Cheng, Lap-Tak; Tam, Wilson; Stevenson, Sylvia H.; Meredith, Gerald R.; Rikken, Geert; Marder, Seth R.; Journal of Physical Chemistry; vol. 95; nb. 26; (1991); p. 10631 - 10643, View in Reaxys 5 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.8

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

various solvent(s)

Fedotov, A. N.; Isaeva, E. S.; Gol'dshtein, I. P.; Russian Journal of Physical Chemistry; vol. 65; nb. 9; (1991); p. 1320 - 1324; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2501 - 2510, View in Reaxys 6 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.4

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

dioxane

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.5

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

CCl4

92/225

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8 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.6

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

benzene

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.1

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

pentane

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.39

Temperature (Electrical Moment) [°C]

Tarasova, G. V.; Khashchina, M. V.; Tyurin, S. A.; Bulgarevich, S. B.; Bogdan, I. G.; Russian Journal of Physical Chemistry; vol. 60; nb. 8; (1986); p. 1235 - 1237; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 2058 - 2061, View in Reaxys 11 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.07

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

CCl4

Austerheim, Asmund; Gramstad, Thor; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 39; nb. 7; (1985); p. 583 - 588, View in Reaxys 12 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.49

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

acetonitrile

93/225

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Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 13 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.62

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

nitromethane

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 14 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.63

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

dimethylformamide

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 15 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.67

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

dimethylsulfoxide

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 16 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.96

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

various solvent(s)

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 17 of 63

Description (Electrical Moment)

Dipole moment

94/225

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Moment (Electrical Moment) [D]

2.48

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

diethylamine

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 18 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.54

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

methyl acetate

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 19 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.26

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

diethyl ether

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 20 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.61

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

triethylamine

Prezhdo, V. V.; Tarasova, G. V.; Prezhdo, L. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2553 2559,2267 - 2272, View in Reaxys 21 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

12.3

Temperature (Electrical Moment) [°C]

95/225

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Solvent (Electrical Moment)

benzene

Exner, Otto; Folli, Ugo; Marcaccioli, Sergio; Vivarelli, Piero; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1983); p. 757 - 760, View in Reaxys 22 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

12.4

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

12.71

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Deshpande, D. K.; Shashidbar, M. A.; Rao, K. Suryanarayana; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 262; nb. 4; (1981); p. 588 - 592, View in Reaxys 24 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.93

Gordon, Michael, D.; Tetrahedron; vol. 36; nb. 88; (1980); p. 2113 - 2118, View in Reaxys 25 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Weisbecker; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 274; (1972); p. 451,453, View in Reaxys; Hanson et al.; Journal of Applied Chemistry and Biotechnology; vol. 25; (1975); p. 727,728, View in Reaxys; Chastrette; Tetrahedron; vol. 35; (1979); p. 1441,1442, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1976); p. 429, View in Reaxys; Weisbecker; Rouquie; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 68; (1971); p. 910, View in Reaxys; Uzhinov; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 2; (1971); p. 82; ; p. 234, View in Reaxys; Juchnowski; Welew; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 4; (1971); p. 333,339, View in Reaxys 26 of 63

Description (Electrical Moment)

Dipole moment

Pancir et al.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 3039,3047, View in Reaxys; Cumper et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 537, View in Reaxys; Weisbecker; Rouquie; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 1059,1062, View in Reaxys; Baraton; Journal of Molecular Structure; vol. 10; (1971); p. 231,233, View in Reaxys; Gramstad; Tjessem; Journal of Molecular Structure; vol. 41; (1977); p. 231,233, 235, 236, View in Reaxys; Vysotskii; Journal of Structural Chemistry; vol. 19; (1978); p. 27,31; ; p. 34, View in Reaxys; Boldeskul et al.; Optics and Spectroscopy; vol. 29; (1970); p. 142; ; p. 270, View in Reaxys; Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys; Cumper; Tetrahedron; vol. 25; (1969); p. 3131, View in Reaxys 27 of 63

Description (Electrical Moment)

Dipole moment

96/225

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Comment (Electrical Moment)

in Hexan, Cyclohexan, CCl4, Benzol, Toluol, CS2

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 28 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Oktansaeureloesung

Grunwald; Journal of the American Chemical Society; vol. 98; (1976); p. 1351,1352, View in Reaxys 29 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ, S.572 nach Ref. 8: J. W. Smith, 'Electric Dipole Moments', Butterworths, London, 1955, p. 209, 215

Colinese et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 570, View in Reaxys 30 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

3.97

Jain; Walker; Journal of Physical Chemistry; vol. 75; (1971); p. 2942, View in Reaxys 31 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

angeregte Zustaende

Huang; Lombardi; Journal of Chemical Physics; vol. 55; (1971); p. 4072, View in Reaxys 32 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (S.109)

Coates; Journal of the Society of Dyers and Colourists; vol. 83; (1967); p. 95, View in Reaxys 33 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

rein

Weaver; Parry; Inorganic Chemistry; vol. 5; (1966); p. 703,708, View in Reaxys 34 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Lsg.

Weaver; Parry; Inorganic Chemistry; vol. 5; (1966); p. 703,708, View in Reaxys 35 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

3.99 D <α; p-Xylol; 15grad u. 60grad bzw. α; Cyclohexan; 15grad>

Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys 36 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

(Dampf): 4.39 D

Charton; Journal of Organic Chemistry; vol. 26; (1961); p. 735, View in Reaxys 37 of 63

Description (Electrical Moment)

Dipole moment

97/225

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Comment (Electrical Moment)

μ = 3.9 D

Zaugg; Journal of the American Chemical Society; vol. 82; (1960); p. 2903,2905, View in Reaxys 38 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

(α; Bzl.): 4.05 D

Cumper; Vogel; Journal of the Chemical Society; (1960); p. 4723,4725, View in Reaxys 39 of 63

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

3.97 D

Schorygin et al.; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 335,338; engl. Ausg.; p. 157, View in Reaxys 40 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.08

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

cyclohexane

Brown; Journal of the American Chemical Society; vol. 81; (1959); p. 3232,3233, View in Reaxys 41 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

del Re; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. <8> 22; (1957); p. 491,493, View in Reaxys 42 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.99

Method (Electrical Moment)

Dielectric constant (α)

Osipow; Zhurnal Fizicheskoi Khimii; vol. 31; (1957); p. 1542,1544; Chem.Abstr.; (1958); p. 5911, View in Reaxys 43 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.39

Solvent (Electrical Moment)

neat (no solvent)

Le Fevre; Rao; Australian Journal of Chemistry; vol. 8; (1955); p. 140, View in Reaxys; Buckingham; Le Fevre; Journal of the Chemical Society; (1952); p. 1932,1935, View in Reaxys 44 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.14

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Method (Electrical Moment)

Stark effect

Lide; Journal of Chemical Physics; vol. 22; (1954); p. 1577, View in Reaxys 45 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.02

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

CCl4

Le Fevre; Le Fevre; Journal of the Chemical Society; (1954); p. 1577,1581; Australian Journal of Chemistry; vol. 7; (1954); p. 33,35, View in Reaxys 46 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.05

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Everard et al.; Journal of the Chemical Society; (1951); p. 2807,2812, View in Reaxys 47 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.26

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Jaffe; Journal of Chemical Physics; vol. 8; (1940); p. 879,887, View in Reaxys; Boettcher; Physica; vol. 6; (1939); p. 59,67, View in Reaxys 48 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.4

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Jaffe; Journal of Chemical Physics; vol. 8; (1940); p. 879,887, View in Reaxys; Boettcher; Physica; vol. 6; (1939); p. 59,67, View in Reaxys 49 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.02

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

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Cowley; Partington; Journal of the Chemical Society; (1936); p. 1184,1185, 1193, View in Reaxys 50 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.37

Method (Electrical Moment)

Dielectric constant (α)

Groves; Sugden; Journal of the Chemical Society; (1935); p. 971,972; Journal of the Chemical Society; (1937); p. 1992,1996, View in Reaxys 51 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.37

Temperature (Electrical Moment) [°C]

109.9

Groves; Sugden; Journal of the Chemical Society; (1934); p. 1094,1097; Journal of the Chemical Society; (1935); p. 972, View in Reaxys 52 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.84

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Martin; Transactions of the Faraday Society; vol. 30; (1934); p. 759,761; Transactions of the Faraday Society; vol. 33; (1937); p. 191,192, 194, View in Reaxys 53 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.94

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Wolf; Strasser; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 21; (1933); p. 389,402, View in Reaxys; Poltz; Steil; Strasser; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 17; (1932); p. 155,156, View in Reaxys 54 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.94

Temperature (Electrical Moment) [°C]

Poltz; Steil; Strasser; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 17; (1932); p. 156, View in Reaxys 55 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.91

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Temperature (Electrical Moment) [°C]

20.6

Bergmann; Engel; Sandor; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 10; (1930); p. 411, View in Reaxys 56 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.88

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Hassel; Naeshagen; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 8; (1930); p. 357,361 Anm. 2, View in Reaxys 57 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.92

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Hassel; Naeshagen; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 8; (1930); p. 357,361 Anm. 2, View in Reaxys 58 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.93

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Hassel; Naeshagen; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 8; (1930); p. 357,361 Anm. 2, View in Reaxys 59 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.91

Temperature (Electrical Moment) [°C]

20.6

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Bergmann; Engel; Sandor; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 10; (1930); p. 397,412, View in Reaxys 60 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.9

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Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (α)

Solvent (Electrical Moment)

benzene

Eide; Hassel; Tidsskr. Kjemi Bergv.; vol. 10; (1930); p. 93, View in Reaxys 61 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.88

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

Werner; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 4; (1929); p. 382,397, View in Reaxys; Eide; Hassel; Chem. Zentralbl.; vol. 101; nb. II; (1930); p. 2234, View in Reaxys; Hassel; Naeshagen; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 8; (1930); p. 361, View in Reaxys 62 of 63

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.92

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.93

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Optical anisotropy

Le Fevre; Rao; Journal of the Chemical Society; (1958); p. 1465, View in Reaxys; Le Fevre; Le Fevre; Journal of the Chemical Society; (1954); p. 1577,1581; Australian Journal of Chemistry; vol. 7; (1954); p. 33,35, View in Reaxys; Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 626, View in Reaxys; Lucas et al.; Molecular Physics; vol. 18; (1970); p. 505,511,513,515,519,520, View in Reaxys; Flory, Paul J.; Navard, Patrick; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 82; (1986); p. 3381 - 3390, View in Reaxys

Atom polarization

Rao; Thyagarajan; Indian Journal of Pure and Applied Physics; vol. 12; (1974); p. 242, View in Reaxys; Austerheim, Asmund; Gramstad, Thor; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 39; nb. 7; (1985); p. 583 - 588, View in Reaxys

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Molar polarization

LeFevre; Journal of the Chemical Society; (1965); p. 2499,2500,2502,2503, View in Reaxys; Jain; Soundararajan; Journal of Inorganic and Nuclear Chemistry; vol. 26; (1964); p. 1255,1257, View in Reaxys

Electrochemical Behaviour (8) Description (Elec- Comment (Electrotrochemical Behav- chemical Behaviour) iour)

References

Basicity

Coetzee; McGuire; Journal of Physical Chemistry; vol. 67; (1963); p. 1810, View in Reaxys; Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Acidity

Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Thermodynamic parameters for dissociation / protonation

Meot-Ner (Mautner), Michael; Kafafi, Sherif A.; Journal of the American Chemical Society; vol. 110; nb. 19; (1988); p. 6297 - 6303, View in Reaxys

Electrolytic dissociation / protonation equilibrium

Holcman; Sehested; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 71; (1975); p. 1211,1212, View in Reaxys; Fraser, Robert R.; Bresse, Monique; Mansour, Tarek S.; Journal of the American Chemical Society; vol. 105; nb. 26; (1983); p. 7790 - 7791, View in Reaxys

Proton affinity

Lau; Kebarle; Journal of the American Chemical Society; vol. 98; (1976); p. 7452, View in Reaxys; Freiser; Beauchamp; Journal of the American Chemical Society; vol. 99; (1977); p. 3214, View in Reaxys; Keough, T.; DeStefano, A. J.; Organic Mass Spectrometry; vol. 16; nb. 12; (1981); p. 527 - 533, View in Reaxys

Electrochemical properties

Romanin et al.; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 88; (1978); p. 175,177,180, View in Reaxys; Baranski; Fawcett; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 100; (1979); p. 185,188, View in Reaxys

Polarography

Sewast'janowa; Tomilow; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 2815,2741, View in Reaxys; Pozdeeva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 45; (1975); p. 172,157,158-161, View in Reaxys; Smirnow et al.; Zhurnal Organicheskoi Khimii; vol. 5; (1969); p. 1392,1359, View in Reaxys; Anthoine et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 465, View in Reaxys

Electrolytic dissoci- in wasserfreier ation / protonation H2SO4 bei 25grad. equilibrium

Liler; Kosanovic; Journal of the Chemical Society; (1958); p. 1084,1086,1088,1090, View in Reaxys

Electrochemical Characteristics (18) 1 of 18

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Scialdone, Onofrio; Filardo, Giuseppe; Galia, Alessandro; Mantione, Davide; Silvestri, Giuseppe; Acta Chemica Scandinavica; vol. 53; nb. 10; (1999); p. 800 - 806, View in Reaxys 2 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

1-methyl-pyrrolidin-2-one

Scialdone, Onofrio; Filardo, Giuseppe; Galia, Alessandro; Mantione, Davide; Silvestri, Giuseppe; Acta Chemica Scandinavica; vol. 53; nb. 10; (1999); p. 800 - 806, View in Reaxys 3 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-2 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: vs. SCE; 500 mV/s; TBAF supporting electrolite

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Product

cyanobenzene

Galli, Carlo; Gentili, Patrizia; Acta Chemica Scandinavica; vol. 52; nb. 1; (1998); p. 67 - 76, View in Reaxys 4 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Kowert et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 5538, View in Reaxys; Krasnomolova et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 44; ; p. 85, View in Reaxys; Kojima; Bard; Journal of the American Chemical Society; vol. 97; (1975); p. 6317,6321, View in Reaxys; Ito; Matsuura; Journal of Organic Chemistry; vol. 44; (1979); p. 41,42,43, View in Reaxys; Rehm; Weller; Israel Journal of Chemistry; vol. 8; (1970); p. 259, View in Reaxys; Rieger et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 683,685, View in Reaxys; Loutfy; Yip; Canadian Journal of Chemistry; vol. 51; (1973); p. 1881,1882, View in Reaxys; Griggio; Capobianco; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 94; (1978); p. 67,69, View in Reaxys; Veshewa et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; (1970); p. 1927,1912,1913, View in Reaxys; Mairanovskii; Boltyanskaya; Doklady Physical Chemistry; vol. 244-249; (1979); p. 591,592, View in Reaxys; Pozdeeva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 45; (1975); p. 172,157,158-161, View in Reaxys; Ivanova et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 23; (1974); p. 2385; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 23; (1974); p. 2474, View in Reaxys; Kadhum, Abdul A. H.; Salmon, G. Arthur; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 82; (1986); p. 2521 - 2530, View in Reaxys; Taran, L. A.; Buzykin, B. I.; Mironova, O. Yu.; Gazetdinova, N. G.; Kitaev, Yu. P.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 32; nb. 1; (1983); p. 142 - 145; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 1; (1983); p. 166 - 169, View in Reaxys; Iwai; Takemura; Furue; Nozakura; Bulletin of the Chemical Society of Japan; vol. 57; nb. 3; (1984); p. 763 - 767, View in Reaxys; Van Walree, Cornelis A.; Roest, Martin R.; Schuddeboom, Wouter; Jenneskens, Leonardus W.; Verhoeven, Jan W.; Warman, John M.; Kooijman, Huub; Spek, Anthony L.; Journal of the American Chemical Society; vol. 118; nb. 35; (1996); p. 8395 - 8407, View in Reaxys 5 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-2.23 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: potentiometry. Description: 0.1 M TBABF4, ultramicroectrode or rotating disc electrode, Pt net as counter electrode, vs. SCE

Product

cyanobenzene

Daasbjerg, Kim; Acta Chemica Scandinavica; vol. 47; nb. 4; (1993); p. 398 - 402, View in Reaxys 6 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile

Comment (Electrochemical Characteristics)

-2.7 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: gold electrode, Ag/AgNO3 reference electrode

Product

cyanobenzene

Uosaki, Kohei; Murakoshi, Kei; Kita, Hideaki; Journal of Physical Chemistry; vol. 95; nb. 2; (1991); p. 779 - 783, View in Reaxys 7 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

1.81 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: polarography. Description: Et4NI

Product

cyanobenzene

Kargin, Yu. M.; Budnikova, Yu. G.; Yanilkin, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.1; (1991); p. 1962 1967,1816 - 1820, View in Reaxys 8 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

1.81 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: polarography. Description: Bu4NI

Product

cyanobenzene

Kargin, Yu. M.; Budnikova, Yu. G.; Yanilkin, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.1; (1991); p. 1962 1967,1816 - 1820, View in Reaxys 9 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Comment (Electrochemical Characteristics)

-2.25 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: polarography. Description: amalgamated gold rotating ring-disk electrode, vs. aqueous normal calomel electrode

Product

cyanobenzene

Nekrasov, L. N.; Peregudova, S. M.; Yur'eva, L. P.; Kravtsov, D. N.; Uralets, I. A.; Zaitseva, N. N.; Journal of Organometallic Chemistry; vol. 365; (1989); p. 269 - 284, View in Reaxys 10 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-2.32 V; Product: /BRN= 3935606/. No. of transm. electrons: 1. Method: voltammetry. Description: Bu4NPF6 solution as electrolyte; working electrode: glassy carbon disc electrode with a calomel reference electrode and Pt wire counter electrode.

Product

benzonitrile radical anion

Prest, Rita; Degrand, Chantal; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1989); p. 607 - 612, View in Reaxys 11 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-2.15 V; Type: Reversible half-wave potential. Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: direct current polarography. Description: dropping mercury electrode, saturated calomel electrode, silver perchlorate electrode, 0.1M; tetrabutylammonium perchlorate electrolyte

Product

cyanobenzene

Dunyashev, V. S.; Polenov, E. A.; Minina, N. E.; Kazakova, V. M.; Grigor'ev, G. A.; Yagupol'skii, L. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 58; nb. 1; (1988); p. 200 - 202,178 - 181, View in Reaxys 12 of 18

Description (Electrochemical Characteristics)

redox potential

Ouyang, Jiangbo; Bard, Allen J.; Journal of Physical Chemistry; vol. 91; nb. 15; (1987); p. 4058 - 4062, View in Reaxys; Fukuzumi, Shunichi; Hironaka, Katsuhiko; Nishizawa, Nobuaki; Tanaka, Toshio; Bulletin of the Chemical Society of Japan; vol. 56; nb. 8; (1983); p. 2220 - 2227, View in Reaxys 13 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-2.25 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: Hg electrode versus SDC

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Product

cyanobenzene

Severin, Maria Gabriella; Arevalo, Maria Carmen; Farnia, Giuseppe; Vianello, Elio; Journal of Physical Chemistry; vol. 91; nb. 2; (1987); p. 466 - 472, View in Reaxys 14 of 18

Description (Electrochemical Characteristics)

oxidation potential

Novi, Marino; Petrillo, Giovanni; Dell'Erba, Carlo; Tetrahedron Letters; vol. 28; nb. 12; (1987); p. 1345 - 1348, View in Reaxys 15 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-2.23 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: Pt-electrode (oxidation), Hg-drop (reduction)

Product

cyanobenzene

Eriksen, Jens; Lund, Henning; Nyvad, Annette I.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 37; nb. 5; (1983); p. 459 - 466, View in Reaxys 16 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

Type: Reversible half-wave potential

Ahlberg, Elisabet; Parker, Vernon D.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 37; nb. 8; (1983); p. 723 - 731, View in Reaxys 17 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Comment (Electrochemical Characteristics)

-2.25 V; Product: /BRN= 4178477/. No. of transm. electrons: 1. Method: polarography. Description: gold amalgam electrode

Product

cyanobenzene

Yur'eva, L. P.; Nekrasov, L. N.; Peregudova, S. M.; Doklady Chemistry; vol. 264; (1982); p. 171 - 173; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 264; nb. 4; (1982); p. 876 - 879, View in Reaxys 18 of 18

Description (Electrochemical Characteristics)

polarographic current/voltage curve

v. Stackelberg; Stracke; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 53; (1949); p. 118,121, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Chen; Wentworth; Journal of Chemical Physics; vol. 63; (1975); p. 3183,3189, View in Reaxys; Wentworth et al.; Journal of Physical Chemistry; vol. 79; (1975); p. 1161,1163, 1165, View in Reaxys; Zlatkis; Lee; Wentworth; Chen; Analytical Chemistry; vol. 55; nb. 9; (1983); p. 1596 - 1599, View in Reaxys

Energy Data (MCS) (58) 1 of 58

Description (Energy Data (MCS))

Entropy of mixtures

Temperature (Energy Data (MCS)) [°C]

24.95

Partner (Energy Data (MCS))

5,11,17,23-tetrakis(1,1-dimethylethyl)-25,27-bis[2-(methylthio)ethoxy]-26,28-bis[(pyrid-2-ylmethyl)oxy]calix(4)arene

Danil de Namor, Angela F.; Al Rawi, Nawar; Piro, Oscar E.; Castellano, Eduardo E.; Gil, Elizabet; Journal of Physical Chemistry B; vol. 106; nb. 4; (2002); p. 779 - 787, View in Reaxys 2 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

106/225

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Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

1,3,5-trimethyl-benzene

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1027 - 1033, View in Reaxys 3 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

toluene

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1027 - 1033, View in Reaxys 4 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

o-xylene

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1027 - 1033, View in Reaxys 5 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

m-xylene

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1027 - 1033, View in Reaxys 6 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

para-xylene

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1027 - 1033, View in Reaxys 7 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

107/225

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Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

ethylbenzene

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1027 - 1033, View in Reaxys 8 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Pressure (Energy Data (MCS)) [Torr]

750.06

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

methanol

Letcher; Naicker; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1035 - 1047, View in Reaxys 9 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Pressure (Energy Data (MCS)) [Torr]

750.06

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

ethanol

Letcher; Naicker; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1035 - 1047, View in Reaxys 10 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Pressure (Energy Data (MCS)) [Torr]

750.06

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

propan-1-ol

Letcher; Naicker; Journal of Chemical Thermodynamics; vol. 33; nb. 9; (2001); p. 1035 - 1047, View in Reaxys 11 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

50 - 140

Pressure (Energy Data (MCS)) [Torr]

11100.9 - 11625.9

Partner (Energy Data (MCS))

benzene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 12 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

108/225

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Temperature (Energy Data (MCS)) [°C]

50 - 140

Pressure (Energy Data (MCS)) [Torr]

10575.8 - 11100.9

Partner (Energy Data (MCS))

toluene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 13 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

20 - 30

Partner (Energy Data (MCS))

toluene

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 14 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

20 - 30

Partner (Energy Data (MCS))

benzene

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 15 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

20 - 30

Partner (Energy Data (MCS))

benzene

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 16 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

20 - 30

Partner (Energy Data (MCS))

toluene

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys 17 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

chlorobenzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 18 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

chlorobenzene

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Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 19 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

benzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 20 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

benzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 21 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

toluene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 22 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

toluene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 23 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

SOCl2

Kanonerov; Tsvetkov; Lelekov; Biryukova; Russian Journal of General Chemistry; vol. 67; nb. 7; (1997); p. 1088 - 1091, View in Reaxys 24 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

SO2Cl2

Kanonerov; Tsvetkov; Lelekov; Biryukova; Russian Journal of General Chemistry; vol. 67; nb. 7; (1997); p. 1088 - 1091, View in Reaxys 25 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

triethylamine

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Borisover, M. D.; Stolov, A. A.; Cherkasov, A. R.; Izosimova, S. V.; Solomonov, B. N.; Russian Journal of Physical Chemistry; vol. 68; nb. 1; (1994); p. 48 - 53; Zhurnal Fizicheskoi Khimii; vol. 68; nb. 1; (1994); p. 56 - 62, View in Reaxys 26 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

benzylamine

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

isopropylamine

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

hexyl-methyl-ketone

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

triethyl phosphate

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

N,N,N,N,N,N-hexamethylphosphoric triamide

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

acetyl chloride

Karsakova, N. A.; Ivanov, A. V.; Tsvetkov, V. G.; Russian Journal of General Chemistry; vol. 64; nb. 2.1; (1994); p. 170 - 172; Zhurnal Obshchei Khimii; vol. 64; nb. 2; (1994); p. 193 - 196, View in Reaxys 32 of 58

Description (Energy Data (MCS))

Enthalpy of solution

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Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

acetic acid

Borisover, M. D.; Solomonov, B. N.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 2.1; (1991); p. 329 341,294 - 305, View in Reaxys 33 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Partner (Energy Data (MCS))

water

Description (Energy Data (MCS))

Enthalpy of solution

Partner (Energy Data (MCS))

Hexadecane

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

nitrobenzene

Breus, V. A.; Khafizov, F. T.; Borisover, M. D.; Solomonov, B. N.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 60; nb. 5; (1990); p. 1147 - 1151,1020 - 1024, View in Reaxys 36 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

Dipropyl ether

Solomonov, B. N.; Borisover, M. D.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 2; (1987); p. 423 431,368 - 374, View in Reaxys 37 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

sulfolane

Pansini; Jannell; Journal of Chemical and Engineering Data; vol. 31; nb. 2; (1986); p. 157 - 160, View in Reaxys 38 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

N,N-dimethyl acetamide

Solomonov, B. N.; Borisover, M. D.; Konovalova, L. K.; Pavlova, A. A.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 6; (1986); p. 1345 - 1349,1190 - 1193, View in Reaxys 39 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

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Partner (Energy Data (MCS))

iso-butanol

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

tert.-butylhydroperoxide

Makitra, R.G.; Tsvetkov, V.G.; Pirig, Ya.N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 7; (1986); p. 1452 - 1457,1286 1290, View in Reaxys 41 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

tetrachloromethane

Solomonov, B. N.; Borisover, M. D.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 1; (1986); p. 3 - 14,1 11, View in Reaxys 42 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

hexan-1-ol

Solomonov, B. N.; Borisover, M. D.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 1; (1986); p. 3 - 14,1 11, View in Reaxys 43 of 58

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

10 - 45

Partner (Energy Data (MCS))

cyclohexane

Tanaka, Reiji; Nakamichi, Toru; Murakami, Sachio; Journal of Solution Chemistry; vol. 14; nb. 11; (1985); p. 795 - 804, View in Reaxys 44 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

298

Partner (Energy Data (MCS))

HNO3

Tsvetkov, V. G.; Marchenko, G. N.; Sopin, V. F.; Tsverkova, L. Ya.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 2; (1985); p. 233 - 238,201 - 205, View in Reaxys 45 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Partner (Energy Data (MCS))

perfluoropropylene

Makitra, R. G.; Politanakaya, T. I.; Moin, F. B.; J. Appl. Chem. USSR (Engl. Transl.); vol. 56; nb. 12; (1983); p. 2754 2755,2568 - 2569, View in Reaxys 46 of 58

Description (Energy Data (MCS))

Enthalpy of solution

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Partner (Energy Data (MCS))

Hexafluoropropene oxide

Makitra, R. G.; Politanakaya, T. I.; Moin, F. B.; J. Appl. Chem. USSR (Engl. Transl.); vol. 56; nb. 12; (1983); p. 2754 2755,2568 - 2569, View in Reaxys 47 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

bromine

Makitra, R. G.; Pirig, Ya. N.; Tsvetkov, V. G.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 4; (1983); p. 727 - 732,633 638, View in Reaxys 48 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

46.9

Partner (Energy Data (MCS))

phenol

Tsvetkov, V. G.; Perov, V. A.; Gatilov, Yu. F.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 6; (1981); p. 1376 - 1379,1166 - 1168, View in Reaxys 49 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

bromine

Tsvetkov, V. G.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 2; (1980); p. 258 - 262,201 - 205, View in Reaxys 50 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Apter et al.; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 577; ; p. 1020, View in Reaxys 51 of 58

Description (Energy Data (MCS))

Enthalpy of mixtures

Addison et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1974); p. 999,1000, View in Reaxys 52 of 58

Description (Energy Data (MCS))

Excess thermochemical parameter

Tran Ha-Phuong et al.; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 12; (1972); p. 234, View in Reaxys; Vernier et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 960, View in Reaxys; Tanaka et al.; Journal of Chemical Thermodynamics; vol. 6; (1974); p. 209,210,216, View in Reaxys 53 of 58

Description (Energy Data (MCS))

Enthalpy of solution

Fuchs; Rodewald; Journal of the American Chemical Society; vol. 95; (1973); p. 5897,5898, View in Reaxys; Genkin et al.; Doklady Physical Chemistry; vol. 160-165; (1965); p. 732; Doklady Akademii Nauk SSSR; vol. 164; (1965); p. 1089, View in Reaxys 54 of 58

Description (Energy Data (MCS))

Thermodynamic properties of system with

Amaya; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1278,1281, 1284, View in Reaxys; Iogansen; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 249,253; ; p. 302, View in Reaxys 55 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

benzene

Luzkii et al.; Zhurnal Fizicheskoi Khimii; vol. 32; (1958); p. 720; Chem.Abstr.; (1958); p. 14313, View in Reaxys 56 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

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Partner (Energy Data (MCS))

chloroform

Marvel; Copley; Ginsberg; Journal of the American Chemical Society; vol. 62; (1940); p. 3109, View in Reaxys 57 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

1,1,2,2-tetrachloroethane

Marvel; Copley; Ginsberg; Journal of the American Chemical Society; vol. 62; (1940); p. 3109, View in Reaxys 58 of 58

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

0.2 percent H2O containing H2SO4

Hantzsch; Chemische Berichte; vol. 64; (1931); p. 667,674, View in Reaxys Enthalpy of Combustion (3) Enthalpy of ComTemperature (Enbustion [Jmol-1] thalpy of Combustion) [°C]

Pressure (Enthalpy of Combustion) [Torr]

-3.6323E+06

760

-3.63476E+06

Comment (Enthalpy of Combustion)

References

Lebedev, B. V.; Bykova, T. A.; Kiparisova, E. G.; Chernomordik, Yu. A.; Kurapov, A. S.; Sergeev, V. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 34; nb. 2; (1985); p. 274 - 279; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 2; (1985); p. 301 - 306, View in Reaxys; Lebedev, B. V.; Bykova, T. A.; Kiparisova, E. G.; Pankratov, V. A.; Mitina, L. M.; Korshak, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 6; (1984); p. 1352 1358,1209 - 1214, View in Reaxys Standard.

-3.62367E+06

Evans et al.; Transactions of the Faraday Society; vol. 55; (1959); p. 255,258, View in Reaxys Berthelot; Petit; Annales de Chimie (Cachan, France); vol. <6>18; (1889); p. 112, View in Reaxys

Enthalpy of Formation (3) Enthalpy of Forma- Temperature (Ention [Jmol-1] thalpy of Formation) [°C]

Pressure (Enthalpy of Formation) [Torr]

163200

760

Comment (Enthalpy of Formation)

References

Lebedev, B. V.; Bykova, T. A.; Kiparisova, E. G.; Chernomordik, Yu. A.; Kurapov, A. S.; Sergeev, V. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 34; nb. 2; (1985); p. 274 - 279; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 2; (1985); p. 301 - 306, View in Reaxys Lebedeva et al.; Zhurnal Organicheskoi Khimii; vol. 12; (1976); p. 1618,1594, View in Reaxys; Williams; Bowen; Organic Mass Spectrometry; vol. 11; (1976); p. 223,224, View in Reaxys

163285

Standard.

Evans et al.; Transactions of the Faraday Society; vol. 55; (1959); p. 255,258, View in Reaxys

Enthalpy of Fusion (3) Enthalpy of Fusion References [Jmol-1] 10980

9085.35

Brooks; Pilcher; Journal of the Chemical Society; (1959); p. 1535,1539, View in Reaxys

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10467

Timmermans; Kasanin; Bulletin des Societes Chimiques Belges; vol. 68; (1959); p. 527,537, View in Reaxys

Enthalpy of Vaporization (3) Enthalpy of Vapori- Temperature (Enzation [Jmol-1] thalpy of Vaporization) [°C]

References

49404.2

24.9

Solomonov, B. N.; Borisover, M. D.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 1; (1986); p. 3 - 14,1 - 11, View in Reaxys

52300

Kiselev, V. D.; Veisman, E. A.; Zabotina, O. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 2; (1983); p. 333 - 342,289 - 297, View in Reaxys

45980.6

Philip; Waterton; Journal of the Chemical Society; (1930); p. 2783, View in Reaxys

Further Information (156) Description (FurReferences ther Information) Further information Beitz; Miller; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1979); p. 4579, View in Reaxys Further information Zyss; Journal of Chemical Physics; vol. 70; (1979); p. 3333,3347, View in Reaxys Further information Vuks; Optics and Spectroscopy; vol. 47; (1979); p. 502; Optika i Spektroskopiya; p. 907, View in Reaxys Further information Baldwin; Organic Mass Spectrometry; vol. 14; (1979); p. 601,602, View in Reaxys Further information Kolling; Analytical Chemistry; vol. 50; (1978); p. 212, View in Reaxys Further information Rossarie et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 63,71, View in Reaxys Further information Morgan; Green; International Journal of Mass Spectrometry and Ion Physics; vol. 28; (1978); p. 171, View in Reaxys Further information Redchenko; Egorova; Journal of Applied Spectroscopy; vol. 29; (1978); p. 858, View in Reaxys Further information Gadzhiev et al.; Journal of Applied Spectroscopy; vol. 29; (1978); p. 830,831,832, View in Reaxys Further information Griggio; Capobianco; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 94; (1978); p. 67,69, View in Reaxys Further information Vysotskii; Journal of Structural Chemistry; vol. 19; (1978); p. 27,31; ; p. 34, View in Reaxys Further information Kuwae; Machida; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 34; (1978); p. 785,787,788, View in Reaxys Further information Dorrepaal; Louw; International Journal of Chemical Kinetics; vol. 10; (1978); p. 249,255, View in Reaxys Further information Egorochkin et al.; Doklady Chemistry; vol. 243; (1978); p. 532,533; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 243; (1978); p. 368, View in Reaxys Further information Korableva; Panachev; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 555; ; p. 943, View in Reaxys Further information Lipei et al.; High Energy Chemistry; vol. 11; (1977); p. 181,182, View in Reaxys Further information Gramstad; Tjessem; Journal of Molecular Structure; vol. 41; (1977); p. 231,233, 235, 236, View in Reaxys Further information Oudar et al.; Journal of Chemical Physics; vol. 67; (1977); p. 1626,1630, View in Reaxys Further information Whittenburg; Wang; Journal of Chemical Physics; vol. 67; (1977); p. 3844, View in Reaxys Further information Baryshev; Journal of Applied Spectroscopy; vol. 26; (1977); p. 120, View in Reaxys Further information Kamlet,M.J. et al.; Journal of the American Chemical Society; vol. 99; (1977); p. 6027 - 6038, View in Reaxys Further information Vakhrin; Grechishkin; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 187; ; p. 314, View in Reaxys Further information Medved et al.; Chemical Physics; vol. 15; (1976); p. 295,298, View in Reaxys Further information Korol'; High Energy Chemistry; vol. 10; (1976); p. 87, View in Reaxys Further information Grunwald et al.; Journal of Physical Chemistry; vol. 80; (1976); p. 2935, View in Reaxys Further information Vysotskii; Journal of Structural Chemistry; vol. 17; (1976); p. 453; ; p. 525, View in Reaxys Further information Bodrikov et al.; Doklady Chemistry; vol. 227; (1976); p. 253; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 227; (1976); p. 863, View in Reaxys Further information Meot-Ner; Field; Chemical Physics Letters; vol. 44; (1976); p. 484, View in Reaxys Further information Lutskii et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 812; ; p. 1374, View in Reaxys

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Further information Dresvyankin et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 114; ; p. 2584, View in Reaxys Further information Dresvyankin et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 144; ; p. 2584, View in Reaxys Further information de la Calle et al.; Anales de Quimica (1968-1979); vol. 71; (1975); p. 243, View in Reaxys Further information Dresvyankin; Journal of Structural Chemistry; vol. 16; (1975); p. 444; ; p. 478, View in Reaxys Further information Gordon; Reid; International Journal of Mass Spectrometry and Ion Physics; vol. 18; (1975); p. 379, View in Reaxys Further information Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys Further information Deeming; Hasso; Journal of Organometallic Chemistry; vol. 88; (1975); p. C21, View in Reaxys Further information Park; Bard; Journal of the American Chemical Society; vol. 97; (1975); p. 2978,2980, View in Reaxys Further information Kanamura et al.; Chemical Physics Letters; vol. 26; (1974); p. 174, View in Reaxys Further information Grechishkin et al.; Russian Journal of Physical Chemistry; vol. 48; (1974); p. 931; ; p. 1580, View in Reaxys Further information Irving; Lewis; Chemica Scripta; vol. 5; (1974); p. 202,204, View in Reaxys Further information Tanaka; Ogata; Inorganic and Nuclear Chemistry Letters; vol. 10; (1974); p. 511,514, View in Reaxys Further information Cooks et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 15; (1974); p. 271,273, View in Reaxys Further information Ivanova et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 23; (1974); p. 2385; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 23; (1974); p. 2474, View in Reaxys Further information Pancir et al.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 3039,3047, View in Reaxys Further information Tolopko et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 39; nb. 4; (1973); p. 395,94, View in Reaxys Further information Weisbecker; Rouquie; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 1059,1062, View in Reaxys Further information Stegeman; Stoicheff; Physical Review A: Atomic, Molecular, and Optical Physics; vol. 7; (1973); p. 3-1160,1170,1171,1173, View in Reaxys Further information McLafferty et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 2120,2127, View in Reaxys Further information Higasi et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 1579,1581, View in Reaxys Further information Gibson; Canadian Journal of Chemistry; vol. 51; (1973); p. 3065,3066, View in Reaxys Further information Tan; Thistlethwaite; Journal of Chemical Physics; vol. 58; (1973); p. 4408, View in Reaxys Further information Burnett et al.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 69; (1973); p. 864, View in Reaxys Further information De Jong; Journal of Magnetic Resonance (1969-1992); vol. 9; (1973); p. 185, View in Reaxys Further information De Young; Mc Lean; Journal of Magnetic Resonance (1969-1992); vol. 11; (1973); p. 373, View in Reaxys Further information Schlossarczyk,H. et al.; Helvetica Chimica Acta; vol. 56; (1973); p. 875 - 944, View in Reaxys Further information Kinlin et al.; Journal of Agricultural and Food Chemistry; vol. 20; (1972); p. 1021,1023, View in Reaxys Further information Mitsky et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 3442,3443, View in Reaxys Further information Sloane; Cook; Applied Spectroscopy; vol. 26; (1972); p. 589,591, View in Reaxys Further information Greffe; Barriol; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1579,1584, 1585, View in Reaxys Further information Kawamura; Inokuchi; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 710,712, View in Reaxys Further information Mallan et al.; Journal of Chemical and Engineering Data; vol. 17; (1972); p. 412,414, View in Reaxys Further information Fluck; Steck; Phosphorus and Sulfur and the Related Elements; vol. 1; (1972); p. 283, View in Reaxys Further information Murata; Mataga; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 354,355-360, View in Reaxys Further information Naff et al.; Journal of Chemical Physics; vol. 54; (1971); p. 212,220, View in Reaxys Further information Merbach; Baenzli; Chimia; vol. 25; (1971); p. 222, View in Reaxys

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Further information Hendra; Loader; Transactions of the Faraday Society; vol. 67; (1971); p. 828,835, View in Reaxys Further information Migahed; Beckey; International Journal of Mass Spectrometry and Ion Physics; vol. 7; (1971); p. 1, View in Reaxys Further information Sebastian; Grunwell; Canadian Journal of Chemistry; vol. 49; (1971); p. 1779,1780, View in Reaxys Further information Srivastava et al.; Indian Journal of Pure and Applied Physics; vol. 9; (1971); p. 364, View in Reaxys Further information Fruwert et al.; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 11; (1971); p. 396, View in Reaxys Further information Ichikawa; Tamaru; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1451, View in Reaxys Further information Torgunakov et al.; Sov. Phys. J. (Engl. Transl.); vol. 14; nb. 8; (1971); p. 92,1093, View in Reaxys Further information Scarlett et al.; Australian Journal of Chemistry; vol. 23; (1970); p. 1333,1338,1344, View in Reaxys Further information Brand; Knight; Journal of Molecular Spectroscopy; vol. 36; (1970); p. 328,329,331,334, View in Reaxys Further information Buchs; Helvetica Chimica Acta; vol. 53; (1970); p. 2026, View in Reaxys Further information Bobykina; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 1198, View in Reaxys Further information Davies et al.; Transactions of the Faraday Society; vol. 66; (1970); p. 273,291, View in Reaxys Further information Boldeskul et al.; Optics and Spectroscopy; vol. 29; (1970); p. 142; ; p. 270, View in Reaxys Further information Rehm; Weller; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 69; (1970); p. 183,193,196, View in Reaxys Further information Heerma; Dijkstra; Organic Mass Spectrometry; vol. 3; (1970); p. 379,381, View in Reaxys Further information Kawamura et al.; Chemical Physics Letters; vol. 5; (1970); p. 80, View in Reaxys Further information Bellamy; Pace; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 319,322, View in Reaxys Further information Gramstad; Sandstroem; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 31,33, View in Reaxys Further information Becher; Hoefler; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 1703,1705, View in Reaxys Further information Howe; Williams; Journal of the American Chemical Society; vol. 91; (1969); p. 7137,7141, View in Reaxys Further information Ben-Reuven; Gershon; Journal of Chemical Physics; vol. 51; (1969); p. 893, View in Reaxys Further information Cumper; Tetrahedron; vol. 25; (1969); p. 3131, View in Reaxys Further information Gray et al.; Journal of Chemical Physics; vol. 48; (1968); p. 1145,1148, View in Reaxys Further information Davies; Williams; Transactions of the Faraday Society; vol. 64; (1968); p. 529,543, View in Reaxys Further information Lugg; Analytical Chemistry; vol. 40; (1968); p. 1072,1074, View in Reaxys Further information Gol'dshtein et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 38; (1968); p. 1984,1925,1926, View in Reaxys Further information Hartmann; Schmidt; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 62; (1968); p. 312, View in Reaxys Further information Shorygin et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 555,556; ; p. 1057, View in Reaxys Further information Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys Further information Craddock et al.; Molecular Physics; vol. 14; (1968); p. 373, View in Reaxys Further information Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys Further information Beens; Weller; Acta Physica Polonica; vol. 34; (1968); p. 593,595, 596, View in Reaxys Further information Baranov; Sechkarev; Sov. Phys. J. (Engl. Transl.); vol. 11; nb. 3; (1968); p. 51,29, View in Reaxys Further information Davies et al.; Transactions of the Faraday Society; vol. 64; (1968); p. 847,857, 858, View in Reaxys Further information Baker et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 22, View in Reaxys Further information Ichikawa et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 1015, View in Reaxys Further information Kuntz; Johnston; Journal of the American Chemical Society; vol. 89; (1967); p. 6008,6010, View in Reaxys Further information Matthews; Sangster; Journal of Physical Chemistry; vol. 71; (1967); p. 4587, View in Reaxys Further information Charlamowa et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 37; (1967); p. 303,284, View in Reaxys

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Further information Zaitsev; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 145,146, View in Reaxys Further information Klaboe et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 3667,3670, 3674, View in Reaxys Further information Voronkov et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 2; (1966); p. 5,8; Khimiya Geterotsiklicheskikh Soedinenii; vol. 2; (1966); p. 8, View in Reaxys Further information Bertin; Lumbroso; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 263; (1966); p. 181, View in Reaxys Further information Roos; Orchin; Journal of Organic Chemistry; vol. 31; (1966); p. 3015, View in Reaxys Further information Sherman; Journal of the American Chemical Society; vol. 88; (1966); p. 1567, View in Reaxys Further information Fraser; Renaud; Journal of the American Chemical Society; vol. 88; (1966); p. 4365,4367, View in Reaxys Further information Brownlee et al.; Journal of the American Chemical Society; vol. 88; (1966); p. 1413,1415, 1416, View in Reaxys Further information Kazitsyna,L.A. et al.; Doklady Chemistry; vol. 160; (1965); p. 92 - 95; Doklady Akademii Nauk SSSR; vol. 160; (1965); p. 600 - 603, View in Reaxys Further information Lorenzelli; Gazzetta Chimica Italiana; vol. 95; (1965); p. 218,220, View in Reaxys Further information Adema; Schrama; Analytical Chemistry; vol. 37; (1965); p. 229,230, View in Reaxys Further information Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 3180,3182, View in Reaxys Further information Zhdanov; Doklady Chemistry; vol. 162; (1965); p. 603,604; Doklady Akademii Nauk SSSR; vol. 162; (1965); p. 1314, View in Reaxys Further information Stevenson; Journal of Molecular Spectroscopy; vol. 15; (1965); p. 220,232, View in Reaxys Further information Issleib; Bleck; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 336; (1965); p. 234,242, View in Reaxys Further information Janz; Ahmad; Venkatasetty; Journal of Physical Chemistry; vol. 68; (1964); p. 889,891, View in Reaxys Further information Becker; Timpe; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 4; (1964); p. 304, View in Reaxys Further information Beringer; Falk; Journal of the Chemical Society; (1964); p. 4442,4449, View in Reaxys Further information Voigt; Reid; Journal of the American Chemical Society; vol. 86; (1964); p. 3930,3932, View in Reaxys Further information Deverse; King; Journal of Chemical Physics; vol. 41; (1964); p. 3833,3835, View in Reaxys Further information Trosman; Bagdasar'jan; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 73; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 141, View in Reaxys Further information Caronna; Marino; Gazzetta Chimica Italiana; vol. 94; (1964); p. 31,33, 34, View in Reaxys Further information Delorme; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 61; (1964); p. 1439,1449, 1453, View in Reaxys Further information Minisci et al.; Tetrahedron Letters; (1963); p. 785,788, View in Reaxys Further information Woronkow; Deitsch; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 214,221, View in Reaxys Further information Schwetlick; Pietzsch; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 125,127, View in Reaxys Further information Greber; Egle; Makromolekulare Chemie; vol. 59; (1963); p. 174,176, View in Reaxys Further information Schindlbauer; Monatshefte fuer Chemie; vol. 94; (1963); p. 99,105, View in Reaxys Further information Kagarlizkii et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 36; (1963); p. 1848,1787, View in Reaxys Further information Pesez et al.; Bulletin de la Societe Chimique de France; (1962); p. 719, View in Reaxys Further information Srivastavan; Lal; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 86, View in Reaxys Further information Amaya; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 1067, View in Reaxys Further information Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys Further information Hidalgo; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 2; (1962); p. 801, View in Reaxys Further information Venkateswarlu; Radhakrishnan; Spectrochimica Acta; vol. 18; (1962); p. 1433,1438,1439, View in Reaxys Further information Schmid; Zeitschrift fuer Elektrochemie; vol. 66; (1962); p. 53, View in Reaxys Further information Sobhanadri; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 14, View in Reaxys

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Further information Francois; Bulletin de la Societe Chimique de France; (1962); p. 511, View in Reaxys Further information Derkatsch et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 3002,2951, View in Reaxys Further information Klaboe; Journal of the American Chemical Society; vol. 84; (1962); p. 3458, View in Reaxys Further information Huisgen et al.; Tetrahedron Letters; (1961); p. 587, View in Reaxys Further information Naveau,J.; Bulletin des Societes Chimiques Belges; vol. 70; (1961); p. 662 - 689, View in Reaxys Further information Inami et al.; Journal of the American Chemical Society; vol. 83; (1961); p. 4745,4748, View in Reaxys Further information Decroocq; Jungers; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 252; (1961); p. 1454,1455, View in Reaxys Further information Bloor; Canadian Journal of Chemistry; vol. 39; (1961); p. 2256,2259, View in Reaxys Further information Chandra; Journal of the American Chemical Society; vol. 83; (1961); p. 4177, View in Reaxys Further information Brown; Korytnik; Journal of the American Chemical Society; vol. 82; (1960); p. 3866,3868, View in Reaxys Further information Wiberley et al.; Analytical Chemistry; vol. 32; (1960); p. 217,219, View in Reaxys Further information Crable et al.; Analytical Chemistry; vol. 32; (1960); p. 13,16, View in Reaxys Further information Bralsford et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 258; (1960); p. 459,464, View in Reaxys Further information Bak; Nielsen; Zeitschrift fuer Elektrochemie; vol. 64; (1960); p. 560, View in Reaxys Further information Astle; Pierce; Analytical Chemistry; vol. 32; (1960); p. 1322, View in Reaxys Heat Capacity Cp (11) Heat Capacity Cp Temperature (Heat [Jmol-1K-1] Capacity Cp) [°C]

References

163.43

9.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

164.61

14.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

165.82

19.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

167.06

24.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

168.32

29.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

169.59

34.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

170.87

39.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

172.15

44.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

163.9

11.99

Lei, Yuntao; Chen, Zhiyun; An, Xueqin; Huang, Meijun; Shen, Weiguo; Journal of Chemical and Engineering Data; vol. 55; nb. 10; (2010); p. 4154 - 4161, View in Reaxys

166.9

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys

167.14

Wilhelm, Emmerich; Egger; Vencour; Roux; Polednicek; Grolier; Journal of Chemical Thermodynamics; vol. 30; nb. 12; (1998); p. 1509 - 1532, View in Reaxys

Heat Capacity Cp0 (2) Heat Capacity Cp0 Temperature (Heat [Jmol-1K-1] Capacity Cp0) [°C] 0.32 - 173.4

-268.2 - 56.9

References Lebedev, B. V.; Bykova, T. A.; Kiparisova, E. G.; Chernomordik, Yu. A.; Kurapov, A. S.; Sergeev, V. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 34; nb. 2; (1985); p. 274 - 279; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 2; (1985); p. 301 - 306, View in Reaxys

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-12.8

Interatomic Distances and Angles (2) Description References Interatomic distances and angles

Domenicano; Tetrahedron Letters; (1976); p. 1029, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1976); p. 429, View in Reaxys; Juchnowski; Welew; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 4; (1971); p. 333,339, View in Reaxys; Dixon et al.; Spectrochimica Acta; vol. 18; (1962); p. 1369, View in Reaxys; Bak et al.; Journal of Chemical Physics; vol. 37; (1962); p. 2027,2029, 2030, View in Reaxys; Portalone, Gustavo; Domenicano, Aldo; Schultz, Gyoergy; Hargittai, Istvan; Journal of Molecular Structure; vol. 160; (1987); p. 97 - 108, View in Reaxys

Electron distribution

Yamakawa et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 3059, View in Reaxys; Juchnowski et al.; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 10; (1977); p. 554,558, View in Reaxys; Lyubimov et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 1381, View in Reaxys; Lynch; Canadian Journal of Chemistry; vol. 55; (1977); p. 541,543, View in Reaxys; Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 16; nb. 7; (1968); p. 1187, View in Reaxys; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 1193,1194, View in Reaxys; Wehrli et al.; Helvetica Chimica Acta; vol. 52; (1969); p. 103, View in Reaxys

Ionization Potential (4) Ionization Potential Method (Ionization [eV] Potential) 405.09

9.83

References Buschek, J. M.; Joergensen, F. S.; Brown R. S.; Journal of the American Chemical Society; vol. 104; nb. 19; (1982); p. 5019 - 5025, View in Reaxys Macoll, Allan; Mathur, Deepak; Organic Mass Spectrometry; vol. 16; nb. 6; (1981); p. 261 263, View in Reaxys Medved et al.; Chemical Physics; vol. 14; (1976); p. 345, View in Reaxys; Redchenko; Egorova; Journal of Applied Spectroscopy; vol. 29; (1978); p. 858, View in Reaxys; Gross; Organic Mass Spectrometry; vol. 6; (1972); p. 827, View in Reaxys; Lipei et al.; High Energy Chemistry; vol. 11; (1977); p. 181,182, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys; Gibson; Canadian Journal of Chemistry; vol. 51; (1973); p. 3065,3066, View in Reaxys; Johnstone; Mellon; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 36, View in Reaxys; Buchs; Helvetica Chimica Acta; vol. 53; (1970); p. 2026, View in Reaxys; Conway et al.; Faraday Discussions of the Chemical Society; vol. 56; (1974); p. 210,216, View in Reaxys; Gilbert; Taylor; Journal of the Chemical Society, Chemical Communications; (1977); p. 242, View in Reaxys; Cooks et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 11; (1973); p. 490, View in Reaxys; Kobayashi; Nagakura; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 2563, View in Reaxys; Crable; Kearns; Journal of Physical Chemistry; vol. 66; (1962); p. 436,437, View in Reaxys; Baldwin; Organic Mass Spectrometry; vol. 14; (1979); p. 601,602, View in Reaxys; Baker et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 22, View in Reaxys

9.95

Electron impact

Morrison; Nicholson; Journal of Chemical Physics; vol. 20; (1952); p. 1021, View in Reaxys

Liquid Phase (3) Description (Liquid References Phase) Radial distribution function

Katayama, Misaki; Komori, Kohei; Ozutsumi, Kazuhiko; Ohtaki, Hitoshi; Zeitschrift fur Physikalische Chemie; vol. 218; nb. 6; (2004); p. 659 - 677, View in Reaxys

Self-association in solution

Kedziora, P.; Jadzyn, J.; Bonnet, P.; Berichte der Bunsen-Gesellschaft; vol. 97; nb. 7; (1993); p. 864 - 867, View in Reaxys; Tsarevskaya, M. N.; Tsarevskii, N. A.; Danil'chenko, S. M.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 5; (1985); p. 1155 - 1159,1029 - 1033, View in Reaxys; Lu; Kong, Rita; Chan; Journal of Chemical Physics; vol. 110; nb. 2-12; (1999); p. 3003 - 3008, View in Reaxys; Ishikawa, Seiichi; Ebata, Takayuki; Mikami, Naohiko; Journal of Chemical Physics; vol. 110; nb. 19; (1999); p. 9504 - 9515, View in Reaxys

Rotational correlation time

Rothschild; Journal of Chemical Physics; vol. 57; (1972); p. 991, View in Reaxys; Daragan, V. A.; Il'ina, E. E.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 36; nb. 4; (1987); p. 710 - 713; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 4; (1987); p. 782 - 786, View in Reaxys; Evilia, R. F.; Robert, J. M.; Whittenburg, S. L.; Journal of Physical Chemistry; vol. 93; nb. 17; (1989); p. 6550 6552, View in Reaxys

Liquid/Liquid Systems (MCS) (64) 1 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS))

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Partner (Liquid/Liquid Systems (MCS))

poly(vinyl chloride); water

Chen, Zhi; Weber, Stephen G.; Analytical Chemistry; vol. 79; nb. 3; (2007); p. 1043 - 1049, View in Reaxys 2 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Hexadecane

Wang, Nong; Mao, Chunfeng; Peng, Xuhong; An, Xueqin; Shen, Weiguo; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 732 - 738, View in Reaxys 3 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Hexadecane

Wang, Nong; Mao, Chunfeng; Peng, Xuhong; An, Xueqin; Shen, Weiguo; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 732 - 738, View in Reaxys 4 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethyl acetate

Del Carmen Grande, Maria; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1324 - 1327, View in Reaxys 5 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

acetic acid butyl ester

Del Carmen Grande, Maria; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1324 - 1327, View in Reaxys 6 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

acetone

Grande, Maria del C.; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 48; nb. 5; (2003); p. 1191 1193, View in Reaxys 7 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

acetone

Grande, Maria del C.; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 48; nb. 5; (2003); p. 1191 1193, View in Reaxys 8 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS))

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

dimethyl sulfoxide

Grande, Maria del C.; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 48; nb. 5; (2003); p. 1191 1193, View in Reaxys 9 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

dimethyl sulfoxide

Grande, Maria del C.; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 48; nb. 5; (2003); p. 1191 1193, View in Reaxys 10 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethanol

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys 11 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

methanol

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys 12 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

propan-1-ol

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys 13 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

methanol

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys 14 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS))

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethanol

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys 15 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

propan-1-ol

Letcher, Trevor M.; Naicker, Pavan K.; Journal of Chemical and Engineering Data; vol. 46; nb. 6; (2001); p. 1436 - 1441, View in Reaxys 16 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

3-methylbutyric acid

Letcher; Redhi; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1555 - 1565, View in Reaxys 17 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

propionic acid

Letcher; Redhi; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1555 - 1565, View in Reaxys 18 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

isobutyric Acid

Letcher; Redhi; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1555 - 1565, View in Reaxys 19 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

valeric acid

Letcher; Redhi; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1555 - 1565, View in Reaxys 20 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

124/225

2018-05-24 12:11:44

Pressure (Liquid/Liquid Systems (MCS)) [Torr]

759811

Partner (Liquid/Liquid Systems (MCS))

triethylene glycol + H2O/hexane + further comp.

Venter, Denise L.; Nieuwoudt, Izak; Journal of Chemical and Engineering Data; vol. 46; nb. 4; (2001); p. 813 - 822, View in Reaxys 21 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

aq. phosphate buffer

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate; H2O

Khaledi; Kelly; Burns; Analytical Chemistry; vol. 73; nb. 24; (2001); p. 6057 - 6062, View in Reaxys 22 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O; gas

Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate

Bel'skii; Russian Chemical Bulletin; vol. 49; nb. 2; (2000); p. 251 - 255, View in Reaxys 23 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

acetonitrile; various solvent(s)

Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

immobilized artificial membrane (IAC)

Valko, Klara; Du, Chau My; Bevan, Christopher D.; Reynolds, Derek P.; Abraham, Michael H.; Journal of Pharmaceutical Sciences; vol. 89; nb. 8; (2000); p. 1085 - 1096, View in Reaxys 24 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

chloroform

Barril; Munoz; Luque; Orozco; Physical Chemistry Chemical Physics; vol. 2; nb. 21; (2000); p. 4897 - 4905, View in Reaxys 25 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

hexadecane

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

octadecafluorodecahydronaphthalene (cis+trans)

Leshchev; Novik; Russian Journal of Applied Chemistry; vol. 73; nb. 11; (2000); p. 1887 - 1889, View in Reaxys 26 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS))

125/225

2018-05-24 12:11:44

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

acetonitrile

Grande, Maria Del C.; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 686 - 688, View in Reaxys 27 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

propiononitrile

Grande, Maria Del C.; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 686 - 688, View in Reaxys 28 of 64

Description (Liquid/Liquid Solution equilibrium Systems (MCS)) Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys 29 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys 30 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

poly(N-isopropylacrylamide) (P-125K)

Matsubara; Saitoh; Iwaki; Suzuki; Yoshida; Matsudo; Fujiwara; Dobashi; Analytical Chemistry; vol. 71; nb. 20; (1999); p. 4506 - 4512, View in Reaxys 31 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

gas

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

39.2

Partner (Liquid/Liquid Systems (MCS))

apolane

Weckwerth, Jeff D.; Carr, Peter W.; Vitha, Mark F.; Nasehzadeh, Asad; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3712 - 3716, View in Reaxys 32 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

126/225

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Partner (Liquid/Liquid Systems (MCS))

formamide

Grande; Marschoff; Journal of Chemical and Engineering Data; vol. 43; nb. 6; (1998); p. 1030 - 1033, View in Reaxys 33 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

N-Methylformamide

Grande; Marschoff; Journal of Chemical and Engineering Data; vol. 43; nb. 6; (1998); p. 1030 - 1033, View in Reaxys 34 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

N,N-dimethyl-formamide

Grande; Marschoff; Journal of Chemical and Engineering Data; vol. 43; nb. 6; (1998); p. 1030 - 1033, View in Reaxys 35 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

dibutyl ether; H2O

Pagliara, Alessandra; Caron, Giulia; Lisa, Giuseppe; Fan, Weizheng; Gaillard, Patrick; Carrupt, Pierre-Alain; Testa, Bernard; Abraham, Michael H.; Journal of the Chemical Society. Perkin Transactions 2; nb. 12; (1997); p. 2639 - 2643, View in Reaxys 36 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

isopropyl alcohol; H2O

Grande; Barrero; Roble; Marschoff; Journal of Chemical and Engineering Data; vol. 41; nb. 4; (1996); p. 926 - 928, View in Reaxys 37 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

isopropyl alcohol; H2O

Grande; Barrero; Roble; Marschoff; Journal of Chemical and Engineering Data; vol. 41; nb. 4; (1996); p. 926 - 928, View in Reaxys 38 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

butan-1-ol; H2O

Grande; Barrero; Roble; Marschoff; Journal of Chemical and Engineering Data; vol. 41; nb. 4; (1996); p. 926 - 928, View in Reaxys

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39 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

butan-1-ol; H2O

Grande; Barrero; Roble; Marschoff; Journal of Chemical and Engineering Data; vol. 41; nb. 4; (1996); p. 926 - 928, View in Reaxys 40 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

octanol; H2O

Garst; Journal of Pharmaceutical Sciences; vol. 73; nb. 11; (1984); p. 1623 - 1629, View in Reaxys; Ishihama, Yasushi; Oda, Yoshiya; Uchikawa, Kiyohiko; Asakawa, Naoki; Analytical Chemistry; vol. 67; nb. 9; (1995); p. 1588 - 1595, View in Reaxys 41 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate; butan-1-ol; n-heptane; H2O

Ishihama, Yasushi; Oda, Yoshiya; Uchikawa, Kiyohiko; Asakawa, Naoki; Analytical Chemistry; vol. 67; nb. 9; (1995); p. 1588 - 1595, View in Reaxys 42 of 64

Description (Liquid/Liquid Solution equilibrium Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

N-ethyl-4-cyanopyridinium iodide; benzene

Laha, Ashis Kumar; Banerjee, Debashis; Bagchi, Sanjib; Indian Journal of Chemistry, Section A: Inorganic, Bio-inorganic, Physical, Theoretical & Analytical Chemistry; vol. 34; nb. 5; (1995); p. 335 - 341, View in Reaxys 43 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

ethanol; H2O

Grande, M. C.; Fresco, J.; Marschoff, C. M.; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1165 - 1167, View in Reaxys 44 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

propan-1-ol; H2O

Grande, M. C.; Fresco, J.; Marschoff, C. M.; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1165 - 1167, View in Reaxys 45 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

octanol / water

Ishihama; Oda; Uchikawa; Asakawa; Chemical and Pharmaceutical Bulletin; vol. 42; nb. 7; (1994); p. 1525 - 1527, View in Reaxys

128/225

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46 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Hexadecane; water

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.9 - 59.9

Partner (Liquid/Liquid Systems (MCS))

octanol; water

Kramer, C.-R.; Henze, U.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 3; (1990); p. 503 - 513, View in Reaxys 48 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

19.9

Partner (Liquid/Liquid Systems (MCS))

octanol; water

Kramer, C. R.; Henze, U.; Schelenz, Th.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 6; (1990); p. 1155 1167, View in Reaxys 49 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

methanol; water

Botto; Agaras; Marschoff; Journal of Chemical and Engineering Data; vol. 34; nb. 4; (1989); p. 382 - 384, View in Reaxys 50 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

methanol; water

Botto; Agaras; Marschoff; Journal of Chemical and Engineering Data; vol. 34; nb. 4; (1989); p. 382 - 384, View in Reaxys 51 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

methanol; water

Botto; Agaras; Marschoff; Journal of Chemical and Engineering Data; vol. 34; nb. 4; (1989); p. 382 - 384, View in Reaxys 52 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

129/225

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Partner (Liquid/Liquid Systems (MCS))

octanol

Minick; Frenz; Patrick; Brent; Journal of Medicinal Chemistry; vol. 31; nb. 10; (1988); p. 1923 - 1933, View in Reaxys 53 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

octanol

Leahy; Journal of pharmaceutical sciences; vol. 75; nb. 7; (1986); p. 629 - 636, View in Reaxys 54 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

50 - 130

Partner (Liquid/Liquid Systems (MCS))

water, ammonia

Pryanikova, R.O.; Markina, I.A.; Russian Journal of Physical Chemistry; vol. 59; nb. 9; (1985); p. 1306 - 1308; Zhurnal Fizicheskoi Khimii; vol. 59; (1985); p. 2198 - 2201, View in Reaxys 55 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

octanol; H2O

Garst; Wilson; Journal of Pharmaceutical Sciences; vol. 73; nb. 11; (1984); p. 1616 - 1623, View in Reaxys 56 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

6.9 - 26.9

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Baranowska-Majgier, Helena; Pyzuk, Wieslaw; Jeute, Wojciech; Ziolo, Jerzy; Journal of Chemical & Engineering Data; vol. 26; nb. 1; (1981); p. 51 - 53, View in Reaxys 57 of 64

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Fujita et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 5175,5177, View in Reaxys; Niclas; Kollecker; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 16; (1976); p. 367, View in Reaxys

58 of 64

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Francis; Journal of Chemical and Engineering Data; vol. 10; (1965); p. 145,148, View in Reaxys

59 of 64

Description (Liquid/Liquid Temperature of separation Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

2-Methylhexane

Miller; Industrial and Engineering Chemistry, Analytical Edition; vol. 17; (1945); p. 5,6, View in Reaxys 60 of 64

Description (Liquid/Liquid Temperature of separation Systems (MCS))

130/225

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Partner (Liquid/Liquid Systems (MCS))

2,2-dimethylpentane

Miller; Industrial and Engineering Chemistry, Analytical Edition; vol. 17; (1945); p. 5,6, View in Reaxys 61 of 64

Description (Liquid/Liquid Temperature of separation Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

2,3-dimethyl pentane

Miller; Industrial and Engineering Chemistry, Analytical Edition; vol. 17; (1945); p. 5,6, View in Reaxys 62 of 64

Description (Liquid/Liquid Temperature of separation Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

2,4-dimethylpentane

Miller; Industrial and Engineering Chemistry, Analytical Edition; vol. 17; (1945); p. 5,6, View in Reaxys 63 of 64

Description (Liquid/Liquid Temperature of separation Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

triptane

Miller; Industrial and Engineering Chemistry, Analytical Edition; vol. 17; (1945); p. 5,6, View in Reaxys 64 of 64

Description (Liquid/Liquid Equilibrium of liquid phases Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

auch in Gegenwart von Neutralsalzen.

Partner (Liquid/Liquid Systems (MCS))

sodium ethanolate

Marshall; Harrison; Acree; American Chemical Journal; vol. 49; (1913); p. 385,393, View in Reaxys; Marshall; Acree; American Chemical Journal; vol. 49; (1913); p. 151, View in Reaxys Liquid/Solid Systems (MCS) (15) 1 of 15

Description (Liquid/Solid Systems (MCS))

Melting points

Temperature (Liquid/Solid Systems (MCS)) [°C]

139 - 165

Partner (Liquid/Solid Systems (MCS))

1,1',3,3'-tetramethyl-2,2'-bi-1H-imidazolium bis(tetraphenylborate)

Ono, Katsuhiko; Saito, Katsuhiro; Uchiumi, Hideki; Tomura, Masaaki; Chemistry Letters; nb. 6; (2002); p. 622 - 623, View in Reaxys 2 of 15

Description (Liquid/Solid Systems (MCS))

Liquid-solid phase equilibrium

Temperature (Liquid/Solid Systems (MCS)) [°C]

-36.16 - 5.53

Partner (Liquid/Solid Systems (MCS))

benzene

Lohmann, Juergen; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 333 - 336, View in Reaxys 3 of 15

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Partner (Liquid/Solid Systems (MCS))

benzene

Lohmann, Juergen; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 333 - 336, View in Reaxys

131/225

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4 of 15

Description (Liquid/Solid Systems (MCS))

Liquid-solid phase equilibrium

Temperature (Liquid/Solid Systems (MCS)) [°C]

-67.91 - -13.3

Partner (Liquid/Solid Systems (MCS))

toluene

Lohmann, Juergen; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 333 - 336, View in Reaxys 5 of 15

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Partner (Liquid/Solid Systems (MCS))

toluene

Lohmann, Juergen; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 333 - 336, View in Reaxys 6 of 15

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

butanedinitrile

Timmermans; Naveau; Bulletin des Societes Chimiques Belges; vol. 67; (1958); p. 560,561, View in Reaxys 7 of 15

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Comment (Liquid/Solid Systems (MCS))

Verbindung 1:1.

Partner (Liquid/Solid Systems (MCS))

N2O2

Addison; Sheldon; Journal of the Chemical Society; (1956); p. 1941,1945, View in Reaxys 8 of 15

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

NOCl

Addison; Sheldon; Journal of the Chemical Society; (1956); p. 1941,1945, View in Reaxys 9 of 15

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Temperature (Liquid/Solid Systems (MCS)) [°C]

-67.5

Comment (Liquid/Solid Systems (MCS))

Verbindung 1:1.

Partner (Liquid/Solid Systems (MCS))

chloroform

Murray; Schneider; Canadian Journal of Chemistry; vol. 33; (1955); p. 797,799, View in Reaxys 10 of 15

Description (Liquid/Solid Systems (MCS))

Melting diagram

Comment (Liquid/Solid Systems (MCS))

1 Additionsverbindung (2:1).

Partner (Liquid/Solid Systems (MCS))

titanium tetrachloride

Puschin et al.; Justus Liebigs Annalen der Chemie; vol. 553; (1942); p. 278,280, 281, 282, 284, View in Reaxys 11 of 15

Description (Liquid/Solid Systems (MCS))

Melting diagram

Partner (Liquid/Solid Systems (MCS))

tin(IV) chloride

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Puschin et al.; Justus Liebigs Annalen der Chemie; vol. 553; (1942); p. 278,280, 281, 282, 284, View in Reaxys 12 of 15

Description (Liquid/Solid Systems (MCS))

Melting diagram

Partner (Liquid/Solid Systems (MCS))

antimony (III)-iodide

Puschin et al.; Justus Liebigs Annalen der Chemie; vol. 553; (1942); p. 278,280, 281, 282, 284, View in Reaxys 13 of 15

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Temperature (Liquid/Solid Systems (MCS)) [°C]

-13.2 - 6

Pressure (Liquid/Solid Systems (MCS)) [Torr]

735.5 - 706823

Deffet; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 69, View in Reaxys 14 of 15

Description (Liquid/Solid Systems (MCS))

Melting diagram

Comment (Liquid/Solid Systems (MCS))

5 Additionsverbindungen (3:1, 2:1, 3:2, 6:5, 1:1).

Partner (Liquid/Solid Systems (MCS))

titanium tetrachloride

Hertel; Demmer; Justus Liebigs Annalen der Chemie; vol. 499; (1932); p. 134,138, 142; Justus Liebigs Annalen der Chemie; vol. 553; (1942); p. 286, View in Reaxys 15 of 15

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-63.7

Partner (Liquid/Solid Systems (MCS))

chlorobenzene

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys Liquid/Vapour Systems (MCS) (35) 1 of 35

Description (Liquid/ Vapour Systems (MCS))

Critical temperature

Partner (Liquid/Vapour Systems (MCS))

Hexadecane

Wang, Nong; Mao, Chunfeng; Peng, Xuhong; An, Xueqin; Shen, Weiguo; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 732 - 738, View in Reaxys 2 of 35

Description (Liquid/ Vapour Systems (MCS))

Critical density

Partner (Liquid/Vapour Systems (MCS))

Hexadecane

Wang, Nong; Mao, Chunfeng; Peng, Xuhong; An, Xueqin; Shen, Weiguo; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 732 - 738, View in Reaxys 3 of 35

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

50 - 80

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

5.24292 - 758.686

Partner (Liquid/Vapour Systems (MCS))

benzene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys

133/225

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4 of 35

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour phase diagram

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

50 - 80

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

5.24292 - 758.686

Partner (Liquid/Vapour Systems (MCS))

benzene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 5 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

50 - 80

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

5.24292 - 758.686

Partner (Liquid/Vapour Systems (MCS))

benzene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 6 of 35

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

50 - 80

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

3.8178 - 291.646

Partner (Liquid/Vapour Systems (MCS))

toluene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 7 of 35

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour phase diagram

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

50 - 80

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

3.8178 - 291.646

Partner (Liquid/Vapour Systems (MCS))

toluene

Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 8 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

50 - 80

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

3.8178 - 291.646

Partner (Liquid/Vapour Systems (MCS))

toluene

134/225

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Gmehling; Horstmann; Gardeler; Bolts; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 539 - 543, View in Reaxys 9 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

Hexadecane

Dallas, Andrew J.; Carr, Peter W.; Journal of Physical Chemistry; vol. 98; nb. 18; (1994); p. 4927 - 4939, View in Reaxys 10 of 35

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

40.1 - 120.1

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

45678.6 - 135686

Partner (Liquid/Vapour Systems (MCS))

carbon dioxide

Walther; Maurer; Journal of Chemical and Engineering Data; vol. 38; nb. 2; (1993); p. 247 - 249, View in Reaxys 11 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

24.9

Partner (Liquid/Vapour Systems (MCS))

t-butyl bromide

Abraham, Michael H.; Grellier, Priscilla L.; Nasehzadeh, Asadollah; Walker, Rosemary A.C.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1988); p. 1717 - 1724, View in Reaxys 12 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

24.9

Partner (Liquid/Vapour Systems (MCS))

tertiary butyl chloride

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

octane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 14 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

butanone

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Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 15 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

ethanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 16 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

toluene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 17 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

1,4-dioxane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 18 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

nitromethane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 19 of 35

Description (Liquid/ Vapour Systems (MCS))

Critical data for mixtures

Partner (Liquid/Vapour Systems (MCS))

2,2,4-trimethylpentane

Miller, B. C.; Clerke, E. A.; Greer, S. C.; Journal of Physical Chemistry; vol. 87; nb. 3; (1983); p. 1063 - 1066, View in Reaxys 20 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 21 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

methyl iodide

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Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 22 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

methanol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 23 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethyl bromide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 24 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethyl iodide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 25 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethanol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 26 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

isoprene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 27 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

1-penten

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 28 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

2-methyl-but-2-ene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 29 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

pentane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 30 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 31 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

hexane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 32 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

n-heptane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 33 of 35

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Lekhova; Belousova; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 1627; ; p. 2719, View in Reaxys 34 of 35

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Pul'tsin et al.; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 428; ; p. 751, View in Reaxys 35 of 35

Description (Liquid/ Vapour Systems (MCS))

Critical data for mixtures

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys Magnetic Data (1) Description (Magnetic Data)

References

Magnetic properties Bauer et al.; Monatshefte fuer Chemie; vol. 101; (1970); p. 469,470,473, View in Reaxys Magnetic Susceptibility (3) Magnetic Suscepti- References bility [10-6cm3mol-1] Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 179,182, View in Reaxys; Francois; Bulletin de la Societe Chimique de France; (1962); p. 511, View in Reaxys -65.2

French; Transactions of the Faraday Society; vol. 50; (1954); p. 1320,1321, View in Reaxys

-64.2

Sauret; Lalande; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 236; (1953); p. 2066, View in Reaxys

Mechanical & Physical Properties (MCS) (40) 1 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 300

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

750.06 - 225018

Comment (Mechanical & Physical Properties (MCS))

diagram

Partner (Mechanical & Physical Properties (MCS))

H2O

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Striteska, Lucie; Hnedkovsky, Lubomir; Cibulka, Ivan; Journal of Chemical Thermodynamics; vol. 35; nb. 7; (2003); p. 1199 - 1212, View in Reaxys 2 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 35

Partner (Mechanical & Physical Properties (MCS))

methanol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 3 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

ethanol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 4 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

propan-1-ol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 5 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 6 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

pentan-1-ol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys

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7 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

tert-butyl alcohol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 8 of 40

Description (Mechanical & Physical Properties (MCS))

Ultrasonic velocity

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25.35 - 45.35

Partner (Mechanical & Physical Properties (MCS))

pyridine

Gill, Dip Singh; Singh, Parvinder; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 5; (1999); p. 478 - 481, View in Reaxys 9 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

chlorobenzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 10 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

chlorobenzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 11 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 12 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

140/225

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Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 13 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

toluene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 14 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

toluene

Tanaka, Reiji; Nakamichi, Toru; Journal of Chemical Thermodynamics; vol. 29; nb. 2; (1997); p. 221 - 227, View in Reaxys 15 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 16 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

toluene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 17 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

141/225

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Partner (Mechanical & Physical Properties (MCS))

o-xylene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 18 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

m-xylene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 19 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

para-xylene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 20 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

ethylbenzene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 21 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

styrene

Haijun, Wang; Mingzhi, Chen; Guokang, Zheng; Journal of Chemical Thermodynamics; vol. 27; nb. 1; (1995); p. 57 - 62, View in Reaxys 22 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

142/225

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Partner (Mechanical & Physical Properties (MCS))

methyl cyclohexane

Venkatesulu; Goud; Prabhakara Rao; Journal of Chemical and Engineering Data; vol. 36; nb. 4; (1991); p. 473 - 474, View in Reaxys 23 of 40

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 40

Partner (Mechanical & Physical Properties (MCS))

Bromoform

Joshi, Shrikant S.; Aminabhavi, Tejraj M.; Shukla, Shyam S.; Canadian Journal of Chemistry; vol. 68; (1990); p. 251 - 257, View in Reaxys 24 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

10 - 45

Partner (Mechanical & Physical Properties (MCS))

cyclohexane

Tanaka, Reiji; Nakamichi, Toru; Murakami, Sachio; Journal of Solution Chemistry; vol. 14; nb. 11; (1985); p. 795 - 804, View in Reaxys 25 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

methoxybenzene

Rajkumar, X. Rosario; Raman, K. V.; Arulraj, S. J.; Journal of the Indian Chemical Society; vol. 62; nb. 7; (1985); p. 516 518, View in Reaxys 26 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Partner (Mechanical & Physical Properties (MCS))

nitrobenzene

Jannelli, Liliana; Lopez, Antonio; Saiello, Silvana; Journal of Chemical & Engineering Data; vol. 28; nb. 2; (1983); p. 169 173, View in Reaxys 27 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

143/225

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Partner (Mechanical & Physical Properties (MCS))

propan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 28 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 29 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

pentan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 30 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

isopropyl alcohol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 31 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

2-methyl-propan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 32 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

144/225

2018-05-24 12:11:44

Partner (Mechanical & Physical Properties (MCS))

i-Amyl alcohol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 33 of 40

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

propan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 34 of 40

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 35 of 40

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

pentan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 36 of 40

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

isopropyl alcohol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 37 of 40

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

145/225

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Partner (Mechanical & Physical Properties (MCS))

2-methyl-propan-1-ol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 38 of 40

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

i-Amyl alcohol

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys 39 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

10.6 - 50

Partner (Mechanical & Physical Properties (MCS))

sulfolane

Jannelli, L.; Lopez, A.; Saiello, S.; Journal of Chemical & Engineering Data; vol. 25; nb. 3; (1980); p. 259 - 263, View in Reaxys 40 of 40

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Oswal et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 17; (1979); p. 605, View in Reaxys; Fried et al.; Bulletin of the Chemical Society of Japan; vol. 50; (1977); p. 497, View in Reaxys; Reddy; Naidu; Australian Journal of Chemistry; vol. 31; (1978); p. 2145,2146-2147, View in Reaxys Mechanical Properties (3) Description (MeReferences chanical Properties) Specific volume

Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Molar volume

Miller et al.; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 417,418, 419, View in Reaxys; Reddy; Naidu; Australian Journal of Chemistry; vol. 31; (1978); p. 2145,2146-2147, View in Reaxys; Mayer; Monatshefte fuer Chemie; vol. 110; (1979); p. 191,195, View in Reaxys; Fedotov, A. N.; Isaeva, E. S.; Gol'dshtein, I. P.; Russian Journal of Physical Chemistry; vol. 65; nb. 9; (1991); p. 1320 - 1324; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2501 2510, View in Reaxys; Chawla, B.; Mehta, S. K.; Jasra, R. V.; Suri, S. K.; Canadian Journal of Chemistry; vol. 61; (1983); p. 2147 - 2150, View in Reaxys; Jannelli, L.; Lopez, A.; Saiello, S.; Journal of Chemical & Engineering Data; vol. 25; nb. 3; (1980); p. 259 - 263, View in Reaxys; Jannelli, Liliana; Lopez, Antonio; Saiello, Silvana; Journal of Chemical & Engineering Data; vol. 28; nb. 2; (1983); p. 169 - 173, View in Reaxys

Viscosity

Akhmetkarimov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 458,460, View in Reaxys; Wright; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 454, View in Reaxys

Molecular Deformation (4) Description (MoComment (Molecu- References lecular Deformalar Deformation) tion) Rotational constants

Siglow, Klaus; Neusser, Hans Juergen; Journal of Physical Chemistry A; vol. 105; nb. 33; (2001); p. 7823 - 7827, View in Reaxys

Force constants

Besnainou et al.; Journal of Molecular Spectroscopy; vol. 21; (1966); p. 113,121, View in Reaxys; Csaszar, Attila G.; Fogarasi, Geza; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 45; nb. 8; (1989); p. 845 - 854, View in Reaxys

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Fundamental vibrations

Wilson; Bloor; Spectrochimica Acta; vol. 21; (1965); p. 45, View in Reaxys

Fundamental vibra- des Molekuels. tions

Bass; Journal of Chemical Physics; vol. 18; (1950); p. 1403,1405, View in Reaxys; Whiffen; Spectrochimica Acta; vol. 7; (1956); p. 253,255, View in Reaxys

Optical Rotatory Power (1) 1 of 1

Type (Optical Rotatory Power)

alpha

Chekmareva et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 6; (1970); p. 735; Khimiya Geterotsiklicheskikh Soedinenii; vol. 6; (1970); p. 794, View in Reaxys Optics (12) Description (Optics)

Comment (Optics)

References

Iso-and anisotropic components of Rayleigh scattering

Chang, Yong Joon; Cong, Peijun; Simon, John D.; Journal of Chemical Physics; vol. 106; nb. 21; (1997); p. 8639 - 8649, View in Reaxys

Magnetic birefringence (CottonMouton effect)

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys; Szivessy; Zeitschrift fuer Physik; vol. 18; p. 104; Chem. Zentralbl.; vol. 95; nb. I; (1924); p. 2567, View in Reaxys; Le Fevre et al.; Australian Journal of Chemistry; vol. 24; (1971); p. 1177,1180, View in Reaxys; Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 1315,1316,1320, View in Reaxys; Nikolaev, V. F.; Strobykin, S. I.; Vul'fson, S. G.; Vereshchagin, A. N.; Russian Journal of Physical Chemistry; vol. 63; nb. 3; (1989); p. 447 449; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 813 - 814, View in Reaxys

Linear dichroism

Jede, F.; Stratmann, A. W.; Schrader, B.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 140; (1986); p. 287 - 296, View in Reaxys; Jede, F.; Stratmann, A. W.; Schrader, B.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 140; (1986); p. 297 - 302, View in Reaxys

Rayleigh scattering

Gershon et al.; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 316, View in Reaxys; Whittenburg; Wang; Journal of Chemical Physics; vol. 71; (1979); p. 561, View in Reaxys; Alms; Patterson; Journal of Chemical Physics; vol. 71; (1979); p. 563, View in Reaxys; Goodman, M. A.; Whittenburg, S. L.; Journal of Physical Chemistry; vol. 88; nb. 23; (1984); p. 5653 - 5656, View in Reaxys

Degree of depolarization of Rayleigh scattering

Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 747,748, 752, View in Reaxys; Alms; Patterson; Journal of Chemical Physics; vol. 68; (1978); p. 3440, View in Reaxys; Whittenburg; Wang; Journal of Chemical Physics; vol. 66; (1977); p. 4995, View in Reaxys

Magnetic circular dichroism

Shieh et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 1031,1035, 1036, View in Reaxys; Kaito et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 384,387, View in Reaxys; Foss; McCarville; Journal of the American Chemical Society; vol. 89; (1967); p. 30, View in Reaxys

Magnetorotation

Seamans; Linderberg; Molecular Physics; vol. 24; (1972); p. 1393,1402, View in Reaxys

Electric birefringence (Kerr effect)

LeFevre; Journal of the Chemical Society; (1965); p. 2499,2500,2502,2503, View in Reaxys

Degree of depolarization of Rayleigh scattering

Depolarisationsgrad Le Fevre; Rao; Journal of the Chemical Society; (1958); p. 1465, View in Reaxys des an Gemischen mit CCl4 gestreuten Lichts.

Electric birefringence (Kerr effect)

Kerr-Konstante in CCl4 bei 25grad.

Le Fevre; Le Fevre; Journal of the Chemical Society; (1954); p. 1577,1581; Australian Journal of Chemistry; vol. 7; (1954); p. 33,35, View in Reaxys

Diffraction

von RoentgenStrahlen in fluessigem Benzonitril (vgl. E II 197).

Ishino; Tanaka; Tsuji; Memoirs of the College of Science, Kyoto Imperial University; vol. <A> 13; (1930); p. 1,14, View in Reaxys

Electric birefringence (Kerr effect)

von BenzonitrilLippmann; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 17; Benzol-Gemischen. (1911); p. 15, View in Reaxys

Other Thermochemical Data (6) Description (Other Comment (Other Thermochemical Thermochemical Data) Data)

References

147/225

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Entropy

Cryoscopic constant

Brooks; Pilcher; Journal of the Chemical Society; (1959); p. 1535,1539, View in Reaxys; Witschonke; Analytical Chemistry; vol. 26; (1954); p. 562, View in Reaxys; Lebedev, B. V.; Bykova, T. A.; Kiparisova, E. G.; Pankratov, V. A.; Mitina, L. M.; Korshak, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 6; (1984); p. 1352 - 1358,1209 - 1214, View in Reaxys

Thermodynamic properties

Kojima; Bard; Journal of the American Chemical Society; vol. 97; (1975); p. 6317,6321, View in Reaxys; Popkie; Kaufman; Journal of Chemical Physics; vol. 66; (1977); p. 4827, View in Reaxys; Del Bene; Jaffe; Journal of Chemical Physics; vol. 49; (1968); p. 1221,1226, View in Reaxys; Freiser; B.auchamp; Journal of the American Chemical Society; vol. 98; (1976); p. 265, View in Reaxys; Wright; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 784,786, View in Reaxys; Kaito et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 384,387, View in Reaxys; Rouch et al.; Acta Physica Polonica, A; vol. 50; (1976); p. 503,510,512, View in Reaxys; Madan; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 89; (1974); p. 259, View in Reaxys; Mayer; Monatshefte fuer Chemie; vol. 110; (1979); p. 191,195, View in Reaxys; Mayer; Monatshefte fuer Chemie; vol. 109; (1978); p. 775,776,778,780,782-785, View in Reaxys; Green; Spectrochimica Acta; vol. 17; (1961); p. 607, View in Reaxys

Enthalpy

Bentrude; Macknight; Tetrahedron Letters; (1966); p. 3147,3148, View in Reaxys

Ebullioscopic constant

3.87 (fuer 1000 g Loesungsmittel).

Heat of combustion 865,6 kcal/Mol. at constant volume

Philip; Waterton; Journal of the Chemical Society; (1930); p. 2783, View in Reaxys Berthelot; Petit; Annales de Chimie (Cachan, France); vol. <6>18; (1889); p. 112, View in Reaxys

Partition octan-1-ol/water (MCS) (3) 1 of 3

log POW

1.56

7.4

Comment (Partition octan-1-ol/water (MCS))

aq.buffer

Toulmin, Anita; Wood, J. Matthew; Kenny, Peter W.; Journal of Medicinal Chemistry; vol. 51; nb. 13; (2008); p. 3720 3730, View in Reaxys 2 of 3

log POW

1.5

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys 3 of 3

log POW

-1.56

Valko, Klara; Du, Chau My; Bevan, Christopher D.; Reynolds, Derek P.; Abraham, Michael H.; Journal of Pharmaceutical Sciences; vol. 89; nb. 8; (2000); p. 1085 - 1096, View in Reaxys Solubility (MCS) (5) 1 of 5

Saturation

in pure solvent

Comment (Solubility (MCS))

equation

Jain, Neera; Yalkowsky, Samuel H.; Journal of Pharmaceutical Sciences; vol. 90; nb. 2; (2001); p. 234 - 252, View in Reaxys 2 of 5

Comment (Solubility (MCS))

bei versch. Temp. fuer H2S, SO2

Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys 3 of 5

Comment (Solubility (MCS))

Lsgm.-Parameter, S.462

Fowler et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 460, View in Reaxys 4 of 5

Comment (Solubility (MCS))

Solvatation in CCl4

Figeys; Nasielski; Spectrochimica Acta; vol. 22; (1966); p. 2055,2059, View in Reaxys

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5 of 5

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

1 part(s) of substance.dissolves in:100 parts of solvent.in boiling solvent.

Fehling; Justus Liebigs Annalen der Chemie; vol. 49; (1844); p. 92, View in Reaxys Solution Behaviour (MCS) (19) 1 of 19

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Be- 25 - 45 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

ethyl acetate

Del Carmen Grande, Maria; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1324 - 1327, View in Reaxys 2 of 19

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Be- 25 - 45 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

acetic acid butyl ester

Del Carmen Grande, Maria; Marschoff, Carlos M.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1324 - 1327, View in Reaxys 3 of 19

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

lithium perfluoro-1-octanesufonate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 4 of 19

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

sodium cholate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 5 of 19

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

sodium dodecyl-sulfate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 6 of 19

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Be- 25 - 45 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

ethanol; H2O

Grande, M. C.; Fresco, J.; Marschoff, C. M.; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1165 - 1167, View in Reaxys

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7 of 19

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Be- 25 - 45 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

propan-1-ol; H2O

Grande, M. C.; Fresco, J.; Marschoff, C. M.; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1165 - 1167, View in Reaxys 8 of 19

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Be- 0 - 90 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water

Stephenson; Journal of Chemical and Engineering Data; vol. 39; nb. 2; (1994); p. 225 - 227, View in Reaxys 9 of 19

Description (Solution Behaviour (MCS))

Solubilizing

Solvent (Solution Behaviour (MCS))

H2O

Partner (Solution Behaviour (MCS))

in micellar phases of sodium dodecyl sulfate

Suslov, D. A.; Solomonov, B. N.; Russian Journal of Physical Chemistry; vol. 67; nb. 8; (1993); p. 1446 - 1448; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 8; (1993); p. 1611 - 1614, View in Reaxys 10 of 19

Description (Solution Behaviour (MCS))

Solubilizing

Solvent (Solution Behaviour (MCS))

H2O

Partner (Solution Behaviour (MCS))

in micellar phases of dodecyltrimethylammonium bromide

Description (Solution Behaviour (MCS))

Dissolving capacity

Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 23; (1973); p. 1,8, View in Reaxys; Markowitz et al.; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 325, View in Reaxys; Salomon; Canadian Journal of Chemistry; vol. 54; (1976); p. 1487, View in Reaxys 12 of 19

Description (Solution Behaviour (MCS))

Miscibility

Hollecker et al.; Chemical Physics; vol. 11; (1975); p. 99,100-105, View in Reaxys 13 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- -8 - 100 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

aluminium bromide

Mueller; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 38; (1932); p. 227,230, View in Reaxys 14 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

silver nitrate

Koch; Journal of the Chemical Society; (1928); p. 272, View in Reaxys; Mueller,R.; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 142; (1925); p. 130, View in Reaxys

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15 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

bromine

Naumann; Chemische Berichte; vol. 47; (1914); p. 1369, View in Reaxys 16 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

iodine

Naumann; Chemische Berichte; vol. 47; (1914); p. 1369, View in Reaxys 17 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

sulfur

Naumann; Chemische Berichte; vol. 47; (1914); p. 1369, View in Reaxys 18 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

anorganic salts

Shaw; Journal of Physical Chemistry; vol. 17; (1913); p. 170, View in Reaxys; Naumann; Chemische Berichte; vol. 47; (1914); p. 1369, View in Reaxys 19 of 19

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

tetrapropylammonium iodide

Walden; Chem. Zentralbl.; vol. 84; nb. II; (1913); p. 209, View in Reaxys Sound Properties (5) Description (Sound Comment (Sound Properties) Properties)

References

Ultrasonic velocity

Gill, Dip Singh; Singh, Parvinder; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 5; (1999); p. 478 - 481, View in Reaxys

Velocity of sound

Karunakar, J.; Reddy, K. Dayananda; Rao, M. V. Prabhakara; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 348 - 350, View in Reaxys; Goodman, Mark A.; McClure, Allen W.; Whittenburg, Scott L.; Journal of Chemical & Engineering Data; vol. 29; nb. 3; (1984); p. 247 - 248, View in Reaxys; Gill, Dip Singh; Singh, Rajinder; Ali, Vazid; Singh, Jasbir; Rehani, Sharwan Kumar; Journal of the Chemical Society, Faraday Transactions; vol. 90; nb. 4; (1994); p. 583 - 586, View in Reaxys; Rajkumar, X. Rosario; Raman, K. V.; Arulraj, S. J.; Journal of the Indian Chemical Society; vol. 62; nb. 7; (1985); p. 516 - 518, View in Reaxys; Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 20; nb. 7; (1988); p. 809 - 814, View in Reaxys; Gill, Dip Singh; Singh, Parvinder; Singh, Jasbir; Singh, Pritam; Senanayake, Gamini; Hefter, Glenn T.; Journal of the Chemical Society, Faraday Transactions; vol. 91; nb. 17; (1995); p. 2789 - 2796, View in Reaxys

Sound absorption

Goodman, M. A.; Whittenburg, S. L.; Journal of Physical Chemistry; vol. 88; nb. 23; (1984); p. 5653 - 5656, View in Reaxys

Ultrasonic properties

Patil; Indian Journal of Pure and Applied Physics; vol. 16; nb. 6; (1978); p. 608 - 613, View in Reaxys; Lucas et al.; Molecular Physics; vol. 18; (1970); p. 505,511,513,515,519,520, View in Reaxys

Velocity of sound

in fluessigem Benzonitril bei 28grad: 1581 m/sec.

Bhimasenachar; Venkateswarlu; Proceedings - Indian Academy of Sciences, Section A; nb. 11; (1940); p. 28,29, View in Reaxys

Static Dielectric Constant (5) Static Dielectric Temperature (Static References Constant Dielectric Constant) [°C] 25.17

Buchner; Barthel; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 101; nb. 10; (1997); p. 1509 - 1516, View in Reaxys

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25.2

Ho, Patience C.; Ramsey, J. B.; Journal of Chemical & Engineering Data; vol. 31; nb. 4; (1986); p. 430 - 434, View in Reaxys; Tarasova, G. V.; Khashchina, M. V.; Tyurin, S. A.; Bulgarevich, S. B.; Bogdan, I. G.; Russian Journal of Physical Chemistry; vol. 60; nb. 8; (1986); p. 1235 1237; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 2058 - 2061, View in Reaxys

22.31 - 25.66

20 - 60

Jannelli, Liliana; Lopez, Antonio; Saiello, Silvana; Journal of Chemical & Engineering Data; vol. 28; nb. 2; (1983); p. 169 - 173, View in Reaxys

22.26 - 25.69

20.3 - 60

Jannelli, L.; Lopez, A.; Saiello, S.; Journal of Chemical & Engineering Data; vol. 25; nb. 3; (1980); p. 259 - 263, View in Reaxys Decroocq; Bulletin de la Societe Chimique de France; (1964); p. 127,133, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys

Surface Tension (6) Surface Tension Temperature (Sur[g·s-2] face Tension) [°C]

References

31.61 - 39.52

19.3 - 87

Jeffery; Vogel; Journal of the Chemical Society; (1948); p. 663, View in Reaxys

38.05

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

39.1

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

39.65

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 606; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 321, View in Reaxys

33.89

Turner; Merry; Journal of the Chemical Society; vol. 97; (1910); p. 2076, View in Reaxys; Morgan; Chazal; Journal of the American Chemical Society; vol. 35; (1913); p. 1823, View in Reaxys

38.59

Turner; Merry; Journal of the Chemical Society; vol. 97; (1910); p. 2076, View in Reaxys; Morgan; Chazal; Journal of the American Chemical Society; vol. 35; (1913); p. 1823, View in Reaxys

Transport Data (1) Description (Trans- References port Data) Thermal conductiv- Mallan et al.; Journal of Chemical and Engineering Data; vol. 17; (1972); p. 412,414, View in Reaxys ity Transport Phenomena (MCS) (38) 1 of 38

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Nikam, Pandarinath S.; Kharat, Sanjeevan J.; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 972 - 976, View in Reaxys 2 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

29.85 - 39.85

Partner (Transport Phenomena (MCS))

methanol

Abraham, Roshan; Abdulkhadar, M.; Asokan, C. V.; Journal of Chemical Thermodynamics; vol. 32; nb. 1; (2000); p. 1 - 16, View in Reaxys 3 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

29.85 - 39.85

Partner (Transport Phenomena (MCS))

toluene

Abraham, Roshan; Abdulkhadar, M.; Asokan, C. V.; Journal of Chemical Thermodynamics; vol. 32; nb. 1; (2000); p. 1 - 16, View in Reaxys

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4 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 35

Partner (Transport Phenomena (MCS))

methanol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 5 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 40

Partner (Transport Phenomena (MCS))

ethanol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 6 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 40

Partner (Transport Phenomena (MCS))

propan-1-ol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 7 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 40

Partner (Transport Phenomena (MCS))

butan-1-ol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 8 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 40

Partner (Transport Phenomena (MCS))

pentan-1-ol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 9 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 40

Partner (Transport Phenomena (MCS))

tert-butyl alcohol

Nikam, Pandharinath S.; Jagdale, Bapu S.; Sawant, Arun B.; Hasan, Mehdi; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 214 - 218, View in Reaxys 10 of 38

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

15 - 25

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Partner (Transport Phenomena (MCS))

methoxybenzene

Prasad; Viswanathan; Anand Rao; Journal of Chemical and Engineering Data; vol. 45; nb. 5; (2000); p. 764 - 770, View in Reaxys 11 of 38

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

15 - 25

Partner (Transport Phenomena (MCS))

tert-butyl methyl ether

Prasad; Viswanathan; Anand Rao; Journal of Chemical and Engineering Data; vol. 45; nb. 5; (2000); p. 764 - 770, View in Reaxys 12 of 38

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 45

Partner (Transport Phenomena (MCS))

triethyl phosphite

Gill; Singh; Joshi; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 39; nb. 6; (2000); p. 579 - 583, View in Reaxys 13 of 38

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25.05

Partner (Transport Phenomena (MCS))

methanol

Lu; Kong, Rita; Chan; Journal of Chemical Physics; vol. 110; nb. 2-12; (1999); p. 3003 - 3008, View in Reaxys 14 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25.35 - 45.35

Partner (Transport Phenomena (MCS))

pyridine

Gill, Dip Singh; Singh, Parvinder; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 5; (1999); p. 478 - 481, View in Reaxys 15 of 38

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

neat (no solvent)

Temperature (Transport Phenomena (MCS)) [°C]

-63.1

Partner (Transport Phenomena (MCS))

1,1,3,3,5,5-hexaphenylcyclotrisiloxane

Gauglitz, G.; Hoffmann, V.; Kohlhage, S.; Kramer, M.; Journal of Molecular Structure; vol. 349; (1995); p. 65 - 68, View in Reaxys 16 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

24.9

Partner (Transport Phenomena (MCS))

acetonitrile

Gill, Dip Singh; Singh, Rajinder; Ali, Vazid; Singh, Jasbir; Rehani, Sharwan Kumar; Journal of the Chemical Society, Faraday Transactions; vol. 90; nb. 4; (1994); p. 583 - 586, View in Reaxys

154/225

2018-05-24 12:11:44

17 of 38

Description (Transport Phenomena (MCS))

Diffusion

Partner (Transport Phenomena (MCS))

C12H18N2(1+)

Phelps, Donald K.; Ramm, Michael T.; Wang, Yichun; Nelsen, Stephen F.; Weaver, Michael J.; Journal of Physical Chemistry; vol. 97; nb. 1; (1993); p. 181 - 188, View in Reaxys 18 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

methanol

Gill, Dip Singh; Kaur, Taranjit; Kaur, Harkiran; Joshi, Inder Mohan; Singh, Jasbir; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 11; (1993); p. 1737 - 1740, View in Reaxys 19 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

acetone

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

acetonitrile

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

pyridine

155/225

2018-05-24 12:11:44

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

tetrachloromethane

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

-0.1

Partner (Transport Phenomena (MCS))

1,4,5,8-tetraaminoanthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 26 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

9.9

Partner (Transport Phenomena (MCS))

1,4,5,8-tetraaminoanthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 27 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

19.9

Partner (Transport Phenomena (MCS))

1,4,5,8-tetraaminoanthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 28 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

29.9

Partner (Transport Phenomena (MCS))

1,4,5,8-tetraaminoanthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 29 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

39.9

Partner (Transport Phenomena (MCS))

1,4,5,8-tetraaminoanthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 30 of 38

Description (Transport Phenomena (MCS))

Viscosity

156/225

2018-05-24 12:11:44

Temperature (Transport Phenomena (MCS)) [°C]

-0.1

Partner (Transport Phenomena (MCS))

1,4-diamino-9,10-anthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 31 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

9.9

Partner (Transport Phenomena (MCS))

1,4-diamino-9,10-anthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 32 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

19.9

Partner (Transport Phenomena (MCS))

1,4-diamino-9,10-anthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 33 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

29.9

Partner (Transport Phenomena (MCS))

1,4-diamino-9,10-anthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 34 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

39.9

Partner (Transport Phenomena (MCS))

1,4-diamino-9,10-anthraquinone

Hartman, R. S.; Alavi, D. S.; Waldeck, D. H.; Journal of Physical Chemistry; vol. 95; nb. 20; (1991); p. 7872 - 7880, View in Reaxys 35 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

Bromoform

Joshi, Shrikant S.; Aminabhavi, Tejraj M.; Shukla, Shyam S.; Canadian Journal of Chemistry; vol. 68; (1990); p. 251 - 257, View in Reaxys 36 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

tetrachloromethane

157/225

2018-05-24 12:11:44

Nikolaev, V. F.; Strobykin, S. I.; Vul'fson, S. G.; Vereshchagin, A. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 21; (1989); p. 246 - 252,210 - 215, View in Reaxys 37 of 38

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

thiophenol

Tanner, Dennis D.; Rahimi, Parviz M.; Journal of the American Chemical Society; vol. 104; nb. 1; (1982); p. 225 - 229, View in Reaxys 38 of 38

Description (Transport Phenomena (MCS))

Diffusion

Partner (Transport Phenomena (MCS))

AgNO3

vol. Ag: MVol.B1; 4.24.15, page 254 - 254, View in Reaxys; Klotzkin, M. R. P.; Diss. Rensselaer Polytech. Inst. 1964, S. 1/212; Diss. Abstr. B; vol. 27; (1966); p. 434/5 ; (from Gmelin), View in Reaxys Triple Point (2) Triple Point [°C]

References

-12.88

-12.82

Vapour Pressure (1) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

References

10.32

Martin; Collie; Journal of the Chemical Society; (1932); p. 2658,2662, View in Reaxys

NMR Spectroscopy (115) 1 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

Paragraph 0046; 0060

Patent; (18 pag.); CN107573259; (2018); (A) Chinese, View in Reaxys 2 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

Paragraph 0047; 0060

Patent; (18 pag.); CN107573259; (2018); (A) Chinese, View in Reaxys 3 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Location

Paragraph 0023

158/225

2018-05-24 12:11:44

Patent; Dalian Institute of Chemical Physics; Wang, Feng; Zhang, Zhe; Xu, Jie; Wang, Min; Zhang, Chaofeng; Chen, Haijun; (7 pag.); CN105085315; (2017); (B) Chinese, View in Reaxys 4 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

Paragraph 0028

Patent; Zhejiang University of Technology; Zhang Guofu; Zhao Yiyong; Zhang Guihua; Ding Chengrong; Yu Yidong; Lv Jinghui; (10 pag.); CN106866326; (2017); (A) Chinese, View in Reaxys 5 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

Paragraph 0029

Patent; Zhejiang University of Technology; Zhang Guofu; Zhao Yiyong; Zhang Guihua; Ding Chengrong; Yu Yidong; Lv Jinghui; (10 pag.); CN106866326; (2017); (A) Chinese, View in Reaxys 6 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

Paragraph 0017

Patent; Yancheng Normal College; Wang Jin; Hu Xiao; Wang Wenling; Geng Rongqing; Qiu Qiong; Shao Jin; Jin Wenbin; Yan Yiyu; Zhai Yulin; Zhu Xiaoming; (7 pag.); CN107382771; (2017); (A) Chinese, View in Reaxys 7 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Denton, Ross M.; An, Jie; Lindovska, Petra; Lewis, William; Tetrahedron; vol. 68; nb. 13; (2012); p. 2899 - 2905, View in Reaxys; Rokade, Balaji V.; Malekar, Sanjeev K.; Prabhu, Kandikere Ramaiah; Chemical Communications; vol. 48; nb. 44; (2012); p. 5506 - 5508, View in Reaxys; Zheng, Shuyan; Yu, Chunhui; Shen, Zhengwu; Organic Letters; vol. 14; nb. 14; (2012); p. 3644 - 3647, View in Reaxys; Liu, Li; Li, Jian; Xu, Jiao; Sun, Jiang-Tao; Tetrahedron Letters; vol. 53; nb. 51; (2012); p. 6954 - 6956, View in Reaxys; Quinn, Dylan J.; Haun, Graham J.; Moura-Letts, Gustavo; Tetrahedron Letters; vol. 57; nb. 34; (2016); p. 3844 - 3847, View in Reaxys 8 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

159/225

2018-05-24 12:11:44

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Denton, Ross M.; An, Jie; Lindovska, Petra; Lewis, William; Tetrahedron; vol. 68; nb. 13; (2012); p. 2899 - 2905, View in Reaxys; Rokade, Balaji V.; Malekar, Sanjeev K.; Prabhu, Kandikere Ramaiah; Chemical Communications; vol. 48; nb. 44; (2012); p. 5506 - 5508, View in Reaxys; Zheng, Shuyan; Yu, Chunhui; Shen, Zhengwu; Organic Letters; vol. 14; nb. 14; (2012); p. 3644 - 3647, View in Reaxys; Quinn, Dylan J.; Haun, Graham J.; Moura-Letts, Gustavo; Tetrahedron Letters; vol. 57; nb. 34; (2016); p. 3844 - 3847, View in Reaxys 9 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Yu, Lei; Li, Hongyan; Zhang, Xu; Ye, Jianqing; Liu, Jianping; Xu, Qing; Lautens, Mark; Organic Letters; vol. 16; nb. 5; (2014); p. 1346 - 1349, View in Reaxys; Zhang, Xu; Sun, Jingjing; Ding, Yuanhua; Yu, Lei; Organic Letters; vol. 17; nb. 23; (2015); p. 5840 - 5842, View in Reaxys 10 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Rokade, Balaji V.; Prabhu, Kandikere Ramaiah; Journal of Organic Chemistry; vol. 77; nb. 12; (2012); p. 5364 - 5370, View in Reaxys; Islam, Md. Rafiqul; Takikawa, Yuji; Lim, Kwon Taek; Journal of Heterocyclic Chemistry; vol. 51; nb. 3; (2014); p. 604 - 609, View in Reaxys 12 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

160/225

2018-05-24 12:11:44

Frequency (NMR Spectro- 395.7 scopy) [MHz] Jasem, Yosef Al; Barkhad, Mohamed; Khazali, Mona Al; Butt, Hifsa Pervez; El-Khwass, Noha Ashraf; Azani, Mariam Al; Hindawi, Bassam Al; Thiemann, Thies; Journal of Chemical Research; vol. 38; nb. 2; (2014); p. 80 - 84, View in Reaxys 13 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.5 scopy) [MHz] Jasem, Yosef Al; Barkhad, Mohamed; Khazali, Mona Al; Butt, Hifsa Pervez; El-Khwass, Noha Ashraf; Azani, Mariam Al; Hindawi, Bassam Al; Thiemann, Thies; Journal of Chemical Research; vol. 38; nb. 2; (2014); p. 80 - 84, View in Reaxys 14 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Tan, Da-Wei; Xie, Jing-Bo; Li, Qi; Li, Hong-Xi; Li, Jun-Chi; Li, Hai-Yan; Lang, Jian-Ping; Dalton Transactions; vol. 43; nb. 37; (2014); p. 14061 - 14071, View in Reaxys 15 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Tan, Da-Wei; Xie, Jing-Bo; Li, Qi; Li, Hong-Xi; Li, Jun-Chi; Li, Hai-Yan; Lang, Jian-Ping; Dalton Transactions; vol. 43; nb. 37; (2014); p. 14061 - 14071, View in Reaxys 16 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6; tetrahydrofuran

Frequency (NMR Spectro- 500.1 scopy) [MHz] Location

supporting information

161/225

2018-05-24 12:11:44

Knapp, Spring Melody M.; Sherbow, Tobias J.; Yelle, Robert B.; Zakharov, Lev N.; Juliette, J. Jerrick; Tyler, David R.; Organometallics; vol. 32; nb. 3; (2013); p. 824 - 834, View in Reaxys 17 of 115

Description (NMR Spectroscopy)

2D-NMR

Nucleus (NMR Spectroscopy)

13C; 13C

Coupling Nuclei

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Blechta, Vratislav; Schraml, Jan; Magnetic Resonance in Chemistry; vol. 51; nb. 6; (2013); p. 378 - 381, View in Reaxys 18 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Cao, Yu-Qing; Qu, An-Li; Liu, Rui-Yan; Duan, Chun-Ming; Journal of Chemical Research; nb. 7; (2010); p. 414 - 415, View in Reaxys; Zhu, Jintao; Song, Guangwei; Yao, Guoxin; Chen, Gang; Synthetic Communications; vol. 42; nb. 13; (2012); p. 1934 - 1940, View in Reaxys 19 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Rokade, Balaji V.; Prabhu, Kandikere Ramaiah; Journal of Organic Chemistry; vol. 77; nb. 12; (2012); p. 5364 - 5370, View in Reaxys 20 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Temperature (NMR Spectroscopy) [°C]

Satoh, Yasushi; Yasuda, Kaoru; Obora, Yasushi; Organometallics; vol. 31; nb. 15; (2012); p. 5235 - 5238, View in Reaxys 21 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

24.94

Frequency (NMR Spectro- 500 scopy) [MHz]

162/225

2018-05-24 12:11:44

Location

supporting information

Song, Ren-Jie; Wu, Ji-Cheng; Liu, Yu; Deng, Guo-Bo; Wu, Cui-Yan; Wei, Wen-Ting; Li, Jin-Heng; Synlett; vol. 23; nb. 17; (2012); p. 2491 - 2496,6, View in Reaxys 22 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Liu, Li; Li, Jian; Xu, Jiao; Sun, Jiang-Tao; Tetrahedron Letters; vol. 53; nb. 51; (2012); p. 6954 - 6956, View in Reaxys 23 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Azath, Ismail Abulkalam; Suresh, Palaniswamy; Pitchumani, Kasi; New Journal of Chemistry; vol. 36; nb. 11; (2012); p. 2334 - 2339, View in Reaxys 24 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Azath, Ismail Abulkalam; Suresh, Palaniswamy; Pitchumani, Kasi; New Journal of Chemistry; vol. 36; nb. 11; (2012); p. 2334 - 2339, View in Reaxys 25 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Suzuki, Yusuke; Yoshino, Takumi; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 67; nb. 21; (2011); p. 3809 - 3814, View in Reaxys

163/225

2018-05-24 12:11:44

26 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Suzuki, Yusuke; Yoshino, Takumi; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 67; nb. 21; (2011); p. 3809 - 3814, View in Reaxys 27 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Kalkhambkar, Rajesh G.; Bunge, Scott D.; Laali, Kenneth K.; Tetrahedron Letters; vol. 52; nb. 40; (2011); p. 5184 - 5187, View in Reaxys 28 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Kalkhambkar, Rajesh G.; Bunge, Scott D.; Laali, Kenneth K.; Tetrahedron Letters; vol. 52; nb. 40; (2011); p. 5184 - 5187, View in Reaxys 29 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Allen, C. Liana; Burel, Celine; Williams, Jonathan M.J.; Tetrahedron Letters; vol. 51; nb. 20; (2010); p. 2724 - 2726, View in Reaxys 30 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

164/225

2018-05-24 12:11:44

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Allen, C. Liana; Burel, Celine; Williams, Jonathan M.J.; Tetrahedron Letters; vol. 51; nb. 20; (2010); p. 2724 - 2726, View in Reaxys 31 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Rezaei, Ramin; Mohammadi, Mohammad Kazem; Rastin, Nedaa; Chinese Journal of Chemistry; vol. 28; nb. 6; (2010); p. 993 - 996, View in Reaxys 32 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Telvekar, Vikas N.; Sasane, Kulbhushan A.; Synlett; nb. 18; (2010); p. 2778 - 2780, View in Reaxys 33 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys; Zhu, Chenjie; Ji, Lei; Wei, Yunyang; Synthesis; nb. 18; (2010); p. 3121 3125, View in Reaxys; Zhu, Chenjie; Sun, Chengguo; Wei, Yunyang; Synthesis; nb. 24; (2010); p. 4235 - 4241; Art.No: F14610SS, View in Reaxys 34 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25.04

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Saha, Debasree; Saha, Amit; Ranu, Brindaban C.; Tetrahedron Letters; vol. 50; nb. 44; (2009); p. 6088 - 6091, View in Reaxys

165/225

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35 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25.04

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Saha, Debasree; Saha, Amit; Ranu, Brindaban C.; Tetrahedron Letters; vol. 50; nb. 44; (2009); p. 6088 - 6091, View in Reaxys 36 of 115

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys 37 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Kangani, Cyrous O.; Day, Billy W.; Kelley, David E.; Tetrahedron Letters; vol. 49; nb. 5; (2008); p. 914 - 918, View in Reaxys 38 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Kangani, Cyrous O.; Day, Billy W.; Kelley, David E.; Tetrahedron Letters; vol. 49; nb. 5; (2008); p. 914 - 918, View in Reaxys 39 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

benzene-d6

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

166/225

2018-05-24 12:11:44

Sarkar, Soumya; Abboud, Khalil A.; Veige, Adam S.; Journal of the American Chemical Society; vol. 130; nb. 48; (2008); p. 16128 - 16129, View in Reaxys 40 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 60 scopy) [MHz] Arote, Nitin D.; Bhalerao, Dinesh S.; Akamanchi, Krishnacharya G.; Tetrahedron Letters; vol. 48; nb. 21; (2007); p. 3651 3653, View in Reaxys 41 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Burgess,H.; Donnelly,J.A.; Tetrahedron; vol. 47; (1991); p. 111, View in Reaxys; Tsuboi, Sadao; Ishii, Naomi; Sakai, Takashi; Tari, Isao; Utaka, Masanori; Bulletin of the Chemical Society of Japan; vol. 63; nb. 7; (1990); p. 1888 - 1893, View in Reaxys; Schumann, Hans; Speis, Martin; Bosman, W. P.; Smits, J. M. M.; Beurskens, Paul T.; Journal of Organometallic Chemistry; vol. 403; nb. 1.2; (1991); p. 165 - 182, View in Reaxys; Card, Roger J.; Schmitt, J. Lawrence; Journal of Organic Chemistry; vol. 46; (1981); p. 754 - 757, View in Reaxys; Audit, M.; Davoust, D.; Goasdoue, N.; Platzer, N.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 33 - 40, View in Reaxys; Sugimoto, Osamu; Mori, Miho; Moriya, Keisuke; Tanji, Ken-Ichi; Helvetica Chimica Acta; vol. 84; nb. 5; (2001); p. 1112 - 1118, View in Reaxys; Takahashi, Tatsuya; Sugimoto, Osamu; Koshio, Jiro; Tanji, Ken-ichi; Heterocycles; vol. 68; nb. 9; (2006); p. 1973 - 1979, View in Reaxys 42 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Venkat Narsaiah; Nagaiah; Advanced Synthesis and Catalysis; vol. 346; nb. 11; (2004); p. 1271 - 1274, View in Reaxys; Golebiewski; Gucma; Journal of Heterocyclic Chemistry; vol. 43; nb. 2; (2006); p. 509 - 513, View in Reaxys 43 of 115

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Venkat Narsaiah; Nagaiah; Advanced Synthesis and Catalysis; vol. 346; nb. 11; (2004); p. 1271 - 1274, View in Reaxys 44 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Frequency (NMR Spectro- 300 scopy) [MHz] Kusurkar, Radhika; Goswami, Shailesh; Vyas, Sandhya; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 42; nb. 12; (2003); p. 3148 - 3151, View in Reaxys 45 of 115

Description (NMR Spectroscopy)

Chemical shifts

167/225

2018-05-24 12:11:44

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Aitken; Farrell; Kirton; Chemistry of Heterocyclic Compounds; vol. 37; nb. 12; (2001); p. 1526 - 1531, View in Reaxys 46 of 115

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Aitken; Farrell; Kirton; Chemistry of Heterocyclic Compounds; vol. 37; nb. 12; (2001); p. 1526 - 1531, View in Reaxys 47 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Aitken; Farrell; Kirton; Chemistry of Heterocyclic Compounds; vol. 37; nb. 12; (2001); p. 1526 - 1531, View in Reaxys 48 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 400 scopy) [MHz] Abraham, Raymond J.; Reid, Matthew; Magnetic Resonance in Chemistry; vol. 38; nb. 7; (2000); p. 570 - 579, View in Reaxys 49 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Burgess,H.; Donnelly,J.A.; Tetrahedron; vol. 47; (1991); p. 111, View in Reaxys; Jackowski; Les; Dambska; Adamowicz; Polish Journal of Chemistry; vol. 72; nb. 7 SUPPL.; (1998); p. 1624 - 1629, View in Reaxys 50 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Creary; Sky; Journal of the American Chemical Society; vol. 112; nb. 1; (1990); p. 368 - 374, View in Reaxys; Schumann, Hans; Speis, Martin; Bosman, W. P.; Smits, J. M. M.; Beurskens, Paul T.; Journal of Organometallic Chemistry; vol. 403; nb. 1.2; (1991); p. 165 - 182, View in Reaxys; Bromilow, John; Brownlee, Robert T. C.; Craik, David J.; Sadek, Maruse; Taft, Robert W.; Journal of Organic Chemistry; vol. 45; nb. 12; (1980); p. 2429 - 2438, View in Reaxys; Dias, A. R.; Garcia, M. Helena; Robalo, M. Paula; Green, M. L. H.; Lai, K. K.; et al.; Journal of Organometallic Chemistry; vol. 453; nb. 2;

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(1993); p. 241 - 247, View in Reaxys; Audit, M.; Davoust, D.; Goasdoue, N.; Platzer, N.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 33 - 40, View in Reaxys; Bailey, William F.; Cioffi, Eugene A.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 181 - 183, View in Reaxys; Bromilow, John; Brownlee, Robert T. C.; Craik, David J.; Sadek, Maruse; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 862 - 871, View in Reaxys; Haupt, Erhard T. K.; Leibfritz, Dieter; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 45; nb. 2; (1989); p. 119 - 122, View in Reaxys; Bilkis, Isaak I.; Vaganova, Tamara A.; Panteleeva, Elena V.; Salnikov, Georgij E.; Tananakin, Andrej P.; et al.; Journal of Physical Organic Chemistry; vol. 7; nb. 3; (1994); p. 153 - 161, View in Reaxys; Cook, Iain B.; Australian Journal of Chemistry; vol. 42; nb. 9; (1989); p. 1493 - 1518, View in Reaxys; Osborne, Alan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 53; nb. 14; (1997); p. 2475 - 2480, View in Reaxys 51 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetonitrile; CD3CN

Temperature (NMR Spectroscopy) [°C]

De Kowalewski, Dora G.; Kowalewski, Valdemar J.; Botek, Edith; Contreras, Ruben H.; Facelli, Julio C.; Magnetic Resonance in Chemistry; vol. 35; nb. 6; (1997); p. 351 - 356, View in Reaxys 52 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-13C.

Haupt, Erhard T. K.; Leibfritz, Dieter; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 45; nb. 2; (1989); p. 119 - 122, View in Reaxys; Osborne, Alan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 53; nb. 14; (1997); p. 2475 - 2480, View in Reaxys 53 of 115

Description (NMR Spectroscopy)

Linewidth of NMR absorption

Osborne, Alan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 53; nb. 14; (1997); p. 2475 2480, View in Reaxys 54 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

D2O; acetone-d6

Temperature (NMR Spectroscopy) [°C]

Kaminskaia, Natalia V.; Kostic, Nenad M.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); nb. 18; (1996); p. 3677 - 3686, View in Reaxys 55 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Frequency (NMR Spectro- 30.4 scopy) [MHz] Thorn; Pettigrew; Goldenberg; Weber; Environmental Science and Technology; vol. 30; nb. 9; (1996); p. 2764 - 2775, View in Reaxys 56 of 115

Description (NMR Spectroscopy)

Chemical shifts

169/225

2018-05-24 12:11:44

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

acetone-d6

Dias, A. R.; Garcia, M. Helena; Robalo, M. Paula; Green, M. L. H.; Lai, K. K.; et al.; Journal of Organometallic Chemistry; vol. 453; nb. 2; (1993); p. 241 - 247, View in Reaxys 57 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Exner, Otto; Budesinsky, Milos; Collection of Czechoslovak Chemical Communications; vol. 56; nb. 11.1; (1991); p. 2234 2250, View in Reaxys 58 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Comment (NMR Spectroscopy)

1H-1H.

Exner, Otto; Budesinsky, Milos; Collection of Czechoslovak Chemical Communications; vol. 56; nb. 11.1; (1991); p. 2234 2250, View in Reaxys 59 of 115

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

FUNG,B.M.; Journal of the American Chemical Society; vol. 105; (1983); p. 5713, View in Reaxys; Creary; Sky; Journal of the American Chemical Society; vol. 112; nb. 1; (1990); p. 368 - 374, View in Reaxys 60 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Exner, Otto; Budesinsky, Milos; Magnetic Resonance in Chemistry; vol. 27; nb. 1; (1989); p. 27 - 36, View in Reaxys; Terui, Yoshihiro; Yamakawa, Masumi; Honma, Tsunetoshi; Tada, Yukio; Tori, Kazuo; Heterocycles; vol. 19; nb. 2; (1982); p. 221 - 228, View in Reaxys 61 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3; dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

170/225

2018-05-24 12:11:44

Exner, Otto; Budesinsky, Milos; Magnetic Resonance in Chemistry; vol. 27; nb. 1; (1989); p. 27 - 36, View in Reaxys 62 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

CDCl3

Audit, M.; Davoust, D.; Goasdoue, N.; Platzer, N.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 33 - 40, View in Reaxys; Haupt, Erhard T. K.; Leibfritz, Dieter; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 45; nb. 2; (1989); p. 119 - 122, View in Reaxys 63 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Wrackmeyer, Bernd; Zeitschrift fuer Naturforschung, B: Chemical Sciences; vol. 43; nb. 7; (1988); p. 923 - 926, View in Reaxys 64 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

benzene-d6

Wrackmeyer, Bernd; Zeitschrift fuer Naturforschung, B: Chemical Sciences; vol. 43; nb. 7; (1988); p. 923 - 926, View in Reaxys 65 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

benzene-d6

Comment (NMR Spectroscopy)

15N-13C.

Wrackmeyer, Bernd; Zeitschrift fuer Naturforschung, B: Chemical Sciences; vol. 43; nb. 7; (1988); p. 923 - 926, View in Reaxys 66 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

Faure, Robert; Llinares, Jeanine; Elguero, Jose; Goya, Pilar; Bulletin des Societes Chimiques Belges; vol. 96; nb. 8; (1987); p. 603 - 618, View in Reaxys 67 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

171/225

2018-05-24 12:11:44

Banks, Malcolm R.; Brown, Charles; Hudson, Robert F.; Record, Keith A. F.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1986); p. 1501 - 1508, View in Reaxys 68 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Comment (NMR Spectroscopy)

13C-13C.

Krishnamurthy, V. V.; Prakash, G. K. Surya; Iyer, Pradeep S.; Olah, Georg A.; Journal of the American Chemical Society; vol. 108; nb. 7; (1986); p. 1575 - 1579, View in Reaxys; Olah, George A.; Iyer, Pradeep S.; Prakash, G. K. Surya; Krishnamurthy, V. V.; Journal of the American Chemical Society; vol. 106; nb. 23; (1984); p. 7073 - 7077, View in Reaxys 70 of 115

Description (NMR Spectroscopy)

NMR with shift reagents

Beaute et al.; Journal of the Chemical Society [Section] D: Chemical Communications; (1971); p. 700, View in Reaxys; Diehl, P.; Amrein, J.; Veracini, C. A.; Organic Magnetic Resonance; vol. 20; nb. 4; (1982); p. 276 - 278, View in Reaxys; Audit, M.; Davoust, D.; Goasdoue, N.; Platzer, N.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 33 - 40, View in Reaxys; Raber, Douglas J.; Caines, G. Herbert; Johnston, Milton D.; Raber, Nancy K.; Journal of Magnetic Resonance (1969-1992); vol. 47; nb. 1; (1982); p. 38 - 50, View in Reaxys 71 of 115

Description (NMR Spectroscopy)

Spin-lattice relaxation time (T1)

Lippmaa et al.; Chemical Physics Letters; vol. 11; (1971); p. 120, View in Reaxys; Wehrli; Journal of Magnetic Resonance (1969-1992); vol. 32; (1978); p. 451,452, 453, 454, View in Reaxys; Sterk et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 34; (1979); p. 375, View in Reaxys; Audit, M.; Davoust, D.; Goasdoue, N.; Platzer, N.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 33 - 40, View in Reaxys 72 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Schuster, Ingeborg I.; Journal of Organic Chemistry; vol. 50; nb. 10; (1985); p. 1656 - 1662, View in Reaxys 73 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CH2Cl2

Temperature (NMR Spectroscopy) [°C]

172/225

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Guillaume, F.; Seguin, J. P.; Nadjo, L.; Uzan, R.; Membrey, F.; Doucet, J.P.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1984); p. 1139 - 1144, View in Reaxys 74 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

methanol; aq. NaOH

Temperature (NMR Spectroscopy) [°C]

Description (NMR Spectroscopy)

NMR in liquid-crystal phase

FUNG,B.M.; Journal of the American Chemical Society; vol. 105; (1983); p. 5713, View in Reaxys; Haloui; Canet; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 275; (1972); p. 447, View in Reaxys 76 of 115

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

FUNG,B.M.; Journal of the American Chemical Society; vol. 105; (1983); p. 5713, View in Reaxys 77 of 115

Description (NMR Spectroscopy)

CIDNP

Becker, Heinz G. O.; Pfeifer, Dietmar; Radeglia, Reiner; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 38; nb. 12; (1983); p. 1591 - 1597, View in Reaxys 78 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CCl4

Bothner-By; Glick; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1652, View in Reaxys; Keumi, Takashi; Yamamoto, Takayoshi; Saga, Hiroshi; Kitajima, Hidehiko; Bulletin of the Chemical Society of Japan; vol. 54; nb. 5; (1981); p. 1579 1580, View in Reaxys; Raber, Douglas J.; Caines, G. Herbert; Johnston, Milton D.; Raber, Nancy K.; Journal of Magnetic Resonance (1969-1992); vol. 47; nb. 1; (1982); p. 38 - 50, View in Reaxys 79 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

acetone

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 80 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

acetonitrile

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 81 of 115

Description (NMR Spectroscopy)

Chemical shifts

173/225

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Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

dioxane

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 82 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

methanol

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 83 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

CH2Cl2

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 84 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

dimethylformamide

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 85 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectroscopy)

nitromethane

Casewit, Carla; Roberts, John D.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 47; nb. 15; (1982); p. 2875 2878, View in Reaxys 86 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

benzene-d6

Comment (NMR Spectroscopy)

1H-1H, 13C-1H, 15N-1H.

Diehl, P.; Amrein, J.; Veracini, C. A.; Organic Magnetic Resonance; vol. 20; nb. 4; (1982); p. 276 - 278, View in Reaxys 87 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Temperature (NMR Spectroscopy) [°C]

29.9

Comment (NMR Spectroscopy)

1H-1H, 13C-1H, 15N-1H. Solvent(s): further solvent(s)

Diehl, P.; Amrein, J.; Veracini, C. A.; Organic Magnetic Resonance; vol. 20; nb. 4; (1982); p. 276 - 278, View in Reaxys

174/225

2018-05-24 12:11:44

88 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

methanol

Chawla,B.; Pollak,S.K.; Lebrilla,C.B.; Journal of the American Chemical Society; vol. 103; (1981); p. 6924, View in Reaxys 89 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

13C-13C.

Wray, V.; Ernst, L.; Lund, T.; Jakobsen, H. J.; Journal of Magnetic Resonance (1969-1992); vol. 40; nb. 1; (1980); p. 55 - 68, View in Reaxys 90 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

des p-C-Atoms im 13C-NMR in versch. Lsgm. gegenueber Benzol als Standard (Tab.I)

Bromilow et al.; Journal of Organic Chemistry; vol. 44; (1979); p. 4766, View in Reaxys 91 of 115

Description (NMR Spectroscopy)

NMR

Huegel,H.M. et al.; Australian Journal of Chemistry; vol. 32; (1979); p. 1511 - 1519, View in Reaxys; Thiem,K.-W.; Chemische Berichte; vol. 103; (1970); p. 3842 - 3849, View in Reaxys; Bravo,P. et al.; Tetrahedron; vol. 26; (1970); p. 1315 - 1330, View in Reaxys; Casanova,J. et al.; Journal of Organic Chemistry; vol. 31; (1966); p. 3473 - 3482, View in Reaxys; Boleslawski,M. et al.; Journal of Organometallic Chemistry; vol. 161; (1978); p. 279 - 288, View in Reaxys; Becker,W. et al.; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 25; (1970); p. 1332 - 1337, View in Reaxys; Retcofsky; Friedel; Journal of Physical Chemistry; vol. 71; (1967); p. 3592, View in Reaxys; Long Jr.; Goldstein; Organic Magnetic Resonance; vol. 9; (1977); p. 148, View in Reaxys; Syrova; Sheinker; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 8; (1972); p. 313; Khimiya Geterotsiklicheskikh Soedinenii; vol. 8; (1972); p. 345, View in Reaxys; Sosnovsky et al.; Synthesis; (1979); p. 722, View in Reaxys; Trickes et al.; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 32; (1977); p. 956, View in Reaxys; Gramstad; Vikane; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 28; (1972); p. 2131,2137, View in Reaxys; Takai et al.; Chemical and Pharmaceutical Bulletin; vol. 26; (1978); p. 1303,1306, View in Reaxys; Brown; Butcher; Australian Journal of Chemistry; vol. 25; (1972); p. 149,164, View in Reaxys; Castellano; Sun; Journal of the American Chemical Society; vol. 88; (1966); p. 4742, View in Reaxys; Veracini et al.; Chemical Physics Letters; vol. 19; (1973); p. 592, View in Reaxys; Deno et al.; Journal of Organic Chemistry; vol. 31; (1966); p. 1968, View in Reaxys; Fischer; Leupold; Chemische Berichte; vol. 105; (1972); p. 599,608, View in Reaxys; Inamoto et al.; Tetrahedron Letters; (1977); p. 737,739, View in Reaxys; Brown et al.; Journal of the Chemical Society, Chemical Communications; (1977); p. 540, View in Reaxys; Long; Goldstein; Journal of Magnetic Resonance (1969-1992); vol. 34; (1979); p. 361,364, View in Reaxys; Miyajima et al.; Chemical and Pharmaceutical Bulletin; vol. 19; (1971); p. 2301,2305, View in Reaxys; Bromilow et al.; Australian Journal of Chemistry; vol. 30; (1977); p. 351,352, 354, View in Reaxys; Shkurko; Zhurnal Organicheskoi Khimii; vol. 13; (1977); p. 918,842,844, View in Reaxys; Inamoto; Masuda; Tetrahedron Letters; (1977); p. 3287, View in Reaxys; Zanger; Organic Magnetic Resonance; vol. 4; (1972); p. 1,7, View in Reaxys; Nesmeyanov et al.; Journal of Structural Chemistry; vol. 14; (1973); p. 42,45; ; p. 49, View in Reaxys; Vysotskii; Journal of Structural Chemistry; vol. 16; (1975); p. 907,908; ; p. 985, View in Reaxys; Veracini et al.; Molecular Physics; vol. 23; (1972); p. 59, View in Reaxys; Nelson et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 3089,3090, View in Reaxys; Sosnovsky; Krogh; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 34; (1979); p. 511,512, View in Reaxys; Farnell et al.; Journal of the Chemical Society, Chemical Communications; (1972); p. 1159, View in Reaxys; Heberhold; Brabetz; Chemische Berichte; vol. 103; (1970); p. 3896,3900, View in Reaxys; Glukhikh; Voronkov; Doklady Physical Chemistry; vol. 244-249; (1979); p. 744, View in Reaxys; Fedorov et al.; Journal of Structural Chemistry; vol. 19; (1978); p. 549,551; ; p. 633, View in Reaxys; Bromilow; Brownlee; Journal of Organic Chemistry; vol. 44; (1979); p. 1261, View in Reaxys; Coulson; Journal of the American Chemical Society; vol. 98; (1976); p. 3111,3112, View in Reaxys; Beistel; Edwards; Journal of Physical Chemistry; vol. 80; (1976); p. 2023, View in Reaxys; Lee; Wheeler; Journal of Organic Chemistry; vol. 37; (1972); p. 497, View in Reaxys; Bromilow et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 2020, View in Reaxys; Sosnovsky; Krogh; Synthesis; (1978); p. 703, View in Reaxys; Dvoryantseva et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1968); p. 951,952; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1968); p. 994, View in Reaxys; Lynch; Canadian Journal of Chemistry; vol. 55; (1977); p. 541,543, View in Reaxys; Ernst et al.; Journal of Magnetic Resonance (1969-1992); vol. 25; (1977); p. 123,126,128, View in Reaxys; Lebel et al.; Analytical Chemistry; vol. 43; (1971); p. 1500, View in Reaxys; Ledaal; Tetrahedron Letters; (1968); p. 1683, View in Reaxys; Witanowski; Tetrahedron; vol. 23; (1967); p. 4299, View in Reaxys

175/225

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92 of 115

Description (NMR Spectroscopy)

Spin-spin coupling constants

Lippmaa et al.; Chemical Physics Letters; vol. 11; (1971); p. 120, View in Reaxys; Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys; Jacobsen; Schaumburg; Molecular Physics; vol. 28; (1974); p. 1505,1509,1510,1511,1513, View in Reaxys; Fraser; Canadian Journal of Chemistry; vol. 44; (1966); p. 2737,2739, View in Reaxys; Ernst et al.; Journal of Magnetic Resonance (1969-1992); vol. 25; (1977); p. 123,126,128, View in Reaxys; Lazzeretti et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 7989,7992, View in Reaxys; Frei; Bernstein; Journal of Chemical Physics; vol. 38; (1963); p. 1216,1220, 1224, View in Reaxys 93 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

Inamoto et al.; Tetrahedron Letters; (1976); p. 3707, View in Reaxys 94 of 115

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

Jacobsen; Schaumburg; Molecular Physics; vol. 28; (1974); p. 1505,1509,1510,1511,1513, View in Reaxys 95 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Jacobsen; Schaumburg; Molecular Physics; vol. 28; (1974); p. 1505,1509,1510,1511,1513, View in Reaxys; Nomura et al.; Tetrahedron Letters; (1969); p. 639, View in Reaxys 96 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

C-13 chem. shifts

Yonemoto; Journal of Magnetic Resonance (1969-1992); vol. 12; (1973); p. 93, View in Reaxys 97 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

N-14 chem. shifts

Yonemoto; Journal of Magnetic Resonance (1969-1992); vol. 12; (1973); p. 93, View in Reaxys 98 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-NMR chem. shifts

Smith; Deavenport; Journal of Magnetic Resonance (1969-1992); vol. 7; (1972); p. 364, View in Reaxys 99 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Aromatic Solvent Induced Shifts (sF partially deuterated)

Robinson et al.; Journal of Magnetic Resonance (1969-1992); vol. 5; (1971); p. 328, View in Reaxys 100 of 115

Description (NMR Spectroscopy)

NOE

Lippmaa et al.; Chemical Physics Letters; vol. 11; (1971); p. 120, View in Reaxys 101 of 115

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

13C (Bezieh.zur α-Elektronendichte)

Wehrli et al.; Helvetica Chimica Acta; vol. 52; (1969); p. 103, View in Reaxys

176/225

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102 of 115

Description (NMR Spectroscopy)

Spectrum

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys 103 of 115

Description (NMR Spectroscopy)

Chemical shifts

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys; Frei; Bernstein; Journal of Chemical Physics; vol. 38; (1963); p. 1216,1220, 1224, View in Reaxys 104 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

NMR-Abs.

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys 105 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

NMR-Daten (chem.shifts) in div. Lsgn.

Laszlo et al.; Journal of Chemical Physics; vol. 48; (1968); p. 1732,1733, View in Reaxys 106 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

1H-NMR-Absorption (chem. Verschiebung ber.)

Schug; Journal of Chemical Physics; vol. 46; (1967); p. 2447, View in Reaxys 107 of 115

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

14N-NMR-Abs.

Herbison-Evans; Richards; Molecular Physics; vol. 8; (1964); p. 19,26, View in Reaxys 108 of 115

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

Einfluss auf die chemische Verschiebung im 1H-NMR-Spektrum von in Benzonitril geloestem Cyclohexan, Iodmethan und Triiodmethan

Abraham; Molecular Physics; vol. 4; (1961); p. 369,371, View in Reaxys 109 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CHCl3

Bothner-By; Glick; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1652, View in Reaxys 110 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dioxane

Bothner-By; Glick; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1652, View in Reaxys 111 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

177/225

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Solvents (NMR Spectroscopy)

CH3I

Bothner-By; Glick; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1652, View in Reaxys 112 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

acetone

Corio; Dailey; Journal of Chemical Physics; vol. 25; (1956); p. 1291, View in Reaxys; Bothner-By; Glick; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1652, View in Reaxys 113 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

cyclohexane

Corio; Dailey; Journal of Chemical Physics; vol. 25; (1956); p. 1291, View in Reaxys 114 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CS2

Corio; Dailey; Journal of Chemical Physics; vol. 25; (1956); p. 1291, View in Reaxys 115 of 115

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Corio; Dailey; Journal of Chemical Physics; vol. 25; (1956); p. 1291, View in Reaxys; Bothner-By; Glick; Journal of the American Chemical Society; vol. 78; (1956); p. 1071; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1654, View in Reaxys IR Spectroscopy (88) 1 of 88

Description (IR Spectroscopy)

Bands; Spectrum

Location

supporting information

Comment (IR Spectroscopy)

film

Quinn, Dylan J.; Haun, Graham J.; Moura-Letts, Gustavo; Tetrahedron Letters; vol. 57; nb. 34; (2016); p. 3844 - 3847, View in Reaxys 2 of 88

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

178/225

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Jasem, Yosef Al; Barkhad, Mohamed; Khazali, Mona Al; Butt, Hifsa Pervez; El-Khwass, Noha Ashraf; Azani, Mariam Al; Hindawi, Bassam Al; Thiemann, Thies; Journal of Chemical Research; vol. 38; nb. 2; (2014); p. 80 - 84, View in Reaxys 4 of 88

Description (IR Spectroscopy)

Bands

Krasnomolova et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 44; ; p. 85, View in Reaxys; Nuttall et al.; Spectrochimica Acta; vol. 17; (1961); p. 947,948, View in Reaxys; Figeys; Mahieu; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1553,1555, View in Reaxys; Gadzhiev et al.; Journal of Applied Spectroscopy; vol. 29; (1978); p. 830,831,832, View in Reaxys; Martin et al.; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 797,799, View in Reaxys; Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Gillis; Occolowitz; Spectrochimica Acta; vol. 19; (1963); p. 873,874, View in Reaxys; Deady et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 1671,1672, View in Reaxys; Baryshev; Journal of Applied Spectroscopy; vol. 26; (1977); p. 120, View in Reaxys; Uzhinov; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 2; (1971); p. 82; ; p. 234, View in Reaxys; Higuchi; Tanaka; Spectroscopy Letters; vol. 13; (1980); p. 127,132, View in Reaxys; Pasynkiewicz; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 21; (1964); p. 1,66, View in Reaxys; Rao et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 685,686, View in Reaxys; Reid; Chemical Physics Letters; vol. 66; (1979); p. 517,520, View in Reaxys; Deady et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 115,120, View in Reaxys; Urano et al.; Yuki Gosei Kagaku Kyokaishi; vol. 30; (1972); p. 154,158,159, View in Reaxys; Brutan; Fadeev; Sov. Phys. J. (Engl. Transl.); vol. 21; nb. 8; (1978); p. 148,1102, View in Reaxys; Arnaud; Bulletin de la Societe Chimique de France; (1961); p. 1050, View in Reaxys; Figeys-Fauconnier et al.; Spectrochimica Acta; vol. 18; (1962); p. 689,690, View in Reaxys; Figeys; Nasielski; Spectrochimica Acta; vol. 22; (1966); p. 2055,2059, View in Reaxys; Kusurkar, Radhika; Goswami, Shailesh; Vyas, Sandhya; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 42; nb. 12; (2003); p. 3148 - 3151, View in Reaxys; Rad, Mohammad Navid Soltani; Khalafi-Nezhad, Ali; Behrouz, Somayeh; Amini, Zohreh; Behrouz, Marzieh; Synthetic Communications; vol. 40; nb. 16; (2010); p. 2429 - 2440, View in Reaxys; Habibi, Davood; Heydari, Somayyeh; Nasrollahzadeh, Mahmoud; ; vol. 36; nb. 10; (2012); p. 573 - 574,2, View in Reaxys 5 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Zhu, Chenjie; Ji, Lei; Wei, Yunyang; Synthesis; nb. 18; (2010); p. 3121 - 3125, View in Reaxys; Zhu, Chenjie; Sun, Chengguo; Wei, Yunyang; Synthesis; nb. 24; (2010); p. 4235 - 4241; Art.No: F14610SS, View in Reaxys; Zheng, Shuyan; Yu, Chunhui; Shen, Zhengwu; Organic Letters; vol. 14; nb. 14; (2012); p. 3644 - 3647, View in Reaxys 6 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

neat liquid

Rezaei, Ramin; Mohammadi, Mohammad Kazem; Rastin, Nedaa; Chinese Journal of Chemistry; vol. 28; nb. 6; (2010); p. 993 - 996, View in Reaxys; Telvekar, Vikas N.; Sasane, Kulbhushan A.; Synlett; nb. 18; (2010); p. 2778 - 2780, View in Reaxys; Suzuki, Yusuke; Yoshino, Takumi; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 67; nb. 21; (2011); p. 3809 - 3814, View in Reaxys; Rokade, Balaji V.; Prabhu, Kandikere Ramaiah; Journal of Organic Chemistry; vol. 77; nb. 12; (2012); p. 5364 - 5370, View in Reaxys 7 of 88

Description (IR Spectroscopy)

Bands

Location

supporting information

Kalkhambkar, Rajesh G.; Bunge, Scott D.; Laali, Kenneth K.; Tetrahedron Letters; vol. 52; nb. 40; (2011); p. 5184 - 5187, View in Reaxys; Begue, Didier; Qiao, Greg Guanghua; Wentrup, Curt; Journal of the American Chemical Society; vol. 134; nb. 11; (2012); p. 5339 - 5350, View in Reaxys 8 of 88

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat liquid

Rokade, Balaji V.; Malekar, Sanjeev K.; Prabhu, Kandikere Ramaiah; Chemical Communications; vol. 48; nb. 44; (2012); p. 5506 - 5508, View in Reaxys 9 of 88

Description (IR Spectroscopy)

Bands; Spectrum

Solvent (IR Spectroscopy)

tetrahydrofuran

179/225

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Liu, Yonglin; Evans, Anthony S.; Toscano, John P.; Physical Chemistry Chemical Physics; vol. 14; nb. 30; (2012); p. 10438 10444, View in Reaxys 10 of 88

Description (IR Spectroscopy)

Bands; Spectrum

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Azath, Ismail Abulkalam; Suresh, Palaniswamy; Pitchumani, Kasi; New Journal of Chemistry; vol. 36; nb. 11; (2012); p. 2334 - 2339, View in Reaxys 11 of 88

Description (IR Spectroscopy)

2D-IR; Spectrum

Solvent (IR Spectroscopy)

methanol

Ghosh, Ayanjeet; Remorino, Amanda; Tucker, Matthew J.; Hochstrasser, Robin M.; Chemical Physics Letters; vol. 469; nb. 4-6; (2009); p. 325 - 330, View in Reaxys 12 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

neat (no solvent)

Saha, Debasree; Saha, Amit; Ranu, Brindaban C.; Tetrahedron Letters; vol. 50; nb. 44; (2009); p. 6088 - 6091, View in Reaxys 13 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Arote, Nitin D.; Bhalerao, Dinesh S.; Akamanchi, Krishnacharya G.; Tetrahedron Letters; vol. 48; nb. 21; (2007); p. 3651 3653, View in Reaxys 14 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Tao, Feng; Wang, Zhong Hai; Xu, Guo Qin; Journal of Physical Chemistry B; vol. 106; nb. 14; (2002); p. 3557 - 3563, View in Reaxys; Venkat Narsaiah; Nagaiah; Advanced Synthesis and Catalysis; vol. 346; nb. 11; (2004); p. 1271 - 1274, View in Reaxys; Golebiewski; Gucma; Journal of Heterocyclic Chemistry; vol. 43; nb. 2; (2006); p. 509 - 513, View in Reaxys 15 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Woltermann, Christopher J.; Shechter, Harold; Helvetica Chimica Acta; vol. 88; nb. 2; (2005); p. 354 - 369, View in Reaxys 16 of 88

Description (IR Spectroscopy)

Near IR spectrum

Assmann; Von Benten; Charvat; Abel; Journal of Physical Chemistry A; vol. 107; nb. 27; (2003); p. 5291 - 5297, View in Reaxys 17 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

2-methyl-tetrahydro-furan

Comment (IR Spectroscopy)

Stark effect

Andrews, Steven S.; Boxer, Steven G.; Journal of Physical Chemistry A; vol. 104; nb. 51; (2000); p. 11853 - 11863, View in Reaxys 18 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CH2Cl2

Comment (IR Spectroscopy)

2250 cm**(-1)

Aitken, R. Alan; Karodia, Nazira; European Journal of Organic Chemistry; nb. 1; (1999); p. 251 - 254, View in Reaxys

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19 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

diethyl ether

Comment (IR Spectroscopy)

2228 1/cm

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gaseous matrix

Comment (IR Spectroscopy)

3100 - 1000 1/cm

Ishikawa, Seiichi; Ebata, Takayuki; Mikami, Naohiko; Journal of Chemical Physics; vol. 110; nb. 19; (1999); p. 9504 - 9515, View in Reaxys 21 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gaseous matrix

Comment (IR Spectroscopy)

3082.0 - 1001.5 1/cm

Ishikawa, Seiichi; Ebata, Takayuki; Mikami, Naohiko; Journal of Chemical Physics; vol. 110; nb. 19; (1999); p. 9504 - 9515, View in Reaxys 22 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

800 - 600 cm**(-1)

Jordanov; Rogojerov; Schrader; Journal of Molecular Structure; vol. 408-409; (1997); p. 309 - 314, View in Reaxys 23 of 88

Description (IR Spectroscopy)

Polarization of IR bands

Jordanov; Rogojerov; Schrader; Journal of Molecular Structure; vol. 408-409; (1997); p. 309 - 314, View in Reaxys 24 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

2300 - 400 cm**(-1)

Rogojerov, M.; Kolev, D.; Jordanov, B.; Journal of Molecular Structure; vol. 349; (1995); p. 447 - 450, View in Reaxys 25 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gaseous matrix

Temperature (IR Spectroscopy) [°C]

-263.2

Comment (IR Spectroscopy)

2236 - 549 cm**(-1)

Morawietz, Jens; Sander, Wolfram; Traeubel, Michael; Journal of Organic Chemistry; vol. 60; nb. 20; (1995); p. 6368 6378, View in Reaxys

181/225

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26 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2231 cm**(-1)

Gomez, Virginia; Perez-Medrano, Arturo; Muchowski, Joseph M.; Journal of Organic Chemistry; vol. 59; nb. 5; (1994); p. 1219 - 1221, View in Reaxys 27 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

solid matrix

Temperature (IR Spectroscopy) [°C]

-261.2

Comment (IR Spectroscopy)

1495 - 921 cm**(-1)

Wentrup, Curt; Kambouris, Peter; Evans, Richard A.; Owen, David; Macfarlane, Graham; Chuche, Josselin; Pommelet, Jean Claude; Cheikh, Abdelhamid Ben; Plisnier, Michel; Flammang, Robert; Journal of the American Chemical Society; vol. 113; nb. 8; (1991); p. 3130 - 3135, View in Reaxys 28 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

1,2-dichloro-ethane

Comment (IR Spectroscopy)

2230 cm**(-1)

Schumann, Hans; Speis, Martin; Bosman, W. P.; Smits, J. M. M.; Beurskens, Paul T.; Journal of Organometallic Chemistry; vol. 403; nb. 1.2; (1991); p. 165 - 182, View in Reaxys 29 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

2229 cm**(-1)

Burgess,H.; Donnelly,J.A.; Tetrahedron; vol. 47; (1991); p. 111, View in Reaxys 30 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

solid

Temperature (IR Spectroscopy) [°C]

-196

Comment (IR Spectroscopy)

2500 - 500 cm**(-1)

Ohno, Keiichi; Matsuura, Hiroatsu; Journal of Molecular Structure; vol. 242; nb. 1; (1991); p. 303 - 314, View in Reaxys 31 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CH2Cl2

Comment (IR Spectroscopy)

2230 cm**(-1)

Jochims, Johannes C.; Glocker, Michael O.; Chemische Berichte; vol. 123; nb. 7; (1990); p. 1537 - 1544, View in Reaxys; Bodrikov, I. V.; Michurin, A. N.; Vasyanina, G. I.; Bochkareva, N. N.; Krasnoj, V. L.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 12; (1980); p. 2123 - 2133; Zhurnal Organicheskoi Khimii; vol. 16; nb. 12; (1980); p. 2492 2503, View in Reaxys 32 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

2230 - 1442 cm**(-1)

182/225

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Tsuboi, Sadao; Ishii, Naomi; Sakai, Takashi; Tari, Isao; Utaka, Masanori; Bulletin of the Chemical Society of Japan; vol. 63; nb. 7; (1990); p. 1888 - 1893, View in Reaxys 33 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2210 cm**(-1)

Keumi, Takashi; Shimada, Masakazu; Morita, Toshio; Kitajima, Hidehiko; Bulletin of the Chemical Society of Japan; vol. 63; nb. 8; (1990); p. 2252 - 2256, View in Reaxys 34 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

2240 cm**(-1)

Kitagawa; Kawaguchi; Iwasaki; Chemical and Pharmaceutical Bulletin; vol. 38; nb. 9; (1990); p. 2583 - 2585, View in Reaxys 35 of 88

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

2300 - 300 cm**(-1)

Csaszar, Attila G.; Fogarasi, Geza; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 45; nb. 8; (1989); p. 845 - 854, View in Reaxys 36 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

2240 cm**(-1)

Rao, C. Someswara; Rambabu, M.; Srinivasan, P. S.; Synthetic Communications; vol. 19; nb. 7,8; (1989); p. 1431 - 1436, View in Reaxys 37 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2227 cm**(-1)

Thomas, C. W.; Leveson, L. L.; Routley, H. A.; Tetrahedron Letters; vol. 29; nb. 7; (1988); p. 811 - 812, View in Reaxys 38 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

paraffin

Comment (IR Spectroscopy)

2222 cm**(-1)

Naddaka, V. I.; Avenesyan, K. V.; Cherkinskaya, M. L.; Minkin, V. I.; Journal of Organic Chemistry USSR (English Translation); vol. 24; nb. 8; (1988); p. 1426 - 1429; Zhurnal Organicheskoi Khimii; vol. 24; nb. 8; (1988); p. 1581 - 1585, View in Reaxys 39 of 88

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

2245 cm**(-1)

Mitrasov, Yu. N.; Mikhailova, O. N.; Yal'tseva, N. S.; Nikiforov, N. G.; Kormachev, V. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 6; (1987); p. 1417 - 1418,1268, View in Reaxys 40 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

2210 cm**(-1)

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Rao, C. Someswara; Rambabu, M.; Srinivasan, P. S.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 26; nb. 1-12; (1987); p. 407 - 411, View in Reaxys 41 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

2220 cm**(-1)

Liguori, Angelo; Sindona, Giovanni; Romeo, Giovanni; Uccella, Nicola; Synthesis; nb. 2; (1987); p. 168, View in Reaxys 42 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2220 cm**(-1)

Furukawa, Naomichi; Fukumura, Mitsuo; Akasaka, Takeshi; Yoshimura, Toshiaki; Oae, Shigeru; Tetrahedron Letters; vol. 21; nb. 8; (1980); p. 761 - 762, View in Reaxys; Gokou, Celestin Tea; Pradere, Jean-Paul; Quiniou, Herve; Journal of Organic Chemistry; vol. 50; nb. 9; (1985); p. 1545 - 1547, View in Reaxys; Kolodyazhnyi, O. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 52; nb. 6; (1982); p. 1314 - 1318,1156 - 1159, View in Reaxys 43 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2225 cm**(-1)

Greig, Derek J.; McPherson, Michael; Paton, Michael R.; Crosby, John; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1985); p. 1205 - 1208, View in Reaxys; Schmidpeter, Alfred; Klehr, Hubert; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 38; nb. 11; (1983); p. 1484 - 1487, View in Reaxys 44 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Comment (IR Spectroscopy)

2231 cm**(-1)

Nakashima, Michio; Mikuriya, Masahiro; Muto, Yoneichiro; Bulletin of the Chemical Society of Japan; vol. 58; nb. 3; (1985); p. 968 - 973, View in Reaxys 45 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2230 cm**(-1)

Alvarez-Valdes, A.; Masaguer, J. R.; Garcia-Vazquez, J. A.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 10; (1984); p. 995 - 998, View in Reaxys 46 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

Temperature (IR Spectroscopy) [°C]

-125 - 25

Comment (IR Spectroscopy)

2215 - 2245 cm**(-1)

Baranova, G. I.; Solov'eva, L. A.; Journal of Applied Spectroscopy; vol. 39; nb. 1; (1983); p. 786 - 793; Zhurnal Prikladnoi Spektroskopii; vol. 39; nb. 1; (1983); p. 61 - 69, View in Reaxys 47 of 88

Description (IR Spectroscopy)

Intensity of IR bands

Brownlee et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 557,559, View in Reaxys; Tunitsyn et al.; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 1,2, 5, View in Reaxys; Ritchie et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4687, View in Reaxys; Caldow et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 254; (1960); p. 17,22, View in Reaxys; Schmid; Bellanato; Zeitschrift fuer Elektrochemie; vol. 65; (1961); p. 362, View in Reaxys; Brownlee; Journal of the American Chemical Society; vol. 87; (1965); p. 3260,3261, View in Reaxys; Gillis; Occolowitz; Spectrochimica Acta; vol. 19; (1963); p. 873,874, View in Reaxys; Deady et

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al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 115,120, View in Reaxys; Binev, Ivan G.; Kuzmanova, Rositsa B.; Kaneti, Jose; Juchnovski, Ivan N.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1533 - 1536, View in Reaxys 48 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

50 - 140 cm**(-1)

Gadzhiev, A. Z.; Russian Journal of Physical Chemistry; vol. 56; nb. 7; (1982); p. 1008 - 1011; Zhurnal Fizicheskoi Khimii; vol. 56; nb. 7; (1982); p. 1660 - 1664, View in Reaxys 49 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

dimethylsulfoxide

Comment (IR Spectroscopy)

2227 cm**(-1)

Binev, Ivan G.; Kuzmanova, Rositsa B.; Kaneti, Jose; Juchnovski, Ivan N.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1533 - 1536, View in Reaxys 50 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

hexamethylphosphoric acid triamide

Comment (IR Spectroscopy)

2227 cm**(-1)

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2220 - 1490 cm**(-1)

Keumi, Takashi; Yamamoto, Takayoshi; Saga, Hiroshi; Kitajima, Hidehiko; Bulletin of the Chemical Society of Japan; vol. 54; nb. 5; (1981); p. 1579 - 1580, View in Reaxys 52 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

Temperature (IR Spectroscopy) [°C]

-188.2

Comment (IR Spectroscopy)

2500 - 1500 cm**(-1)

Toubro, Nils Henrik; Holm, Arne; Journal of the American Chemical Society; vol. 102; nb. 6; (1980); p. 2093 - 2094, View in Reaxys 53 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

solid

Temperature (IR Spectroscopy) [°C]

-160

Comment (IR Spectroscopy)

2200 - 2300 cm**(-1)

Brutan, E. G.; Fadeev, Yu. A.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 586 - 587; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1025 - 1027, View in Reaxys 54 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

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Temperature (IR Spectroscopy) [°C]

230

Comment (IR Spectroscopy)

2200 - 2300 cm**(-1)

Brutan, E. G.; Fadeev, Yu. A.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 586 - 587; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1025 - 1027, View in Reaxys 55 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

2200 - 2300 cm**(-1)

Brutan, E. G.; Fadeev, Yu. A.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 586 - 587; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1025 - 1027, View in Reaxys 56 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

2250 cm**(-1)

Narasimhan, N. S.; Wadia, M. S.; Shete, N. R.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 19; nb. 7; (1980); p. 556 - 560, View in Reaxys 57 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

2250 - 1600 cm**(-1)

Gelas-Mialhe, Yvonne; Vessiere, Roger; Synthesis; nb. 12; (1980); p. 1005 - 1007, View in Reaxys 58 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

decahydronaphthalene

Temperature (IR Spectroscopy) [°C]

19.9

Comment (IR Spectroscopy)

100 - 44 cm**(-1)

Reid, Colin J.; Evans, Myron; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 733 - 738, View in Reaxys 59 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Temperature (IR Spectroscopy) [°C]

19.9

Comment (IR Spectroscopy)

100 - 50 cm**(-1)

Reid, Colin J.; Evans, Myron; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 733 - 738, View in Reaxys 60 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

19.9

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Comment (IR Spectroscopy)

100 - 50 cm**(-1)

Reid, Colin J.; Evans, Myron; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 733 - 738, View in Reaxys 61 of 88

Description (IR Spectroscopy)

Brownlee,R.T.C. et al.; Journal of the American Chemical Society; vol. 90; nb. 7; (1968); p. 1757 - 1767, View in Reaxys; Olah,A.; Kiovsky,T.E.; Journal of the American Chemical Society; vol. 90; (1968); p. 4666 - 4672, View in Reaxys; Bravo,P. et al.; Tetrahedron; vol. 26; (1970); p. 1315 - 1330, View in Reaxys; Butruille,D. et al.; Tetrahedron; vol. 27; (1971); p. 2055 2067, View in Reaxys; Wolkoff,P.; Hammerum,S.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 30; (1976); p. 831 - 836, View in Reaxys; Mukaiyama,T. et al.; Journal of Organic Chemistry; vol. 26; (1961); p. 2202 - 2206, View in Reaxys; Monahan,A.S. et al.; Journal of Organic Chemistry; vol. 43; nb. 2; (1978); p. 232 - 238, View in Reaxys; Sheludyakov,V.D. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 2259 - 2266,2061 - 2067, View in Reaxys; Slavinskaya,R.A. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 206 - 212,182 - 187, View in Reaxys; Becker,W. et al.; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 25; (1970); p. 1332 - 1337, View in Reaxys; Perregaard,J. et al.; Bulletin des Societes Chimiques Belges; vol. 86; (1977); p. 321 - 328, View in Reaxys; Hudson,R.F.; Record,K.A.F.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1978); p. 1167 - 1171, View in Reaxys; Deady et al.; Tetrahedron Letters; (1973); p. 1881,1883, View in Reaxys; Kanaoka et al.; Chemical and Pharmaceutical Bulletin; vol. 18; (1970); p. 397,398, View in Reaxys; Seydel et al.; Arzneimittel Forschung; vol. 13; (1963); p. 200,203, View in Reaxys; Ikeda et al.; Synthesis; (1978); p. 301, View in Reaxys; Ahmad; Synthesis; (1976); p. 418, View in Reaxys; Juchnovski et al.; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 33; (1978); p. 557,561, View in Reaxys; Joeckle et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 21; (1966); p. 1906,1909-1910, 1912-1913, View in Reaxys; Bayer; Haefelinger; Chemische Berichte; vol. 99; (1966); p. 1689, View in Reaxys; Griffiths; Derwish; Journal of Molecular Spectroscopy; vol. 13; (1964); p. 393,397, View in Reaxys; Exner; Bocek; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 50,53, View in Reaxys; Rider; Hammaker; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 501, View in Reaxys; Fini; Mirone; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 625,626, View in Reaxys; Isaac et al.; Applied Spectroscopy; vol. 17; (1963); p. 90,93, View in Reaxys; Brown; Butcher; Australian Journal of Chemistry; vol. 25; (1972); p. 149,164, View in Reaxys; Juchnowski et al.; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 10; (1977); p. 554,558, View in Reaxys; Rothschild; Journal of Chemical Physics; vol. 57; (1972); p. 991, View in Reaxys; McDevitt; Fateley; Journal of Molecular Structure; vol. 5; (1970); p. 477,484, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Tretyakov; Filimonov; Kinetics and Catalysis; vol. 11; (1970); p. 815,818, View in Reaxys; Jakobsen; Brasch; Journal of the American Chemical Society; vol. 86; (1964); p. 3571, View in Reaxys; Datta; Barrow; Journal of Chemical Physics; vol. 48; (1968); p. 4662,4664, View in Reaxys; Favero et al.; Gazzetta Chimica Italiana; vol. 103; (1973); p. 297,300, View in Reaxys; Augdahl; Klaboe; Spectrochimica Acta; vol. 19; (1963); p. 1665,1669, View in Reaxys; Fischer; Leupold; Chemische Berichte; vol. 105; (1972); p. 599,608, View in Reaxys; Chatt et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1971); p. 1169,1172, View in Reaxys; Hohmann; Tom Dieck; Journal of Organometallic Chemistry; vol. 85; (1975); p. 47,50, View in Reaxys; Holm; Huge-Jensen; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 28; (1974); p. 705,706, View in Reaxys; Martin; Brause; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 812, View in Reaxys; Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Laurence; Wojtkowiak; Bulletin de la Societe Chimique de France; (1971); p. 3124,3125-3129, View in Reaxys; Thistlewaite; Australian Journal of Chemistry; vol. 30; (1977); p. 1595, View in Reaxys; Wilson; Bloor; Spectrochimica Acta; vol. 21; (1965); p. 45, View in Reaxys; Deady et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 1671,1672, View in Reaxys; Tatsumi et al.; Inorganic Chemistry; vol. 14; (1975); p. 2530, View in Reaxys; Le Bel; La Posa; Journal of Molecular Spectroscopy; vol. 41; (1972); p. 249,250-290, View in Reaxys; Larsson; Folkesson; Chemica Scripta; vol. 9; (1976); p. 148, View in Reaxys; Hill; Schmookler; Journal of Organic Chemistry; vol. 32; (1967); p. 4025, View in Reaxys; Vincent-Geisse; Lecomte; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 1; (1962); p. 104,107, View in Reaxys; Wright; Robson; Nature (London, United Kingdom); vol. 222; (1969); p. 290, View in Reaxys; Sosnovsky; Krogh; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 34; (1979); p. 511,512, View in Reaxys; Heberhold; Brabetz; Chemische Berichte; vol. 103; (1970); p. 3896,3900, View in Reaxys; Jain; Walker; Journal of Physical Chemistry; vol. 75; (1971); p. 2942, View in Reaxys; Orlov et al.; Kinetics and Catalysis; vol. 14; (1973); p. 1077,1078, View in Reaxys; Reid; Evans; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 75; (1979); p. 1218,1226, View in Reaxys; Davies et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 75; (1979); p. 1428,1432, 1436, 1437, View in Reaxys; Yukhnovskii; Doklady Physical Chemistry; vol. 166-171; (1966); p. 393; vol. 168; p. 1117, View in Reaxys; Ashby et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 4896,4899, View in Reaxys; Gadzhiev et al.; Theoretical and Experimental Chemistry; vol. 11; (1975); p. 549,551, 553, View in Reaxys; Angell; Howell; Journal of Physical Chemistry; vol. 73; (1969); p. 2551, View in Reaxys; Kroon; van der Elsken; Chemical Physics Letters; vol. 1; (1967); p. 285, View in Reaxys; Anderson; Griffiths; Analytical Chemistry; vol. 47; (1975); p. 2339,2344, View in Reaxys; Mamatov; Yagudaev; Journal of Applied Spectroscopy; vol. 8; (1968); p. 498; ; p. 825, View in Reaxys; Yamato; Sugasawa; Tetrahedron Letters; (1970); p. 4383, View in Reaxys; Hindle et al.; Journal of Chemical Physics; vol. 62; (1975); p. 3230, View in Reaxys; Moharram; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 248; (1971); p. 137,140,141, View in Reaxys; Moharram; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 251; (1972); p. 33,35,38, View in Reaxys; Oranskaya; Filimonov; Doklady Physical Chemistry; vol. 194; (1970); p. 675; ; p. 140, View in Reaxys; Green; Harrison; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 1279,1284,1285, View in Reaxys; Sosnovsky; Krogh; Synthesis; (1978); p. 703,

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View in Reaxys; Chekunov; Polyakova; Journal of Applied Spectroscopy; vol. 10; (1969); p. 523; ; p. 784, View in Reaxys; Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 2; (1965); p. 18; Chem.Abstr.; vol. 63; nb. 13111; (1965), View in Reaxys; Martin; Franz; Journal of the American Chemical Society; vol. 97; (1975); p. 6137,6138, View in Reaxys; Zecchina et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1969); p. 2196, View in Reaxys; Anderson; Griffiths; Analytical Chemistry; vol. 50; (1978); p. 1804,1806, View in Reaxys; Deady et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 115,120, View in Reaxys; Juchnovski; Binev; Tetrahedron; vol. 33; (1977); p. 2993, View in Reaxys; Pasynkiewicz; Starowieyski; Roczniki Chemii; vol. 38; (1964); p. 331, View in Reaxys; Delorme; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 256; (1963); p. 3272, View in Reaxys; McWhinnie; Poller; Spectrochimica Acta; vol. 22; (1966); p. 501,503, View in Reaxys; Benson et al.; Canadian Journal of Chemistry; vol. 50; (1972); p. 2610, View in Reaxys; Chastrette et al.; Journal of Organometallic Chemistry; vol. 78; (1974); p. 303,304-306,308,309, View in Reaxys; LLoyd; Wade; Journal of the Chemical Society; (1965); p. 2662,2665,2666,2668, View in Reaxys; Oranskaya et al.; Kinetics and Catalysis; vol. 11; (1970); p. 1068,1069, View in Reaxys; Schiemenz; Tetrahedron Letters; (1966); p. 3023,3025, View in Reaxys; Bagnell et al.; Australian Journal of Chemistry; vol. 27; (1974); p. 2577,2580, View in Reaxys; Kupletskaya et al.; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 2594,2610, View in Reaxys; Cabana et al.; Journal of Physical Chemistry; vol. 64; (1960); p. 1941,1942, View in Reaxys; Cassar et al.; Gazzetta Chimica Italiana; vol. 104; (1974); p. 665,666, View in Reaxys; Seydel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 16; (1961); p. 419, View in Reaxys; Juchnovski; Binev; Journal of Molecular Structure; vol. 7; (1971); p. 490,491,493, View in Reaxys; Gadzhiev; Journal of Applied Spectroscopy; vol. 18; (1973); p. 323; ; p. 437, View in Reaxys; Brasch; Jacobsen; Spectrochimica Acta; vol. 20; (1964); p. 1644, View in Reaxys; Kanaoka et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 280,283,284, View in Reaxys 62 of 88

Description (IR Spectroscopy)

Spectrum

Grigat,E. et al.; Chemische Berichte; vol. 98; (1965); p. 3777 - 3784, View in Reaxys; Wright; Nature; vol. 209; nb. 5023; (1966); p. 571 - 572, View in Reaxys; Freymann et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 265; (1967); p. 771, View in Reaxys; Michielsen; Ketelaar; Molecular Physics; vol. 24; (1972); p. 1181, View in Reaxys; Muirhead et al.; Journal of Chemical Physics; vol. 56; (1972); p. 4385, View in Reaxys; Wiberley et al.; Analytical Chemistry; vol. 32; (1960); p. 217,219, View in Reaxys; Lebas; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 59; (1962); p. 1072,1073, View in Reaxys; Quintard; Applied Spectroscopy; vol. 29; nb. 2; (1975); p. 201 - 204, View in Reaxys; Ham; Willis; Spectrochimica Acta; vol. 16; (1960); p. 279,292,296,300, View in Reaxys; Juchnovski et al.; Monatshefte fuer Chemie; vol. 100; (1969); p. 1980,1985, View in Reaxys 63 of 88

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

700 - 250 cm**(-1)

Hidalgo; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 249; (1959); p. 395, View in Reaxys 64 of 88

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

2400 - 2100 cm**(-1)

Hidalgo; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 249; (1959); p. 395, View in Reaxys 65 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

CN-Valenzschwingung und der CN-Deformationsschwingung.

Hidalgo; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 249; (1959); p. 395, View in Reaxys 66 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Bayliss et al.; Spectrochimica Acta; vol. 15; (1959); p. 12,15, View in Reaxys 67 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Sensi; Gallo; Gazzetta Chimica Italiana; vol. 85; (1955); p. 235,243, View in Reaxys; Katritzky; Recueil des Travaux Chimiques des Pays-Bas; vol. 78; (1959); p. 995,997, View in Reaxys; Thompson; Steel; Transactions of the Faraday Society; vol. 52;

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(1956); p. 1451,1453, View in Reaxys; Brown; Journal of the American Chemical Society; vol. 80; (1958); p. 794,795; Spectrochimica Acta; vol. 10; (1958); p. 149,152, View in Reaxys 68 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

1600 - 1000 cm**(-1)

Katritzky; Lagowski; Journal of the Chemical Society; (1958); p. 4155,4158, View in Reaxys 69 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

pyridine

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Brown; Journal of the American Chemical Society; vol. 80; (1958); p. 794,795; Spectrochimica Acta; vol. 10; (1958); p. 149,152, View in Reaxys 70 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

tetrachloroethene

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Brown; Journal of the American Chemical Society; vol. 80; (1958); p. 794,795; Spectrochimica Acta; vol. 10; (1958); p. 149,152, View in Reaxys; Mander; Thompson; Transactions of the Faraday Society; vol. 53; (1957); p. 1402,1403, View in Reaxys 71 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

hexane

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Brown; Journal of the American Chemical Society; vol. 80; (1958); p. 794,795; Spectrochimica Acta; vol. 10; (1958); p. 149,152, View in Reaxys 72 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Skinner; Thompson; Journal of the Chemical Society; (1955); p. 487, View in Reaxys; Brown; Journal of the American Chemical Society; vol. 80; (1958); p. 794,795; Spectrochimica Acta; vol. 10; (1958); p. 149,152, View in Reaxys; Mander; Thompson; Transactions of the Faraday Society; vol. 53; (1957); p. 1402,1403, View in Reaxys 73 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CH2Cl2

Comment (IR Spectroscopy)

Druckabhaengigkeit (1040-9140 at) der CN-Valenzschwingungsfrequenz.

Wiederkehr; Drickamer; Journal of Chemical Physics; vol. 28; (1958); p. 311,312, View in Reaxys 74 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nitromethane

Comment (IR Spectroscopy)

Intensitaet der CN-Valenzschwingungsbande.

Mander; Thompson; Transactions of the Faraday Society; vol. 53; (1957); p. 1402,1403, View in Reaxys

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75 of 88

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3200 - 650 cm**(-1)

Josien; Lebas; Bulletin de la Societe Chimique de France; (1956); p. 53, View in Reaxys 76 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

2326 - 2083 cm**(-1)

Anderson; Le Fevre; Savage; Journal of the Chemical Society; (1947); p. 449, View in Reaxys 77 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CS2

Comment (IR Spectroscopy)

1613 - 699 cm**(-1)

Anderson; Le Fevre; Savage; Journal of the Chemical Society; (1947); p. 449, View in Reaxys 78 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5000 - 714 cm**(-1)

Bell; A.P.I. Res. Project; vol. 44; nb. 541; (1947), View in Reaxys 79 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1818 - 1111 cm**(-1)

Barnes; Liddel; Williams; Industrial and Engineering Chemistry, Analytical Edition; vol. 15; (1943); p. 659,687, View in Reaxys 80 of 88

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 6250 cm**(-1)

Suhrmann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 50; (1941); p. 23,58, View in Reaxys 81 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1333 - 500 cm**(-1)

Lecomte; Journal de Physique et le Radium; vol. <7> 8; (1937); p. 489,492, View in Reaxys; Lecomte; Freymann; Bulletin de la Societe Chimique de France; vol. <5> 8; (1941); p. 612,616, View in Reaxys 82 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

paraffin

Comment (IR Spectroscopy)

400 - 200 cm**(-1)

Barchewitz; Parodi; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 209; (1939); p. 30, View in Reaxys

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83 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

11494 cm**(-1)

Barchewitz; Annales de Physique (Paris, France); vol. <11>11; (1939); p. 335; Annales de l'Office National des Combustibles Liquides (France); vol. 13; (1938); p. 517; Chem. Zentralbl.; vol. 110; nb. I; (1939); p. 1743, View in Reaxys 84 of 88

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

14286 cm**(-1)

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

500 - 200 cm**(-1)

Barchewitz; Parodi; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 207; (1938); p. 903; Journal de Physique et le Radium; vol. <7> 10; (1939); p. 143,150, View in Reaxys 86 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3704 - 1961 cm**(-1)

Gordy; Williams; Journal of Chemical Physics; vol. 4; (1936); p. 86, View in Reaxys 87 of 88

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5000 - 833 cm**(-1)

Bell; Journal of the American Chemical Society; vol. 57; (1935); p. 1024, View in Reaxys 88 of 88

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 667 cm**(-1)

Coblentz,W. W.; Investigations of Infra-red Spectra <Washington 1905>, S. 157, 159, 244, View in Reaxys Mass Spectrometry (32) Description (Mass Location Spectrometry) spectrum

Comment (Mass Spectrometry)

Paragraph 0017

References Patent; Yancheng Normal College; Wang Jin; Hu Xiao; Wang Wenling; Geng Rongqing; Qiu Qiong; Shao Jin; Jin Wenbin; Yan Yiyu; Zhai Yulin; Zhu Xiaoming; (7 pag.); CN107382771; (2017); (A) Chinese, View in Reaxys

electrospray ionisa- supporting information (ESI); spection trum

Azath, Ismail Abulkalam; Suresh, Palaniswamy; Pitchumani, Kasi; New Journal of Chemistry; vol. 36; nb. 11; (2012); p. 2334 - 2339, View in Reaxys; Quinn, Dylan J.; Haun, Graham J.; Moura-Letts, Gustavo; Tetrahedron Letters; vol. 57; nb. 34; (2016); p. 3844 - 3847, View in Reaxys

electron impact (EI); spectrum

Liu, Li; Li, Jian; Xu, Jiao; Sun, Jiang-Tao; Tetrahedron Letters; vol. 53; nb. 51; (2012); p. 6954 - 6956, View in Reaxys; Zhang, Xu; Sun, Jingjing; Ding, Yuanhua; Yu, Lei; Organic Letters; vol. 17; nb. 23; (2015); p. 5840 5842, View in Reaxys

supporting information

191/225

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electron impact (EI); gas chromatography mass spectrometry (GCMS); spectrum

supporting information

Yu, Lei; Li, Hongyan; Zhang, Xu; Ye, Jianqing; Liu, Jianping; Xu, Qing; Lautens, Mark; Organic Letters; vol. 16; nb. 5; (2014); p. 1346 1349, View in Reaxys

electron impact (EI); spectrum

Spectrum

Zhu, Jintao; Song, Guangwei; Yao, Guoxin; Chen, Gang; Synthetic Communications; vol. 42; nb. 13; (2012); p. 1934 - 1940, View in Reaxys

gas chromatography mass spectrometry (GCMS); spectrum

GCMS (Gas chromatography mass spectrometry); Spectrum

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys; Zhu, Chenjie; Ji, Lei; Wei, Yunyang; Synthesis; nb. 18; (2010); p. 3121 - 3125, View in Reaxys; Zhu, Chenjie; Sun, Chengguo; Wei, Yunyang; Synthesis; nb. 24; (2010); p. 4235 - 4241; Art.No: F14610SS, View in Reaxys; Kalkhambkar, Rajesh G.; Bunge, Scott D.; Laali, Kenneth K.; Tetrahedron Letters; vol. 52; nb. 40; (2011); p. 5184 - 5187, View in Reaxys

EI (Electron impact); Doubly charged ions; Spectrum

Zins, Emilie-Laure; Schroeder, Detlef; International Journal of Mass Spectrometry; vol. 299; nb. 1; (2011); p. 53 - 58, View in Reaxys

EI (Electron impact); Spectrum

Zins, Emilie-Laure; Schroeder, Detlef; Journal of Physical Chemistry A; vol. 114; nb. 19; (2010); p. 5989 - 5996, View in Reaxys

CID (collision-induced dissociation); EI (Electron impact); Spectrum

Zins, Emilie-Laure; Schroeder, Detlef; Journal of Physical Chemistry A; vol. 114; nb. 19; (2010); p. 5989 - 5996, View in Reaxys

spectrum; electron impact (EI)

Agafonov, N. E.; Sedishev, I. P.; Dudin, A. V.; Kutin, A. A.; Stashina, G. A.; Zhulin, V. M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 40; nb. 2.2; (1991); p. 366 - 372; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 2; (1991); p. 426 - 433, View in Reaxys; Aitken; Farrell; Kirton; Chemistry of Heterocyclic Compounds; vol. 37; nb. 12; (2001); p. 1526 - 1531, View in Reaxys; Venkat Narsaiah; Nagaiah; Advanced Synthesis and Catalysis; vol. 346; nb. 11; (2004); p. 1271 - 1274, View in Reaxys; Kangani, Cyrous O.; Day, Billy W.; Kelley, David E.; Tetrahedron Letters; vol. 49; nb. 5; (2008); p. 914 - 918, View in Reaxys

spectrum

Pzhevotskii, K.; Voronkov, M. G.; Pzhevotskaya, L.; Malinskii, E.; Usov, V. A.; Russian Journal of Organic Chemistry; vol. 29; nb. 3.2; (1993); p. 472 - 475; Zhurnal Organicheskoi Khimii; vol. 29; nb. 3; (1993); p. 565 569, View in Reaxys; Lijser, H. J. P. de; Arnold, Donald R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1997); p. 1369 - 1380, View in Reaxys; Aitken, R. Alan; Karodia, Nazira; European Journal of Organic Chemistry; nb. 1; (1999); p. 251 - 254, View in Reaxys; Klaic, Lada; Aleskovic, Marija; Veljkovic, Jelena; Mlinaric-Majerski, Kata; Journal of Physical Organic Chemistry; vol. 21; nb. 4; (2008); p. 299 - 305, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

Pongsuwan, Wipawee; Bamba, Takeshi; Kobayashi, Akio; Fukusaki, Eiichiro; Yonetani, Tsutomu; Journal of Agricultural and Food Chemistry; vol. 56; nb. 3; (2008); p. 744 - 750, View in Reaxys

GCMS (Gas chromatography mass spectrometry)

Molecular peak

Patent; IHARA CHEMICAL INDUSTRY CO., LTD.; EP1555257; (2005); (A1) English, View in Reaxys

192/225

2018-05-24 12:11:44

spectrum; chemical ionization (CI)

Daishima, Shigeki; Iida, Yoshio; Kanda, Fujihiro; Organic Mass Spectrometry; vol. 26; nb. 5; (1991); p. 486 - 492, View in Reaxys; Srinivas, R.; Vairamani, M.; Rao, G. K. Viswanadha; Mirza, U. A.; Organic Mass Spectrometry; vol. 24; (1989); p. 435 - 438, View in Reaxys; Vairamani, M.; Organic Mass Spectrometry; vol. 28; nb. 12; (1993); p. 1498 - 1503, View in Reaxys; Tsuji, Masaharu; Arikawa, Takeshi; Nishimura, Yukio; Bulletin of the Chemical Society of Japan; vol. 72; nb. 2; (1999); p. 293 302, View in Reaxys; Zhu, Hua-Jie; Lu, Kai-Tao; Sun, Guang-Ri; He, Jin-Bao; Li, Hai-Qing; Pittman Jr., Charles U.; New Journal of Chemistry; vol. 27; nb. 2; (2003); p. 409 - 413, View in Reaxys

time-of-flight mass spectra (TOFMS)

Balucani; Asvany; Chang; Lin; Lee; Kaiser; Bettinger; Schleyer; Schaefer III; Journal of Chemical Physics; vol. 111; nb. 16; (1999); p. 7457 - 7471, View in Reaxys

chemical ionization (CI); spectrum

Hunt, Donald F.; Sethi, Satinder K.; Journal of the American Chemical Society; vol. 102; nb. 23; (1980); p. 6953 - 6963, View in Reaxys; Kadentsev, V. I.; Kolotyrkina, N. G.; Stomakhin, A. A.; Chizhov, O. S.; Russian Chemical Bulletin; vol. 44; nb. 9; (1995); p. 1698 - 1704; Izvestiya Akademi Nauk, Seriya Khimicheskaya; nb. 9; (1995); p. 1767 - 1773, View in Reaxys

electron impact (EI)

collisional activation; metastable ions

McLafferty; Bente III; Kornfeld; Tsai; Howe; Journal of Mass Spectrometry; vol. 30; nb. 6; (1995); p. 797 - 806, View in Reaxys

spectrum; chemical ionization (CI)

collisional activation

Adams, Gregory W.; Bowie, John H.; Hayes, Roger N.; Gross, Michael L.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 6; (1992); p. 897 - 901, View in Reaxys; Nielsen, Lawrence T.; Srivastava, R. M.; Silva, Leda M. M. e; Organic Mass Spectrometry; vol. 18; nb. 9; (1983); p. 367 - 372, View in Reaxys; Bortolini, Olga; Yang, Sheng Sheng; Cooks, R. G.; Organic Mass Spectrometry; vol. 28; nb. 11; (1993); p. 1313 - 1322, View in Reaxys

fragmentation pattern; spectrum

Boerboom, A. J. H.; Organic Mass Spectrometry; vol. 26; nb. 11; (1991); p. 929 - 935, View in Reaxys Bravo,P. et al.; Tetrahedron; vol. 26; (1970); p. 1315 - 1330, View in Reaxys; Krasnomolova et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 44; ; p. 85, View in Reaxys; Kinlin et al.; Journal of Agricultural and Food Chemistry; vol. 20; (1972); p. 1021,1023, View in Reaxys; Maquestiau et al.; Bulletin des Societes Chimiques Belges; vol. 84; (1975); p. 1179,1182, View in Reaxys; Large; Knof; Organic Mass Spectrometry; vol. 11; (1976); p. 582,593, View in Reaxys; Subba Rao; Fenselau; Analytical Chemistry; vol. 50; (1978); p. 511, View in Reaxys; Goldenfeld et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 11; (1973); p. 9, View in Reaxys; Brown; Butcher; Australian Journal of Chemistry; vol. 25; (1972); p. 149,164, View in Reaxys; Hickling; Jennings; Organic Mass Spectrometry; vol. 3; (1970); p. 1499,1501, View in Reaxys; Franchetti et al.; Organic Mass Spectrometry; vol. 13; (1978); p. 106, View in Reaxys; Morgan; Green; International Journal of Mass Spectrometry and Ion Physics; vol. 28; (1978); p. 171, View in Reaxys; Schug; Journal of Chemical Physics; vol. 40; (1964); p. 1283, View in Reaxys; Fischer; Leupold; Chemische Berichte; vol. 105; (1972); p. 599,608, View in Reaxys; Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 3180,3182, View in Reaxys; Blumenthal et al.; Australian Journal of Chemistry; vol. 26; (1973); p. 2019,2022, View in Reaxys; Howe; Williams; Journal of the American Chemical Society; vol. 91; (1969); p. 7137,7141, View in Reaxys; Levsen; Beckey; Organic Mass Spectrometry; vol. 9; (1974); p. 570,575, View in Reaxys; Brown; Organic Mass Spectrometry; vol. 3; (1970); p. 639,641, View in Reaxys; Migahed; Beckey; Organic Mass Spectrometry; vol. 5; (1971); p. 453,459, View in Reaxys; Hunt et al.; Analytical Chemistry; vol. 47; (1975); p. 1730, View in Reaxys; Gordon; Reid; International Journal of Mass Spectrometry and Ion Physics; vol. 18; (1975); p. 379, View in Reaxys; Cooks et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 15; (1974); p. 271,273, View in Reaxys; Andlauer; Ottinger; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 27; (1972); p. 293,299, View in Reaxys; Kambara; Kanomata; International Journal of Mass Spectrometry and Ion Physics; vol. 24; (1977); p. 453, View in Reaxys; Kemp et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 21; (1976); p. 93,100,

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2018-05-24 12:11:44

View in Reaxys; Behan et al.; Organic Mass Spectrometry; vol. 11; (1976); p. 207,208, View in Reaxys; Williams; Bowen; Organic Mass Spectrometry; vol. 11; (1976); p. 223,224, View in Reaxys; Nagiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 4; (1978); p. 20,22; Chem.Abstr.; vol. 91; nb. 20077; (1979), View in Reaxys; Mechtiew et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 4; (1965); p. 70,71; Chem.Abstr.; vol. 64; nb. 10539; (1966), View in Reaxys; Klots; Journal of Chemical Physics; vol. 64; (1976); p. 4269,4271, View in Reaxys; Howe; Williams; Organic Mass Spectrometry; vol. 2; (1969); p. 1141, View in Reaxys; Bentley et al.; Journal of the Chemical Society, Chemical Communications; (1973); p. 510, View in Reaxys; Heerma; Dijkstra; Organic Mass Spectrometry; vol. 3; (1970); p. 379,381, View in Reaxys; Korostyshevskii et al.; Theoretical and Experimental Chemistry; vol. 8; (1972); p. 640; ; p. 777, View in Reaxys; Momigny; Memoires de la Societe Royale des Sciences de Liege, Collection in 8.degree; vol. 13; (1966); p. 1,2-248; Chem.Abstr.; vol. 65; nb. 8137; (1966), View in Reaxys; McLafferty; Fairweather; Journal of the American Chemical Society; vol. 90; (1968); p. 5915, View in Reaxys; Howe; Williams; Journal of the Chemical Society [Section] B: Physical Organic; (1990); p. 6759, View in Reaxys

spectrum

field ionization

Nelson, P. R.; Abbey, L. E.; Moran, T. F.; Organic Mass Spectrometry; vol. 24; (1989); p. 22 - 26, View in Reaxys

collisional activation

Bozorgzadeh, M. H.; Lapp, R. L.; Gross, M. L.; Organic Mass Spectrometry; vol. 23; (1988); p. 712 - 718, View in Reaxys

collisional activation

Maquestiau, Andre; Haverbeke, Yves Van; Flammang, Robert; Meyrant, Philippe; Organic Mass Spectrometry; vol. 15; nb. 2; (1980); p. 80 83, View in Reaxys; Molenaar-Langeveld, Tineke A.; Fokkens, Roel H.; Nibbering, Nico M. M.; Organic Mass Spectrometry; vol. 21; (1986); p. 15 - 22, View in Reaxys

fragmentation pattern; spectrum; electron impact (EI)

Molenaar-Langeveld, Tineke A.; Fokkens, Roel H.; Nibbering, Nico M. M.; Organic Mass Spectrometry; vol. 21; (1986); p. 15 - 22, View in Reaxys

chemical ionization (CI)

MIKE (mass ion ki- Molenaar-Langeveld, Tineke A.; Fokkens, Roel H.; Nibbering, Nico M. netic energy); meta- M.; Organic Mass Spectrometry; vol. 21; (1986); p. 15 - 22, View in Reaxys stable ions

appearance potentials

Medved et al.; Chemical Physics; vol. 14; (1976); p. 345, View in Reaxys; Hickling; Jennings; Organic Mass Spectrometry; vol. 3; (1970); p. 1499,1501, View in Reaxys; Gross; Organic Mass Spectrometry; vol. 6; (1972); p. 827, View in Reaxys; Occolowitz et al.; Organic Mass Spectrometry; vol. 8; (1974); p. 61,69, View in Reaxys; Hertel; Ottinger; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 22; (1967); p. 40, View in Reaxys; Macoll, Allan; Mathur, Deepak; Organic Mass Spectrometry; vol. 16; nb. 6; (1981); p. 261 - 263, View in Reaxys metastable ions

Zaretskii, Ze'Ev V. I.; Dan, Pnina; Organic Mass Spectrometry; vol. 16; nb. 8; (1981); p. 372 - 373, View in Reaxys

positive secondary Hunt, Donald F.; Sethi, Satinder K.; Journal of the American Chemical ions; charge exSociety; vol. 102; nb. 23; (1980); p. 6953 - 6963, View in Reaxys change with positive ions; collisional activation spectrum; chemical ionization (CI)

MIKE (mass ion ki- Maquestiau, Andre; Haverbeke, Yves Van; Flammang, Robert; Meyrnetic energy) ant, Philippe; Organic Mass Spectrometry; vol. 15; nb. 2; (1980); p. 80 83, View in Reaxys

negative ion spectroscopy

Large; Knof; Organic Mass Spectrometry; vol. 11; (1976); p. 582,593, View in Reaxys

UV/VIS Spectroscopy (34) 1 of 34

Description (UV/VIS Spectroscopy)

UV two-photon absorption; Band assignment; Spectrum

Balmer, Franziska A.; Ottiger, Philipp; Leutwyler, Samuel; Chimia; vol. 70; nb. 4; (2016); p. 284 - 287, View in Reaxys 2 of 34

Description (UV/VIS Spectroscopy)

Spectrum

194/225

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Solvent (UV/VIS Spectroscopy)

ethyl acetate

Comment (UV/VIS Spectroscopy)

Remark: 293 - 393 K

Kawski; Kuklinski; Bojarski; Chemical Physics Letters; vol. 419; nb. 4-6; (2006); p. 309 - 312, View in Reaxys 3 of 34

Description (UV/VIS Spectroscopy)

Absorption spectrum

Absorption Maxima (UV/ VIS) [nm]

224; 271

Log epsilon

4.11; 3

Patent; Gao, Xiaolian; US6965040; (2005); (B1) English, View in Reaxys 4 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

various solvent(s)

Assmann; Von Benten; Charvat; Abel; Journal of Physical Chemistry A; vol. 107; nb. 27; (2003); p. 5291 - 5297, View in Reaxys 5 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

190 - 320 nm

Lueck, Horst B.; Swinney, Tim C.; Hudson, Bruce S.; Friedrich, Donald M.; Chemical Physics Letters; vol. 258; nb. 1-2; (1996); p. 80 - 86, View in Reaxys 6 of 34

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

221.24; 270.27; 229.89; 276.24

Ext./Abs. Coefficient [l·mol-1cm-1]

12000; 620

Van Walree, Cornelis A.; Roest, Martin R.; Schuddeboom, Wouter; Jenneskens, Leonardus W.; Verhoeven, Jan W.; Warman, John M.; Kooijman, Huub; Spek, Anthony L.; Journal of the American Chemical Society; vol. 118; nb. 35; (1996); p. 8395 - 8407, View in Reaxys 7 of 34

Description (UV/VIS Spectroscopy)

Oscillator strength

Kaito et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 384,387, View in Reaxys; Chia, Lucille; Goodman, Lionel; Philis, John G.; Journal of Chemical Physics; vol. 79; nb. 2; (1983); p. 593 - 602, View in Reaxys 8 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

265 - 570 nm

Chia, Lucille; Goodman, Lionel; Philis, John G.; Journal of Chemical Physics; vol. 79; nb. 2; (1983); p. 593 - 602, View in Reaxys 9 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

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Comment (UV/VIS Spectroscopy)

290 - 320 nm

Anunziata, J.; Singh, J.; Silber, J. J.; Canadian Journal of Chemistry; vol. 59; (1981); p. 1291 - 1296, View in Reaxys 10 of 34

Description (UV/VIS Spectroscopy)

UV/VIS

Holm et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6197,6201, View in Reaxys; Grunwell; Baker; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 1542, View in Reaxys; Cohen; Takahashi; Journal of the American Chemical Society; vol. 95; (1973); p. 443,444, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Tsuzuki; Asabe; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 108,109, View in Reaxys; Brett; Gold; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 1437, View in Reaxys; Yamakawa et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 1046,1047,1050, View in Reaxys; Panayotov; Tsvetanov; Monatshefte fuer Chemie; vol. 101; (1970); p. 1672,1676, 1679, View in Reaxys; Kahane-Paillous; Leach; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 1; (1962); p. 398, View in Reaxys; Kaito et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 384,387, View in Reaxys; Holcman; Sehested; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 71; (1975); p. 1211,1212, View in Reaxys; Arnold et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 2728,2730, View in Reaxys; Exner; Vetesnik; Collection of Czechoslovak Chemical Communications; vol. 43; (1978); p. 2763,2766, View in Reaxys; Ratovskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 548,479,480,481, View in Reaxys; Ostrovskii et al.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 1027,1015, View in Reaxys; Schiemenz; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 439,441, View in Reaxys; Freiser; Beauchamp; Journal of the American Chemical Society; vol. 99; (1977); p. 3214, View in Reaxys; Sharma; Pathak; Applied Spectroscopy; vol. 21; (1967); p. 423, View in Reaxys 11 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Baly; Collie; Journal of the Chemical Society; vol. 87; (1905); p. 1342, View in Reaxys; Baly; Tryhorn; Journal of the Chemical Society; vol. 107; (1915); p. 1067, View in Reaxys; Strasser; Chem. Zentralbl.; vol. 86; nb. I; (1915); p. 1159, View in Reaxys; Purvis; Journal of the Chemical Society; vol. 107; (1915); p. 505, View in Reaxys; Krasnomolova et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 44; ; p. 85, View in Reaxys; Freiser; B.auchamp; Journal of the American Chemical Society; vol. 98; (1976); p. 265, View in Reaxys; Shorygin et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 555,556; ; p. 1057, View in Reaxys; Brand; Knight; Journal of Molecular Spectroscopy; vol. 36; (1970); p. 328,329,331,334, View in Reaxys; Lui; McGlynn; Journal of Luminescence; vol. 9; (1974); p. 449,450,454,455, View in Reaxys; Jordan; Burrow; Accounts of Chemical Research; vol. 11; (1978); p. 341,347, View in Reaxys; Freiser et al.; Chemical Physics Letters; vol. 39; (1976); p. 49, View in Reaxys; Ogata; Nakajima; Tetrahedron; vol. 20; (1964); p. 2751,2753, View in Reaxys; Kuehnel; Dunken; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 6; (1966); p. 195, View in Reaxys; Lim; Spectrochimica Acta; vol. 19; (1963); p. 1967,1968, 1971, View in Reaxys; Luzkii; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 1601,1562, View in Reaxys; Kimura; Nagakura; Theoretica Chimica Acta; vol. 3; (1965); p. 164,165, 166, View in Reaxys; Ishitani; Nagakura; Theoretica Chimica Acta; vol. 4; (1966); p. 236,243, View in Reaxys; Egorochkin et al.; Doklady Chemistry; vol. 243; (1978); p. 532,533; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 243; (1978); p. 368, View in Reaxys 12 of 34

Description (UV/VIS Spectroscopy)

Absorption maxima

Bloor,J.E.; Buraway,A.; Tetrahedron; vol. 20; (1964); p. 861 - 869, View in Reaxys; Rao; Hayon; Journal of the American Chemical Society; vol. 96; (1974); p. 1287,1289, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys; Stenberg et al.; Spectroscopy Letters; vol. 11; (1978); p. 731,733,734, View in Reaxys; Schindlbauer; Monatshefte fuer Chemie; vol. 94; (1963); p. 99,105, View in Reaxys; Schiemenz; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 465,468, View in Reaxys; Schorygin et al.; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 335,338; engl. Ausg.; p. 157, View in Reaxys 13 of 34

Description (UV/VIS Spectroscopy)

Triplet-triplet band

Achiba; Kimura; Chemical Physics Letters; vol. 48; (1977); p. 107,108,109, View in Reaxys 14 of 34

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

heptane

Absorption Maxima (UV/ VIS) [nm]

223; 272

Schorygin; Ilitschewa; Izvestiya Akademii Nauk SSSR, Seriya Fizicheskaya; vol. 22; (1958); p. 1058,1062;engl.Ausg.S.1046,1050, View in Reaxys 15 of 34

Description (UV/VIS Spectroscopy)

Spectrum

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Solvent (UV/VIS Spectroscopy)

ethanol; cyclohexane

Comment (UV/VIS Spectroscopy)

220 - 290 nm

Leandri; Spinelli; Bollettino Scientifico della Facolta di Chimica Industriale di Bologna; vol. 15; (1957); p. 90,93, View in Reaxys 16 of 34

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

2,2,4-trimethyl-pentane

Absorption Maxima (UV/ VIS) [nm]

276.32

Ferguson; Journal of Chemical Physics; vol. 24; (1956); p. 1263, View in Reaxys 17 of 34

Description (UV/VIS Spectroscopy)

Absorption maxima

Comment (UV/VIS Spectroscopy)

0.0-Uebergang.

Absorption Maxima (UV/ VIS) [nm]

273.85

Ferguson; Journal of Chemical Physics; vol. 24; (1956); p. 1263, View in Reaxys 18 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

220 - 290 nm

Grammaticakis; Bulletin de la Societe Chimique de France; (1953); p. 207,208, View in Reaxys 19 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

200 - 330 nm

Hirt; King; Journal of Chemical Physics; vol. 20; (1952); p. 1821, View in Reaxys 20 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

200 - 330 nm

Hirt; King; Journal of Chemical Physics; vol. 20; (1952); p. 1821, View in Reaxys 21 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

240 - 280 nm

Hirt; Howe; Journal of Chemical Physics; vol. 16; (1948); p. 480,481, 483, View in Reaxys 22 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

110 - 270 nm; des Dampfes.

Walsh; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 191; (1947); p. 32,34, 38, View in Reaxys

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23 of 34

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methanol; H2O

Absorption Maxima (UV/ VIS) [nm]

224; 271

Doub; Vandenbelt; Journal of the American Chemical Society; vol. 69; (1947); p. 2714,2717, View in Reaxys 24 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

273 - 282 nm

Masaki; Bulletin of the Chemical Society of Japan; vol. 11; (1936); p. 346, View in Reaxys 25 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Comment (UV/VIS Spectroscopy)

240 - 285 nm

Wolf; Strasser; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 21; (1933); p. 389,402, View in Reaxys 26 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

heptane

Comment (UV/VIS Spectroscopy)

220 - 280 nm

Wolf; Strasser; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 21; (1933); p. 389,402, View in Reaxys 27 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

diethyl ether

Comment (UV/VIS Spectroscopy)

225 - 240 nm

Hantzsch; Chemische Berichte; vol. 64; (1931); p. 667,674, View in Reaxys 28 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2SO4; H2O

Comment (UV/VIS Spectroscopy)

230 - 265 nm

Hantzsch; Chemische Berichte; vol. 64; (1931); p. 667,674, View in Reaxys 29 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

des Dampfes.

Acly; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 135; (1928); p. 256, View in Reaxys 30 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Scheibe; Chemische Berichte; vol. 59; (1926); p. 2624; Chemische Berichte; vol. 60; (1927); p. 1417, View in Reaxys

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31 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Scheibe; Chemische Berichte; vol. 59; (1926); p. 2624; Chemische Berichte; vol. 60; (1927); p. 1417, View in Reaxys 32 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CCl4

Scheibe; Chemische Berichte; vol. 59; (1926); p. 2624; Chemische Berichte; vol. 60; (1927); p. 1417, View in Reaxys 33 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Ley; v. Engelhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 39, View in Reaxys; Purvis; Journal of the Chemical Society; vol. 107; (1915); p. 505, View in Reaxys; Purvis; Pr. Cambridge phil. Soc.; vol. 21; p. 786; Chem. Zentralbl.; vol. 95; nb. I; (1924); p. 1484, View in Reaxys 34 of 34

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

HCl; benzonitrile

Baly; Tryhorn; Journal of the Chemical Society; vol. 107; (1915); p. 1067, View in Reaxys ESR Spectroscopy (4) 1 of 4

Description (ESR Spectro- Signals scopy) Solvents (ESR Spectrosco- ethanol py) Temperature (ESR Spectroscopy) [°C]

-196.2

Wagner, Peter J.; May, Mary L.; Journal of Physical Chemistry; vol. 95; nb. 25; (1991); p. 10317 - 10321, View in Reaxys 2 of 4

Description (ESR Spectro- ESR scopy) Rieger; Fraenkel; Journal of Chemical Physics; vol. 37; (1962); p. 2795,2800, View in Reaxys; Kowert et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 5538, View in Reaxys; Stasko et al.; Organic Magnetic Resonance; vol. 9; (1977); p. 269, View in Reaxys; Buick et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1969); p. 666, View in Reaxys; Greatorex et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 1762,1764, View in Reaxys; Hirota et al.; Molecular Physics; vol. 29; (1975); p. 903,907,909,911,915, View in Reaxys; Mao et al.; Chemical Physics Letters; vol. 13; (1972); p. 199, View in Reaxys; Arnold et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 2728,2730, View in Reaxys; Wagner; May; Chemical Physics Letters; vol. 39; (1976); p. 350, View in Reaxys

3 of 4

Description (ESR Spectro- ESR-hyperfine coupling constants scopy) Ludwig et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 4568,4571, View in Reaxys; Rieger et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 683,685, View in Reaxys; Carrington; Todd; Molecular Physics; vol. 6; (1963); p. 161,162, View in Reaxys

4 of 4

Description (ESR Spectro- Spectrum scopy) Carrington; Todd; Molecular Physics; vol. 6; (1963); p. 161,162, View in Reaxys; Ludwig; Adams; Journal of Chemical Physics; vol. 37; (1962); p. 828, View in Reaxys

NQR Spectroscopy (2) Description (NQR References Spectroscopy) Nuclear quadrupole Negita; Bray; Journal of Chemical Physics; vol. 33; (1960); p. 1876, View in Reaxys; Lucken; Journal of Molecular resonance Structure; vol. 19; (1973); p. 43,46,47, View in Reaxys; Colligiani et al.; Molecular Physics; vol. 14; (1968); p. 89,90,

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View in Reaxys; Colligiani et al.; Journal of Chemical Physics; vol. 54; (1971); p. 5442, View in Reaxys; Colligiani; Ambrosetti; Journal of Magnetic Resonance (1969-1992); vol. 32; (1978); p. 93,98, View in Reaxys Nuclear quadrupole Dinesh; Rogers; Journal of Magnetic Resonance (1969-1992); vol. 7; (1972); p. 30, View in Reaxys coupling constants Rotational Spectroscopy (3) Description (Rota- Comment (Rotational Spectroscotional Spectroscopy) py)

References

Microwave spectrum

Davies et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 75; (1979); p. 1428,1432, 1436, 1437, View in Reaxys; Casado et al.; Journal of Molecular Structure; vol. 8; (1971); p. 211,213, 219, 220, 221, View in Reaxys; Bak et al.; Journal of Chemical Physics; vol. 37; (1962); p. 2027,2029, 2030, View in Reaxys; Firman, P.; Marchetti, A.; Xu, M.; Eyring, Edward M.; Petrucci, S.; Journal of Physical Chemistry; vol. 95; nb. 18; (1991); p. 7055 - 7061, View in Reaxys

Stark effect

Muirhead et al.; Journal of Chemical Physics; vol. 56; (1972); p. 4385, View in Reaxys; Madan; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 89; (1974); p. 259, View in Reaxys

Microwave spectrum

(19100-25700 MHz).

Raman Spectroscopy (18) Description (Ram- Solvent (Raman an Spectroscopy) Spectroscopy)

Lide; Journal of Chemical Physics; vol. 22; (1954); p. 1577, View in Reaxys; Erlandsson; Journal of Chemical Physics; vol. 22; (1954); p. 1152; Ark. Fysik; vol. 9; (1955); p. 399,429, View in Reaxys Comment (Raman Spectroscopy)

References

Spectrum

neat (no solvent)

Raghuvansh; Srivastava, Sunil K.; Singh, Ranjan K.; Asthana; Kiefer; Physical Chemistry Chemical Physics; vol. 6; nb. 3; (2004); p. 531 - 536, View in Reaxys

Bands

neat (no solvent)

Raghuvansh; Srivastava, Sunil K.; Singh, Ranjan K.; Asthana; Kiefer; Physical Chemistry Chemical Physics; vol. 6; nb. 3; (2004); p. 531 - 536, View in Reaxys

Bands

neat liquid

Mrozek; Wasileski; Weaver; Journal of the American Chemical Society; vol. 123; nb. 51; (2001); p. 12817 - 12825, View in Reaxys

Spectrum

Sloane; Cook; Applied Spectroscopy; vol. 26; (1972); p. 589,591, View in Reaxys; Michel; Gueibe; Bulletin des Societes Chimiques Belges; vol. 70; (1961); p. 330, View in Reaxys; McDevitt; Fateley; Journal of Molecular Structure; vol. 5; (1970); p. 477,484, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Venkateswarlu; Balasubramanian; Proceedings - Indian Academy of Sciences, Section A; vol. 51; (1960); p. 151,152, View in Reaxys; Venkateswarlu; Balasubramanian; Proceedings - Indian Academy of Sciences, Section A; vol. 53; (1961); p. 202,203, View in Reaxys; Kuwae; Machida; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 34; (1978); p. 785,787,788, View in Reaxys; Venkateswarlu; Radhakrishnan; Spectrochimica Acta; vol. 18; (1962); p. 1433,1438,1439, View in Reaxys; Ratovskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 548,479,480,481, View in Reaxys; Baranov; Sechkarev; Sov. Phys. J. (Engl. Transl.); vol. 11; nb. 3; (1968); p. 51,29, View in Reaxys; Alia, J. M.; Edwards, H. G. M.; Moore, J.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 12; (1995); p. 2039 - 2056, View in Reaxys; Chang, Yong Joon; Cong, Peijun; Simon, John D.; Journal of Chemical Physics; vol. 106; nb. 21; (1997); p. 8639 - 8649, View in Reaxys

Spectrum

acetonitrile

Lueck, Horst B.; Swinney, Tim C.; Hudson, Bruce S.; Friedrich, Donald M.; Chemical Physics Letters; vol. 258; nb. 1-2; (1996); p. 80 - 86, View in Reaxys

Spectrum

methanol

Vacque; Dupuy; Sombret; Huvenne; Legrand; Journal of Molecular Structure; vol. 384; nb. 2-3; (1996); p. 165 - 174, View in Reaxys

Raman resonance effect

Lueck, Horst B.; Swinney, Tim C.; Hudson, Bruce S.; Friedrich, Donald M.; Chemical Physics Letters; vol. 258; nb. 1-2; (1996); p. 80 - 86, View in Reaxys

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Degree of depolarization of Raman bands Spectrum

Simons; Comment. phys. math. Helsingfors; vol. 6; nb. 13; (1932); p. 1,45, View in Reaxys; Colaianni, S.E. May; Nielsen, O. Faurskov; Journal of Molecular Structure; vol. 347; (1995); p. 267 - 284, View in Reaxys neat (no solvent)

Raman intensities

Gao, Xiaoping; Davies, John P.; Weaver, Michael J.; Journal of Physical Chemistry; vol. 94; nb. 17; (1990); p. 6858 - 6864, View in Reaxys; Colaianni, S.E. May; Nielsen, O. Faurskov; Journal of Molecular Structure; vol. 347; (1995); p. 267 - 284, View in Reaxys Schmid, Eduard D.; Topsom, Ronald D.; Journal of the American Chemical Society; vol. 103; nb. 7; (1981); p. 1628 - 1632, View in Reaxys; Korobeinicheva, I. K.; Fugaeva, O. M.; Furin, G. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 36; nb. 8; (1987); p. 1634 - 1637; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 8; (1987); p. 1766 - 1769, View in Reaxys; Proutiere, A.; Legoff, D.; Chabanel, M.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 167; (1989); p. 39 - 50, View in Reaxys; Colaianni, S.E. May; Nielsen, O. Faurskov; Journal of Molecular Structure; vol. 347; (1995); p. 267 - 284, View in Reaxys

Bands

neat (no solvent)

Gao, Xiaoping; Davies, John P.; Weaver, Michael J.; Journal of Physical Chemistry; vol. 94; nb. 17; (1990); p. 6858 - 6864, View in Reaxys

Bands

CCl4

Schmid, Eduard D.; Topsom, Ronald D.; Journal of the American Chemical Society; vol. 103; nb. 7; (1981); p. 1628 - 1632, View in Reaxys; Proutiere, A.; Legoff, D.; Chabanel, M.; Megnassan, E.; Journal of Molecular Structure; vol. 178; (1988); p. 49 - 62, View in Reaxys; Proutiere, A.; Legoff, D.; Chabanel, M.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 167; (1989); p. 39 - 50, View in Reaxys

Raman

Lippincott; et al.; Spectrochimica Acta; vol. 22; (1966); p. 1493,1495, View in Reaxys; Fini; Mirone; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 625,626, View in Reaxys; El-Sayed et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 227, View in Reaxys; Thistlewaite; Australian Journal of Chemistry; vol. 30; (1977); p. 1595, View in Reaxys; Whittenburg; Wang; Journal of Chemical Physics; vol. 66; (1977); p. 4995, View in Reaxys; Green; Harrison; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 1279,1284,1285, View in Reaxys; Shorygin; Lopatin; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 1533; ; p. 2868, View in Reaxys

Bands

Hendra; Loader; Transactions of the Faraday Society; vol. 67; (1971); p. 828,835, View in Reaxys; Schorygin et al.; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 335,338; engl. Ausg.; p. 157, View in Reaxys

Raman intensities

(3000-170 cmE-1) in CCl4.

Behringer; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 62; (1958); p. 544,559, View in Reaxys; Schorygin; Egorowa; Doklady Akademii Nauk SSSR; vol. 117; (1957); p. 856,857; Doklady Physical Chemistry; 112-117 <1957> 785, 786, View in Reaxys; Behringer; Brandmueller; Annalen der Physik (Weinheim, Germany); vol. <7> 4; (1959); p. 234,235, View in Reaxys; Chalilow; Schorygin; Doklady Akademii Nauk SSSR; vol. 78; (1951); p. 87; Chem.Abstr.; (1951); p. 8891, View in Reaxys

Raman intensities

Intensitaet der Raman-Banden in Abhaengigkeit von der Anregungsfrequenz.

Chalilow; Schorygin; Doklady Akademii Nauk SSSR; vol. 81; (1951); p. 1031; Chem.Abstr.; (1952); p. 3409, View in Reaxys

Spectrum

bei -150grad

Bishui; Indian Journal of Physics (1926-1976); vol. 22; (1948); p. 170; Chem.Abstr.; (1948); p. 8651, View in Reaxys

Spectrum

bei 20grad

Bishui; Indian Journal of Physics (1926-1976); vol. 22; (1948); p. 170; Chem.Abstr.; (1948); p. 8651, View in Reaxys; Kohlrausch; Monatshefte fuer Chemie; vol. 76; (1947); p. 231,240, View in Reaxys; Kohlrausch; Pongratz; Monatshefte fuer Chemie; vol. 63; (1933); p. 427,437, View in Reaxys

Luminescence Spectroscopy (9)

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Description (Luminescence Spectroscopy)

Comment (Luminescence Spectroscopy)

Luminescence quantum yield

References

Luminescence quenching

Quenching with proton (aq.HClO4)

Pincock, J. A.; Redden, P. R.; Canadian Journal of Chemistry; vol. 67; (1989); p. 710 - 719, View in Reaxys

Luminescence quenching

Quenching with hexamethyldisilane

Horn, Keith A.; Whitenack, Anne A.; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3875 - 3880, View in Reaxys

Luminescence lifetime

Mao et al.; Chemical Physics Letters; vol. 13; (1972); p. 199, View in Reaxys; Achiba; Kimura; Chemical Physics Letters; vol. 48; (1977); p. 107,108,109, View in Reaxys; Devolder; Journal of Luminescence; vol. 21; (1980); p. 177,180, View in Reaxys; Kobayashi, Tohru; Honma, Kenji; Kajimoto, Okitsugu; Tsuchiya, Soji; Journal of Chemical Physics; vol. 86; nb. 3; (1987); p. 1111 - 1117, View in Reaxys

Luminescence quenching

Padwa et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 2653, View in Reaxys; Wagner, Peter J.; Lam, Henry M. H.; Journal of the American Chemical Society; vol. 102; nb. 12; (1980); p. 4167 - 4172, View in Reaxys; Iwai; Takemura; Furue; Nozakura; Bulletin of the Chemical Society of Japan; vol. 57; nb. 3; (1984); p. 763 - 767, View in Reaxys

Lasing properties

Hadni et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 71,72, View in Reaxys; Mizugai, Yoshihiro; Katayama, Mikio; Journal of the American Chemical Society; vol. 102; nb. 21; (1980); p. 6424 - 6426, View in Reaxys

Luminescence

Steffen et al.; Physics Letters; vol. 20; (1966); p. 20, View in Reaxys; Le Bel; La Posa; Journal of Molecular Spectroscopy; vol. 41; (1972); p. 249,250-290, View in Reaxys; Lui; McGlynn; Journal of Luminescence; vol. 9; (1974); p. 449,450,454,455, View in Reaxys

Emission spectrum in the infrared region

Kahane-Paillovs; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 57; (1960); p. 587, View in Reaxys; Tsuji et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 3380,3381, View in Reaxys

Degree of depolarization of luminescence

Suppan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1161,1163, View in Reaxys

Fluorescence Spectroscopy (15) Description (Fluo- Solvent (Fluoresrescence Spectrocence Spectroscoscopy) py)

Temperature (Fluorescence Spectroscopy) [°C]

Spectrum

neat liquid

19.85

Spectrum

ethyl acetate

19.85 - 119.85

Comment (Fluores- References cence Spectroscopy) Kawski; Kuklinski; Bojarski; Chemical Physics Letters; vol. 419; nb. 4-6; (2006); p. 309 - 312, View in Reaxys concentration dependence

Kawski; Kuklinski; Bojarski; Chemical Physics Letters; vol. 419; nb. 4-6; (2006); p. 309 - 312, View in Reaxys

Fluorescence excitation spectrum

Clara; Siglow; Neusser; Zeitschrift fur Physikalische Chemie; vol. 215; nb. 6; (2001); p. 765 - 776, View in Reaxys

Fluorescence excitation spectrum; Spectrum

Sakota, Kenji; Nishi, Kaori; Ohashi, Kazuhiko; Sekiya, Hiroshi; Chemistry Letters; nb. 6; (2000); p. 618 - 619, View in Reaxys

Spectrum

Maxima

274.73 - 267.38 nm Mordzinski, Andrzej; Sobolewski, Andrzej L.; Levy, Donald H.; Journal of Physical Chemistry A; vol. 101; nb. 44; (1997); p. 8221 - 8226, View in Reaxys cyclohexane

289.02 nm; 294.99 nm

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Maxima

acetonitrile

289 nm

Horn, Keith A.; Whitenack, Anne A.; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3875 3880, View in Reaxys

Maxima

273.88 nm; 270.04 nm; 268.68 nm; 266.96 nm; 266.77 nm

Kobayashi, Tohru; Honma, Kenji; Kajimoto, Okitsugu; Tsuchiya, Soji; Journal of Chemical Physics; vol. 86; nb. 3; (1987); p. 1111 - 1117, View in Reaxys

Maxima

268.68 nm; 274.33 nm; 276.14 nm; 277.58 nm; 277.8 nm

Kobayashi, Tohru; Kajimoto, Okitsugu; Journal of Chemical Physics; vol. 86; nb. 3; (1987); p. 1118 1124, View in Reaxys

Maxima

270.04 nm; 274.1 nm; 274.72 nm; 275.07 nm; 277.5 nm

Kobayashi, Tohru; Kajimoto, Okitsugu; Journal of Chemical Physics; vol. 86; nb. 3; (1987); p. 1118 1124, View in Reaxys

Maxima

273.88 nm; 277.31 nm; 281.54 nm; 283.06 nm; 285.2 nm

Kobayashi, Tohru; Kajimoto, Okitsugu; Journal of Chemical Physics; vol. 86; nb. 3; (1987); p. 1118 1124, View in Reaxys

Fluorescence

Yoshida et al.; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 2399, View in Reaxys; Le Bel; La Posa; Journal of Molecular Spectroscopy; vol. 41; (1972); p. 249,250-290, View in Reaxys; Stenberg et al.; Spectroscopy Letters; vol. 11; (1978); p. 731,733,734, View in Reaxys; Yoshita et al.; Bulletin of the Chemical Society of Japan; vol. 49; (1976); p. 1697,1698, View in Reaxys

Spectrum

270 - 300 nm

Maxima

bei Bestrahlung mit Newcomer; Journal of the American Chemical SociRoentgenstrahlen. ety; vol. 42; (1920); p. 2002, View in Reaxys

Spectrum

ethanol

Phosphorescence Spectroscopy (3) Description (Phos- Solvent (Phosphorphorescence Spec- escence Spectrotroscopy) scopy) Maxima

ethanol

Ley; v. Engelhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 39, View in Reaxys Comment (Phosphorescence Spectroscopy)

References

370 nm; 410 nm; 471 nm

Wagner, Peter J.; May, Mary L.; Journal of Physical Chemistry; vol. 95; nb. 25; (1991); p. 10317 - 10321, View in Reaxys

Phosphorescence

Spectrum

Bass; Journal of Chemical Physics; vol. 18; (1950); p. 1403,1405, View in Reaxys

Harrigan et al.; Chemical Physics Letters; vol. 14; (1972); p. 549, View in Reaxys; Le Bel; La Posa; Journal of Molecular Spectroscopy; vol. 41; (1972); p. 249,250-290, View in Reaxys; Faure et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 269; (1969); p. 431, View in Reaxys; Hirota et al.; Molecular Physics; vol. 29; (1975); p. 903,907,909,911,915, View in Reaxys; Arnold et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 2728,2730, View in Reaxys; Devolder; Journal of Luminescence; vol. 21; (1980); p. 177,180, View in Reaxys; Takei; Kanda; Spectrochimica Acta; vol. 18; (1962); p. 1201,1215, View in Reaxys ethanol

bei -190grad.

de Kowalski; de Dzierzbicki; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 152; (1911); p. 84, View in Reaxys

Other Spectroscopic Methods (3) Description (Other References Spectroscopic Methods) Electronic state studies

Siglow, Klaus; Neusser, Hans Juergen; Journal of Physical Chemistry A; vol. 105; nb. 33; (2001); p. 7823 - 7827, View in Reaxys

Photoelectron spec- Orlowski et al.; Chemical Physics; vol. 16; (1976); p. 439, View in Reaxys; Rao; Tetrahedron; vol. 32; (1976); p. trum 1561,1564, View in Reaxys; Bock et al.; Angewandte Chemie; vol. 90; (1978); p. 986, View in Reaxys; Cody; Freiser;

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Analytical Chemistry; vol. 51; (1979); p. 547,548-550, View in Reaxys; Freiser; Beauchamp; Chemical Physics Letters; vol. 42; (1976); p. 380,381, View in Reaxys; Ohta et al.; Chemical Physics Letters; vol. 32; (1975); p. 369, View in Reaxys; Krogh-Jespersen; Ratner; Journal of Chemical Physics; vol. 65; (1976); p. 1305, View in Reaxys; Burckett-St. Laurent, James C.T.R.; King, Michael A.; Kroto, Harold W.; Nixon, John F.; Suffolk, Roger J.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1983); p. 755 - 760, View in Reaxys; Bock, Hans; Wittmann, Joerg; Arpe, Hans-Juergen; Chemische Berichte; vol. 115; nb. 6; (1982); p. 2326 - 2337, View in Reaxys; Mizugai, Yoshihiro; Katayama, Mikio; Journal of the American Chemical Society; vol. 102; nb. 21; (1980); p. 6424 - 6426, View in Reaxys; Bender, Harald; Carnovale Frank; Peel Barrie J.; Wentrup, Curt; Journal of the American Chemical Society; vol. 110; nb. 11; (1988); p. 3458 - 3461, View in Reaxys; Ouyang, Jiangbo; Bard, Allen J.; Journal of Physical Chemistry; vol. 91; nb. 15; (1987); p. 4058 - 4062, View in Reaxys; Palmer, Michael H.; Moyes, William; Spiers, Martin; Journal of Molecular Structure; vol. 62; (1980); p. 165 - 188, View in Reaxys; Araki, Mitsunori; Sato, Shin-Ichiro; Kimura, Katsumi; Journal of Physical Chemistry; vol. 100; nb. 25; (1996); p. 10542 - 10546, View in Reaxys ESCA

Ohta et al.; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 2017, View in Reaxys; Larsson; Folkesson; Chemica Scripta; vol. 9; (1976); p. 148, View in Reaxys; Yumatov, V. D.; Salakhutdinov, N. F.; Russian Chemical Bulletin; vol. 43; nb. 7; (1994); p. 1186 - 1190; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 7; (1994); p. 1251 - 1254, View in Reaxys

Exposure Assessment (2) Exposure Sources presence in emissions

References

heating of nitrogen- Watanabe, Mafumi; Nakata, Chisto; Wu, Wei; Kawamoto, Katsuya; Noma, Yukio; Chemocontaining plastics sphere; vol. 68; nb. 11; (2007); p. 2063 - 2072, View in Reaxys such as acetonitrilebutadiene-styrene at low temp. (<=300 deg C); table presence in clean offgas; waste incineration plant; Germany

Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys

Concentration in the Environment (2) 1 of 2

Media (Concentration in the Environment)

clean offgas

Location

Germany

Contamination Concentration

0.30 ng/l

Method, Remarks (Concentration in the Environment)

municipal waste incineration plant; water vapor condensation; XAD-resin filters; adsorption/thermodesorption; adsorption/elution; GC-FID analysis

Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys 2 of 2

Media (Concentration in the Environment)

smoke condensate

Contamination Concentration

0 - 0.06 mg/g

Method, Remarks (Concentration in the Environment)

mean emission factor based on mass of fuel consumed from three separate fires; fuels: ponderosa pine sapwood, needles, bark, litter, duff, and humus; fires: smolder, self-sustained smolder, flaming; bench-scale fires; condensed at -45 deg C

McKenzie; Wei Min Hao; Richards; Ward; Environmental Science and Technology; vol. 29; nb. 8; (1995); p. 2047 - 2054, View in Reaxys Transport and Distribution (11) 1 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficient (Kip) at 15 deg C: 6.01E-03 m3/g at 75percent relative humidity

Method, Remarks (Transport and Distribution)

ambient particles collected Berlin, Germany using high volume air sampler with silylated Teflon glass fiber filters; Apr. 10-18, 2006; Kip determ. by inverse gas chromatography using washed (water) particle loaded fiber filters as stationary phase

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Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 2 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 8.64E-03 - 1.18E-02, 1.12E-02 and 9.65E-03 m3/g at 50, 70 and 90percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Roost, Untersiggental, Switzerland using high vol. air sampler with silylated Teflon glass fiber filter; Nov. 5-12, 2006; Kip determ. by inverse gas chromatography with particle loaded filter stationary phase at diff. RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 3 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 4.04E-03, 4.93E-03 and 7.22E-03 m3/g at 50, 70 and 90percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Berlin, Germany using high volume air sampler with silylated Teflon glass fiber filters; Apr. 10-18, 2006; Kip determ. by inverse gas chromatography using particle loaded fiber filters as stationary phase at various RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 4 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 5.00E-03, 5.89E-03 and 7.94E-03 m3/g at 50, 70 and 90percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Duebendorf, Switzerland using high volume air sampler with silylated Teflon glass fiber filter; June 15-20, 2006; Kip determ. by inverse gas chromatography using particle loaded filters as stationary phase at various RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 5 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 2.42E-02 and 2.59E-02 m3/g at 50percent and 70percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Aspvreten, Sweden using high volume air sampler with silylated Teflon glass fiber filter; Mar. 13-Apr. 3, 2006; Kip determ. by inverse gas chromatography with particle loaded filters as stationary phase at various RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 6 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 9.37E-03 and 1.14E-02 m3/g in unwashed and washed inverse gas chromatography (IGC) column resp.

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Method, Remarks (Transport and Distribution)

ambient particles collected from Zurich, Switzerland using high volume air sampler with silylated Teflon glass fiber filter; Feb. 2-3, 2006; Kip determ. by IGC with particle loaded fiber filter as stationary phase with or without washing (water)

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 7 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 4.53E4 - 6.35E4 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated at least 48 h; <0.01 percent-98 percent relative humidity; 15 deg C; relative humidity effect on partition equilibrium

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 8 of 11

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - Leonardite humic acid

Results

experimental sorption enthalpy, ΔabsHi = -46.3 kJ/mol

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5 to 75 deg C

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 9 of 11

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 8.58E3 - 9.45E4 l/kgHA; no glass transitions below 75 deg C that had an effect on the sorption properties of humic acid as indicated by linear van't Hoff plot

Method, Remarks (Transport and Distribution)

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 10 of 11

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - snow

Results

log Ki snow surface/air (m3/m2): -2.85; Ki snow surface/air: air/snow surface sorption coefficient

Method, Remarks (Transport and Distribution)

snow from Central Swiss Alp collected on January 10, 2003; 46 deg 37' 02" N, 8 deg 35' 38" E; altitude: ca. 2278 m above sea level; sorption coefficient determined from retention volume; -6.8 deg C; inverse gas chromatography analysis

Roth, Christine M.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 15; (2004); p. 4078 - 4084, View in Reaxys 11 of 11

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

water-landfill

Results

retardation factor, relative to water, from breakthrough curves: 0.8-1.3

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Method, Remarks (Transport and Distribution)

pilot-scale landfill contained 540 m3 of ordinary household waste; LiBr as tracer; ca. 500 g title comp. applied at the top of landfill; waste irrigated with 10 mm of water per day; leachate collected at depths of 0.5-4.0 m for 78 days

Oeman, Cecilia; Rosqvist, Hakan; Water Research; vol. 33; nb. 10; (1999); p. 2247 - 2254, View in Reaxys Biodegradation (12) 1 of 12

Type (Biodegradation)

bottle test

Inoculum

Rhodococcus erythropolis 9675

Concentration (Biodegradation)

Ca. 30 μmol/l

Degradation Rate (Biodegradation) [%]

100 percent

Exposure Period (Biodegradation)

Ca. 0.1 d

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

culture grown in R2A-based broth under orbital shaking (100 rpm, 24 h); title comp. in DMSO incub. with inoculum in test tubes with mineral salt medium containing sodium succinate under orbital shaking (100 rpm) in the dark; HPLC-UV; diagrams

Degradation Product (Biodegradation)

benzamide

Holtze, Maria Sommer; Sorensen, Jan; Hansen, Hans Christian B.; Aamand, Jens; Biodegradation; vol. 17; nb. 6; (2006); p. 503 - 510, View in Reaxys 2 of 12

Type (Biodegradation)

bottle test

Inoculum

Rhodococcus erythropolis 9685

Concentration (Biodegradation)

Ca. 30 μmol/l

Degradation Rate (Biodegradation) [%]

100 percent

Exposure Period (Biodegradation)

Ca. 0.1 d

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

Degradation Product (Biodegradation)

benzamide

Holtze, Maria Sommer; Sorensen, Jan; Hansen, Hans Christian B.; Aamand, Jens; Biodegradation; vol. 17; nb. 6; (2006); p. 503 - 510, View in Reaxys 3 of 12

Type (Biodegradation)

bottle test

Inoculum

Rhizobium radiobacter 9674

Concentration (Biodegradation)

Ca. 25 μmol/l

Degradation Rate (Biodegradation) [%]

100 percent

Exposure Period (Biodegradation)

0.5 d

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

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Degradation Product (Biodegradation)

benzamide

Holtze, Maria Sommer; Sorensen, Jan; Hansen, Hans Christian B.; Aamand, Jens; Biodegradation; vol. 17; nb. 6; (2006); p. 503 - 510, View in Reaxys 4 of 12

Type (Biodegradation)

bottle test

Inoculum

Rhizobium sp. 11401

Concentration (Biodegradation)

Ca. 30 μmol/l

Degradation Rate (Biodegradation) [%]

100 percent

Exposure Period (Biodegradation)

1.0 d

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

culture grown in R2A-based broth under orbital shaking (100 rpm, 24 h); title comp. in DMSO incub. with inoculum in glass test tubes with mineral salt medium containing sodium succinate under orbital shaking (100 rpm) in the dark; HPLC-UV; diagrams

Degradation Product (Biodegradation)

benzamide

Holtze, Maria Sommer; Sorensen, Jan; Hansen, Hans Christian B.; Aamand, Jens; Biodegradation; vol. 17; nb. 6; (2006); p. 503 - 510, View in Reaxys 5 of 12

Type (Biodegradation)

bottle test

Inoculum

Pseudomonas fluorescens 11387

Concentration (Biodegradation)

Ca. 35 μmol/l

Degradation Rate (Biodegradation) [%]

100 percent

Exposure Period (Biodegradation)

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

Degradation Product (Biodegradation)

benzamide

Holtze, Maria Sommer; Sorensen, Jan; Hansen, Hans Christian B.; Aamand, Jens; Biodegradation; vol. 17; nb. 6; (2006); p. 503 - 510, View in Reaxys 6 of 12

Type (Biodegradation)

aerobic

Inoculum

Agrobacterium radiobacter 8/4

Concentration (Biodegradation)

50 mg/l

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

in DMSO; soil microorganism; A. radiobacter cells cultured on LB medium; samples taken at 1, 2 and 4 h; nitrile hydratase action; degradation in the cell-free extract and growing culture experiments: + and +, resp.

Vosahlova; Pavlu; Vosahlo; Brenner; Pesticide Science; vol. 49; nb. 3; (1997); p. 303 - 306, View in Reaxys 7 of 12

Type (Biodegradation)

aerobic

Inoculum

activated sewage sludge

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Concentration (Biodegradation)

15 - 240 mg/l

Method, Remarks (Biodegradation)

according to MITI and OECD standard test; growth kinetic parameter values measurement: maximum observed relative growth rate of microorganisms, μmax, 1.2-2.4 d-1, half-saturation constant, Ks, < 1-36 mg ThOD/l

Blok; Struys; Ecotoxicology and Environmental Safety; vol. 33; nb. 3; (1996); p. 217 - 227, View in Reaxys 8 of 12

Type (Biodegradation)

aerobic

Inoculum

industrial treatment plant sludge

Concentration (Biodegradation)

100 mg/l

Method, Remarks (Biodegradation)

according to MITI and OECD standard test; growth kinetic parameter values measurement: maximum observed relative growth rate of microorganisms, μmax, 1.5 d-1, half-saturation constant, Ks, 36 mg ThOD/l

Blok; Struys; Ecotoxicology and Environmental Safety; vol. 33; nb. 3; (1996); p. 217 - 227, View in Reaxys 9 of 12

Type (Biodegradation)

aerobic

Inoculum

municipal treatment plant sludge

Concentration (Biodegradation)

100 mg/l

Method, Remarks (Biodegradation)

according to MITI and OECD standard test; growth kinetic parameter values measurement: maximum observed relative growth rate of microorganisms, μmax, 2.0 d-1, half-saturation constant, Ks, 2.6 mg ThOD/l

Blok; Struys; Ecotoxicology and Environmental Safety; vol. 33; nb. 3; (1996); p. 217 - 227, View in Reaxys 10 of 12

Type (Biodegradation)

aerobic

Inoculum

activated sewage sludge

Concentration (Biodegradation)

100 mg/l

Method, Remarks (Biodegradation)

according to MITI and OECD standard test; growth kinetic parameter values measurement: maximum observed relative growth rate of microorganisms, μmax, 1.8 d-1, half-saturation constant, Ks, 43 mg ThOD/l

Blok; Struys; Ecotoxicology and Environmental Safety; vol. 33; nb. 3; (1996); p. 217 - 227, View in Reaxys 11 of 12

Type (Biodegradation)

anaerobic

Inoculum

freshwater sediment extract; Athens, Georgia

Concentration (Biodegradation)

1E-5 mol/l

Temperature (Biodegradation) [°C]

Half-life Time (Biodegradation)

7.4 d

Method, Remarks (Biodegradation)

sediment extracting with 20 percent glycerol solution; HPLC

Masunaga, Shigeki; Wolfe, N. Lee; Carriera, Laura; Environmental Toxicology and Chemistry; vol. 14; nb. 11; (1995); p. 1827 - 1838, View in Reaxys 12 of 12

Type (Biodegradation)

anaerobic

Inoculum

freshwater sediment slurry; Athens, Georgia

Concentration (Biodegradation)

1E-05 - 5E-05 mol/l

Temperature (Biodegradation) [°C]

5 - 115

Half-life Time (Biodegradation)

62.3 d

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Method, Remarks (Biodegradation)

incubation for several days and resorufin adding for anaerobicity; benzonitrile in methanol; HPLC; temperature effect investigation

Masunaga, Shigeki; Wolfe, N. Lee; Carriera, Laura; Environmental Toxicology and Chemistry; vol. 14; nb. 11; (1995); p. 1827 - 1838, View in Reaxys Abiotic Degradation, Hydrolysis (2) 1 of 2

Type (Abiotic Degradation, Hydrolysis)

hydrolysis

Temperature (Abiotic Deg- 85 radation, Hydrolysis) [°C] Rate Constant

0.045 per day

pH-Value (Abiotic Degradation, Hydrolysis)

7.7

Half-life Time (Abiotic Degradation, Hydrolysis) [h]

369.6

Method, Remarks (Abiotic in distilled water; phosphate buffer; monitoring for 28 days; HPLC Degradation, Hydrolysis) Degradation Product (Abiotic Degradation, Hydrolysis)

benzoic acid

Masunaga, Shigeki; Wolfe, N. Lee; Hayase, Kohji; Environmental Toxicology and Chemistry; vol. 14; nb. 9; (1995); p. 1457 1464, View in Reaxys 2 of 2

Type (Abiotic Degradation, Hydrolysis)

hydrolysis

Concentration (Abiotic Degradation, Hydrolysis)

1E-5 mol/l

Temperature (Abiotic Deg- 25 radation, Hydrolysis) [°C] Method, Remarks (Abiotic autoclave-sterilized sediment; HPLC Degradation, Hydrolysis) Masunaga, Shigeki; Wolfe, N. Lee; Carriera, Laura; Environmental Toxicology and Chemistry; vol. 14; nb. 11; (1995); p. 1827 - 1838, View in Reaxys Use (22) Laboratory Use and Use Pattern Handling

Location

References

Chemical processes/laboratory use

Page/Page column title page; 10

Patent; SCG CHEMICALS COMPANY LIMITED; THIRASAK, Attapong; KAMMAFOO, Alisa; PROMBUNGLUM, Arnat; (15 pag.); WO2016/36326; (2016); (A1) English, View in Reaxys

extractive agent for a process for separation of ethylbenzene from a mixture comprising C8 aromatics

Page/Page column title page; 10

Patent; SCG CHEMICALS COMPANY LIMITED; THIRASAK, Attapong; KAMMAFOO, Alisa; PROMBUNGLUM, Arnat; (15 pag.); WO2016/36326; (2016); (A1) English, View in Reaxys

Solvent for preparation of diazonaphtoquinonesulfonyl ester

Patent; COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH; MINISTRY OF INFORMATION TECHNOLOGY; WO2007/26374; (2007); (A1) English, View in Reaxys

Ligand

Patent; The Regents of the University of California; US2007/78280; (2007); (A1) English, View in Reaxys

solvent for preparing N-acetylaminoacetophenones

Patent; DSM FINE CHEMICALS AUSTRIA NFG GMBH and CO KG; WO2007/39034; (2007); (A1) English, View in Reaxys

solvent for ozonolysis

Patent; DSM FINE CHEMICALS AUSTRIA NFG GMBH and CO KG; WO2007/39034; (2007); (A1) English, View in Reaxys

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distillation aid for separating crude chlorosilane streams of lowerboiling chlorosilanes and higherboiling chlorosilanes

Patent; DOW CORNING CORPORATION; WO2007/67723; (2007); (A1) English, View in Reaxys

polymerization solvent

Patent; INDIAN INSTITUTE OF TECHNOLOGY BOMBAY; KUMAR, Anil; MISHRA, Sarada, Prasad; SAHOO, Rabindra; SREELEKHA, P., G.; JASMINE; WO2007/66353; (2007); (A2) English, View in Reaxys

Solvent for chemical oxidative polymerization

Patent; INDIAN INSTITUTE OF TECHNOLOGY BOMBAY; KUMAR, Anil; MISHRA, Sarada, Prasad; SAHOO, Rabindra; SREELEKHA, P., G.; JASMINE; WO2007/66353; (2007); (A2) English, View in Reaxys

Inert liquid suitable for use during electrochemical oxidation of 3,4-propylenedioxythiophene compounds

Patent; INDIAN INSTITUTE OF TECHNOLOGY BOMBAY; KUMAR, Anil; MISHRA, Sarada, Prasad; SAHOO, Rabindra; SREELEKHA, P., G.; JASMINE; WO2007/66353; (2007); (A2) English, View in Reaxys

Agent for solubilizing the rhodium-organophosphorus ligand complex and free organophosphorus ligand

Patent; DOW GLOBAL TECHNOLOGIES INC.; WO2007/133379; (2007); (A1) English, View in Reaxys

Promoter in the direct synthesis of trialkoxysilane

Patent; Lewis, Kenrick M.; Cameron, Rudolph A.; Ritscher, James S.; Ritscher, Karen; US2007/287850; (2007); (A1) English, View in Reaxys

Solvent

Patent; DAICEL CHEMICAL INDUSTRIES, LTD.; EP1681284; (2006); (A1) English, View in Reaxys

Liquefying agent

Patent; ALBEMARLE CORPORATION; WO2006/11873; (2006); (A1) English, View in Reaxys

Solvent for preparing a 2-hydroxy carboxilic acid

Patent; Chaudhari, Raghunath Vitthal; Tonde, Sunil Sopana; US2005/143600; (2005); (A1) English, View in Reaxys

Decoy agent

Patent; Wyeth; US2005/228179; (2005); (A1) English, View in Reaxys

substrate for iodination

Patent; MITSUBISHI GAS CHEMICAL COMPANY, INC.; EP1595862; (2005); (A1) English, View in Reaxys

Carrier

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys

facilitating encapsulation of the phytoactive compound within the adjuvant

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys

Solvent for synthesis of acylphosphines

Patent; BASF AKTIENGESELLSCHAFT; WO2004/94439; (2004); (A2) German, View in Reaxys

Normalpotential Eo, Geschw. Konst. (eTransfer): als Katalysator bei der elektroch. Red. von Brombenzol, Chlorbenzol, 2-Bromopyridin

Andrieux et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 3431,3434,3436,3437, View in Reaxys

Inhibitor bei der Polymerisation von

Sinizyna; Bagdasar'jan; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 1110,1113; engl. Ausgabe; p. 528, View in Reaxys

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Vinylacetat (kinet. Angaben) Isolation from Natural Product (2) Isolation from Nat- References ural Product aus Kakaoaroma durch Gaschromatographie

Marion et al.; Helvetica Chimica Acta; vol. 50; (1967); p. 1509, View in Reaxys

Im Steinkohlenteer

Kraemer; Spilker; Chemische Berichte; vol. 23; (1890); p. 84, View in Reaxys

Quantum Chemical Calculations (1) Calculated Proper- Method (Quantum ties Chemical Calculations) Atom distances, an- Ab initio calcns. gles (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Location

References

supporting informa- Chu, Jiaxiang; Kefalidis, Christos E.; Maron, Laurent; Leng, Xuebing; tion Chen, Yaofeng; Journal of the American Chemical Society; vol. 135; nb. 22; (2013); p. 8165 - 8168, View in Reaxys

Medchem (48) 1 of 48

Substance Effect

Pheromone activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Conotrachelus nenuphar, plum curculioBioassay : title comp. evaluated in 12 replicates run consecutively over a 24-day period; RI: response index field experiments using baited cotton dental wick attached to boll-weevil traps placed on the ground beneath the canopy of unsprayed apple trees; open-air indoor conditions at 26-28 deg C for 96 hr; title comp. in mineral oil; solvent control

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

release-rate 11.33 mg/day; RI=33.0

Measurement Parameter

qualitative

Leskey, Tracy C.; Prokopy, Ronald J.; Wright, Starker E.; Phelan, P. Larry; Haynes, Leroy W.; Journal of Chemical Ecology; vol. 27; nb. 1; (2001); p. 1 - 17, View in Reaxys 2 of 48

Substance Effect

Pheromone activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Conotrachelus nenuphar, plum curculioBioassay : title comp. in hexane; a dual-choice stillair system of enclosed Pettri dishes employed to test; tests conducted at 26 deg C, 65-80 percent RH, at beginning of scotophase of the 16L:6D; solvent control; RI: response index labor. bioassay; overwintered plum curculio (PC) adults collected in the field in May-June 1998 and 2000 from populations present on unsprayed wild plum or apple trees in Hampshire County, Massachusetts; 12 PCs tested individually in bioassay dishes

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

no significant differences between males and females in response to title compound at any of the 5 concentrations tested; RI=-29.2, -10.0, 11.7, -16.7 at 1.00, 0.10, 0.01, 0.001 percent concentrations, respectively; repellent effects

Measurement Parameter

qualitative

Leskey, Tracy C.; Prokopy, Ronald J.; Wright, Starker E.; Phelan, P. Larry; Haynes, Leroy W.; Journal of Chemical Ecology; vol. 27; nb. 1; (2001); p. 1 - 17, View in Reaxys 3 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

506893View in Reaxys

Substance Name

28214

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Qualitative Results

testing as an inducer of a diaminomaleonitrile-degrading enzyme in Trichoderma sp. MB 519

Measurement Parameter

qualitative

Kuwahara, Masaaki; Yanase, Hideshi; Agricultural and Biological Chemistry; vol. 49; nb. 1; (1985); p. 125 - 132, View in Reaxys 4 of 48

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : mortalityBioassay : LC50 vs time dependence; 14-day semichronic experiment; bioconcentration and reactive models; comparison

Biological Species/NCBI ID

guppy

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

LC50

Unit

Quantitative value

1.35 - 2.42

Measurement pX

2.87

Verhaar, Henk J. M.; De Wolf, Watze; Legierse, Karin C. H. M.; Seinen, Willem; Hermens, Joop L. M.; Environmental Science and Technology; vol. 33; nb. 5; (1999); p. 758 - 763, View in Reaxys 5 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : fibril formation; inhibition ofTarget : recombinant transthyretinBioassay : fibril formation in the absence of title comp. assigned as 100 percent; complete inhibition was equivalent to 0 percent fibril formation transthyretin incubated with title comp. in phosphate buffer, pH 7.2 at 37 deg C for 30 min; pH lowered to pH 4.4 by addition of acetate buffer, pH 4.2; incubated at 37 deg C for 72 h; quantified by turbidity measurements

Substance RN

506893View in Reaxys

Substance Name

28214

Substance Dose

1.44000 mM

Qualitative Results

94 percent fibril formation

Measurement Parameter

qualitative

Johnson, Steven M.; Petrassi, H. Michael; Palaninathan, Satheesh K.; Mohamedmohaideen, Nilofar N.; Purkey, Hans E.; Nichols, Christopher; Chiang, Kyle P.; Walkup, Traci; Sacchettini, James C.; Sharpless, K. Barry; Kelly, Jeffery W.; Journal of Medicinal Chemistry; vol. 48; nb. 5; (2005); p. 1576 - 1587, View in Reaxys 6 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

binding to bovine serum albumin

Measurement Parameter

qualitative

Garst; Journal of Pharmaceutical Sciences; vol. 73; nb. 11; (1984); p. 1623 - 1629, View in Reaxys 7 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

no nematicidal activity against Bursaphelenchus lignicolus

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Measurement Parameter

qualitative

Nagase; Kuwahara; Tominaga; Sugawara; Agricultural and Biological Chemistry; vol. 46; nb. 1; (1982); p. 167 - 172, View in Reaxys 8 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : ambient particles collected Berlin, Germany using high volume air sampler with silylated Teflon glass fiber filters; Apr. 10-18, 2006; Kip determ. by inverse gas chromatography using washed (water) particle loaded fiber filters as stationary phase

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition gas/particle equilibrium partition coefficient (Kip) at 15 deg C: 6.01E-03 m3/g at 75% relative humidity

Measurement Parameter

qualitative

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 9 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : ambient particles collected from Aspvreten, Sweden using high volume air sampler with silylated Teflon glass fiber filter; Mar. 13-Apr. 3, 2006; Kip determ. by inverse gas chromatography with particle loaded filters as stationary phase at various RH

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 2.42E-02 and 2.59E-02 m3/g at 50% and 70% relative humidity (RH) resp.

Measurement Parameter

qualitative

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 10 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : ambient particles collected from Berlin, Germany using high volume air sampler with silylated Teflon glass fiber filters; Apr. 10-18, 2006; Kip determ. by inverse gas chromatography using particle loaded fiber filters as stationary phase at various RH

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 4.04E-03, 4.93E-03 and 7.22E-03 m3/g at 50, 70 and 90% relative humidity (RH) resp.

Measurement Parameter

qualitative

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 11 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : ambient particles collected from Duebendorf, Switzerland using high volume air sampler with silylated Teflon glass fiber filter; June 15-20, 2006; Kip determ. by inverse gas chromatography using particle loaded filters as stationary phase at various RH

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 5.00E-03, 5.89E-03 and 7.94E-03 m3/g at 50, 70 and 90% relative humidity (RH) resp.

Measurement Parameter

qualitative

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Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 12 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : ambient particles collected from Roost, Untersiggental, Switzerland using high vol. air sampler with silylated Teflon glass fiber filter; Nov. 5-12, 2006; Kip determ. by inverse gas chromatography with particle loaded filter stationary phase at diff. RH

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 8.64E-03 - 1.18E-02, 1.12E-02 and 9.65E-03 m3/g at 50, 70 and 90% relative humidity (RH) resp.

Measurement Parameter

qualitative

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 13 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : ambient particles collected from Zurich, Switzerland using high volume air sampler with silylated Teflon glass fiber filter; Feb. 2-3, 2006; Kip determ. by IGC with particle loaded fiber filter as stationary phase with or without washing (water)

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 9.37E-03 and 1.14E-02 m3/g in unwashed and washed inverse gas chromatography (IGC) column resp.

Measurement Parameter

qualitative

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 14 of 48

Substance Effect

Antihelmintic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : mortalityTarget : Caenorhabditis elegans strain N2Bioassay : assay on free living nematode as model with important genetic similarities to parasitic nematodes; C. elegans maintenance on solid NGM medium; E. coli culture: 5 times concentrated overnight culture of E. coli WP2 (uvr A trp malB) in S medium between 20 and 50 nematodes in 500 μl S medium with 30 μl E. coli culture placing in wells; 10 μl title comp. DMSO soln. addition; nematode survival measurement 4-5 h and 12-13 h after title comp. addn.; controls with DMSO alone

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

LC90

Unit

µM

Quantitative value

19000

Measurement pX

2.68

Kermanshai, Rohan; McCarry, Brian E.; Rosenfeld, Jack; Summers, Peter S.; Weretilnyk, Elizabeth A.; Sorger, George J.; Phytochemistry; vol. 57; nb. 3; (2001); p. 427 - 435, View in Reaxys 15 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : microtubule assembly; inhibition ofTarget : microtubule protein of porcine brainBioassay : effect of title comp. on microtubule assembly/disassembly determined during temperature cycles from 4 to 37 and back to 4 deg C by turbidity assay

Substance RN

506893View in Reaxys

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Substance Name

28214

Measurement Parameter

NOAEC

Unit

Quantitative value

Measurement pX

2.3

Stoiber, Thomas; Unger, Eberhard; Dorn, Susanne B.; Degen, Gisela H.; Bolt, Hermann M.; Archives of Toxicology; vol. 82; nb. 9; (2008); p. 601 - 606, View in Reaxys 16 of 48

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Spirostomum ambiguum, protozoaBioassay : Spirotox test, polystyrene microplates, pH 7.4, hardness 2.8 mg CaCO3/l, incubation in the darkness 25 deg C

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

LC50

Unit

Quantitative value

9.33 - 12.1

Measurement pX

2.03

Nalecz-Jawecki, Grzegorz; Sawicki, Jozef; Chemosphere; vol. 38; nb. 14; (1999); p. 3211 - 3218, View in Reaxys 17 of 48

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Spirostomum ambiguum, protozoaBioassay : Spirotox test, polystyrene microplates, pH 7.4, hardness 2.8 mg CaCO3/l, incubation in the darkness 25 deg C

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

EC50

Unit

Quantitative value

3.9 - 4.83

Measurement pX

2.41

Nalecz-Jawecki, Grzegorz; Sawicki, Jozef; Chemosphere; vol. 38; nb. 14; (1999); p. 3211 - 3218, View in Reaxys 18 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

Radioprotective activity in mice. Dose: LD(50)/2 mg/kg/i.p. Mean survival time (day): 13.7 <control: 10.3>; Increase (percent) of survival (30 day): 17; Survival (percent, 30 day): 10

Measurement Parameter

qualitative

Fernandez, J. P.; Robbe, Y.; Chapat, J. P.; Cassanas, G.; Fatome, M.; Sentenac-Roumanou, H.; Farmaco, Edizione Scientifica; vol. 41; nb. 1; (1986); p. 41 - 48, View in Reaxys 19 of 48

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

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Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |enzyme; inhib. of Bioassay : title comp. and enzyme incubated at 25 deg C for 2 h; assayed for remaining activity using benzamidine substrate

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

remaining activity 48.1%; class of inhibition: amidase dead-end inhibition

Measurement Parameter

qualitative

Substance Effect

Genotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : B6C3F1 mouseBioassay : PCE: polychromatic erythrocytes; NCE: normochromatic erythrocytes; MN: micronucleus; control (C): without title comp.; dose: highest negative exposure level in vivo; 7-10 mice per group were treated with title comp.; blood collected and stained; MN frequencies (PCE and NCE) determined using ca. 1000 cells by epifluorescence microscopy

Substance RN

506893View in Reaxys

Substance Name

28214

Substance Dose

37.5000 mg/kg

Substance Route of Adm.

oral administration

Qualitative Results

MN-NCE/1000 NCE: (dose, mg/kg): 1.10 (C), 1.27 (37.5), 0.85 (75), 1.19 (150), 1.08 (300), 1.26 (600); percent PCE (dose, mg/kg): 1.95 (C), 1.68 (37.5), 2.10 (75), 1.86 (150), 2.00 (300), 1.78 (600); dose: 600 mg/kg

Measurement Parameter

qualitative

Witt, Kristine L.; Knapton, Alan; Wehr, Carol M.; Hook, Graham J.; Mirsalis, Jon; Shelby, Michael D.; MacGregor, James T.; Environmental and Molecular Mutagenesis; vol. 36; nb. 3; (2000); p. 163 - 194, View in Reaxys 21 of 48

Substance Effect

Genotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : B6C3F1 mouseBioassay : PCE: polychromatic erythrocytes; NCE: normochromatic erythrocytes; MN: micronucleus; control (C): without title comp.; dose: highest negative exposure level in vivo; 9-10 mice per group were treated with title comp.; blood collected and stained; MN frequencies (PCE and NCE) determined using ca. 1000 cells by epifluorescence microscopy

Substance RN

506893View in Reaxys

Substance Name

28214

Substance Dose

37.5000 mg/kg

Substance Route of Adm.

oral administration

Qualitative Results

MN-NCE/1000 NCE: (dose, mg/kg): 1.60 (C), 1.51 (37.5), 1.24 (75), 1.27 (150), 1.49 (300), 1.58 (600); percent PCE (dose, mg/kg): 1.93 (C), 2.05 (37.5), 1.70 (75), 1.72 (150), 1.85 (300), 1.93 (600); dose: 600 mg/kg

Measurement Parameter

qualitative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : pilot-scale landfill contained 540 m3 of ordinary household waste; LiBr as tracer; ca. 500 g title comp. applied at the top of landfill; waste irrigated with 10 mm of water per day; leachate collected at depths of 0.5-4.0 m for 78 days

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Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

sorption retardation factor, relative to water, from breakthrough curves: 0.8-1.3

Measurement Parameter

qualitative

Oeman, Cecilia; Rosqvist, Hakan; Water Research; vol. 33; nb. 10; (1999); p. 2247 - 2254, View in Reaxys 23 of 48

Substance Effect

Antialgae

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Pseudokirchneriella subcapitata UTEX 1648, algaeBioassay : control: acetone; DO: dissolved oxygen; EC50: title comp. conc. that reduced final DO to half of that obtained by the control closed algal toxicity testing with no headspace in BOD bottles with dilution water, growth medium and title comp.; bottles placed in orbital shaker at 100 rpm for 48 h; initial DO level: ca. 1-3 mg/l; DO production determ.; US EPA (1996)

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

29.175

Measurement pX

3.55

Huang, Chun-Pin; Wang, Yun-Ju; Chen, Chung-Yuan; Ecotoxicology and Environmental Safety; vol. 67; nb. 3; (2007); p. 439 - 446, View in Reaxys 24 of 48

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Pseudokirchneriella subcapitata UTEX 1648, algaeBioassay : control: acetone; EC50: title comp. conc. that reduced growth rate to half of that obtained by the control closed algal toxicity testing with no headspace in BOD bottles with dilution water, growth medium and title comp.; bottles placed in orbital shaker at 100 rpm for 48 h; initial cell density: 15000 cells/ml; growth rate determ.; US EPA (1996)

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

33.251

Measurement pX

3.49

Huang, Chun-Pin; Wang, Yun-Ju; Chen, Chung-Yuan; Ecotoxicology and Environmental Safety; vol. 67; nb. 3; (2007); p. 439 - 446, View in Reaxys 25 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

in vitro metabolism using rat liver subcellular fractions: oxidative metabolism to produce ring-hydroxylated metabolites

Measurement Parameter

qualitative

Markus; Kwon; Journal of Pharmaceutical Sciences; vol. 83; nb. 12; (1994); p. 1729 - 1734, View in Reaxys 26 of 48

Target Name

Transthyretin

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27 of 48

Target Synonyms

attr; crocttr; palb; prealbumin; t-t3bp; tadpole t3-binding protein; tbpa; thbp; transthyretin; tt; ttr; xttr

Target, Subunit, Species

Transthyretin

Target Mutant/Chimera Details

Transthyretin:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : transthyretin (TTR) amyloid fibril formation; inhibition ofBioassay : Fibril Formation Assay; Wild type TTR was purified from an Escherichia coli expression system as described previously (Lashuel, H. A.; et al. Biochemistry 1999, 38, 13560-13573). Disposable cuvettes (Fisher No.14 385 938) were charged with 495 μL of a 0.4 mg/mL stock of TTR (7.2 μM) in 10 mM phosphate

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

the extent of fibril formation in the presence of title compound (7.2 μmol/l): 94 %

Measurement Parameter

qualitative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : snow from Central Swiss Alp collected on January 10, 2003; 46 deg 37' 02" N, 8 deg 35' 38" E; altitude: ca. 2278 m above sea level; sorption coefficient determined from retention volume; -6.8 deg C; inverse gas chromatography analysis

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

sorption log Ki snow surface/air (m3/m2): -2.85; Ki snow surface/air: air/snow surface sorption coefficient

Measurement Parameter

qualitative

Roth, Christine M.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 15; (2004); p. 4078 - 4084, View in Reaxys 28 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated at least 48 h; <0.01 percent-98 percent relative humidity; 15 deg C; relative humidity effect on partition equilibrium

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition Leonardite humic acid/air partition coefficient, KHA,air = 4.53E4 - 6.35E4 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

Measurement Parameter

qualitative

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 29 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5 to 75 deg C

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

sorption experimental sorption enthalpy, ΔabsHi = -46.3 kJ/mol

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Measurement Parameter

qualitative

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 30 of 48

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Substance RN

506893View in Reaxys

Substance Name

28214

Qualitative Results

partition Leonardite humic acid/air partition coefficient, KHA,air = 8.58E3 - 9.45E4 l/kgHA; no glass transitions below 75 deg C that had an effect on the sorption properties of humic acid as indicated by linear van't Hoff plot

Measurement Parameter

qualitative

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 31 of 48

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |enzyme; inhib. of Bioassay : formation of <14C>guanosine 5'-monophosphate determined in vitro; inhibition of T. gondii guanine phosphoribosyltransferase activity evaluated; 4 μmol/l <8-14C>guanine (spec. act.: 55 Ci/mol); 4 mmol/l 5'-phosphoribosyl-1-pyrophosphate; assay buffer, pH 7.4; 37 deg C

Substance RN

506893View in Reaxys

Substance Name

28214

Substance Dose

0 mM

Measurement Parameter

Ki (inhibition constant)

Unit

µM

Quantitative value

580

Measurement pX

3.24

Naguib; Iltzsch; El Kouni; Panzica; Biochemical Pharmacology; vol. 50; nb. 10; (1995); p. 1685 - 1693, View in Reaxys 32 of 48

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |enzyme; inhib. of Bioassay : formation of <14C>xanthosine 5'-monophosphate determined in vitro; inhibition of T. gondii xanthine phosphoribosyltransferase activity evaluated; 10 μmol/l <8-14C>xanthine (spec. act.: 55 Ci/mol); 4 mmol/l 5'-phosphoribosyl-1-pyrophosphate; assay buffer, pH 7.4; 37 deg C

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Substance RN

506893View in Reaxys

Substance Name

28214

Substance Dose

0 mM

Measurement Parameter

Ki (inhibition constant)

Unit

µM

Quantitative value

870

Measurement pX

3.06

Naguib; Iltzsch; El Kouni; Panzica; Biochemical Pharmacology; vol. 50; nb. 10; (1995); p. 1685 - 1693, View in Reaxys 33 of 48

Substance Effect

Antialgae

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Pseudokirchneriella subcapitata, UTEX 1648Bioassay : growth medium without EDTA; BOD: biochemical-oxygen-demand; EC50: median effective conc.; % inhibition = <(Xt - Xo)/Xc Xo)>*100; Xt and Xc denote final cell densities for treatment and control, resp.; Xo: initial cell in sealed BOD bottles filled with dilution H2O with growth medium (pH 7.5); no headspace; test-system exposed to title comp. for 48 h at 24 deg C, 65 μEm-2s-1 with shaking at 100 rpm; % inhibition rate

Substance RN

506893View in Reaxys

Substance Name

28214

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

23.33

Measurement pX

3.65

Tsai, Kuo-Pei; Chen, Chung-Yuan; Environmental Toxicology and Chemistry; vol. 26; nb. 9; (2007); p. 1931 - 1939, View in Reaxys 34 of 48

Bioassay Category

Pharmacokinetic

Bioassay Details

In vitro area under plasma concentration time curve was determined in rat upon oral administration of the compound

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Substance Route of Adm.

oral administration

Measurement Parameter

qualitative

Measurement Object

Area under plasma concentration

Qualitative value

Not Published

Leach, Andrew G.; Jones, Huw D.; Cosgrove, David A.; Kenny, Peter W.; Ruston, Linette; MacFaul, Philip; Wood, J. Matthew; Colclough, Nicola; Law, Brian; Journal of Medicinal Chemistry; vol. 49; nb. 23; (2006); p. 6672 - 6682, View in Reaxys 35 of 48

Bioassay Category

Pharmacokinetic

Bioassay Details

In vitro area under plasma concentration time curve was determined in rat upon oral administration of the compound

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Substance Route of Adm.

oral administration

Measurement Parameter

qualitative

Measurement Object

Area under plasma concentration

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Qualitative value

Not Published

Quantitative value

37 of 48

Target Name

Serum albumin [taurine cattle]

Target Synonyms

alb; bsa; serum albumin

Target Uniprot ID

p02769

Target PDB ID

2l7u; 3v03; 4f5s; 4jk4; 4or0

Target, Subunit, Species

Serum albumin [taurine cattle]

Target Mutant/Chimera Details

Serum albumin [taurine cattle]:Wild

Target Species (Bioactivity)

taurine cattle

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Concentration of the compound required for binding to bovine serum albumin

Biological Species/NCBI ID

taurine cattle

Substance RN

506893View in Reaxys

Measurement Parameter

pIC50

Quantitative value

3.23

Measurement pX

3.23

Bioassay Category

Pharmacokinetic

Bioassay Details

In vitro area under plasma concentration time curve was determined in rat upon oral administration of the compound

Substance RN

506893View in Reaxys

Substance Route of Adm.

oral administration

Measurement Parameter

qualitative

Measurement Object

Area under plasma concentration

Qualitative value

Not Published

Bioassay Category

Pharmacokinetic

Bioassay Details

In vitro area under plasma concentration time curve was determined in rat upon oral administration of the compound

Substance RN

506893View in Reaxys

Substance Route of Adm.

oral administration

Measurement Parameter

qualitative

Measurement Object

Area under plasma concentration

Qualitative value

Not Published

Quantitative value

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39 of 48

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

Metabolism/Transport

Bioassay Details

Binding affinity of the compound towards rat plasma protein

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Measurement Parameter

Ki (inhibition constant)

Unit

Qualitative value

Quantitative value

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

Metabolism/Transport

Bioassay Details

Binding affinity of the compound towards rat plasma protein

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Measurement Parameter

pKi

Unit

Qualitative value

Quantitative value

-0.06

Deviation

0.4

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

Metabolism/Transport

Bioassay Details

Binding affinity of the compound towards rat plasma protein

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Measurement Parameter

percentage

Unit

Measurement Object

log Ki

Qualitative value

Quantitative value

-0.06

Deviation

0.4

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose in rat

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Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

Quantitative value

1200

Material Safety Data Sheet, View in Reaxys 43 of 48

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published lethal dose

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Unit

mg/kg

Measurement Object

Lowest published lethal dose

Qualitative value

Quantitative value

720

Material Safety Data Sheet, View in Reaxys 44 of 48

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published lethal concentration;Inhalation

Biological Species/NCBI ID

Rattus norvegicus

Substance RN

506893View in Reaxys

Substance Route of Adm.

inhalational administration

Measurement Parameter

qualitative

Qualitative value

Not Published

Material Safety Data Sheet, View in Reaxys 45 of 48

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Oral lethal dose

Biological Species/NCBI ID

Mus musculus

Substance RN

506893View in Reaxys

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

Quantitative value

971

Material Safety Data Sheet, View in Reaxys 46 of 48

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Toxicity of the compound determined as negative log of inhibitory growth concentration in Tetrahymena pyriformis

Biological Species/NCBI ID

Tetrahymena pyriformis

Substance RN

506893View in Reaxys

Qualitative Results

pIGC50 not calculated

Measurement Parameter

qualitative

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Measurement Object

pIGC50

Perez Gonzalez, Maykel; Gonzalez Diaz, Humberto; Cabrera, Miguel Angel; Molina Ruiz, Reinaldo; Bioorganic and Medicinal Chemistry; vol. 12; nb. 4; (2004); p. 735 - 744, View in Reaxys 47 of 48

Target Name

Serum albumin [taurine cattle]

Target Synonyms

alb; bsa; serum albumin

Target Uniprot ID

p02769

Target PDB ID

2l7u; 3v03; 4f5s; 4jk4; 4or0

Target, Subunit, Species

Serum albumin [taurine cattle]

Target Mutant/Chimera Details

Serum albumin [taurine cattle]:Wild

Target Species (Bioactivity)

taurine cattle

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Binding constant of the compound towards bovine serum albumin

Biological Species/NCBI ID

taurine cattle

Substance RN

506893View in Reaxys

Measurement Parameter

pIC50

Quantitative value

3.23

Measurement pX

3.23

Minick; Frenz; Patrick; Brent; Journal of Medicinal Chemistry; vol. 31; nb. 10; (1988); p. 1923 - 1933, View in Reaxys 48 of 48

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Concentration that causes 50% mortality in the fathead minnow (Pimephales promelas)

Biological Species/NCBI ID

Pimephales promelas

Substance RN

506893View in Reaxys

Measurement Parameter

qualitative

Measurement Object

Concentration that causes 50% mortality

Qualitative value

Not Published

Martin; Young; Chemical Research in Toxicology; vol. 14; nb. 10; (2001); p. 1378 - 1385, View in Reaxys

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