Bromobenzene [C6H5Br] by Asch

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2018-06-17 20h:43m:35s (UTC)

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Reaxys ID 1236661 View in Reaxys

1/1 CAS Registry Number: 108-86-1 Chemical Name: bromobenzene; phenyl bromide; monobromobenzene Linear Structure Formula: (C6H5)Br Molecular Formula: C6H5Br Molecular Weight: 157.01 Type of Substance: isocyclic InChI Key: QARVLSVVCXYDNA-UHFFFAOYSA-N Note:

Substance Label (273) Label References 2a

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A&n%

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1b'

Liu, Yongjun; Xiao, Shuhuan; Qi, Yan; Du, Feng; Chemistry - An Asian Journal; vol. 12; nb. 6; (2017); p. 673 - 678, View in Reaxys

Ma, Ben; Chu, Zhaowei; Huang, Ben; Liu, Zhenli; Liu, Lu; Zhang, Junliang; Angewandte Chemie - International Edition; vol. 56; nb. 10; (2017); p. 2749 - 2753; Angew. Chem.; vol. 129; nb. 10; (2017); p. 2793 - 2797,5, View in Reaxys

II-a

Patent; Sichuan Univeristy; Fu, Haiyan; Ceng, Yang; Chen, Hua; Zheng, Xueli; Yuan, Maolin; Li, Ruixiang; (20 pag.); CN106336375; (2017); (A) Chinese, View in Reaxys

Liu, Zhihao; Wei, Wei; Xiong, Lu; Feng, Qiang; Shi, Yaojie; Wang, Ningyu; Yu, Luoting; New Journal of Chemistry; vol. 41; nb. 8; (2017); p. 3172 - 3176, View in Reaxys

1-2

Patent; CHANGCHUN HAIPU RUNSI TECHNOLOGY CO., LTD.; Liu, Xiqing; Guo, JianHua; (30 pag.); CN106279184; (2017); (A) Chinese, View in Reaxys; Patent; Changchun Haipu Runsi Technology Co., Ltd.; Liu, Xiqing; Guo, Jianhua; (35 pag.); CN106187944; (2016); (A) Chinese, View in Reaxys

Cumine, Florimond; Zhou, Shengze; Tuttle, Tell; Murphy, John A.; Organic and Biomolecular Chemistry; vol. 15; nb. 15; (2017); p. 3324 - 3336, View in Reaxys

Patent; CANON INCORPORATED; NISHIDE, YOSUKE; IWAWAKI, HIRONOBU; KAMATANI, JUN; (34 pag.); JP2017/19730; (2017); (A) Japanese, View in Reaxys

Lee, Yeosan; Baek, Seung-Yeol; Park, Jinyoung; Kim, Seoung-Tae; Tussupbayev, Samat; Kim, Jeongho; Baik, Mu-Hyun; Cho, Seung Hwan; Journal of the American Chemical Society; vol. 139; nb. 2; (2017); p. 975 - 984, View in Reaxys

3-2

Patent; Hyun, Sug Hak; Im, Sook Kyung; Kim, Jin Yeon; Ahn, Tae Ho; Jang, Hwa Young; (43 pag.); KR2017/18251; (2017); (A) Korean, View in Reaxys

Iwasaki, Masayuki; Araki, Yasuhiro; Nishihara, Yasushi; Journal of Organic Chemistry; vol. 82; nb. 12; (2017); p. 6242 - 6258, View in Reaxys

Jia, Tiezheng; Zhang, Mengnan; McCollom, Samuel P.; Bellomo, Ana; Montel, Sonia; Mao, Jianyou; Dreher, Spencer D.; Welch, Christopher J.; Regalado, Erik L.; Williamson, R. Thomas; Manor, Brian C.; Tomson, Neil

18/219

2018-06-17 20:44:10

C.; Walsh, Patrick J.; Journal of the American Chemical Society; vol. 139; nb. 24; (2017); p. 8337 - 8345, View in Reaxys Sub 5-1

Patent; DUK SAN NEOLUX CO., LTD.; Mun, Soung-Yun; Lee, Sun-Hui; Kim, Hye-Ryeong; Choi, Yeon-Hui; Kim, Seul-Gi; Park, Chi-Hyun; (45 pag.); KR2017/57526; (2017); (A) Korean, View in Reaxys

2b'

Kalari, Saradhi; Babar, Dattatraya A.; Karale, Uttam B.; Makane, Vitthal B.; Rode, Haridas B.; Tetrahedron Letters; vol. 58; nb. 29; (2017); p. 2818 - 2821, View in Reaxys

16c

Alazet, Sébastien; Le Vaillant, Franck; Nicolai, Stefano; Courant, Thibaut; Waser, Jerome; Chemistry - A European Journal; vol. 23; nb. 40; (2017); p. 9501 - 9504, View in Reaxys

Wang, Bingbing; Sun, Song; Yu, Jin-Tao; Jiang, Yan; Cheng, Jiang; Organic Letters; vol. 19; nb. 16; (2017); p. 4319 - 4322, View in Reaxys

Gensch, Tobias; Teders, Michael; Glorius, Frank; Journal of Organic Chemistry; vol. 82; nb. 17; (2017); p. 9154 9159, View in Reaxys

Patent; Tsingtao Yuntian Biological Co., Ltd.; Wang Chuanxiu; (7 pag.); CN106432053; (2017); (A) Chinese, View in Reaxys; Patent; China Petroleum Gas Co., Ltd.; Li Xinle; Li Botian; Lang Xiaomei; Xue Shan; Hu Hongfan; Ran Yin; Xin Shixuan; Zhou Shengyuan; Sun Xin; Zhang Xueqin; (15 pag.); CN106905224; (2017); (A) Chinese, View in Reaxys; Patent; China Petroleum Gas Co., Ltd.; Li Xinle; Li Botian; Lang Xiaomei; Xue Shan; Hu Hongfan; Ran Yin; Xin Shixuan; Zhou Shengyuan; Sun Xin; Zhang Xueqin; (17 pag.); CN106905223; (2017); (A) Chinese, View in Reaxys

Zhang, Hu; Buchwald, Stephen L.; Journal of the American Chemical Society; vol. 139; nb. 33; (2017); p. 11590 11594, View in Reaxys

2.1

Rao, Maddali L. N.; Ramakrishna, Boddu S.; European Journal of Organic Chemistry; vol. 2017; nb. 34; (2017); p. 5080 - 5093, View in Reaxys

20a

Shen, Guodong; Wang, Yichen; Zhao, Xiliang; Huangfu, Xinlei; Tian, Yanmeng; Zhang, Tongxin; Yang, Bingchuan; Synlett; vol. 28; nb. 15; (2017); p. 2030 - 2035; Art.No: ST-2017-W0197-L, View in Reaxys

Beesam, Raghavendra; Nareddula, Dastagiri Reddy; Applied Organometallic Chemistry; vol. 31; nb. 9; (2017); Art.No: E3696, View in Reaxys

Guan, Liangyu; Holl, Maxwell Gargiulo; Pitts, Cody Ross; Struble, Mark D.; Siegler, Maxime A.; Lectka, Thomas; Journal of the American Chemical Society; vol. 139; nb. 42; (2017); p. 14913 - 14916, View in Reaxys

Xu, Hang; Hu, Yu-Kun; Guo, Meng-Bi; Huang, Ai-Su; Su, Xin; Guo, Chun; Chemical Papers; vol. 71; nb. 12; (2017); p. 2455 - 2463, View in Reaxys

Compound 8

Patent; Shandong Yuxin Pharmaceutical Co., Ltd.; Liu Zhenteng; Sun Yiwei; Li Zhen; Xu Guichao; Leng Xiangxiang; Huang Chunyan; (9 pag.); CN107266370; (2017); (A) Chinese, View in Reaxys

compound 8

Patent; Shandong Yuxin Pharmaceutical Co., Ltd.; Liu Zhenteng; Sun Yiwei; Li Hua; Gong Wenju; Wang Libiao; (10 pag.); CN107325055; (2017); (A) Chinese, View in Reaxys

Forster, Francis; Metsänen, Toni T.; Irran, Elisabeth; Hrobárik, Peter; Oestreich, Martin; Journal of the American Chemical Society; vol. 139; nb. 45; (2017); p. 16334 - 16342, View in Reaxys

Patent; Changchun Hai Purunsi Technology Co., Ltd.; Cai Hui; Zhang Hong; (32 pag.); CN107400111; (2017); (A) Chinese, View in Reaxys; Patent; Changchun Hai Purunsi Technology Co., Ltd.; Zhang Hong; Cai Hui; (33 pag.); CN107488184; (2017); (A) Chinese, View in Reaxys

2d'

Martinez-Amezaga; Delpiccolo; Mata; RSC Advances; vol. 7; nb. 56; (2017); p. 34994 - 35003, View in Reaxys

Raw Material U

Patent; Jiangsu March Optoelectric Technology Co., Ltd.; Tang Dandan; Xing Zongren; Li Chong; Zhang Xiaoqing; Zhang Zhaochao; (40 pag.); CN107337680; (2017); (A) Chinese, View in Reaxys

Ortega-Jiménez, Fernando; Penieres-Carrillo, José Guillermo; López-Cortés, José Guadalupe; Carmen OrtegaAlfaro; Lagunas-Rivera, Selene; Chinese Journal of Chemistry; vol. 35; nb. 12; (2017); p. 1881 - 1888, View in Reaxys

S1-1

Li, Chunsheng; Li, Meng; Li, Jianxiao; Wu, Wanqing; Jiang, Huanfeng; Chemical Communications; vol. 54; nb. 1; (2017); p. 66 - 69, View in Reaxys

Zhu, Pengju; Fu, Huansheng; Fang, Hao; Letters in Drug Design and Discovery; vol. 14; nb. 12; (2017); p. 1382 1390, View in Reaxys

Patent; Jiangsu March Optoelectric Technology Co., Ltd.; Tang Dandan; Zhang Zhaochao; Zhang Xiaoqing; Wang Lichun; (45 pag.); CN107522705; (2017); (A) Chinese, View in Reaxys

Sub 1-5

Patent; Duksan Neolux Co.,Ltd.; Moon Seong-yun; Kim Seul-gi; Lee Seon-hui; Choi Yeon-hui; Park Chi-hyeon; (81 pag.); KR2017/120233; (2017); (A) Korean, View in Reaxys

19/219

2018-06-17 20:44:10

Patent; LG Chem, Ltd.; Jeong Min-u; Lee Dong-hun; Jang Bun-jae; Huh Dong-uk; (23 pag.); KR2017/134252; (2017); (A) Korean, View in Reaxys

Milanesi, Silvia; Fagnoni, Maurizio; Albini, Angeld; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 603 610, View in Reaxys; Yucel, Baris; Walsh, Patrick J.; IUBMB Life; vol. 356; nb. 17; (2014); p. 3659 - 3667, View in Reaxys; Yucel, Baris; Walsh, Patrick J.; Advanced Synthesis and Catalysis; vol. 356; nb. 17; (2014); p. 3659 3667, View in Reaxys; Subramanian, Parthasarathi; Kaliappan, Krishna P.; European Journal of Organic Chemistry; vol. 2014; nb. 27; (2014); p. 5986 - 5997, View in Reaxys; Li, Zhijie; Wen, Quan; Zhou, Lihong; Deng, Xingmei; Zeng, Qingle; Synthesis (Germany); vol. 47; nb. 23; (2015); p. 3751 - 3757; Art.No: SS-2015-H0391-OP, View in Reaxys; Ouyang, Jia-Sheng; Li, Yan-Fang; Shen, Dong-Sheng; Ke, Zhuofeng; Liu, Feng-Shou; Dalton Transactions; vol. 45; nb. 38; (2016); p. 14919 - 14927, View in Reaxys

Sadygov; Alimardanov; Chalabiev; Russian Journal of Organic Chemistry; vol. 41; nb. 11; (2005); p. 1631 - 1636, View in Reaxys; Cvijetić, Ilija N.; Tanç, Muhammet; Juranić, Ivan O.; Verbić, Tatjana Ž.; Supuran, Claudiu T.; Drakulić, Branko J.; Bioorganic and Medicinal Chemistry; vol. 23; nb. 15; (2015); p. 4649 - 4659, View in Reaxys; Patent; Liu, Zhihua; (11 pag.); CN106117265; (2016); (A) Chinese, View in Reaxys; Patent; Liu, Zhihua; (11 pag.); CN106083917; (2016); (A) Chinese, View in Reaxys

Kosmrlj, Berta; Sket, Boris; Organic Letters; vol. 9; nb. 20; (2007); p. 3993 - 3996, View in Reaxys; Patel, Leena; Chandrasekhar, Jayaraman; Evarts, Jerry; Haran, Aaron C.; Ip, Carmen; Kaplan, Joshua A.; Kim, Musong; Koditek, David; Lad, Latesh; Lepist, Eve-Irene; McGrath, Mary E.; Novikov, Nikolai; Perreault, Stephane; Puri, Kamal D.; Somoza, John R.; Steiner, Bart H.; Stevens, Kirk L.; Therrien, Joseph; Treiberg, Jennifer; Villaseor, Armando G.; Yeung, Arthur; Phillips, Gary; Journal of Medicinal Chemistry; vol. 59; nb. 7; (2016); p. 3532 - 3548, View in Reaxys

Beletskaya, Irina P.; Sigeev, Alexander S.; Peregudov, Alexander S.; Petrovskii, Pavel V.; Synthesis; nb. 16; (2007); p. 2534 - 2538, View in Reaxys; Kebede, Eshetu; Tadikonda, Ramu; Nakka, Mangarao; Inkollu, Bhargavi; Vidavalur, Siddaiah; European Journal of Organic Chemistry; vol. 2015; nb. 27; (2015); p. 5929 - 5933, View in Reaxys; Grünberg, Matthias F.; Jia, Fan; Rivas-Nass, Andreas; Gooßen, Lukas J.; Advanced Synthesis and Catalysis; vol. 358; nb. 10; (2016); p. 1589 - 1594, View in Reaxys

Goriya, Yogesh; Ramana, Chepuri V.; Chemistry--A European Journal; vol. 18; nb. 42; (2012); p. 13288 - 13292,5, View in Reaxys; Goriya, Yogesh; Ramana, Chepuri V.; Chemistry - A European Journal; vol. 18; nb. 42; (2012); p. 13288 - 13292, View in Reaxys; Christakakou, Maria; Schön, Michael; Schnürch, Michael; Mihovilovic, Marko D.; Synlett; vol. 24; nb. 18; (2013); p. 2411 - 2418; Art.No: ST-2013-D0723-L, View in Reaxys; Bose, Shubhankar Kumar; Deissenberger, Andrea; Eichhorn, Antonius; Steel, Patrick G.; Lin, Zhenyang; Marder, Todd B.; Angewandte Chemie - International Edition; vol. 54; nb. 40; (2015); p. 11843 - 11847; Angew. Chem.; vol. 127; nb. 40; (2015); p. 12009 - 12014,6, View in Reaxys; Amaya, Toru; Hata, Dai; Moriuchi, Toshiyuki; Hirao, Toshikazu; Chemistry - A European Journal; vol. 21; nb. 46; (2015); p. 16427 - 16433, View in Reaxys; Yao, Wubing; Fang, Huaquan; Peng, Sihan; Wen, Huanan; Zhang, Lei; Hu, Aiguo; Huang, Zheng; Organometallics; vol. 35; nb. 10; (2016); p. 1559 - 1564, View in Reaxys; Mir, Sajjad Husain; Ochiai, Bungo; ChemistryOpen; vol. 5; nb. 3; (2016); p. 213 218, View in Reaxys; Shen, Chao; Shen, Hongyun; Yang, Ming; Xia, Chengcai; Zhang, Pengfei; Green Chemistry; vol. 17; nb. 1; (2015); p. 225 - 230, View in Reaxys

Luo, Qun-Li; Tan, Jian-Ping; Li, Zhi-Fu; Nan, Wen-Hui; Xiao, Dong-Rong; Journal of Organic Chemistry; vol. 77; nb. 18; (2012); p. 8332 - 8337, View in Reaxys; Wandler, Angela E. E.; Bräse, Stefan; Advanced Synthesis and Catalysis; vol. 358; nb. 24; (2016); p. 4125 - 4128, View in Reaxys

Presset, Marc; Oehlrich, Daniel; Rombouts, Frederik; Molander, Gary A.; Organic Letters; vol. 15; nb. 7; (2013); p. 1528 - 1531, View in Reaxys; Lévêque, Christophe; Chenneberg, Ludwig; Corcé, Vincent; Ollivier, Cyril; Fensterbank, Louis; Chemical Communications; vol. 52; nb. 64; (2016); p. 9877 - 9880, View in Reaxys; Ravi, Chitrakar; Reddy, N. Naresh Kumar; Pappula, Venkatanarayana; Samanta, Supravat; Adimurthy, Subbarayappa; Journal of Organic Chemistry; vol. 81; nb. 20; (2016); p. 9964 - 9972, View in Reaxys

Hansmann, Max M.; Pernpointner, Markus; Doepp, Rene; Hashmi, A. Stephen K.; Chemistry - A European Journal; vol. 19; nb. 45; (2013); p. 15290 - 15303, View in Reaxys; Omar, Mohamed A.; Conrad, Juergen; Beifuss, Uwe; Tetrahedron; vol. 70; nb. 18; (2014); p. 3061 - 3072, View in Reaxys; Chen, C. Chun; Waser, Jerome; Organic Letters; vol. 17; nb. 3; (2015); p. 736 - 739, View in Reaxys; Ghosh, Ketaki; Ranjit, Sadananda; Mal, Dipakranjan; Tetrahedron Letters; vol. 56; nb. 37; (2015); p. 5199 - 5202, View in Reaxys; Zell, Daniel; Warratz, Svenja; Gelman, Dmitri; Garden, Simon J.; Ackermann, Lutz; Chemistry - A European Journal; vol. 22; nb. 4; (2016); p. 1248 - 1252, View in Reaxys; Min, Byul-Hana; Kim, Dong-Su; Park, Hyo-Soon; Jun, Chul-Ho; Chemistry - A European Journal; vol. 22; nb. 18; (2016); p. 6234 - 6238, View in Reaxys

Jia, Tiezheng; Bellomo, Ana; Montel, Sonia; Zhang, Mengnan; El Baina, Kawtar; Zheng, Bing; Walsh, Patrick J.; Angewandte Chemie - International Edition; vol. 53; nb. 1; (2014); p. 260 - 264; Angew. Chem.; vol. 126; nb. 1; (2014); p. 264 - 268,5, View in Reaxys; Puthiaraj, Pillaiyar; Ahn, Wha-Seung; Catalysis Science and Technology; vol. 6; nb. 6; (2016); p. 1701 - 1709, View in Reaxys

Raghunadh, Akula; Meruva, Suresh Babu; Mekala, Ramamohan; Raghavendra Rao; Krishna, Thalishetti; Gangadhara Chary; Vaikunta Rao; Syam Kumar; Tetrahedron Letters; vol. 55; nb. 18; (2014); p. 2986 - 2990, View in Reaxys; Singh, Gurpreet; Kumar, Manoj; Sharma, Kamaldeep; Bhalla, Vandana; Green Chemistry; vol.

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18; nb. 11; (2016); p. 3278 - 3285, View in Reaxys; Seo, Yong-Sik; Kim, Dong-Su; Jun, Chul-Ho; Chemistry - An Asian Journal; vol. 11; nb. 24; (2016); p. 3508 - 3512, View in Reaxys 7a

Chung, Sheng-Hsuan; Lin, Ting-Ju; Hu, Qian-Yu; Tsai, Chia-Hua; Pan, Po-Shen; Molecules; vol. 18; nb. 10; (2013); p. 12346 - 12367, View in Reaxys; Wang, Chan; Huang, Kaimeng; Wang, Junying; Wang, Hongkai; Liu, Lingyan; Chang, Weixing; Li, Jing; Advanced Synthesis and Catalysis; vol. 357; nb. 13; (2015); p. 2795 - 2802, View in Reaxys; Ortega-Jiménez, Fernando; Penieres-Carrillo, José Guillermo; Lagunas-Rivera, Selene; LópezCortés, José G.; Álvarez-Toledano, Cecilio; Ortega-Alfaro, M. Carmen; RSC Advances; vol. 5; nb. 99; (2015); p. 80911 - 80918, View in Reaxys; Xie, Yang; Zhang, Ping; Zhou, Lei; Journal of Organic Chemistry; vol. 81; nb. 5; (2016); p. 2128 - 2134, View in Reaxys; Steinkamp, Anne-Dorothee; Wiezorek, Stefan; Brosge, Felix; Bolm, Carsten; Organic Letters; vol. 18; nb. 20; (2016); p. 5348 - 5351, View in Reaxys

Suresh; Baburajan, Poongavanam; Ahmed, Mansur; Tetrahedron Letters; vol. 56; nb. 34; (2015); p. 4864 - 4867; Art.No: 46446, View in Reaxys; Gao, Yongjun; Tang, Pei; Zhou, Hu; Zhang, Wei; Yang, Hanjun; Yan, Ning; Hu, Gang; Mei, Donghai; Wang, Jianguo; Ma, Ding; Angewandte Chemie - International Edition; vol. 55; nb. 9; (2016); p. 3124 - 3128; Angew. Chem.; vol. 128; nb. 9; (2016); p. 3176 - 3180,5, View in Reaxys

He, Xiao-Xi; Li, Yan-Fang; Huang, Ju; Shen, Dong-Sheng; Liu, Feng-Shou; Journal of Organometallic Chemistry; vol. 803; (2016); p. 58 - 66, View in Reaxys; Johnston, Adam J. S.; Ling, Kenneth B.; Sale, David; Lebrasseur, Nathalie; Larrosa, Igor; Organic Letters; vol. 18; nb. 23; (2016); p. 6094 - 6097, View in Reaxys

ArX

Wang, Junke; Zong, Yingxiao; Wang, Xicun; Hu, Yulai; Yue, Guoren; Pan, Yi; Green Chemistry; vol. 18; nb. 4; (2016); p. 967 - 973, View in Reaxys

19a

Hieda, Yuhzo; Hatae, Noriyuki; Anraku, Makoto; Matsuura, Nobuyasu; Uemura, Kazuhide; Hibino, Satoshi; Choshi, Tominari; Tomida, Hisao; Hori, Osamu; Fujioka, Haruto; Heterocycles; vol. 92; nb. 1; (2016); p. 120 - 132, View in Reaxys

1a''

Smyth, Lynette A.; Phillips, Eric M.; Chan, Vincent S.; Napolitano, José G.; Henry, Rodger; Shekhar, Shashank; Journal of Organic Chemistry; vol. 81; nb. 3; (2016); p. 1285 - 1294, View in Reaxys

Jiang, Hui; Jia, Tiezheng; Zhang, Mengnan; Walsh, Patrick J.; Organic Letters; vol. 18; nb. 5; (2016); p. 972 - 975, View in Reaxys

10b

Li, Minyan; Yucel, Baris; Jiménez, Jacqueline; Rotella, Madeline; Fu, Yue; Walsh, Patrick J.; Advanced Synthesis and Catalysis; vol. 358; nb. 12; (2016); p. 1910 - 1915, View in Reaxys

6(1')

Traficante, Carla I.; Fagundez, Catherine; Serra, Gloria L.; Mata, Ernesto G.; Delpiccolo, Carina M. L.; ACS Combinatorial Science; vol. 18; nb. 5; (2016); p. 225 - 229, View in Reaxys

Sub 5-3-5; Sub 5-4-5; Sub 9-1

Patent; DS Neolux Co. Ltd.; Kim, Yu Ri; Lee, Seon Hui; Kim, Won Sam; Kim, Hye Ryeong; Jeong, Ho Yeong; Park, Jeong Hwan; Hwang, Seon Pil; (58 pag.); KR2016/10878; (2016); (A) Korean, View in Reaxys

Compound 7

Patent; Industrial Technology Research Institute; Huang, Helong; Zhao, Dengzhi; (17 pag.); CN102911211; (2016); (B) Chinese, View in Reaxys

III

Patent; Shandong Shenghua Electronic New Material Co., Ltd.; Wu, Shengxi; Du, Kaichang; Wu, Hua; Hou, Juan; Liang, Bin; Sun, Yonghe; Wang, Zuopeng; (12 pag.); CN105348037; (2016); (A) Chinese, View in Reaxys; Patent; Weifang Medical University; Wang, Lin; (12 pag.); CN104610108; (2016); (B) Chinese, View in Reaxys

Patent; LG Display Co., Ltd.; Liang, Zhonghuan; Yin, Jiongchen; Lu, Xiaozhen; Yin, Dawei; Shen, Renai; Jin, Zunyan; (39 pag.); CN105524071; (2016); (A) Chinese, View in Reaxys

Compound VIII

Patent; INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE; RITDISPLAY CORPORATION; CHAO, TENG CHIH; CHANG, MENG HAO; YEH, HAN CHENG; CHOU, CHING HUI; (31 pag.); TWI520967; (2016); (B) Chinese, View in Reaxys

11b

Subba Rao; Venkateswara Rao, Anna; Krishna; Murthy; Rajesh; Raghunadh; RSC Advances; vol. 6; nb. 72; (2016); p. 67534 - 67539, View in Reaxys; Sivák, Ivan; Berkeš, Dušan; Kožíšek, Jozef; Kolarovič, Andrej; Tetrahedron Letters; vol. 57; nb. 10; (2016); p. 1079 - 1082, View in Reaxys

Tan, Bryan Yong-Hao; Teo, Yong-Chua; Tetrahedron; vol. 72; nb. 42; (2016); p. 6646 - 6653, View in Reaxys

Li, Jin Jing; Wu, Kong; Zhou, Wei; Wang, Hong; Cui, Dong-Mei; Zhang, Chen; Synlett; vol. 27; nb. 13; (2016); p. 1993 - 1996; Art.No: ST-2016-W0172-L, View in Reaxys

Southgate, Emma H.; Pospech, Jola; Fu, Junkai; Holycross, Daniel R.; Sarlah, David; Nature Chemistry; vol. 8; nb. 10; (2016); p. 922 - 928, View in Reaxys

7aa

Gazzola, Silvia; Beccalli, Egle M.; Bernasconi, Alice; Borelli, Tea; Broggini, Gianluigi; Mazza, Alberto; European Journal of Organic Chemistry; vol. 2016; nb. 26; (2016); p. 4534 - 4544, View in Reaxys

Patent; University of Washington; US7425643; (2008); (B1) English, View in Reaxys; Heinz, Luisa G.; Yushchenko, Oleksandr; Neuburger, Markus; Vauthey, Eric; Wenger, Oliver S.; Journal of Physical Chemistry A; vol. 119; nb. 22; (2015); p. 5676 - 5684, View in Reaxys

21/219

2018-06-17 20:44:10

Ph-Br

Hajipour, Abdol R.; Rahimi, Hannaneh; Rafiee, Fatemeh; Applied Organometallic Chemistry; vol. 26; nb. 9; (2012); p. 467 - 470, View in Reaxys; Sabounchei, Seyyed Javad; Ahmadi, Mohsen; Nasri, Zahra; Journal of Coordination Chemistry; vol. 66; nb. 3; (2013); p. 411 - 423, View in Reaxys; Hajipour, Abdol R.; Rafiee, Fatemeh; Najafi, Narges; Applied Organometallic Chemistry; vol. 28; nb. 4; (2014); p. 217 - 220, View in Reaxys; Kim, Byeong-Seon; Hussain, Mahmud M.; Hussain, Nusrah; Walsh, Patrick J.; Chemistry - A European Journal; vol. 20; nb. 37; (2014); p. 11726 - 11739, View in Reaxys; Hopkins; Wolfe; Chemical Science; vol. 5; nb. 12; (2014); p. 4840 - 4844, View in Reaxys; Zhao, Yang; Weix, Daniel J.; Journal of the American Chemical Society; vol. 137; nb. 9; (2015); p. 3327 - 3340, View in Reaxys; Günay, Muhammet Emin; Çoʇaşlioʇlu, Gülcan Gençay; Firinci, Rukiye; Turkish Journal of Chemistry; vol. 39; nb. 6; (2015); p. 1310 - 1316, View in Reaxys

Huang, Manna; Wang, Leilei; Zhu, Xinhai; Mao, Zuxing; Kuang, Daizhi; Wan, Yiqian; European Journal of Organic Chemistry; nb. 26; (2012); p. 4897 - 4901, View in Reaxys; Verma, Akhilesh K.; Jha, Rajeev R.; Chaudhary, Ritu; Tiwari, Rakesh K.; Danodia, Abhinandan K.; Advanced Synthesis and Catalysis; vol. 355; nb. 2-3; (2013); p. 421 - 438, View in Reaxys; Khazaei, Ardeshir; Rahmati, Sadegh; Hekmatian, Zahra; Saeednia, Shahnaz; Journal of Molecular Catalysis A: Chemical; vol. 372; (2013); p. 160 - 166, View in Reaxys; Chen, Junmin; Zhang, Yimin; Hao, Wenyan; Zhang, Rongli; Yi, Fei; Tetrahedron; vol. 69; nb. 2; (2013); p. 613 - 617, View in Reaxys; Xu, Kai; Yang, Fan; Zhang, Guodong; Wu, Yangjie; Green Chemistry; vol. 15; nb. 4; (2013); p. 1055 - 1060, View in Reaxys; Khazaei, Ardeshir; Rahmati, Sadegh; Ghaderi, Arash; Roshani, Leila; Journal of the Iranian Chemical Society; vol. 11; nb. 1; (2014); p. 263 - 269, View in Reaxys; Zhang, Leilei; Wang, Aiqin; Miller, Jeffrey T.; Liu, Xiaoyan; Yang, Xiaofeng; Wang, Wentao; Li, Lin; Huang, Yanqiang; Mou, Chung-Yuan; Zhang, Tao; ACS Catalysis; vol. 4; nb. 5; (2014); p. 1546 - 1553, View in Reaxys; Zhang, Sheng; Wang, Liangguang; Feng, Xiujuan; Bao, Ming; Organic and Biomolecular Chemistry; vol. 12; nb. 37; (2014); p. 7233 - 7237, View in Reaxys; Iranpoor, Nasser; Firouzabadi, Habib; Etemadi-Davan, Elham; Rostami, Abed; Rajabi Moghadam, Khashayar; Applied Organometallic Chemistry; vol. 29; nb. 11; (2015); p. 719 - 724, View in Reaxys

Khemnar, Ashok B.; Bhanage, Bhalchandra M.; RSC Advances; vol. 4; nb. 26; (2014); p. 13405 - 13408, View in Reaxys; Guo, Tenglong; Jiang, Quanbin; Yu, Likun; Yu, Zhengkun; Chinese Journal of Catalysis; vol. 36; nb. 1; (2015); p. 78 - 85, View in Reaxys; Zhang, Chen; Huang, Bo; Bao, Ai-Qing; Li, Xiao; Guo, Shunna; Zhang, Jin-Quan; Xu, Jun-Zhi; Zhang, Rihao; Cui, Dong-Mei; Organic and Biomolecular Chemistry; vol. 13; nb. 47; (2015); p. 11432 - 11437, View in Reaxys

11a

Nadaf, Rashid N.; Seapy, Dave G.; Synthetic Communications; vol. 44; nb. 14; (2014); p. 2012 - 2020, View in Reaxys; Nallasivam, Jothi L.; Fernandes, Rodney A.; European Journal of Organic Chemistry; vol. 2015; nb. 16; (2015); p. 3558 - 3567, View in Reaxys

Jakab, Alexandra; Dalicsek, Zoltn; Sos, Tibor; European Journal of Organic Chemistry; vol. 2015; nb. 1; (2015); p. 56 - 59, View in Reaxys

BrBz

Gotthardt, Meike A.; Schoch, Roland; Brunner, Tobias S.; Bauer, Matthias; Kleist, Wolfgang; ChemPlusChem; vol. 80; nb. 1; (2015); p. 188 - 195, View in Reaxys

Du, Zhi-Jun; Guan, Jing; Wu, Guo-Jie; Xu, Peng; Gao, Lian-Xun; Han, Fu-She; Journal of the American Chemical Society; vol. 137; nb. 2; (2015); p. 632 - 635, View in Reaxys

10d

Hsu, Yu-Chen; Shen, Jiun-Shian; Lin, Bo-Chao; Chen, Wen-Ching; Chan, Yi-Tsu; Ching, Wei-Min; Yap, Glenn P. A.; Hsu, Chao-Ping; Ong, Tiow-Gan; Angewandte Chemie - International Edition; vol. 54; nb. 8; (2015); p. 2420 2424; Angew. Chem.; vol. 127; nb. 8; (2015); p. 2450 - 2454,5, View in Reaxys

1; 1a

Kathiravan, Subban; Nicholls, Ian A.; Organic Letters; vol. 17; nb. 8; (2015); p. 1874 - 1877, View in Reaxys

133A

Patent; BIOMARIN PHARMACEUTICAL INC.; WANG, Bing; CHU, Daniel; BRIDGES, Alexander, James; WO2015/42397; (2015); (A1) English, View in Reaxys

Sato, Azusa; Han, Jianlin; Ono, Taizo; Wzorek, Alicja; Aceña, José Luis; Soloshonok, Vadim A.; Chemical Communications; vol. 51; nb. 27; (2015); p. 5967 - 5970, View in Reaxys

1c'

Jawale, Dhanaji V.; Gravel, Edmond; Boudet, Caroline; Shah, Nimesh; Geertsen, Valérie; Li, Haiyan; Namboothiri, Irishi N. N.; Doris, Eric; Catalysis Science and Technology; vol. 5; nb. 4; (2015); p. 2388 - 2392, View in Reaxys

T1E9S1

Movahed, Siyavash Kazemi; Shariatipour, Monire; Dabiri, Minoo; RSC Advances; vol. 5; nb. 42; (2015); p. 33423 33431, View in Reaxys

3a'

Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu; Organic Letters; vol. 17; nb. 11; (2015); p. 2860 - 2863, View in Reaxys

24c

Nencetti, Susanna; Ciccone, Lidia; Rossello, Armando; Nuti, Elisa; Milanese, Claudio; Orlandini, Elisabetta; Journal of Enzyme Inhibition and Medicinal Chemistry; vol. 30; nb. 3; (2015); p. 406 - 412, View in Reaxys

1b; 2; 4a

Sharma, Kamaldeep; Kumar, Manoj; Bhalla, Vandana; Chemical Communications; vol. 51; nb. 63; (2015); p. 12529 - 12532, View in Reaxys

Davidson, Samuel J.; Barker, David; Tetrahedron Letters; vol. 56; nb. 30; (2015); p. 4549 - 4553; Art.No: 46407, View in Reaxys

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1a, X = Br

Song, Guang-Lin; Zhang, Zhang; Da, Yu-Xia; Wang, Xi-Cun; Tetrahedron; vol. 71; nb. 46; (2015); p. 8823 - 8829; Art.No: 27088, View in Reaxys

S-5u

Sun, Yin-Wei; Tang, Xiang-Ying; Shi, Min; Chemical Communications; vol. 51; nb. 73; (2015); p. 13937 - 13940, View in Reaxys

Barker, Graeme; Webster, Stacey; Johnson, David G.; Curley, Rachel; Andrews, Matthew; Young, Paul C.; MacGregor, Stuart A.; Lee, Ai-Lan; Journal of Organic Chemistry; vol. 80; nb. 20; (2015); p. 9807 - 9816, View in Reaxys

39f

Brogi, Simone; Brindisi, Margherita; Joshi, Bhupendra P.; Sanna Coccone, Salvatore; Parapini, Silvia; Basilico, Nicoletta; Novellino, Ettore; Campiani, Giuseppe; Gemma, Sandra; Butini, Stefania; Bioorganic and Medicinal Chemistry Letters; vol. 25; nb. 22; (2015); p. 5412 - 5418, View in Reaxys

2; PhBr

Ackerman, Laura K. G.; Lovell, Matthew M.; Weix, Daniel J.; Nature; vol. 524; nb. 7566; (2015); p. 454 - 457, View in Reaxys

13; 24

Walia, Preet Kamal; Pramanik, Subhamay; Bhalla, Vandana; Kumar, Manoj; Chemical Communications; vol. 51; nb. 97; (2015); p. 17253 - 17256, View in Reaxys

13n

Kundu, Priyanka; Mondal, Amrita; Das, Bimolendu; Chowdhury, Chinmay; Advanced Synthesis and Catalysis; vol. 357; nb. 16-17; (2015); p. 3737 - 3752, View in Reaxys

E31

Patent; CANON KABUSHIKI KAISHA; KAMATANI, Jun; KOSUGE, Tetsuya; ITABASHI, Masumi; NISHIDE, Yosuke; MIYASHITA, Hirokazu; YAMADA, Naoki; TAKAHASHI, Tetsuo; SHIOBARA, Satoru; (69 pag.); WO2015/198579; (2015); (A1) English, View in Reaxys

1f; 1j; 1k

Shang, Ning-Zhao; Gao, Shu-Tao; Feng, Cheng; Wang, Chun; Wang, Zhi; Letters in Organic Chemistry; vol. 12; nb. 10; (2015); p. 693 - 698, View in Reaxys

Sub 2-13

Patent; DUK SAN NEOLUX CO LTD; MUN, SOUNG YUN; LEE, SUN HEE; PARK, JUNG CHEOL; KIM, DAE SUNG; LEE, BUM SUNG; KWON, JAE TAEK; (50 pag.); KR2015/117399; (2015); (A) Korean, View in Reaxys

Sub 2-1(1)

Patent; DUK SAN NEOLUX CO., LTD.; PARK, JEONG KEUN; KIM, SEUL GI; PARK, HYOUNG KEUN; CHO, HYE MIN; PARK, JONG GWANG; KIM, SEOK HYEON; MOON, SOUNG YOON; LEE, TAE WON; (60 pag.); KR2015/121394; (2015); (A) Korean, View in Reaxys

Sub 1-6-1

Patent; Duksan NeoluxCo., Ltd.; PARK, JUNG GUEN; LEE, SON HEE; PARK, HYUNG GUEN; JO, HAY MIN; LEE, DAE WON; PARK, SUNG JAY; (38 pag.); KR2015/49004; (2015); (A) Korean, View in Reaxys

51-C

Patent; Samsung Display Co., Ltd.; Kim, Su Yeon; Hwang, Suk Hwan; Kim, Young Kuk; Jung, Hay Jin; Park, Jun Ha; Lee, Uhn Young; Kim, Jong Woo; Im, Jin Oh; Han, Sang Hyun; Kim, Kwang Hyun; Jung, Uhn Jae; Lee, Jong Hyuk; (82 pag.); KR2015/19391; (2015); (A) Korean, View in Reaxys

XVII

Patent; Merck Patent GmbH; Anemian, Remi Manouk; Matsuda, Noriyuki; (86 pag.); JP2015/509918; (2015); (A) Japanese, View in Reaxys

4a'

Uozumi, Yasuhiro; Danjo, Hiroshi; Hayashi, Tamio; Journal of Organic Chemistry; vol. 64; nb. 9; (1999); p. 3384 3388, View in Reaxys; Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi; Organic Letters; vol. 15; nb. 13; (2013); p. 3294 - 3297, View in Reaxys; Jiao, Jiao; Hyodo, Keita; Hu, Hao; Nakajima, Kiyohiko; Nishihara, Yasushi; Journal of Organic Chemistry; vol. 79; nb. 1; (2014); p. 285 - 295, View in Reaxys

BrB

Mennes, W. C.; Holsteijn, C. W. M. van; Iersel, A. A. J. van; Yap, S. H.; Noordhoek, J.; Blaauboer, B. J.; Human & Experimental Toxicology; vol. 13; nb. 6; (1994); p. 415 - 422, View in Reaxys; Manautou, Jose E.; Silva, Vanessa M.; Hennig, Gayle E.; Whiteley, Herbert E.; Toxicology; vol. 127; nb. 1-3; (1998); p. 1 - 10, View in Reaxys; Wang, Yong-Fa; Hu, Miao-Lin; Food and Chemical Toxicology; vol. 38; nb. 5; (2000); p. 451 - 458, View in Reaxys; Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys; Zurita, Jorge L.; Jos, Angeles; Peso, Ana del; Salguero, Manuel; Lopez-Artiguez, Miguel; Repetto, Guillermo; Food and Chemical Toxicology; vol. 45; nb. 4; (2007); p. 575 - 584, View in Reaxys; Yuan, Haixia; Pan, Huxiang; Shi, Jin; Li, Hongjing; Dong, Wenbo; Asian Journal of Chemistry; vol. 26; nb. 14; (2014); p. 4211 - 4214, View in Reaxys

Tamba, Shunsuke; Ide, Kenji; Shono, Keisuke; Sugie, Atsushi; Mori, Atsunori; Synlett; vol. 24; nb. 9; (2013); p. 1133 - 1136; Art.No: ST-2013-U0171-L, View in Reaxys; Taber, Douglass F.; Paquette, Craig M.; Gu, Peiming; Tian, Weiwei; Journal of Organic Chemistry; vol. 78; nb. 19; (2013); p. 9772 - 9780, View in Reaxys; Firouzabadi, Habib; Iranpoor, Nasser; Ghaderi, Arash; Gholinejad, Mohammad; Rahimi, Sajjad; Jokar, Safura; RSC Advances; vol. 4; nb. 53; (2014); p. 27674 - 27682, View in Reaxys

Bellina, Fabio; Lessi, Marco; Manzini, Chiara; European Journal of Organic Chemistry; nb. 25; (2013); p. 5621 5630, View in Reaxys; Jiang, Haizhen; Lu, Wenjun; Yang, Kun; Ma, Guobin; Xu, Minjun; Li, Jian; Yao, Jianhua; Wan, Wen; Deng, Hongmei; Wu, Shaoxiong; Zhu, Shizheng; Hao, Jian; Chemistry - A European Journal; vol. 20; nb. 32; (2014); p. 10084 - 10092, View in Reaxys

2; 4

Huang, Wei-Sheng; Xu, Rongsong; Dodd, Rory; Shakespeare, William C.; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 441 - 444, View in Reaxys

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Pal, Rammyani; Sarkar, Swarbhanu; Chatterjee, Nivedita; Sen, Asish Kumar; Tetrahedron Letters; vol. 55; nb. 8; (2014); p. 1452 - 1455, View in Reaxys

(XIII)

Patent; MERCK PATENT GMBH; ANEMIAN, Rémi, Manouk; PAEK, Jong-Hyub; WO2014/15936; (2014); (A1) English, View in Reaxys

Strueben, Jan; Gates, Paul J.; Staubitz, Anne; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p. 1719 - 1728, View in Reaxys

1aBr

Komati, Rajesh; Jursic, Branko S.; Tetrahedron Letters; vol. 55; nb. 9; (2014); p. 1523 - 1527, View in Reaxys

Zong, Chenglong; Liu, Jianli; Chen, Shengyan; Zeng, Runsheng; Zou, Jianping; Chinese Journal of Chemistry; vol. 32; nb. 3; (2014); p. 212 - 218, View in Reaxys

Gigant, Nicolas; Baeckvall, Jan-E.; Organic Letters; vol. 16; nb. 6; (2014); p. 1664 - 1667, View in Reaxys

3a; PhBr

Hussain, Nusrah; Frensch, Gustavo; Zhang, Jiadi; Walsh, Patrick J.; Angewandte Chemie - International Edition; vol. 53; nb. 14; (2014); p. 3693 - 3697; Angew. Chem.; vol. 126; nb. 14; (2014); p. 3767 - 3771,5, View in Reaxys

14a

Roiban, Gheorghe-Doru; Mehler, Gerlinde; Reetz, Manfred T.; European Journal of Organic Chemistry; vol. 2014; nb. 10; (2014); p. 2070 - 2076, View in Reaxys

XIb

Gharibyan; Makaryan; Hovhannisyan; Kinoyan; Chobanyan; Russian Journal of General Chemistry; vol. 84; nb. 3; (2014); p. 457 - 464; Zh. Obshch. Khim.; vol. 84; nb. 3; (2014); p. 399 - 406,8, View in Reaxys

Huang, Yuxing; Moret, Marc-Etienne; Klein Gebbink, Robertus J. M.; European Journal of Organic Chemistry; vol. 2014; nb. 18; (2014); p. 3788 - 3793, View in Reaxys

Wang, Yuanxiang; Frett, Brendan; Li, Hong-Yu; Organic Letters; vol. 16; nb. 11; (2014); p. 3016 - 3019, View in Reaxys

Yang, Yun-Chin; Toy, Patrick H.; Synlett; vol. 25; nb. 9; (2014); p. 1319 - 1324; Art.No: ST-2014-W0084-L, View in Reaxys

2a; 3a

Frensch, Gustavo; Hussain, Nusrah; Marques, Francisco A.; Walsh, Patrick J.; Advanced Synthesis and Catalysis; vol. 356; nb. 11-12; (2014); p. 2517 - 2524, View in Reaxys

sm of Table-2, entry 9

Gholinejad, Mohammad; Shahsavari, Hamid R.; Inorganica Chimica Acta; vol. 421; (2014); p. 433 - 438, View in Reaxys

p-BrPh

Egorov, Ilya N.; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 69; nb. 8; (2014); p. 899 - 905, View in Reaxys

C-2; D-2

Patent; Samsung Display Co., Ltd.; Lee, Jung-Sub; EP2772493; (2014); (A1) English, View in Reaxys

1a&1%

Zhong, Wei; Liu, Xiaoming; Tetrahedron Letters; nb. 35; (2014); p. 4909 - 4911, View in Reaxys

Ang, Wei Jie; Lo, Lee-Chiang; Lam, Yulin; Tetrahedron; vol. 70; nb. 45; (2014); p. 8545 - 8558, View in Reaxys

El Bahhaj, Fatima; Dsir, Jrme; Blanquart, Christophe; Martinet, Nadine; Zwick, Vincent; Simes-Pires, Claudia; Cuendet, Muriel; Grgoire, Marc; Bertrand, Philippe; Tetrahedron; vol. 70; nb. 51; (2014); p. 9702 - 9708, View in Reaxys

2b; PhBr

Mao, Jianyou; Jia, Tiezheng; Frensch, Gustavo; Walsh, Patrick J.; Organic Letters; vol. 16; nb. 20; (2014); p. 5304 5307, View in Reaxys

MeNO&2%

Brzozowski, Martin; Forni, Jose A.; Paul Savage; Polyzos, Anastasios; Chemical Communications; vol. 51; nb. 2; (2014); p. 334 - 337, View in Reaxys

16b

Konda, Saidulu; Rao, Pallavi; Oruganti, Srinivas; RSC Advances; vol. 4; nb. 109; (2014); p. 63962 - 63965, View in Reaxys

Hildebrand; Hartmann; Popp; Bomhard; Archives of Toxicology; vol. 71; nb. 6; (1997); p. 351 - 359, View in Reaxys; Shrestha, Ruja; Mukherjee, Paramita; Tan, Yichen; Litman, Zachary C.; Hartwig, John F.; Journal of the American Chemical Society; vol. 135; nb. 23; (2013); p. 8480 - 8483, View in Reaxys

Patent; PLEXXIKON, INC.; WO2008/79909; (2008); (A1) English, View in Reaxys; Li, Yifan; Brand, Jonathan P.; Waser, Jerome; Angewandte Chemie - International Edition; vol. 52; nb. 26; (2013); p. 6743 - 6747, View in Reaxys

Kuroboshi, Manabu; Yamamoto, Takashi; Tanaka, Hideo; Synlett; vol. 24; nb. 2; (2013); p. 197 - 200; Art.No: ST-2012-U0872-L, View in Reaxys

Fleury, Lauren M.; Kosal, Andrew D.; Masters, James T.; Ashfeld, Brandon L.; Journal of Organic Chemistry; vol. 78; nb. 2; (2013); p. 253 - 269, View in Reaxys

Bochatay, Valentin N.; Boissarie, Patrick J.; Murphy, John A.; Suckling, Colin J.; Lang, Stuart; Journal of Organic Chemistry; vol. 78; nb. 4; (2013); p. 1471 - 1477, View in Reaxys; Aitken, Harry R. M.; Furkert, Daniel P.; Hubert,

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2018-06-17 20:44:10

Jonathan G.; Wood, James M.; Brimble, Margaret A.; Organic and Biomolecular Chemistry; vol. 11; nb. 31; (2013); p. 5147 - 5155, View in Reaxys 1h; PhBr

Zhang, Yimin; Liu, Li; Chen, Junmin; Journal of Chemical Research; vol. 37; nb. 1; (2013); p. 19 - 21, View in Reaxys

1b; PhBr

Budén, María E.; Guastavino, Javier F.; Rossi, Roberto A.; Organic Letters; vol. 15; nb. 6; (2013); p. 1174 - 1177, View in Reaxys

5a; PhBr

Uenishi, Ami; Nakagawa, Yuya; Osumi, Hironobu; Harada, Toshiro; Chemistry - A European Journal; vol. 19; nb. 15; (2013); p. 4896 - 4905, View in Reaxys

1a'

Liu, Wei; Tian, Fei; Wang, Xiaolei; Yu, Hao; Bi, Yanlan; Chemical Communications; vol. 49; nb. 29; (2013); p. 2983 - 2985, View in Reaxys

1k'

Gu, Liuqun; Lu, Ting; Zhang, Mingyun; Tou, Lijuan; Zhang, Yugen; Advanced Synthesis and Catalysis; vol. 355; nb. 6; (2013); p. 1077 - 1082, View in Reaxys

for 3i

Millet, Anthony; Larini, Paolo; Clot, Eric; Baudoin, Olivier; Chemical Science; vol. 4; nb. 5; (2013); p. 2241 - 2247, View in Reaxys

Patent; CANON KABUSHIKI KAISHA; MIYASHITA, Hirokazu; KAMATANI, Jun; KOSUGE, Tetsuya; SAITOH, Akihito; WO2013/58137; (2013); (A1) English, View in Reaxys

E1; E7

Patent; CANON KABUSHIKI KAISHA; MIYASHITA, Hirokazu; KAMATANI, Jun; SAITOH, Akihito; NISHIDE, Yosuke; WO2013/77142; (2013); (A1) English, View in Reaxys

Mosset, Paul; Gree, Rene; Synlett; vol. 24; nb. 9; (2013); p. 1142 - 1146; Art.No: ST-2013-D0140-L, View in Reaxys

12b

Patent; JIANGSU HENGRUI MEDICINE CO., LTD.; SHANGHAI HENGRUI PHARMACEUTICAL CO., LTD.; Yang, Fanglong; Tang, Peng Cho; Dong, Qing; Tu, Wangyang; Fan, Jiang; Guan, Dongliang; Shen, Guangyuan; Wang, Yang; Yuan, Jijun; Zhang, Limin; US2013/130997; (2013); (A1) English, View in Reaxys

Parshina; Tantsyrev; Grishchenko; Trofimov; Russian Journal of Organic Chemistry; vol. 49; nb. 3; (2013); p. 412 416; Zh. Org. Khim.; vol. 49; nb. 3; (2013); p. 425 - 428,4, View in Reaxys

Khaibulova, T. Sh.; Boyarskaya; Boyarskii; Russian Journal of Organic Chemistry; vol. 49; nb. 3; (2013); p. 360 365; Zh. Org. Khim.; vol. 49; nb. 3; (2013); p. 373 - 378, View in Reaxys

Iranpoor, Nasser; Firouzabadi, Habib; Riazi, Asma; Shakerpoor, Alireza; Applied Organometallic Chemistry; vol. 27; nb. 8; (2013); p. 451 - 458, View in Reaxys

30a

Heinrich, Annika C. J.; Thiedemann, Birk; Gates, Paul J.; Staubitz, Anne; Organic Letters; vol. 15; nb. 18; (2013); p. 4666 - 4669, View in Reaxys

Ponzano, Stefano; Bertozzi, Fabio; Mengatto, Luisa; Dionisi, Mauro; Armirotti, Andrea; Romeo, Elisa; Berteotti, Anna; Fiorelli, Claudio; Tarozzo, Glauco; Reggiani, Angelo; Duranti, Andrea; Tarzia, Giorgio; Mor, Marco; Cavalli, Andrea; Piomelli, Daniele; Bandiera, Tiziano; Journal of Medicinal Chemistry; vol. 56; nb. 17; (2013); p. 6917 6934, View in Reaxys

2j; PhBr

Cui, Weijian; Mao, Mengyi; He, Zuying; Zhu, Gangguo; Journal of Organic Chemistry; vol. 78; nb. 19; (2013); p. 9815 - 9821, View in Reaxys

Tian, Yulin; Jin, Jing; Wang, Xiaojian; Han, Weijuan; Li, Gang; Zhou, Wanqi; Xiao, Qiong; Qi, Jianguo; Chen, Xiaoguang; Yin, Dali; MedChemComm; vol. 4; nb. 9; (2013); p. 1267 - 1274, View in Reaxys

Bhat, Aparna P. I.; Inam, Fawad; Bhat, Badekai Ramachandra; RSC Advances; vol. 3; nb. 44; (2013); p. 22191 22198, View in Reaxys

BnBr

Wu, Chao; Huang, Wangyong; He, Weimin; Xiang, Jiannan; Chemistry Letters; vol. 42; nb. 10; (2013); p. 1233 1234, View in Reaxys; Zhang, Hanmo; Hay, E. Ben; Geib, Steven J.; Curran, Dennis P.; Journal of the American Chemical Society; vol. 135; nb. 44; (2013); p. 16610 - 16617, View in Reaxys

Leyva-Perez, Antonio; Oliver-Meseguer, Judit; Rubio-Marques, Paula; Corma, Avelino; Angewandte Chemie - International Edition; vol. 52; nb. 44; (2013); p. 11554 - 11559; Angew. Chem.; vol. 125; nb. 44; (2013); p. 11768 11773,6, View in Reaxys

Ar25

Kumar, Sarvesh; Thornton, Paul D.; Santini, Conrad; ACS Combinatorial Science; vol. 15; nb. 11; (2013); p. 564 571, View in Reaxys

Rennison, David; Conole, Daniel; Tingle, Malcolm D.; Yang, Junpeng; Eason, Charles T.; Brimble, Margaret A.; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 24; (2013); p. 6629 - 6635, View in Reaxys

T-3-R-1

Asachenko, Andrey F.; Sorochkina, Kristina R.; Dzhevakov, Pavel B.; Topchiy, Maxim A.; Nechaev, Mikhail S.; Advanced Synthesis and Catalysis; vol. 355; nb. 18; (2013); p. 3553 - 3557, View in Reaxys

T-1,E-4-6-Sm

Keles, Mustafa; Yilmaz, Mustafa Kemal; Heteroatom Chemistry; vol. 23; nb. 5; (2012); p. 466 - 471, View in Reaxys

25/219

2018-06-17 20:44:10

12g

Izgu, Enver Cagri; Hoye, Thomas R.; Tetrahedron Letters; vol. 53; nb. 37; (2012); p. 4938 - 4941, View in Reaxys

Kumar, Ambati Ashok; Illyes, Tuende Zita; Koever, Katalin E.; Szilagyi, Laszlo; Carbohydrate Research; vol. 360; (2012); p. 8 - 18, View in Reaxys

5d; PhBr

Bagley, Mark C.; Fusillo, Vincenzo; Hills, Edward G.B.; Mulholland, Alex T.; Newcombe, Joseph; Pentecost, Leanne J.; Radley, Emily L.; Stephens, Bethan R.; Turrell, Christopher C.; Arkivoc; vol. 2012; nb. 7; (2012); p. 294 - 313, View in Reaxys

Nishina, Yuta; Takami, Keishi; Green Chemistry; vol. 14; nb. 9; (2012); p. 2380 - 2383, View in Reaxys

Phe-Br

Elmalem, Einat; Biedermann, Frank; Johnson, Kerr; Friend, Richard H.; Huck, Wilhelm T. S.; Journal of the American Chemical Society; vol. 134; nb. 42; (2012); p. 17769 - 17777, View in Reaxys

compound S-12

Patent; LG Chem, Ltd.; EP2332911; (2011); (A2) English, View in Reaxys

Patent; ASTERAND UK LIMITED; US2010/130556; (2010); (A1) English, View in Reaxys

3-1

Patent; MERCK and CO., INC.; WO2009/143041; (2009); (A1) English, View in Reaxys

T3, run 1, BrArH

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Fleck, Thomas J.; Chen, Jiong Jack; Lu, Cuong V.; Hanson, Kari J.; Organic Process Research and Development; vol. 10; nb. 2; (2006); p. 334 - 338, View in Reaxys

Table 1. Ent.4a,b, ArX

Moncada, Adriana I.; Khan, Masood A.; Slaughter, LeGrande M.; Tetrahedron Letters; vol. 46; nb. 9; (2005); p. 1399 - 1403, View in Reaxys

tab.1.entries 7-12

Frey, Guido D.; Reisinger, Claus-Peter; Herdtweck, Eberhardt; Herrmann, Wolfgang A.; Journal of Organometallic Chemistry; vol. 690; nb. 13; (2005); p. 3193 - 3201, View in Reaxys

Table 1, starting

Simuste, Hannes; Panov, Dmitri; Tuulmets, Ants; Nguyen, Binh T.; Journal of Organometallic Chemistry; vol. 690; nb. 12; (2005); p. 3061 - 3066, View in Reaxys

Tab. 2, entry 3

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Tab. 10, entry 4

Denmark, Scott E.; Ober, Michael H.; Advanced Synthesis and Catalysis; vol. 346; nb. 13-15; (2004); p. 1703 - 1714, View in Reaxys

Table 1 compound 3

McMillian, Michael; Nie, Alex Y.; Parker, J. Brandon; Leone, Angelique; Bryant, Stewart; Kemmerer, Michael; Herlich, Judy; Liu, Yanhong; Yieh, Lynn; Bittner, Anton; Liu, Xuejun; Wan, Jackson; Johnson, Mark D.; Biochemical Pharmacology; vol. 68; nb. 11; (2004); p. 2249 - 2261, View in Reaxys

Tab. 4, entry 9

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Tab. 2, entry 10

Alimardanov, Asaf; Schmieder-Van De Vondervoort, Lizette; De Vries, Andre H. M.; De Vries, Johannes G.; Advanced Synthesis and Catalysis; vol. 346; nb. 13-15; (2004); p. 1812 - 1817, View in Reaxys

Tab.1, run 3

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Termaten, Arjan; Van der Sluis, Marcel; Bickelhaupt, Friedrich; European Journal of Organic Chemistry; nb. 11; (2003); p. 2049 - 2055, View in Reaxys

prod., Tab. 4, entry 6

Firouzabadi; Iranpoor; Shiri; Tetrahedron Letters; vol. 44; nb. 49; (2003); p. 8781 - 8785, View in Reaxys

tab2 run7

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arene(table 3, entry13)

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C6H5Br

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tab. 1, entry 3

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3, Table 1, entry 1

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1, R=H, X=Br

Heidenreich, Roland G.; Koehler, Klaus; Krauter, Juergen G. E.; Pietsch, Joerg; Synlett; nb. 7; (2002); p. 1118 1122, View in Reaxys

1, R=H

Koehler, Klaus; Heidenreich, Roland G.; Krauter, Juergen G. E.; Pietsch, Joerg; Chemistry - A European Journal; vol. 8; nb. 3; (2002); p. 622 - 631, View in Reaxys

iii

Patent; E.I. DU PONT DE NEMOURS AND COMPANY; EP1178040; (2002); (A1) English, View in Reaxys

Table 1. Aryl halide Artamkina, Galina A.; Sergeev, Alexey G.; Beletskaya, Irina P.; Tetrahedron Letters; vol. 42; nb. 26; (2001); p. 4381 7 - 4384, View in Reaxys C6H5-Br

Boehm, Volker P. W.; Herrmann, Wolfgang A.; Chemistry - A European Journal; vol. 7; nb. 19; (2001); p. 4191 4197, View in Reaxys

1, R=p-Br

Manoso; DeShong; Journal of Organic Chemistry; vol. 66; nb. 22; (2001); p. 7449 - 7455, View in Reaxys

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

arene R=4-Br

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Mottino, Aldo; Tuchweber, Beatriz; Plaa, Gabriel L.; Yousef, Ibrahim M.; Toxicology Letters; vol. 116; nb. 1-2; (2000); p. 69 - 77, View in Reaxys

PhX, X=Br

Mukhopadhyay, Sudip; Rothenberg, Gadi; Gitis, Diana; Baidossi, Mubeen; Ponde, Datta E.; Sasson, Yoel; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2000); p. 1809 - 1812, View in Reaxys

4, R=Br/6, R=H

Smith, Keith; El-Hiti, Gamal A.; Hammond, Mark E.W.; Bahzad, Dawoud; Li, Zhaoqiang; Siquet, Christophe; Journal of the Chemical Society, Perkin Transactions 1; nb. 16; (2000); p. 2745 - 2752, View in Reaxys

1, X=Br

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

BrC6H5

Reis; Silva; Frausto da Silva; Pombeiro; Chemical Communications; nb. 19; (2000); p. 1845 - 1846, View in Reaxys

Table 1 Entry 1, 15 ArX

Budnikova, Yulia; Kargin, Yuri; Nedelec, Jean-Yves; Perichon, Jacques; Journal of Organometallic Chemistry; vol. 575; nb. 1; (1999); p. 63 - 66, View in Reaxys

educt to 1, 3, 4, 5, 8 Cammidge, Andrew N.; Kelsey, Richard D.; King, Amy S.H.; Tetrahedron Letters; vol. 40; nb. 1; (1999); p. 147 148, View in Reaxys educt to 1, 6

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bromide Tab. 1, ent. Wang, Zhongren; Skerlj, Renato T.; Bridger, Gary J.; Tetrahedron Letters; vol. 40; nb. 18; (1999); p. 3543 - 3546, 8 View in Reaxys 1,R=Br

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t.2, 64

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Patent-Specific Data (98) Prophetic ComLocation in Patent pound

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Patent; Lee, So Ha; Ryu, Jae Chun; Yoo, Kyung Ho; El-Deeb, Ibrahim Mustafa; US2010/63281; (2010); (A1) English, View in Reaxys Patent; Bahmanyar, Sogole; Bates, R.J.; Blease, Kate; Calabrese, Andrew Antony; Daniel, Thomas Oran; Delgado, Mercedes; Elsner, Jan; Erdman, Paul; Fahr, Bruce; Ferguson, Gregory; Lee, Branden; Nadolny, Lisa; Packard, Garrick; Papa, Patrick; Plantevin-Krenitsky, Veronique; Riggs, Jennifer; Rohane, Patricia; Sankar, Sabita; Sapienza, John; Satoh, Yoshitaka; Sloan, Victor; Stevens, Randall; Tehrani, Lida; Tikhe, Jayashree; Torres, Eduardo; Wallace, Andrew; Whitefield, Brandon Wade; Zhao, Jingjing; US2010/93698; (2010); (A1) English, View in Reaxys Patent; KOWA COMPANY, LTD.; US2010/144694; (2010); (A1) English, View in Reaxys Patent; SUMITOMO CHEMICAL COMPANY, LIMITED; GENENTECH, INC.; MIKI, Takashi; SHIMASAKI, Yasuharu; BABU, Srinivasan; CHENG, Zhigang; REYNOLDS, Mark, E.; TIAN, Qingping; WO2010/110782; (2010); (A1) English, View in Reaxys Patent; Burke, Martin D.; Gillis, Eric P.; Lee, Suk Joong; Knapp, David M.; Gray, Kaitlyn C.; US2009/30238; (2009); (A1) English, View in Reaxys Patent; Laboratorios del Dr. Esteve S.A.; EP2070933; (2009); (A1) English, View in Reaxys Patent; SALTIGO GMBH; US2009/247764; (2009); (A1) English, View in Reaxys Page/page column 4/2

Patent; Scherer, Stefan; Meudt, Andreas; Nerdinger, Sven; Lehnemann, Bernd Wilhelm; Jagusch, Thomas; Snieckus, Victor; US2009/143586; (2009); (A1) English, View in Reaxys Patent; Yen, Feng Wen; US2008/265746; (2008); (A1) English, View in Reaxys Patent; XEROX CORPORATION; US2008/125607; (2008); (A1) English, View in Reaxys Patent; Muller, Nikolaus; Magerlein, Wolfgang; Cotte, Alain; Beller, Matthias; Schareina, Thomas; Zapf, Alexander; US2008/194829; (2008); (A1) English, View in Reaxys Patent; Meudt, Andreas; Nerdinger, Sven; Lehnemann, Bernd Wilhelm; Vogel, Till; Snieckus, Victor; US2008/221350; (2008); (A1) English, View in Reaxys Patent; BASF SE; WO2008/65145; (2008); (A1) English, View in Reaxys Patent; NOVARTIS AG; NOVARTIS PHARMA GmbH; WO2007/120827; (2007); (A2) English, View in Reaxys Patent; DSM IP ASSETS B.V.; WO2006/9431; (2006); (A1) English, View in Reaxys Patent; BANYU PHARMACEUTICAL CO., LTD; WO2006/38741; (2006); (A1) Japanese, View in Reaxys

prophetic product

Patent; Eli Lilly and Company; US4303591; (1981); (A) English, View in Reaxys; Patent; Wisconsin Alumni Research Foundation; US4448721; (1984); (A) English, View in Reaxys; Patent; Syntex U.S.A. Inc.; US5716954; (1998); (A) English, View in Reaxys; Patent; Hiratsuka, Atsunori; Yano, Kazuyoshi; Karube, Isao; Tsai, Shuo-Wen; Yokoyama, Kenji; Koide, Satoshi; Akimoto, Takuo; US2006/113189; (2006); (A1) English, View in Reaxys Patent; Wehle, Detlef; Forstinger, Klaus; Meudt, Andreas; US2005/1333; (2005); (A1) English, View in Reaxys Patent; MITSUBISHI GAS CHEMICAL COMPANY, INC.; EP1595862; (2005); (A1) English, View in Reaxys Patent; JFE Chemical Corporation; EP1520846; (2005); (A1) English, View in Reaxys Patent; CAMBRIDGE UNIVERSITY TECHNICAL SERVICES LIMITED; ASTRAZENECA UK LIMITED; WO2005/90283; (2005); (A1) English, View in Reaxys Patent; Perichon, Jacques; Gosmini, Corinne; Bastienne, Mylene; Gomes, Paulo; US2004/186328; (2004); (A1) English, View in Reaxys Patent; CELLTECH R and D LIMITED; WO2004/113349; (2004); (A1) English, View in Reaxys Patent; MERCK SHARP and DOHME LIMITED; WO2004/14865; (2004); (A1) English, View in Reaxys Patent; PFIZER LIMITED; PFIZER INC.; WO2004/37809; (2004); (A1) English, View in Reaxys Patent; ASTRAZENECA AB; WO2004/41784; (2004); (A1) English, View in Reaxys

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Patent; SYNGENTA PARTICIPATIONS AG; WO2004/50607; (2004); (A1) English, View in Reaxys Patent; LG LIFE SCIENCES LTD.; WO2004/80979; (2004); (A1) English, View in Reaxys Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2004/101522; (2004); (A1) English, View in Reaxys Patent; Perichon, Jacques; Gosmini, Corinne; Fillon, Hyacinthe; US2004/236155; (2004); (A1) English, View in Reaxys Patent; Takeda Chemical Industries, Ltd.; EP1484320; (2004); (A1) English, View in Reaxys Patent; Treacher, Kevin; Stossel, Philipp; Spreitzer, Hubert; Becker, Heinrich; Falcou, Aurelie; US2004/260090; (2004); (A1) English, View in Reaxys Patent; Zhang, Tony Yantao; Zhang, Hongbin; Proctor, Christophor Scott; US2003/225282; (2003); (A1) English, View in Reaxys Patent; Cellier, Pascal Philippe; Cristau, Henri-Jean; Spindler, Jean-Francis; Taillefer, Marc; US2003/236413; (2003); (A1) English, View in Reaxys Patent; E.I. DU PONT DE NEMOURS AND COMPANY; EP1178040; (2002); (A1) English, View in Reaxys Patent; F. HOFFMANN-LA ROCHE AG; EP1236715; (2002); (A2) English, View in Reaxys prophetic product

Patent; Takasago International Corporation; US6365776; (2002); (B1) English, View in Reaxys Patent; Studiengesellschaft Kohle mbH; US6392111; (2002); (B1) English, View in Reaxys Patent; IDEMITSU KOSAN CO., LTD.; EP1182183; (2002); (A1) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

2.82

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

Lipinski Number

Veber Number

Derivative (32) Comment (Derivative)

References

π-Komplex m. tertPolumbrik; Serguchev; Theoretical and Experimental Chemistry; vol. 14; (1978); p. 104; ; p. 130, View in Reaxys Butylmesitylnitroxid: ΔH0, ΔS0 TCNE-Komplex : Abs.Sp.

Bendig; Kreysig; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 1176, View in Reaxys

Bld.-geschw.-Jodkomplex in CCl4

Clark; Kolb; Journal of Organic Chemistry; vol. 42; (1977); p. 359,360, View in Reaxys

Charge-TransferKomplex mit I2

Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys

Charge-TransferKomplex mit Cl2

Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys

Charge-TransferKomplex mit Br2

Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys

H-Komplex m. tBitman et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 1361,1336,1337, View in Reaxys Butylhydroperoxid: π(S)(OH) π-Komplex mit p-Ni- Berthelot et al.; Journal of Molecular Structure; vol. 18; (1973); p. 435,441, View in Reaxys tro-m-trifluorme-

32/219

2018-06-17 20:44:10

thylphenol (NTP): IR (Tab.2), (Fig.1) Komplex mit TBMN: Gleichgew.-konst., ΔHgrad, ΔSgrad, ΔGgrad (Tab. 1), (Fig. 3)

Burnett et al.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 69; (1973); p. 864, View in Reaxys

TCNE-Komplex: Bock,H. et al.; Chemische Berichte; vol. 105; (1972); p. 3850 - 3864, View in Reaxys vertikale PEIonis.energie u. charge-transferBandenmax (Tab.5) Clathrat m. Dianin: ΔHgrad, NMR

Gregoire; Meinnel; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 272; (1971); p. 347, View in Reaxys

Komplex mit PheKnoesel,R. et al.; Bulletin de la Societe Chimique de France; (1971); p. 4471 - 4480, View in Reaxys nothiazin, C12H9NS*C6H5Br : photochromes Verhalten Einschlussverb. m. Desoxycholsaeure: P.

Csueroes et al.; Acta Chimica Academiae Scientiarum Hungaricae; vol. 63; (1970); p. 425, View in Reaxys

Komplex m. N,NDimethylnitrosamin: NMR, K

Chu; Lin; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 16; (1969); p. 56,65, View in Reaxys

Komplex mit N,NDimethylnitrosoamin: K (Tab.III)

Chu; Lin; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 16; (1968); p. II-55,65, View in Reaxys

CT-Komplex mit Cl-Atom B. Brombenzol, CCl4, radiolytisch; UV

BUehler; Ebert; Nature (London, United Kingdom); vol. 214; (1967); p. 1220, View in Reaxys

Collision Complexes

Horak et al.; Spectrochimica Acta; vol. 21; (1965); p. 919, View in Reaxys

Kompl. m. TetraFarrell; Newton; Journal of Physical Chemistry; vol. 69; (1965); p. 3506, View in Reaxys cyanaethylen: Charge-transfer-Energie (CCl4, 24grad) System m. Toluol: P

Dunken et al.; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 4; (1964); p. 312, View in Reaxys

Komplex mit Phenol (s. Syst.nr. 512)

Wayland; Drago; Journal of the American Chemical Society; vol. 86; (1964); p. 5240,5241, View in Reaxys

Charge-transferKomplexe m. Chloranil/CHCl3

Nepras; Zahradnik; Collection of Czechoslovak Chemical Communications; vol. 29; (1964); p. 1555,1556, View in Reaxys

Charge-transferKomplexe m. Tetracyan-aethylen/ CHCl3

Nepras; Zahradnik; Collection of Czechoslovak Chemical Communications; vol. 29; (1964); p. 1555,1556, View in Reaxys

Verb. m. Tetracyan- Voigt; Journal of the American Chemical Society; vol. 86; (1964); p. 3611,3614, View in Reaxys aethylen (1:1) (Charge-TransferKomplex): UVmax. Elektronen-Donator-Acceptor-Komplex m. Tetracyanaethylen: charge-

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

33/219

2018-06-17 20:44:10

transfer-Sp., charge-transfer-Energie Benzaldehyd-2,4dinitro-phenylhydrazon: F:234-235grad

Sharefkin; Forschirm; Analytical Chemistry; vol. 35; (1963); p. 1616,1618, View in Reaxys

Jod-Komplex: Sta- Plucknett; Richards; Journal of Chemical and Engineering Data; vol. 8; (1963); p. 239, View in Reaxys bilitaetskonstante in Cyclohexan bei 25grad Verbindung m.<81>Brom C6H5Br*<81Br2>: Quadrupolmoment bei 77K

Read et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1778, View in Reaxys

katal. Dehalogenierung: Identifizierung

Thompson et al.; Analytical Chemistry; vol. 34; (1962); p. 154, View in Reaxys

Komplexbildung m. Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 126, View in Reaxys Jod C6H5Br*J2: Gleichgewichtskonstante u. Temperaturabhaengigkeit von 293 bis 333K; freie Bildungsenthalpie u. Bildungsentropie bei 298K Additionsverb. m. Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 91, View in Reaxys Jod C6H5Br*J2: Gleichgewichtskonstante bei 293, 313, 333K; Temperaturabhaengigkeit der Gleichgewichtskonst.; freie Enthalpie, Enthalpie, ΔS Komplexbildung m. Bardamowa; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR; vol. 2; (1960); p. 71,72,73, View in Reaxys Essigsaeure, Buttersaeure, Phenol, Anisol, Dioxan, Me., A. compound with sil- Andrews; Keefer; Journal of the American Chemical Society; vol. 72; (1950); p. 3113, View in Reaxys ver (+); Further Data see Handbook (Electrochemical behaviour) Melting Point (9) 1 of 9

Melting Point [°C]

30 - 31

Schneider, Franziska; Szuppa, Tony; Stolle, Achim; Ondruschka, Bernd; Hopf, Henning; Green Chemistry; vol. 11; nb. 11; (2009); p. 1894 - 1899, View in Reaxys 2 of 9

Angell et al.; Journal of Physical Chemistry; vol. 82; (1978); p. 2622,2626, View in Reaxys; Kresge; Brown; Journal of Organic Chemistry; vol. 32; (1967); p. 756,757, View in Reaxys

3 of 9

Melting Point [°C]

-30.73

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys; Goates et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 217,219, View in Reaxys; Moellmer et al.; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 317,318, 319, View in Reaxys 4 of 9

Melting Point [°C]

-31

Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys

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2018-06-17 20:44:10

5 of 9

Melting Point [°C]

-30.6

Timmermans; Chem. Zentralbl.; vol. 82; nb. II; (1911); p. 1015, View in Reaxys; Bugarszky; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 71; (1910); p. 710, View in Reaxys; Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys; Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys 6 of 9

Melting Point [°C]

-30.82

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 7 of 9

Melting Point [°C]

-30.5

Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys; 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 8 of 9

Melting Point [°C]

-30.6 - -13

Comment (Melting Point)

unter Drucken von 1 at bis 914 at.

Deffet; Bulletin des Societes Chimiques Belges; vol. 49; (1940); p. 223,227, View in Reaxys 9 of 9

Melting Point [°C]

-31.1

Haase; Chemische Berichte; vol. 26; (1893); p. 1053, View in Reaxys Boiling Point (48) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

156

Location

References

Page/Page column 2

Patent; BASF SE; US2011/190510; (2011); (A1) English, View in Reaxys

150

Sadygov; Alimardanov; Chalabiev; Russian Journal of Organic Chemistry; vol. 41; nb. 11; (2005); p. 1631 - 1636, View in Reaxys

154 - 156

Patent; Bedekar, Ashutosh Vasant; Ghosh, Kumar Pushpito; Adimurthy, Subbarayyappa; Ramachandraiah, Gadde; US2005/137431; (2005); (A1) English, View in Reaxys; Patent; COUNCIL OF SCIENTIFIC and INDUSTRIAL RESEARCH; WO2005/61423; (2005); (A1) English, View in Reaxys; Koser; Liu; Journal of Organic Chemistry; vol. 43; (1978); p. 478,479,480, View in Reaxys; Minisci; Gazzetta Chimica Italiana; vol. 90; (1960); p. 1307,1315, View in Reaxys

156

Fujii; Asaba; Nippon Kagaku Kaishi; (1977); p. 599,601, 603, View in Reaxys; Jost et al.; Chemicky Prumysl; vol. 15; (1965); p. 521, View in Reaxys; Gun'kin, I. F.; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 654 - 655; Zhurnal Obshchei Khimii; vol. 67; nb. 4; (1997); p. 699 - 700, View in Reaxys

155.15

Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 128 - 131, View in Reaxys; Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 - 135, View in Reaxys

Kotsuki; Datta; Hayakawa; Suenaga; Synthesis; nb. 11; (1995); p. 1348 1350, View in Reaxys

156.1

760

Zubkov, V. A.; Yudovich, M. E.; Saidov, G. V.; Russian Journal of Physical Chemistry; vol. 62; nb. 1; (1988); p. 77 - 80; Zhurnal Fizicheskoi Khimii; vol. 62; (1988); p. 155 - 159, View in Reaxys

155.9

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys

150 - 170

Banerjee, Amalendu; Banerjee, Gopal Chandra; Adak, Mohini Mohan; Banerjee, Santa; Samaddar, Haraprasad; Journal of the Indian Chemical Society; vol. 58; (1981); p. 985 - 988, View in Reaxys

153 - 155

Banerjee et al.; Journal of the Indian Chemical Society; vol. 56; (1979); p. 518, View in Reaxys

Kabalka; Ferrell; Synthetic Communications; vol. 9; (1979); p. 443,446, 447, View in Reaxys

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2018-06-17 20:44:10

155

Bartlett et al.; Journal of Organometallic Chemistry; vol. 46; (1972); p. 267, View in Reaxys; Patent; Ethyl Corp.; US3283019; (1966); Chem.Abstr.; vol. 66; nb. 55008, View in Reaxys; Bhattacharya; Raj; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 15; (1977); p. 799, View in Reaxys

153

Moodie et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1976); p. 1089,1090, View in Reaxys

155.7

Aronskaya; Bezuglyi; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 268,269, View in Reaxys

155 - 156

760

Mermillod-Blardet; Mauret; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 278; (1974); p. 633, View in Reaxys

156 - 156.1

Peschel; Schnorrer; Berichte der Bunsen-Gesellschaft; vol. 78; (1974); p. 1294,1295, View in Reaxys

154.5

Kumar; Merklin; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 69; (1973); p. 577,579-583, View in Reaxys

130 - 130.5

Kikkawa et al.; Nippon Kagaku Kaishi; (1972); p. 625,626,627, View in Reaxys

156 - 157

Modro; Piekos; Tetrahedron; vol. 28; (1972); p. 3867,3868-3876, View in Reaxys

150 - 152

van Tamelen,E.E. et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 6141 - 6144, View in Reaxys

153 - 156

Dorofeenko; Nauchnye Zapiski Luganskogo Sel'skokhozyaistvennogo Instituta; vol. 7; (1961); p. 203; Chem.Abstr.; vol. 58; nb. 2393g; (1963), View in Reaxys; Wolinski et al.; Roczniki Chemii; vol. 44; (1970); p. 905,906, 907, View in Reaxys

154 - 154.4

Coombes et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 347,349-351, View in Reaxys

155 - 157

Kolpakchi; Babin; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 38; ; p. 69, View in Reaxys

158

Minoura; Toshima; Kogyo Kagaku Zasshi; vol. 72; (1969); p. 984,987; Chem.Abstr.; vol. 71; nb. 61812; (1969), View in Reaxys

154

Krosnar et al.; Collection of Czechoslovak Chemical Communications; vol. 34; (1969); p. 1286,1288, View in Reaxys

155.5

760

Kahlbaum; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 26; (1898); p. 603, View in Reaxys; Seliga; Collection of Czechoslovak Chemical Communications; vol. 33; (1968); p. 999, View in Reaxys

155 - 156

Jackson; Sasse; Journal of the Chemical Society; (1962); p. 3746,3747, View in Reaxys; Goto; Suzuki; Nippon Kagaku Zasshi; vol. 84; (1963); p. 167,168,173; Chem.Abstr.; vol. 59; nb. 15205; (1963), View in Reaxys; Shern et al.; Organic Reactivity (New York, English Translation); vol. 5; (1968); p. 159,162, View in Reaxys

156.2

Evans; Tiley; Journal of the Chemical Society [Section] B: Physical Organic; (1966); p. 134, View in Reaxys

155.5

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys; Bobyl et al.; Sov. Phys. J. (Engl. Transl.); vol. 6; (1965); p. 48,30, View in Reaxys

150 - 154 156

Hey; Tewfik; Journal of the Chemical Society; (1965); p. 2402, View in Reaxys Rylski; Acta Poloniae Pharmaceutica; vol. 20; (1963); p. 156,160, View in Reaxys

764

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

36/219

2018-06-17 20:44:10

156 - 158

Forrest,J.; Journal of the Chemical Society; (1960); p. 589 - 592, View in Reaxys

157 - 160

Forrest,J.; Journal of the Chemical Society; (1960); p. 589 - 592, View in Reaxys

Haszeldine; Sharpe; Journal of the Chemical Society; (1952); p. 993,1000, View in Reaxys

156.06

760

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys

155.5

732

Whitmore et al.; Journal of the American Chemical Society; vol. 69; (1947); p. 236, View in Reaxys

156.07

768

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys

156.2 - 156.3

762

Tsukamoto; Japan. J. Chem.; vol. 2; p. 137; Chem. Zentralbl.; vol. 99; nb. II; (1928); p. 2108, View in Reaxys

156.15

760

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys; Timmermans; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 442, View in Reaxys

Herbst; Koll. Beih.; vol. 23; p. 332; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 2544, View in Reaxys

140

497

Herbst; Koll. Beih.; vol. 23; p. 332; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 2544, View in Reaxys

156.2 - 156.3

Williams; Krchma; Journal of the American Chemical Society; vol. 48; (1926); p. 1891; Journal of the American Chemical Society; vol. 49; (1927); p. 1679, View in Reaxys

155

749

Sugden; Journal of the Chemical Society; vol. 125; (1924); p. 1173, View in Reaxys

Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys

155

760

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

155.6

760

Weger; Justus Liebigs Annalen der Chemie; vol. 221; (1883); p. 83; Journal fuer Praktische Chemie (Leipzig); vol. <2>61; (1900); p. 217 Anm. 3, View in Reaxys

90.54

100

Dreisbach,R.R.; Physical Properties of Chemical Compounds (= Advances in Chemistry Series Nr. 15) <Washington 1955> S. 150, View in Reaxys

Refractive Index (67) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C] 1.559

Comment (Refractive Index)

References

Czech, Anna; Ganicz, Tomasz; Noskowska, Malgorzata; Stanczyk, Wlodzimierz A.; Szelag, Anna; Journal of Organometallic Chemistry; vol. 694; nb. 21; (2009); p. 3386 - 3389, View in Reaxys

1.5598

589

Bobyl et al.; Sov. Phys. J. (Engl. Transl.); vol. 6; (1965); p. 48,30, View in Reaxys; Sadygov; Alimardanov; Chalabiev; Russian Journal of Organic Chemistry; vol. 41; nb. 11; (2005); p. 1631 - 1636, View in Reaxys

1.5569

589

Gun'kin, I. F.; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 654 - 655; Zhurnal Obshchei Khimii; vol. 67; nb. 4; (1997); p. 699 - 700, View in Reaxys

1.56

589

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys; Bugarszky; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 71; (1910); p. 710, View in Reaxys; Minisci; Gazzetta Chimica Italiana; vol. 90; (1960); p.

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2018-06-17 20:44:10

1307,1315, View in Reaxys; Zubkov, V. A.; Yudovich, M. E.; Saidov, G. V.; Russian Journal of Physical Chemistry; vol. 62; nb. 1; (1988); p. 77 - 80; Zhurnal Fizicheskoi Khimii; vol. 62; (1988); p. 155 - 159, View in Reaxys 1.55891

589

19.9

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Halligudi, S. B.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 27; nb. 4; (1988); p. 303 - 307, View in Reaxys

1.56447

546

Abdel-Azim, Abdel-Azim A.; Munk, Petr; Journal of Physical Chemistry; vol. 91; nb. 14; (1987); p. 3910 - 3914, View in Reaxys

1.558

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

1.5601

589

Lacourt et al.; Journal de Pharmacie de Belgique; vol. 8; (1953); p. 535,554; Microchimica Acta; (1953); p. 305,324, View in Reaxys; Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys

1.6585

589

Mermillod-Blardet; Mauret; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 278; (1974); p. 633, View in Reaxys

1.567

589

Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys

1.56

589

1.5602

589

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys; Aronskaya; Bezuglyi; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 268,269, View in Reaxys

1.5547

589

25.5

Deshpande et al.; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 469,470-472, View in Reaxys

Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys

1.66

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

1.56 - 1.561

589

Kolpakchi; Babin; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 38; ; p. 69, View in Reaxys

1.5555

589

Kiersznicki et al.; Roczniki Chemii; vol. 44; (1970); p. 1049, View in Reaxys

1.5575

589

Kochi,J.K. et al.; Tetrahedron; vol. 24; (1968); p. 3503 - 3515, View in Reaxys; Lacourt et al.; Journal de Pharmacie de Belgique; vol. 8; (1953); p. 535,554; Microchimica Acta; (1953); p. 305,324, View in Reaxys

1.5597

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys; Seliga; Collection of Czechoslovak Chemical Communications; vol. 33; (1968); p. 999, View in Reaxys

1.5595

589

Haberditzl; Koeppel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 691, View in Reaxys

38/219

2018-06-17 20:44:10

Dubrowskii; Afonina; J. Gen. Chem. USSR (Engl. Transl.); vol. 36; (1966); p. 1875,1868, View in Reaxys 1.5599

589

Wratschko, Kohler; Monatshefte fuer Chemie; vol. 93; (1962); p. 374,376, View in Reaxys

1.5592

589

Jackson; Sasse; Journal of the Chemical Society; (1962); p. 3746,3747, View in Reaxys

1.5556

589

Tourky et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 216; (1961); p. 176,177, 181, 182, View in Reaxys

1.5602

Luedde; Riechstoffe und Aromen; vol. 10; (1960); p. 193, View in Reaxys

1.5628

589

Lacourt et al.; Journal de Pharmacie de Belgique; vol. 8; (1953); p. 535,554; Microchimica Acta; (1953); p. 305,324, View in Reaxys

1.55774

589

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

1.5571

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys

1.5546

656.3

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

1.5739

486.1

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

1.585

434

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

1.5937 - 1.7042

285 - 420

15.9

Voellmy; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 127; (1927); p. 345, View in Reaxys

1.55711

589

Williams; Krchma; Journal of the American Chemical Society; vol. 48; (1926); p. 1891; Journal of the American Chemical Society; vol. 49; (1927); p. 1679, View in Reaxys

1.557

656.3

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.56252

589

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.57636

486.1

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.58837

434

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.5649

589

10.2

Szivessy; Annalen der Physik (Weinheim, Germany); vol. <4> 68; (1922); p. 150; Zeitschrift fuer Physik; vol. 18; p. 102; Chem. Zentralbl.; vol. 95; nb. I; (1924); p. 2567, View in Reaxys

1.556

656.3

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

1.5578

656.3

13.7

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

39/219

2018-06-17 20:44:10

1.5615

589

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

1.5631

589

13.7

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

1.5753

486.1

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

1.5772

486.1

13.7

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

1.5893

434

13.7

v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys

1.5572

589

Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys

1.5549

656.3

Morgulewa; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 46; (1914); p. 237; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 2137, View in Reaxys

1.5604

589

Morgulewa; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 46; (1914); p. 237; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 2137, View in Reaxys

1.5741

486.1

Morgulewa; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 46; (1914); p. 237; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 2137, View in Reaxys

1.5859

434

Morgulewa; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 46; (1914); p. 237; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 2137, View in Reaxys

1.5569

589

23.5

Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 44; (1912); p. 692; Chem. Zentralbl.; vol. 83; nb. II; (1912); p. 789, View in Reaxys

1.5585

656.3

13.2

Jahn; Moeller; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 13; (1894); p. 393, View in Reaxys

1.5635

589

13.2

Jahn; Moeller; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 13; (1894); p. 393, View in Reaxys

1.5904

434

13.2

Jahn; Moeller; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 13; (1894); p. 393, View in Reaxys

1.51752

656.3

89.2

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.52235

589

89.2

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.5463

430.8

89.2

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.56252

656.3

4.2

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.56796

589

4.2

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.59439

430.8

4.2

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.5578

589

(:18-20 degreeC.

Seubert; Chemische Berichte; vol. 22; (1889); p. 2520, View in Reaxys

1.5715

486.1

(:18-20 degreeC.

Seubert; Chemische Berichte; vol. 22; (1889); p. 2520, View in Reaxys

40/219

2018-06-17 20:44:10

1.5586

589

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

1.561

589

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

1.55439

656.3

Bruehl; Justus Liebigs Annalen der Chemie; vol. 200; (1880); p. 184; Chemische Berichte; vol. 27; (1894); p. 1066, View in Reaxys

1.55977

589

Bruehl; Justus Liebigs Annalen der Chemie; vol. 200; (1880); p. 184; Chemische Berichte; vol. 27; (1894); p. 1066, View in Reaxys

1.58557

434

Bruehl; Justus Liebigs Annalen der Chemie; vol. 200; (1880); p. 184; Chemische Berichte; vol. 27; (1894); p. 1066, View in Reaxys

1.55426

589

Dreisbach,R.R.; Physical Properties of Chemical Compounds (= Advances in Chemistry Series Nr. 15) <Washington 1955> S. 150, View in Reaxys

Density (87) 1 of 87

Density [g·cm-3]

1.43415 - 1.50195

Measurement Temperature 14.99 - 64.99 [°C] Goralski, Pawet; Piekarski, Henryk; Journal of Chemical and Engineering Data; vol. 52; nb. 2; (2007); p. 655 - 659, View in Reaxys 2 of 87

Density [g·cm-3]

1.5012

Reference Temperature [°C]

Measurement Temperature 20 [°C] Sadygov; Alimardanov; Chalabiev; Russian Journal of Organic Chemistry; vol. 41; nb. 11; (2005); p. 1631 - 1636, View in Reaxys 3 of 87

Density [g·cm-3]

1.48838

Measurement Temperature 25 [°C] Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 4 of 87

Density [g·cm-3]

1.48147

Measurement Temperature 30 [°C] Ramadevi; Rao; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 65 - 67, View in Reaxys 5 of 87

Density [g·cm-3]

1.48159

Measurement Temperature 30 [°C] Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 128 131, View in Reaxys; Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 - 135, View in Reaxys 6 of 87

Density [g·cm-3]

1.4965

Measurement Temperature 25 [°C] Singh, R. P.; Sinha, C. P.; Das, J. C.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 2; (1990); p. 419 - 426, View in Reaxys 7 of 87

Density [g·cm-3]

1.48811

Measurement Temperature 25 [°C]

41/219

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Naorem, Homendra; Suri, S. K.; Canadian Journal of Chemistry; vol. 67; (1989); p. 1672 - 1676, View in Reaxys 8 of 87

Density [g·cm-3]

1.447 - 1.4889

Measurement Temperature 30 - 60 [°C] Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 34; nb. 3; (1989); p. 335 - 338, View in Reaxys 9 of 87

Density [g·cm-3]

1.495

Reference Temperature [°C]

Measurement Temperature 20 [°C] Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys; Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Cowley; Partington; Journal of the Chemical Society; (1937); p. 130,131, View in Reaxys; Zubkov, V. A.; Yudovich, M. E.; Saidov, G. V.; Russian Journal of Physical Chemistry; vol. 62; nb. 1; (1988); p. 77 - 80; Zhurnal Fizicheskoi Khimii; vol. 62; (1988); p. 155 - 159, View in Reaxys 10 of 87

Density [g·cm-3]

1.4886

Measurement Temperature 25 [°C] Zainel, Hanaa A.; Al-Azzawi, Souad F.; Swellem, Hassan I.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 84; nb. 10; (1988); p. 3511 - 3516, View in Reaxys 11 of 87

Density [g·cm-3]

1.47639

Measurement Temperature 45 [°C] Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 12 of 87

Density [g·cm-3]

1.4982

Measurement Temperature 25 [°C] Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 13 of 87

Density [g·cm-3]

1.49824

Measurement Temperature 25 [°C] Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 25; nb. 5; (1986); p. 465 - 467, View in Reaxys 14 of 87

Density [g·cm-3]

1.48891

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 15 of 87

Density [g·cm-3]

1.4931

Reference Temperature [°C]

Measurement Temperature 20 [°C] Holm, Torkil; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 464 - 467, View in Reaxys 16 of 87

Density [g·cm-3]

1.4144 - 1.4959

Measurement Temperature 20 - 80 [°C] Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys

42/219

2018-06-17 20:44:10

17 of 87

Density [g·cm-3]

1.475

Measurement Temperature 35 [°C] Oswal et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 17; (1979); p. 605, View in Reaxys 18 of 87

Density [g·cm-3]

1.482

Measurement Temperature 30 [°C] Oswal et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 17; (1979); p. 605, View in Reaxys 19 of 87

Dubrowskii; Afonina; J. Gen. Chem. USSR (Engl. Transl.); vol. 36; (1966); p. 1875,1868, View in Reaxys; Oswal et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 17; (1979); p. 605, View in Reaxys; Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys; Wellek et al.; AIChE Journal; vol. 12; (1966); p. 854,857, View in Reaxys; Miller et al.; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 417,418, 419, View in Reaxys

20 of 87

Density [g·cm-3]

1.48881

Measurement Temperature 25 [°C] Miller et al.; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 417,418, 419, View in Reaxys 21 of 87

Density [g·cm-3]

1.501

Reference Temperature [°C]

Measurement Temperature 20 [°C] Aronskaya; Bezuglyi; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 268,269, View in Reaxys 22 of 87

Density [g·cm-3]

1.4953

Reference Temperature [°C]

Measurement Temperature 20 [°C] Biron; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 42; (1910); p. 178; Chem. Zentralbl.; vol. 81; nb. I; (1910); p. 1913, View in Reaxys; Bruniquel et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 1558, View in Reaxys 23 of 87

Density [g·cm-3]

1.48874

Measurement Temperature 25 [°C] Deshpande et al.; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 469,470-472, View in Reaxys 24 of 87

Density [g·cm-3]

1.483

Measurement Temperature 42 [°C] Curran; Curley; Analytical Chemistry; vol. 43; (1971); p. 118,119, View in Reaxys 25 of 87

Density [g·cm-3]

1.491 - 1.51

Reference Temperature [°C]

Measurement Temperature 20 [°C] Kolpakchi; Babin; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 38; ; p. 69, View in Reaxys 26 of 87

Density [g·cm-3]

1.503

Reference Temperature [°C]

43/219

2018-06-17 20:44:10

Measurement Temperature 20 [°C] Kiersznicki et al.; Roczniki Chemii; vol. 44; (1970); p. 1049, View in Reaxys 27 of 87

Density [g·cm-3]

1.4879

Measurement Temperature 25 [°C] Nigam; Singh; Transactions of the Faraday Society; vol. 65; (1969); p. 950,956, View in Reaxys 28 of 87

Density [g·cm-3]

1.4883

Reference Temperature [°C]

Measurement Temperature 25 [°C] Krosnar et al.; Collection of Czechoslovak Chemical Communications; vol. 34; (1969); p. 1286,1288, View in Reaxys 29 of 87

Density [g·cm-3]

1.499

Reference Temperature [°C]

Measurement Temperature 20 [°C] Seliga; Collection of Czechoslovak Chemical Communications; vol. 33; (1968); p. 999, View in Reaxys 30 of 87

Density [g·cm-3]

1.5219

Measurement Temperature 20 [°C] Haberditzl; Koeppel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 691, View in Reaxys 31 of 87

Type (Density)

crystallographic

Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys 32 of 87

Density [g·cm-3]

1.48148

Reference Temperature [°C]

Measurement Temperature 30 [°C] Tourky et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 216; (1961); p. 176,177, 181, 182, View in Reaxys 33 of 87

Density [g·cm-3]

1.4952

Luedde; Riechstoffe und Aromen; vol. 10; (1960); p. 193, View in Reaxys 34 of 87

Density [g·cm-3]

1.493

Reference Temperature [°C]

Measurement Temperature 20 [°C] Minisci; Gazzetta Chimica Italiana; vol. 90; (1960); p. 1307,1315, View in Reaxys 35 of 87

Density [g·cm-3]

1.5597 - 1.4976

Measurement Temperature -30 - 20 [°C] Kesemenli; Izv. Akad. Azerbajdzansk. S.S.R.; nb. 6; (1959); p. 53,54; Chem.Abstr.; (1961); p. 21714, View in Reaxys 36 of 87

Density [g·cm-3]

1.654

Comment (Density)

bei -180grad.

Biswas; Acta Crystallographica; vol. 11; (1958); p. 882, View in Reaxys

44/219

2018-06-17 20:44:10

37 of 87

Density [g·cm-3]

1.48847

Measurement Temperature 25 [°C] McGlashan; Windgrove; Transactions of the Faraday Society; vol. 52; (1956); p. 470,471, View in Reaxys 38 of 87

Density [g·cm-3]

1.556 - 1.47

Measurement Temperature -25 - 40 [°C] Belinskaja; Uc. Zap. Moskovsk. oblast. pedagog. Inst.; vol. 33; (1955); p. 221,224; Chem.Abstr.; (1958); p. 821, View in Reaxys 39 of 87

Density [g·cm-3]

1.48841

Measurement Temperature 25 [°C] Kohler,Rott; Monatshefte fuer Chemie; vol. 85; (1954); p. 703,11, View in Reaxys 40 of 87

Density [g·cm-3]

1.50189

Measurement Temperature 20 [°C] Kohler,Rott; Monatshefte fuer Chemie; vol. 85; (1954); p. 703,11, View in Reaxys 41 of 87

Density [g·cm-3]

1.4936

Measurement Temperature 25 [°C] Babak; Udowenko; Zhurnal Obshchei Khimii; vol. 20; (1950); p. 2124; engl. Ausg. S. 2203, View in Reaxys 42 of 87

Density [g·cm-3]

1.4312

Measurement Temperature 75 [°C] Babak; Udowenko; Zhurnal Obshchei Khimii; vol. 20; (1950); p. 2124; engl. Ausg. S. 2203, View in Reaxys 43 of 87

Density [g·cm-3]

1.4589

Measurement Temperature 50 [°C] Babak; Udowenko; Zhurnal Obshchei Khimii; vol. 20; (1950); p. 2124; engl. Ausg. S. 2203, View in Reaxys 44 of 87

Density [g·cm-3]

1.4882

Reference Temperature [°C]

Measurement Temperature 25 [°C] Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 45 of 87

Density [g·cm-3]

1.49

Reference Temperature [°C]

Measurement Temperature 25 [°C] Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys 46 of 87

Density [g·cm-3]

1.5075 - 1.4535

Measurement Temperature 10 - 50 [°C] Lagemann; McMillan; Woolf; Journal of Chemical Physics; vol. 17; (1949); p. 370, View in Reaxys 47 of 87

Density [g·cm-3]

1.4939 - 1.4093

Measurement Temperature 20 - 85.2 [°C]

45/219

2018-06-17 20:44:10

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys 48 of 87

Density [g·cm-3]

1.6926

Rozental; Bulletin des Societes Chimiques Belges; vol. 45; (1936); p. 585,600, View in Reaxys 49 of 87

Density [g·cm-3]

1.4974

Reference Temperature [°C]

Measurement Temperature 17 [°C] Vorlaender; Fischer; Chemische Berichte; vol. 65; (1932); p. 1756,1759, View in Reaxys 50 of 87

Density [g·cm-3]

1.489

Reference Temperature [°C]

Measurement Temperature 25 [°C] Martin; Collie; Journal of the Chemical Society; (1932); p. 2658,2662, View in Reaxys 51 of 87

Density [g·cm-3]

1.4887

Reference Temperature [°C]

Measurement Temperature 25 [°C] Harkins; Jordan; Journal of the American Chemical Society; vol. 52; (1930); p. 1751,1760, View in Reaxys 52 of 87

Density [g·cm-3]

1.4875

Reference Temperature [°C]

Measurement Temperature 25 [°C] Tsukamoto; Japan. J. Chem.; vol. 2; p. 137; Chem. Zentralbl.; vol. 99; nb. II; (1928); p. 2108, View in Reaxys 53 of 87

Density [g·cm-3]

1.444

Reference Temperature [°C]

Measurement Temperature 58 [°C] Kerr; Phil. Mag.; vol. <7> 3; (1927); p. 332, View in Reaxys 54 of 87

Density [g·cm-3]

1.4815

Reference Temperature [°C]

Measurement Temperature 30 [°C] Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys 55 of 87

Density [g·cm-3]

1.5017

Reference Temperature [°C]

Measurement Temperature 15 [°C] Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys 56 of 87

Density [g·cm-3]

1.522

Reference Temperature [°C]

46/219

2018-06-17 20:44:10

Measurement Temperature 0 [°C] Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys 57 of 87

Density [g·cm-3]

1.4944

Reference Temperature [°C]

19.9

Measurement Temperature 19.9 [°C] Miller; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 106; (1924); p. 740, View in Reaxys 58 of 87

Density [g·cm-3]

1.5077

Reference Temperature [°C]

8.8

Measurement Temperature 8.8 [°C] Miller; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 106; (1924); p. 740, View in Reaxys 59 of 87

Density [g·cm-3]

1.4986

Reference Temperature [°C]

Measurement Temperature 18.5 [°C] v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys 60 of 87

Density [g·cm-3]

1.5038

Reference Temperature [°C]

Measurement Temperature 13.7 [°C] v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys 61 of 87

Density [g·cm-3]

1.325 - 1.522

Reference Temperature [°C]

Measurement Temperature -0.1 - 142.5 [°C] Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys 62 of 87

Density [g·cm-3]

1.4922

Reference Temperature [°C]

Measurement Temperature 22.2 [°C] Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 44; (1912); p. 709; Chem. Zentralbl.; vol. 83; nb. II; (1912); p. 789, View in Reaxys 63 of 87

Density [g·cm-3]

1.4879

Reference Temperature [°C]

Measurement Temperature 25 [°C] Bugarszky; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 71; (1910); p. 710, View in Reaxys

47/219

2018-06-17 20:44:10

64 of 87

Density [g·cm-3]

1.4946

Reference Temperature [°C]

Measurement Temperature 20 [°C] Bugarszky; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 71; (1910); p. 710, View in Reaxys 65 of 87

Density [g·cm-3]

1.5223

Reference Temperature [°C]

Measurement Temperature 0 [°C] Biron; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 42; (1910); p. 178; Chem. Zentralbl.; vol. 81; nb. I; (1910); p. 1913, View in Reaxys 66 of 87

Density [g·cm-3]

1.5218 - 1.1099

Measurement Temperature 0 - 270 [°C] Young; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 626; Scientific Proceedings of the Royal Dublin Society; vol. 12; (1909); p. 432, View in Reaxys 67 of 87

Density [g·cm-3]

1.52193

Reference Temperature [°C]

Measurement Temperature 0 [°C] Timmermans; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 442, View in Reaxys 68 of 87

Density [g·cm-3]

1.3862

Reference Temperature [°C]

Measurement Temperature 100.6 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 69 of 87

Density [g·cm-3]

1.44313

Reference Temperature [°C]

Measurement Temperature 58.6 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 70 of 87

Density [g·cm-3]

1.46425

Reference Temperature [°C]

Measurement Temperature 42.8 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 71 of 87

Density [g·cm-3]

1.50188

Reference Temperature [°C]

Measurement Temperature 14.3 [°C]

48/219

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Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 72 of 87

Density [g·cm-3]

1.52178

Reference Temperature [°C]

Measurement Temperature 0 [°C] Young; Journal of the Chemical Society; vol. 81; (1902); p. 771,772, View in Reaxys 73 of 87

Density [g·cm-3]

1.4416

Reference Temperature [°C]

100

Measurement Temperature 100 [°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 74 of 87

Density [g·cm-3]

1.4522

Reference Temperature [°C]

Measurement Temperature 75 [°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 75 of 87

Density [g·cm-3]

1.4681

Reference Temperature [°C]

Measurement Temperature 50 [°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 76 of 87

Density [g·cm-3]

1.4886

Reference Temperature [°C]

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 77 of 87

Density [g·cm-3]

1.4991

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 78 of 87

Density [g·cm-3]

1.5103

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 79 of 87

Density [g·cm-3]

1.39638

49/219

2018-06-17 20:44:10

Reference Temperature [°C]

Measurement Temperature 89.2 [°C] Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys 80 of 87

Density [g·cm-3]

1.51

Reference Temperature [°C]

Measurement Temperature 4.2 [°C] Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys 81 of 87

Density [g·cm-3]

1.48972

Reference Temperature [°C]

Measurement Temperature 20 [°C] Seubert; Chemische Berichte; vol. 22; (1889); p. 2520, View in Reaxys 82 of 87

Density [g·cm-3]

1.50242

Reference Temperature [°C]

Measurement Temperature 14.6 [°C] Young; Journal of the Chemical Society; vol. 55; (1889); p. 501; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 422, View in Reaxys 83 of 87

Density [g·cm-3]

1.52182

Reference Temperature [°C]

Measurement Temperature 0 [°C] Young; Journal of the Chemical Society; vol. 55; (1889); p. 501; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 422, View in Reaxys 84 of 87

Density [g·cm-3]

1.49225

Measurement Temperature 23 [°C] Gladstone; Journal of the Chemical Society; vol. 45; (1884); p. 246, View in Reaxys 85 of 87

Density [g·cm-3]

1.4958

Measurement Temperature 16 [°C] Gladstone; Journal of the Chemical Society; vol. 45; (1884); p. 246, View in Reaxys 86 of 87

Density [g·cm-3]

1.5203

Reference Temperature [°C]

Measurement Temperature 0 [°C] Weger; Justus Liebigs Annalen der Chemie; vol. 221; (1883); p. 83; Journal fuer Praktische Chemie (Leipzig); vol. <2>61; (1900); p. 217 Anm. 3, View in Reaxys 87 of 87

Density [g·cm-3]

1.4914

Reference Temperature [°C]

Measurement Temperature 20 [°C]

50/219

2018-06-17 20:44:10

Bruehl; Justus Liebigs Annalen der Chemie; vol. 200; (1880); p. 184; Chemische Berichte; vol. 27; (1894); p. 1066, View in Reaxys Adsorption (MCS) (26) 1 of 26

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

15 - 35

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 2 of 26

Description (Adsorption (MCS))

Enthalpy of adsorption

Temperature (Adsorption (MCS)) [°C]

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 3 of 26

Description (Adsorption (MCS))

Desorption

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

35 μm Supelco Amberchrom CG-1000S

Zhang, Guangming; Hua, Inez; Chemosphere; vol. 46; nb. 1; (2002); p. 59 - 66, View in Reaxys 4 of 26

Description (Adsorption (MCS))

Desorption

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

silica particles

Zhang, Guangming; Hua, Inez; Chemosphere; vol. 46; nb. 1; (2002); p. 59 - 66, View in Reaxys 5 of 26

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

Polysorb-1

Shepelenko; Zibarev; Russian Journal of Physical Chemistry A; vol. 75; nb. 8; (2001); p. 1351 - 1354, View in Reaxys 6 of 26

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

benzene

Temperature (Adsorption (MCS)) [°C]

1.9 - 29.9

Partner (Adsorption (MCS))

magnesium

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 274 - 276, View in Reaxys

51/219

2018-06-17 20:44:10

7 of 26

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

benzene

Temperature (Adsorption (MCS)) [°C]

1.9 - 29.9

Partner (Adsorption (MCS))

magnesium

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 274 - 276, View in Reaxys 8 of 26

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 9 of 26

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 10 of 26

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 11 of 26

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 12 of 26

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

diethyl ether; benzene

Temperature (Adsorption (MCS)) [°C]

19.85

52/219

2018-06-17 20:44:10

Partner (Adsorption (MCS))

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 12; (1998); p. 1876 - 1877, View in Reaxys 13 of 26

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

129.9 - 189.9

Partner (Adsorption (MCS))

graphitized thermal carbon black

Kalashnikova; Lopatkin; Russian Chemical Bulletin; vol. 46; nb. 12; (1997); p. 2060 - 2063, View in Reaxys 14 of 26

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

benzene

Partner (Adsorption (MCS))

magnesium

Maslennikov; Kirillov; Berezina; Spirina; Kondin; Russian Journal of General Chemistry; vol. 67; nb. 5; (1997); p. 667 671, View in Reaxys 15 of 26

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 16 of 26

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 17 of 26

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 18 of 26

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

150

Partner (Adsorption (MCS))

BaSO4

Belyakova, L. D.; Larionov, O. G.; Strokina, L. M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 37; (1988); p. 1315 - 1320; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 7; (1988); p. 1491 - 1497, View in Reaxys 19 of 26

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

27.9

Partner (Adsorption (MCS))

silicalite

Thamm, H.; Journal of Physical Chemistry; vol. 92; nb. 1; (1988); p. 193 - 196, View in Reaxys

53/219

2018-06-17 20:44:10

20 of 26

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

gas

Temperature (Adsorption (MCS)) [°C]

27.9

Partner (Adsorption (MCS))

silicalite

Thamm, H.; Journal of Physical Chemistry; vol. 92; nb. 1; (1988); p. 193 - 196, View in Reaxys 21 of 26

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

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 22 of 26

Description (Adsorption (MCS))

Adsorption isotherm

Wortel et al.; Journal of Catalysis; vol. 60; (1979); p. 110,112, 115, 117, 118, View in Reaxys; Handa et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 255; (1974); p. 245,247, View in Reaxys; Voloshchuk et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 24; (1975); p. 445; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 24; (1975); p. 517, View in Reaxys 23 of 26

Description (Adsorption (MCS))

Adsorption

Wright; Transactions of the Faraday Society; vol. 62; (1966); p. 1275, View in Reaxys; Chopra et al.; Journal of the Indian Chemical Society; vol. 51; (1974); p. 740, View in Reaxys; Handa et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 255; (1974); p. 245,247, View in Reaxys; Tul'bovich; Priimak; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 195; Zhurnal Fizicheskoi Khimii; p. 362, View in Reaxys 24 of 26

Description (Adsorption (MCS))

Enthalpy of adsorption

Kiselev et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 644; ; p. 1235, View in Reaxys; Kiselev et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 705,706; ; p. 1272, View in Reaxys 25 of 26

Description (Adsorption (MCS))

Adsorption to title compound

Partner (Adsorption (MCS))

Davis, H. S.; Crandall, G. P.; Journal of the American Chemical Society; vol. 52; (1930); p. 3757 - 3785, View in Reaxys; vol. O: MVol.3; 63, page 492 - 494 ; (from Gmelin), View in Reaxys 26 of 26

Description (Adsorption (MCS))

Adsorption to title compound

Partner (Adsorption (MCS))

CO2

Just, G.; Z. Physik. Chem.; vol. 37; (1901); p. 342 - 367, View in Reaxys; vol. C: MVol.C1; 215, page 548 - 568 ; (from Gmelin), View in Reaxys Association (MCS) (71) 1 of 71

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(Me2NH2)[Zn2(L)(H2O)]4DMA MOF doped with 0.28 wtpercent[Ir]+ + 0.45 wtpercent [Ru]2+

Zhao, He; Ni, Jun; Zhang, Jian-Jun; Liu, Shu-Qin; Sun, Ying-Ji; Zhou, Huajun; Li, Yan-Qin; Duan, Chun-Ying; Chemical Science; vol. 9; nb. 11; (2018); p. 2918 - 2926, View in Reaxys

54/219

2018-06-17 20:44:10

2 of 71

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

2,2,2-trifluoroethanol

Temperature (Association (MCS)) [°C]

Location

supporting information

Partner (Association (MCS))

(Na(I))42

Sarma, Bidyut Bikash; Avram, Liat; Neumann, Ronny; Chemistry - A European Journal; vol. 22; nb. 43; (2016); p. 15231 15236, View in Reaxys 3 of 71

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

D2O

Partner (Association (MCS))

4Ga(3+)*6[1,5-bis(1,2-di-O(1-)-C6H3-3-CONH)naphthalene]

Hastings, Courtney J.; Pluth, Michael D.; Biros, Shannon M.; Bergman, Robert G.; Raymond, Kenneth N.; Tetrahedron; vol. 64; nb. 36; (2008); p. 8362 - 8367, View in Reaxys 4 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gaseous matrix

Comment (Association (MCS))

decomposition

Partner (Association (MCS))

Mg(1+)

Yang, Xin; Gao, Kelin; Liu, Haichuan; Yang, Shihe; Journal of Chemical Physics; vol. 112; nb. 23; (2000); p. 10236 - 10246, View in Reaxys 5 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

25 - 40

Partner (Association (MCS))

tetrahydrofuran

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 6 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

25 - 40

Partner (Association (MCS))

TETRAHYDROPYRANE

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 7 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

25 - 40

Partner (Association (MCS))

2-methyltetrahydrofuran

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys

55/219

2018-06-17 20:44:10

8 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

25 - 40

Partner (Association (MCS))

2,5-dimethyltetrahydrofuran

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 9 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

acetonitrile

Partner (Association (MCS))

2,4,6-triphenylpyrylium tetrafluoroborate

Jayanthi; Ramamurthy; Journal of Physical Chemistry A; vol. 101; nb. 11; (1997); p. 2016 - 2022, View in Reaxys 10 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

ethenetetracarbonitrile

Frey, John E.; Aiello, Theresa; Fu, Shi-Lin; Hutson, Heather; Journal of Organic Chemistry; vol. 61; nb. 1; (1996); p. 295 300, View in Reaxys 11 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Partner (Association (MCS))

ethenetetracarbonitrile

Frey, John E.; Aiello, Theresa; Fu, Shi-Lin; Hutson, Heather; Journal of Organic Chemistry; vol. 61; nb. 1; (1996); p. 295 300, View in Reaxys 12 of 71

Description (Association (MCS))

UV/VIS spectrum of the complex

Partner (Association (MCS))

ethenetetracarbonitrile

Frey, John E.; Aiello, Theresa; Fu, Shi-Lin; Hutson, Heather; Journal of Organic Chemistry; vol. 61; nb. 1; (1996); p. 295 300, View in Reaxys 13 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

IBr

Drepaul, Ian; Fagundez, Veronica; Guiterrez, Franklin; Lau, Eddy Hung; Joens, Jeffrey A.; Journal of Organic Chemistry; vol. 61; nb. 10; (1996); p. 3571 - 3572, View in Reaxys 14 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

Br2

Drepaul, Ian; Fagundez, Veronica; Guiterrez, Franklin; Lau, Eddy Hung; Joens, Jeffrey A.; Journal of Organic Chemistry; vol. 61; nb. 10; (1996); p. 3571 - 3572, View in Reaxys 15 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

ICl

Drepaul, Ian; Fagundez, Veronica; Guiterrez, Franklin; Lau, Eddy Hung; Joens, Jeffrey A.; Journal of Organic Chemistry; vol. 61; nb. 10; (1996); p. 3571 - 3572, View in Reaxys 16 of 71

Description (Association (MCS))

Further physical properties of the complex

56/219

2018-06-17 20:44:10

Partner (Association (MCS))

acetonitrile

Markovich, Gil; Perera, Lalith; Berkowitz, Max L.; Cheshnovsky, Ori; Journal of Chemical Physics; vol. 105; nb. 7; (1996); p. 2675 - 2685, View in Reaxys 17 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

Hu, Yihua; Lu, Wenyun; Yang, Shihe; Journal of Chemical Physics; vol. 105; nb. 13; (1996); p. 5305 - 5312, View in Reaxys 18 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

2-methoxy-ethanol

Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 135, View in Reaxys 19 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

AlCl3

Omelanczuk, Jan; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 86; nb. 1.4; (1994); p. 93 - 102, View in Reaxys 20 of 71

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

π-cyclodextrin

Sanemasa, Isao; Wu, Yue; Koide, Yuuki; Shigenaga, Masako; Ishibashi, Kazunari; Deguchi, Toshio; Bulletin of the Chemical Society of Japan; vol. 66; nb. 5; (1993); p. 1424 - 1429, View in Reaxys 21 of 71

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

cyclomaltooctaose

57/219

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Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

NOBF4

Bockman; Karpinski; Sankararaman; Kochi; Journal of the American Chemical Society; vol. 114; nb. 6; (1992); p. 1970 1985, View in Reaxys 24 of 71

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

solid

Partner (Association (MCS))

1,1,3,3-Tetrakis(4-tert-butylphenyl)allen

Weber, Edwin; Seichter, Wilhelm; Goldberg, Israel; Chemische Berichte; vol. 123; nb. 4; (1990); p. 811 - 820, View in Reaxys 25 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

Hexadecane

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 26 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 27 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 28 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

58/219

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Partner (Association (MCS))

π-cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 29 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

π-cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 30 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

cyclomaltooctaose

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 31 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

cyclomaltooctaose

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 32 of 71

Description (Association (MCS))

NMR spectrum of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

1-methyl-pyrrolidin-2-one

Zainel, Hanaa A.; Al-Azzawi, Souad F.; Swellem, Hassan I.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 84; nb. 10; (1988); p. 3511 - 3516, View in Reaxys 33 of 71

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 34 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

phenylnitrenium ion

59/219

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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 35 of 71

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

35 - 55

Partner (Association (MCS))

N-(4-ethoxybenzylidene)-4-butylaniline

Chingduang, P.; Bualek, S.; Phaovibul, O.; Schrader, B.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 132; (1986); p. 131 - 142, View in Reaxys 36 of 71

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

2,2,2-trifluoroethyl methyl ether

Ladika, Mladen; Jursic, Branko; Sunko, Dionis E.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 42; nb. 12; (1986); p. 1397 - 1400, View in Reaxys 37 of 71

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

1,1,1,3,3,3-hexafluoro-2-methoxypropane

Ladika, Mladen; Jursic, Branko; Sunko, Dionis E.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 42; nb. 12; (1986); p. 1397 - 1400, View in Reaxys 38 of 71

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

2,2,2-trifluoroethanol

Ladika, Mladen; Jursic, Branko; Sunko, Dionis E.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 42; nb. 12; (1986); p. 1397 - 1400, View in Reaxys 39 of 71

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

1,1,1,3',3',3'-hexafluoro-propanol

Ladika, Mladen; Jursic, Branko; Sunko, Dionis E.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 42; nb. 12; (1986); p. 1397 - 1400, View in Reaxys 40 of 71

Description (Association (MCS))

IR spectrum of the complex

60/219

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Solvent (Association (MCS))

various solvent(s)

Temperature (Association (MCS)) [°C]

-263.2

Partner (Association (MCS))

Davis, Steven R.; Andrews, Lester; Journal of Physical Chemistry; vol. 90; nb. 12; (1986); p. 2600 - 2608, View in Reaxys 41 of 71

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

various solvent(s)

Temperature (Association (MCS)) [°C]

-263.2

Partner (Association (MCS))

Davis, Steven R.; Andrews, Lester; Journal of Physical Chemistry; vol. 90; nb. 12; (1986); p. 2600 - 2608, View in Reaxys 42 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

2,4,6-trinitrochlorobenzene

Basu, Rama; Journal of the Indian Chemical Society; vol. 63; (1986); p. 105 - 107, View in Reaxys 43 of 71

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

ethenetetracarbonitrile

Kubota, Tanekazu; Uno, Bunji; Kano, Kenji; Ninomiya, Yoichi; Molecular Crystals and Liquid Crystals (1969-1991); vol. 126; (1985); p. 111 - 120, View in Reaxys 44 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

ethenetetracarbonitrile

Gol'dshtein, I. P.; Fedotov, A. N.; Starostina, T. A.; Rybakova, L. F.; Gur'yanova, E. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 6; (1984); p. 1363 - 1374,1218 - 1227, View in Reaxys 45 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

chlorobenzene

Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 16; nb. 11; (1984); p. 1031 - 1036, View in Reaxys 46 of 71

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

24.9

61/219

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Partner (Association (MCS))

iodine

Shedbalkar, V. P.; Bhat, S. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 22; nb. 12; (1983); p. 1062 - 1064, View in Reaxys 47 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

-130.7 - -123.4

Partner (Association (MCS))

cis-decalin

Agarwal, C. B.; Mansingh, A.; Journal of Chemical Physics; vol. 76; nb. 9; (1982); p. 4606 - 4610, View in Reaxys 48 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

chloranil

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 49 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

2,3,5,6-tetracyano pyrazine

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 50 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

ethenetetracarbonitrile

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 51 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

maleic anhydride

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 52 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 53 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

trifluoroacetic acid

62/219

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Partner (Association (MCS))

Br2

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 54 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

Br2

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 55 of 71

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

mercury(II) trifluoroacetate

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 56 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

2,3,5,6-tetracyano pyrazine

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 57 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

ethenetetracarbonitrile

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 58 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

chloranil

Fukuzumi, S.; Kochi, J. K.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4116 - 4126, View in Reaxys 59 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

bromine

63/219

2018-06-17 20:44:10

Fukuzumi, S.; Kochi, J. K.; Journal of the American Chemical Society; vol. 103; nb. 24; (1981); p. 7240 - 7252, View in Reaxys 60 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

trifluoroacetic acid

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

bromine

Fukuzumi, S.; Kochi, J. K.; Journal of the American Chemical Society; vol. 103; nb. 24; (1981); p. 7240 - 7252, View in Reaxys 61 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

mercury(II) trifluoroacetate

Fukuzumi, S.; Kochi, J. K.; Journal of the American Chemical Society; vol. 103; nb. 24; (1981); p. 7240 - 7252, View in Reaxys 62 of 71

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Partner (Association (MCS))

π-cyclodextrin

Yamaguchi, Hiroyuki; Abe, Suemi; Journal of Physical Chemistry; vol. 85; nb. 12; (1981); p. 1640 - 1643, View in Reaxys 63 of 71

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

-10

Partner (Association (MCS))

Shereshovets, V. V.; Galimova, L. G.; Komissarov, V. D.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 30; nb. 11; (1981); p. 2055 - 2059; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 11; (1981); p. 2488 - 2492, View in Reaxys 64 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Temperature (Association (MCS)) [°C]

-57 - -10

Partner (Association (MCS))

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Partner (Association (MCS))

anthracene; sodium dodecyl-sulfate

64/219

2018-06-17 20:44:10

Ponomareva; Zaev; Journal of applied spectroscopy; vol. 33; nb. 3; (1980); p. 940 - 944, View in Reaxys 66 of 71

Description (Association (MCS))

Stability constant of the complex with ...

Takayama et al.; Journal of Organic Chemistry; vol. 44; (1979); p. 2871,2872, View in Reaxys 67 of 71

Description (Association (MCS))

Spectrum of the complex

Nigam; Maini; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 14; (1976); p. 605, View in Reaxys 68 of 71

Description (Association (MCS))

Further physical properties of the complex

Rosen et al.; Molecular Physics; vol. 22; (1971); p. 33,42, View in Reaxys; Kudryavtsev; Samgina; Sov. Phys. J. (Engl. Transl.); vol. 9; nb. 5; (1966); p. 12,5, View in Reaxys 69 of 71

Description (Association (MCS))

Dipole moment of the complex

Nigam et al.; Indian Journal of Chemistry; vol. 8; (1970); p. 658, View in Reaxys 70 of 71

Description (Association (MCS))

Association with compound

Horak et al.; Spectrochimica Acta; vol. 21; (1965); p. 919, View in Reaxys; Voigt; Journal of Physical Chemistry; vol. 72; (1968); p. 3300, View in Reaxys; Krueger; Mettee; Canadian Journal of Chemistry; vol. 42; (1964); p. 288,289, View in Reaxys; Marcus; Miller; Journal of Physical Chemistry; vol. 73; (1969); p. 453, View in Reaxys; Watts, V.S; Goldstein, J.H; Journal of Molecular Spectroscopy; vol. 21; nb. 1-4; (1966); p. 260 - 266, View in Reaxys; Olszer; Siekierski; Journal of Inorganic and Nuclear Chemistry; vol. 28; (1966); p. 1991, View in Reaxys; Olszer; Siekierski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 14; (1966); p. 325, View in Reaxys 71 of 71

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

1,3,5-trinitrobenzene

Ferguson; Garner; Journal of the American Chemical Society; vol. 76; (1954); p. 1167, View in Reaxys Azeotropes (MCS) (51) 1 of 51

Temperature (Azeotropes (MCS)) [°C]

93.55

Pressure (Azeotropes (MCS)) [Torr]

300.024

Azeotropes

butan-1-ol

Artigas, Hector; Lafuente, Carlos; Cea, Pilar; Royo, Felix M.; Urieta, Jose S.; Journal of Chemical and Engineering Data; vol. 42; nb. 1; (1997); p. 132 - 136, View in Reaxys 2 of 51

Temperature (Azeotropes (MCS)) [°C]

154.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetamide

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys; Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 19,23, 33, View in Reaxys 3 of 51

Temperature (Azeotropes (MCS)) [°C]

99.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

formic acid

Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 19,23, 33, View in Reaxys 4 of 51

Temperature (Azeotropes (MCS)) [°C]

154.8

65/219

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isovaleric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys; Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 19,23, 33, View in Reaxys 5 of 51

Temperature (Azeotropes (MCS)) [°C]

151.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

hexyl alcohol

Lecat; Ann. Soc. scient. Bruxelles; vol. 48 I; (1928); p. 118, View in Reaxys 6 of 51

Temperature (Azeotropes (MCS)) [°C]

152.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromoacetic acid ethyl ester

Lecat; Ann. Soc. scient. Bruxelles; vol. 48 I; (1928); p. 118, View in Reaxys 7 of 51

Temperature (Azeotropes (MCS)) [°C]

150.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethylene glycol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys; Lecat; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 26, View in Reaxys 8 of 51

Temperature (Azeotropes (MCS)) [°C]

154.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chloroacetic acid

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 112,151,155, View in Reaxys 9 of 51

Temperature (Azeotropes (MCS)) [°C]

154.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propyl isovalerate

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 112,151,155, View in Reaxys 10 of 51

Temperature (Azeotropes (MCS)) [°C]

155

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

camphene

Lecat; Ann. Soc. scient. Bruxelles; vol. 45 I; (1926); p. 174, View in Reaxys 11 of 51

Temperature (Azeotropes (MCS)) [°C]

153.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

furfurol

66/219

2018-06-17 20:44:10

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 622; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16, View in Reaxys 12 of 51

Temperature (Azeotropes (MCS)) [°C]

149.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethyl lactate

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 622; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16, View in Reaxys 13 of 51

Temperature (Azeotropes (MCS)) [°C]

155.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

trichlorohydrin

Lecat; Ann. Soc. scient. Bruxelles; vol. 45 I; (1926); p. 288, View in Reaxys 14 of 51

Temperature (Azeotropes (MCS)) [°C]

131.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl alcohol

Lecat; Ann. Soc. scient. Bruxelles; vol. 45 I; (1926); p. 288, View in Reaxys 15 of 51

Temperature (Azeotropes (MCS)) [°C]

155.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

glycerol-π-dichloro-hydrin

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 622; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16, View in Reaxys 16 of 51

Temperature (Azeotropes (MCS)) [°C]

153.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pinacone

Lecat; Ann. Soc. scient. Bruxelles; vol. 47; p. I, 112, View in Reaxys 17 of 51

Temperature (Azeotropes (MCS)) [°C]

154.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

camphene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 18 of 51

Temperature (Azeotropes (MCS)) [°C]

153.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

π-pinene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 19 of 51

Temperature (Azeotropes (MCS)) [°C]

153.3

Pressure (Azeotropes (MCS)) [Torr]

760

67/219

2018-06-17 20:44:10

Azeotropes

furfural

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 20 of 51

Temperature (Azeotropes (MCS)) [°C]

118

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 21 of 51

Temperature (Azeotropes (MCS)) [°C]

151.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

hexanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 22 of 51

Temperature (Azeotropes (MCS)) [°C]

152.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 23 of 51

Temperature (Azeotropes (MCS)) [°C]

153.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

cyclohexanol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 24 of 51

Temperature (Azeotropes (MCS)) [°C]

155.9

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<155.9gradC; Gewprozent >72.

Azeotropes

π-pinene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 25 of 51

Temperature (Azeotropes (MCS)) [°C]

98.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

formic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 26 of 51

Temperature (Azeotropes (MCS)) [°C]

140.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propionic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 27 of 51

Temperature (Azeotropes (MCS)) [°C]

131.7

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isoamyl alcohol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 28 of 51

Temperature (Azeotropes (MCS)) [°C]

155.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

valeric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 29 of 51

Temperature (Azeotropes (MCS)) [°C]

148.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 30 of 51

Temperature (Azeotropes (MCS)) [°C]

154.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chloroacetic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 31 of 51

Temperature (Azeotropes (MCS)) [°C]

147

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pyruvic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 32 of 51

Temperature (Azeotropes (MCS)) [°C]

153.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-iodo-ethanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 33 of 51

Temperature (Azeotropes (MCS)) [°C]

156

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.1-diacetoxy-ethane

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 34 of 51

Temperature (Azeotropes (MCS)) [°C]

145

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-amino-ethanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 35 of 51

Temperature (Azeotropes (MCS)) [°C]

127.5

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-chloro-ethanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 36 of 51

Temperature (Azeotropes (MCS)) [°C]

155.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2.3-trichloro-propane

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 37 of 51

Temperature (Azeotropes (MCS)) [°C]

135.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1-ethoxy-ethanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 38 of 51

Temperature (Azeotropes (MCS)) [°C]

155.5

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<155.5gradC; Gewprozent <88.

Azeotropes

2.7-dimethyl-octane

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 39 of 51

Temperature (Azeotropes (MCS)) [°C]

150.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

lactic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 40 of 51

Temperature (Azeotropes (MCS)) [°C]

141.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

lactic acid methyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 41 of 51

Temperature (Azeotropes (MCS)) [°C]

153.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

oxalic acid dimethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 42 of 51

Temperature (Azeotropes (MCS)) [°C]

155.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.3-dichloro-propanol-(2)

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

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2018-06-17 20:44:10

43 of 51

Temperature (Azeotropes (MCS)) [°C]

148.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1-propyloxy-ethanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 44 of 51

Temperature (Azeotropes (MCS)) [°C]

142.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2.2-dichloro-ethanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 45 of 51

Temperature (Azeotropes (MCS)) [°C]

154

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

carbamic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 46 of 51

Temperature (Azeotropes (MCS)) [°C]

155.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

lactic acid isopropyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 47 of 51

Temperature (Azeotropes (MCS)) [°C]

155.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromoacetic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 48 of 51

Temperature (Azeotropes (MCS)) [°C]

155.9

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T=155.9gradC(?); Gewprozent =93.5(?).

Azeotropes

1-butyloxy-ethanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 49 of 51

Temperature (Azeotropes (MCS)) [°C]

149.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pyruvic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 50 of 51

Temperature (Azeotropes (MCS)) [°C]

153.5

Pressure (Azeotropes (MCS)) [Torr]

760

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Comment (Azeotropes (MCS))

Verbindung (1)::T<153.5gradC; Gewprozent >80.

Azeotropes

2.3-dimethyl-butanediol-(2.3)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 51 of 51

Temperature (Azeotropes (MCS)) [°C]

155.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetic acid-<2-ethoxy-ethyl ester>

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys Boundary Surface Phenomena (MCS) (11) 1 of 11

Description (Boundary Surface Phenomena (MCS))

Surface tension

Dhillon; Monatshefte fuer Chemie; vol. 110; (1979); p. 847, View in Reaxys; Nigam; Maini; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 14; (1976); p. 605, View in Reaxys 2 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Wolf; Neumann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 219; (1962); p. 60,77,78, View in Reaxys; Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys 3 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser bei Temperaturen von 20grad bis 70grad.

Jasper; Wood; Journal of Physical Chemistry; vol. 60; (1956); p. 1625, View in Reaxys 4 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser bei Temperaturen von 20grad bis 80grad.

Jasper; Wood; Journal of Physical Chemistry; vol. 59; (1955); p. 541, View in Reaxys 5 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser bei Temperaturen von 25grad.

Donahue; Bartell; Journal of Physical Chemistry; vol. 56; (1952); p. 480,483, View in Reaxys 6 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

von Brombenzol.

Dunken; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 47; (1940); p. 195,204, 208; Annalen der Physik (Weinheim, Germany); vol. <5> 41; (1942); p. 567,582, View in Reaxys 7 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

von Brombenzol-Heptan-Gemischen gegen Quecksilber.

Dunken; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 47; (1940); p. 195,204, 208; Annalen der Physik (Weinheim, Germany); vol. <5> 41; (1942); p. 567,582, View in Reaxys

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8 of 11

Description (Boundary Surface Phenomena (MCS))

Spreading pressure

Solvent (Boundary Surface H2O Phenomena (MCS)) Partner (Boundary Surface benzene; bromobenzene Phenomena (MCS)) Keim; Washburn; Journal of the American Chemical Society; vol. 62; (1940); p. 2318, View in Reaxys 9 of 11

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Comment (Boundary Surface Phenomena (MCS))

sowie bei 35grad und bei 50grad.

Partner (Boundary Surface toluene Phenomena (MCS)) Yajnik; Sharma; Bharadwaj; Quart. J. indian chem. Soc.; vol. 3; p. 66; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 2147, View in Reaxys 10 of 11

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser.

Harkins; Feldman; Journal of the American Chemical Society; vol. 44; (1922); p. 2671, View in Reaxys 11 of 11

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface chlorobenzene Phenomena (MCS)) Kremann; Meingast; Monatshefte fuer Chemie; vol. 35; (1914); p. 1360, View in Reaxys Chromatographic Data (3) Chromatographic Location data

References

GC (Gas chromatography)

supporting informa- Nagaki, Aiichiro; Moriwaki, Yuya; Yoshida, Jun-Ichi; Chemical Communications; vol. 48; nb. tion 91; (2012); p. 11211 - 11213, View in Reaxys; Dennig, Alexander; Luelsdorf, Nina; Liu, Haifeng; Schwaneberg, Ulrich; Angewandte Chemie - International Edition; vol. 52; nb. 32; (2013); p. 8459 - 8462; Angew. Chem.; vol. 125; nb. 32; (2013); p. 8617 - 8620,4, View in Reaxys; St. Denis, Jeffrey D.; Scully, Conor C. G.; Lee, C. Frank; Yudin, Andrei K.; Organic Letters; vol. 16; nb. 5; (2014); p. 1338 - 1341, View in Reaxys

HPLC (High performance liquid chromatography)

supporting informa- Wei, Carolyn S.; Davies, Geraint H. M.; Soltani, Omid; Albrecht, Jacob; Gao, Qi; Pathirana, tion Charles; Hsiao, Yi; Tummala, Srinivas; Eastgate, Martin D.; Angewandte Chemie - International Edition; vol. 52; nb. 22; (2013); p. 5822 - 5826; Angew. Chem.; vol. 52; nb. 22; (2013); p. 5822 - 5826,5, View in Reaxys

GC (Gas chromatography)

Collins, Karl D.; Glorius, Frank; Tetrahedron; vol. 69; nb. 36; (2013); p. 7817 - 7825, 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 (14) Description (Com- Comment (Compressibility) pressibility)

References

Isothermal compressibility

Jayalakshmi, T.; Reddy, Kalluru S.; Canadian Journal of Chemistry; vol. 63; (1985); p. 2824 2828, View in Reaxys; Abdel-Azim, Abdel-Azim A.; Munk, Petr; Journal of Physical Chemis-

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try; vol. 91; nb. 14; (1987); p. 3910 - 3914, View in Reaxys; Lanshina; Journal of Structural Chemistry; vol. 43; nb. 6; (2002); p. 1006 - 1010, View in Reaxys Adiabatic compressibility

Lucas et al.; Molecular Physics; vol. 18; (1970); p. 505,511,513,515,519,520, View in Reaxys

Adiabatic compres- aus der SchallDshioew; Trudy Stalinirsk. pedagog. Inst.; vol. 7; (1959); p. 1,8; Chem.Abstr.; vol. 56; (1962); p. sibility geschwindigkeit er- 13565, View in Reaxys mittelt bei Temperaturen von 10grad bis 55grad. Adiabatic compres- von 10grad bis sibility 50grad.

Lagemann; McMillan; Woolf; Journal of Chemical Physics; vol. 17; (1949); p. 370, View in Reaxys

Adiabatic compres- bei 20grad. sibility

Lagemann; Evans; McMillan; Journal of the American Chemical Society; vol. 70; (1948); p. 2997, View in Reaxys

Adiabatic compres- von 32.5grad bis sibility 120grad.

Suryaprakasam; Proceedings - Indian Academy of Sciences, Section A; vol. <A> 12; (1941); p. 341,348, View in Reaxys

Adiabatic compres- bei 28grad. sibility

Parthasarathy; Proceedings - Indian Academy of Sciences, Section A; vol. <A> 3; (1936); p. 519,520, View in Reaxys

Isothermal compressibility

von 0grad bis 95grad unter Drucken bis zu 9000 kg/cm2.

Bridgman; Pr. Am. Acad. Arts Sci.; vol. 66; (1931); p. 185,212, View in Reaxys

Isothermal compressibility

bei 25grad.

Shiba; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 16; (1931); p. 212,220, 222; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 3587, View in Reaxys

Isothermal compressibility

bei 30grad.

Shiba; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 16; (1931); p. 212,220, 222; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 3587, View in Reaxys

Adiabatic compres- bei 25grad. sibility

Shiba; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 16; (1931); p. 212,220, 222; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 3587, View in Reaxys

Adiabatic compres- bei 30grad. sibility

Shiba; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 16; (1931); p. 212,220, 222; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 3587, View in Reaxys

Isothermal compressibility

bei 0 und 8 Atm. Ueberdruck bei 8,37grad: 57.2*10E-6 AtmE-1, bei 17.75grad: 62.28*10E-6 AtmE-1.

Schmidt,K.; Annalen der Physik (Weinheim, Germany); vol. <4> 76; (1925); p. 571, View in Reaxys

Isothermal compressibility

zwischen 0 und 500 Biron; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 44; (1912); p. 105; Chem. Atm. bei 0grad: Zentralbl.; vol. 83; nb. I; (1912); p. 1952, View in Reaxys 50.6*10E-6 Atm.E-1.

Conformation (1) Object of Investiga- References tion Conformation

Russel et al.; Journal of the Chemical Society, Chemical Communications; (1977); p. 427, View in Reaxys

Critical Density (1) Critical Density References [g·cm-3] 0.4853

Herz; Archiv der Pharmazie (Weinheim, Germany); (1927); p. 213, View in Reaxys

Critical Pressure (1) References Evans; Tiley; Journal of the Chemical Society [Section] B: Physical Organic; (1966); p. 134, View in Reaxys Critical Temperature (4) Critical TemperaReferences ture [°C] 396.85

Filippov, L. P.; Laushkina, L. A.; Russian Journal of Physical Chemistry; vol. 58; nb. 5; (1984); p. 654 - 656; Zhurnal Fizicheskoi Khimii; vol. 58; (1984); p. 1072 - 1077, View in Reaxys

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Evans; Tiley; Journal of the Chemical Society [Section] B: Physical Organic; (1966); p. 134, View in Reaxys 397.7

Fischer; Reichel; Mikrochemie; vol. 31; (1943); p. 104; Chem.Abstr.; (1945); p. 2675, View in Reaxys

397

Young; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 626; Scientific Proceedings of the Royal Dublin Society; vol. 12; (1909); p. 432, View in Reaxys

Critical Volume (3) Critical Volume [l/ Comment (Critical mol] Volume) 0.324

References Filippov, L. P.; Laushkina, L. A.; Russian Journal of Physical Chemistry; vol. 58; nb. 5; (1984); p. 654 - 656; Zhurnal Fizicheskoi Khimii; vol. 58; (1984); p. 1072 - 1077, View in Reaxys Joliet; Berthon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 260; (1965); p. 2805, View in Reaxys; Bhagvanth Rao et al.; Journal of the Indian Institute of Science; vol. 53; (1971); p. 99,103, View in Reaxys

Crystal Phase (4) Description (Crystal Phase) Crystal structure determination

2.061 cm3/g.

Comment (Crystal Phase)

References

Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys

Solid state structure properties

Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys

Crystal structure determination

a=14.3 Angstroem, Biswas; Acta Crystallographica; vol. 11; (1958); p. 882, View in Reaxys b=11.48 Angstroem, c=7.5 Angstroem, n=8.; aus dem Roentgen-Diagramm ermittelt bei -180grad.

Crystal structure determination

bei -180grad stabile Biswas; Acta Crystallographica; vol. 11; (1958); p. 882, View in Reaxys Kristalle.

Crystal Property Description (2) Colour & Other Location Properties yellow

Page/Page column

colorless

References Patent; CANON KABUSHIKI KAISHA; Kamatani, Jun; Yamada, Naoki; Kosuge, Tetsuya; Horiuchi, Takayuki; Nishide, Yosuke; Miyashita, Hirokazu; Saitoh, Akihito; US2013/33416; (2013); (A1) English, View in Reaxys Patent; Bedekar, Ashutosh Vasant; Ghosh, Kumar Pushpito; Adimurthy, Subbarayyappa; Ramachandraiah, Gadde; US2005/137431; (2005); (A1) English, View in Reaxys; Patent; COUNCIL OF SCIENTIFIC and INDUSTRIAL RESEARCH; WO2005/61423; (2005); (A1) English, View in Reaxys

Crystal System (1) Crystal System References rhombic

Biswas; Acta Crystallographica; vol. 11; (1958); p. 882, View in Reaxys

Decomposition (1) 1 of 1

Ormrod; Hogg; Journal of Chemical Physics; vol. 34; (1961); p. 624,625, View in Reaxys; Kerr; Hogg; Journal of Chemical Physics; vol. 36; (1962); p. 2109,2110, View in Reaxys

Dielectric Constant (35) Dielectric Constant Frequency (Dielectric Constant) [Hz] 5.55

2E+06

Temperature (Dielectric Constant) [°C]

Comment (Dielectric Constant)

References

Laurence, Christian; Nicolet, Pierre; Dalati, M. Tawfik; Abboud, Jose-Luis M.; Notario, Rafael; Journal of Physical Chemistry; vol. 98; nb. 23; (1994); p. 5807 - 5816, View in Reaxys Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys; Gryczinski; Kawski; Zeitschrift fuer Naturforschung,

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Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 30; (1975); p. 287,290, 291, View in Reaxys; Petrov et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 32; (1977); p. 1487,1180,1181,1184, View in Reaxys; Garg; Smyth; Journal of Chemical Physics; vol. 42; (1965); p. 1397,1398, View in Reaxys; Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Hartmann; Schmidt; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 62; (1968); p. 312, View in Reaxys; Foote; Denny; Journal of the American Chemical Society; vol. 93; (1971); p. 5168, View in Reaxys; Bellomo et al.; Annali di Chimica (Rome, Italy); vol. 55; (1965); p. 832,838, View in Reaxys; Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys; Constant et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 1022, View in Reaxys; Magee; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 3093,3098, 3099, View in Reaxys; Deich; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 975,891, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys; Peschel; Schnorrer; Berichte der Bunsen-Gesellschaft; vol. 78; (1974); p. 1294,1295, View in Reaxys; Zaheeruddin; Pakistan Journal of Scientific and Industrial Research; vol. 20; (1977); p. 212, View in Reaxys; Hanna; Abd-El-Nour; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 246; (1971); p. 292,294, View in Reaxys; Ziolo; Kosiba; Acta Physica Polonica, A; vol. 52; (1977); p. 477, View in Reaxys; Lim; Drago; Journal of the American Chemical Society; vol. 94; (1972); p. 84,86, View in Reaxys; Luedde; Riechstoffe und Aromen; vol. 10; (1960); p. 193, View in Reaxys; Korenman; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 380,394, View in Reaxys; Honda; Sasada; Japanese Journal of Applied Physics; vol. 16; (1977); p. 1775,1776-1778, View in Reaxys; Okabayashi; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 163, View in Reaxys; Nigam; Maini; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 14; (1976); p. 605, View in Reaxys; Forest; Smyth; Journal of Physical Chemistry; vol. 69; (1965); p. 1302, View in Reaxys; Imanow; Sul'fugarzade; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 1314; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 2437, View in Reaxys; Imanov et al.; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 681; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1271, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys; Srivastava; Crossley; Canadian Journal of Chemistry; vol. 54; (1976); p. 1418,1420, 1422, View in Reaxys 3E+09

-20 - 60

van Eick; Poley; Appl. scient. Res.; vol. 6; (1957); p. 359,361, View in Reaxys

3.73599E+10

-20 - 60

van Eick; Poley; Appl. scient. Res.; vol. 6; (1957); p. 359,361, View in Reaxys

7.05882E+06

Ebert; Zeitschrift fuer Analytische Chemie; vol. 140; (1953); p. 161,163, View in Reaxys

3E+09

1 - 75

Branin; Smyth; Journal of Chemical Physics; vol. 20; (1952); p. 1121,1124, View in Reaxys

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2018-06-17 20:44:10

4.9

1E+10

Crouch; Journal of Chemical Physics; vol. 16; (1948); p. 364, View in Reaxys

2.95

2.3622E+10

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4093,4096, View in Reaxys

3.08

2.3622E+10

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4093,4096, View in Reaxys

3.08

2.3622E+10

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4093,4096, View in Reaxys

3.18

2.3622E+10

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4093,4096, View in Reaxys

3.62

9.31677E+09

Hennelly; Heston; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4105, View in Reaxys; Laquer; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4097,4100, View in Reaxys

3.92

9.31677E+09

4.06

9.31677E+09

4.16

9.31677E+09

Audsley; Goss; Journal of the Chemical Society; (1941); p. 864,872, View in Reaxys

Le Fevre; Le Fevre; Journal of the Chemical Society; (1936); p. 1130,1136, View in Reaxys; Martin; Transactions of the Faraday Society; vol. 33; (1937); p. 191,195, View in Reaxys

Danforth; Physical Review; vol. <2>38; (1931); p. 1227, View in Reaxys; Wyman; Journal of the American Chemical Society; vol. 56; (1934); p. 543,544, View in Reaxys

-60 - 60

Heil; Physical Review; vol. <2> 39; (1932); p. 666,669, View in Reaxys

10 - 60

Das; Roy; Indian Journal of Physics (1926-1976); vol. 5; (1930); p. 441,459, View in Reaxys

4.92

Kerr; Phil. Mag.; vol. <7> 3; p. 332; Chem. Zentralbl.; vol. 98; nb. II; (1927); p. 388, View in Reaxys

5.4

Williams; Krchma; Journal of the American Chemical Society; vol. 48; (1926); p. 1891; Journal of the American Chemical Society; vol. 49; (1927); p. 1679, View in Reaxys

77/219

2018-06-17 20:44:10

26.6 5.47

Grenacher; Annalen der Physik (Weinheim, Germany); vol. <4> 77; (1925); p. 154, View in Reaxys at:12-14 degreeC.

Walden; Ulich; Werner; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 116; (1925); p. 264, View in Reaxys

4.56

100

Bergholm; Annalen der Physik (Weinheim, Germany); vol. <4>65; (1921); p. 137, View in Reaxys

5.53

Bergholm; Annalen der Physik (Weinheim, Germany); vol. <4>65; (1921); p. 137, View in Reaxys

5.9

Bergholm; Annalen der Physik (Weinheim, Germany); vol. <4>65; (1921); p. 137, View in Reaxys

6.4

-20

Bergholm; Annalen der Physik (Weinheim, Germany); vol. <4>65; (1921); p. 137, View in Reaxys

5.52

Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 44; (1912); p. 692; Chem. Zentralbl.; vol. 83; nb. II; (1912); p. 789, View in Reaxys

20.5

Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 125; Chem. Zentralbl.; vol. 82; nb. I; (1911); p. 955, View in Reaxys

4.64

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

5.21

23.5

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

5.46

1.2

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

5.66

Bugarszky; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 71; (1910); p. 710, View in Reaxys

Dissociation Energy (5) Dissociation Ener- Bond Type gy [Jmol-1]

References

345829

C-Br

Galli, Carlo; Pau, Tullia; Tetrahedron; vol. 54; nb. 12; (1998); p. 2893 - 2904, View in Reaxys

345829

Ph-Br

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

349598

C-Br

Chen, Edward C. M.; Albyn, Keith; Dussack, Laurie; Wentworth, W. E.; Journal of Physical Chemistry; vol. 93; nb. 18; (1989); p. 6827 - 6832, View in Reaxys

5.61

5E+08

Kominar et al.; Canadian Journal of Chemistry; vol. 56; (1978); p. 1589, View in Reaxys 296844

C6H5-Br

Dynamic Viscosity (20) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

Szwarc; Williams; Journal of Chemical Physics; vol. 20; (1952); p. 1171, View in Reaxys; Ladacki; Szwarc; Journal of Chemical Physics; vol. 20; (1952); p. 1814, View in Reaxys References

0.00985

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys; Collins; Raffel; Journal of Chemical Physics; vol. 22; (1954); p. 1728,1732, View in Reaxys; Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 - 135, View in Reaxys

0.007129 - 0.00985

30 - 60

Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 34; nb. 3; (1989); p. 335 - 338, View in Reaxys

78/219

2018-06-17 20:44:10

1.081

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys; Manjeshwar; Aminabhavi; Journal of Chemical and Engineering Data; vol. 33; nb. 2; (1988); p. 184 - 185, View in Reaxys

0.008536

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys

0.01081

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys

0.01128 - 0.02399

-30 - 20

Kesemenli; Izv. Akad. Azerbajdzansk. S.S.R.; nb. 6; (1959); p. 53,54; Chem.Abstr.; (1961); p. 21714, View in Reaxys

0.00967 - 0.02644

-25 - 40

Belinskaja; Uc. Zap. Moskovsk. oblast. pedagog. Inst.; vol. 33; (1955); p. 221,224; Chem.Abstr.; (1958); p. 821, View in Reaxys

0.005941

Babak; Udowenko; Zhurnal Obshchei Khimii; vol. 20; (1950); p. 2124; engl. Ausg. S. 2203, View in Reaxys

0.007683

Babak; Udowenko; Zhurnal Obshchei Khimii; vol. 20; (1950); p. 2124; engl. Ausg. S. 2203, View in Reaxys

0.010619

Babak; Udowenko; Zhurnal Obshchei Khimii; vol. 20; (1950); p. 2124; engl. Ausg. S. 2203, View in Reaxys

0.0074 - 0.0155

1 - 55

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

0.00969

31.2

Ebert; Tschamler; Monatshefte fuer Chemie; vol. 80; (1949); p. 873, View in Reaxys

0.0108

Hennelly; Heston; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4105, View in Reaxys

0.0272

-30.6

Andrade; Pr. phys. Soc. London; vol. 52; (1940); p. 748,753, View in Reaxys

0.01401

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys

0.01196

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

0.01133

19.9

Miller; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 106; (1924); p. 740, View in Reaxys

0.01306

8.8

Miller; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 106; (1924); p. 740, View in Reaxys

0.00385 - 0.01566

-0.1 - 142.5

Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys

0.015

Ssachanow; Rjachowski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 47; (1915); p. 129; Chem. Zentralbl.; vol. 87; nb. I; (1916); p. 729, View in Reaxys; Ssachanow; Rjachowski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 46; (1914); p. 84; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 1625, View in Reaxys

Electrical Data (24) 1 of 24

Description (Electrical Da- Dielectric relaxation time ta) Magee; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 3093,3098, 3099, View in Reaxys; Kramer; Zeitschrift fuer Naturforschung; vol. 15a; (1960); p. 552, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys; Demau et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 212,216, 217, View in Reaxys; Jackson; Simic-Glavaski; Molecular Physics; vol. 18; (1970); p. 393, View in Reaxys; Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys; Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 1; (1991); p. 47 - 51; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 93 101, View in Reaxys

2 of 24

Description (Electrical Da- Dielectric loss ta) Garg; Smyth; Journal of Chemical Physics; vol. 42; (1965); p. 1397,1398, View in Reaxys; Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Garg; Kadaba; Journal of Physical Chemistry; vol. 69; (1965); p. 674, View in Reaxys; Magee; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 3093,3098, 3099, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys; Kramer; Zeitschrift fuer Naturforschung; vol. 15a; (1960); p. 552, View in Reaxys; Forest; Smyth; Journal of Physical Chem-

79/219

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istry; vol. 69; (1965); p. 1302, View in Reaxys; Reid, C. J.; Evans, M. W.; Journal of Chemical Physics; vol. 76; nb. 5; (1982); p. 2576 - 2584, View in Reaxys 3 of 24

Description (Electrical Da- Electrical properties ta) Madan; Canadian Journal of Physics; vol. 51; (1973); p. 1815,1817,1818, View in Reaxys; Kastha et al.; Indian Journal of Physics (1926-1976); vol. 41; (1967); p. 313,319, View in Reaxys; Sinha et al.; Indian Journal of Physics (1926-1976); vol. 40; (1966); p. 101,114, View in Reaxys; Bhattacharyya et al.; Indian Journal of Physics (1926-1976); vol. 40; (1966); p. 187,191, View in Reaxys; Mitra; Misra; Mehrotra; Indian Journal of Pure and Applied Physics; vol. 16; nb. 6; (1978); p. 604 - 607, View in Reaxys

4 of 24

Description (Electrical Da- Cole-Cole diagram ta) Poley; Chem. Weekb.; vol. 52; (1956); p. 464,466, View in Reaxys; Heineken; Bruin; Physica; vol. 23; (1957); p. 57,60, View in Reaxys; Baba; Kamiyoshi; Journal of Physical Chemistry; vol. 81; (1977); p. 1872,1874, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys

5 of 24

Description (Electrical Da- Electrical conductivity ta) Di Ciommox; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 44; (1903); p. 508, View in Reaxys; Kopylev et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 1571; ; p. 2955, View in Reaxys; Ahmed et al.; Journal of Applied Chemistry; vol. 20; (1970); p. 109, View in Reaxys; Kopylov; Yanchenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 243; ; p. 421, View in Reaxys; Kopylov et al.; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 262; ; p. 491, View in Reaxys; Romanez; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 592; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1102, View in Reaxys; Kopylov; Trofimova; Sov. Phys. J. (Engl. Transl.); vol. 9; nb. 1; (1966); p. 85,53, View in Reaxys

6 of 24

Description (Electrical Da- Dielectric anisotropy ta) Ziolo; Piotrowska-Szczepaniak; Acta Physica Polonica; vol. 35; (1969); p. 949, View in Reaxys

7 of 24

Description (Electrical Da- Photoconductivity ta) Kopylov; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 24; (1960); p. 223; ; p. 237, View in Reaxys; Romanez; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 592; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1102, View in Reaxys

8 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Loesungen in Benzol bei 30grad Wellenlaengen von 1,22 cm bis 3,21 cm. Rao; Journal of Scientific and Industrial Research; vol. 18 B; (1959); p. 133,135, View in Reaxys

9 of 24

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Benzol geloestem Brombenzol bei 30grad. Rao; Journal of Scientific and Industrial Research; vol. 18 B; (1959); p. 133,135, View in Reaxys; Murty; Rao; Journal of Scientific and Industrial Research; vol. 15 B; (1956); p. 346,349; Current Science; vol. 25; (1956); p. 49, View in Reaxys

10 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von unverduenntem Brombenzol bei Temperaturen von -20grad bis +60grad und Wellenlaengen von 0.803 cm bis 10cm. van Eick; Poley; Appl. scient. Res.; vol. 6; (1957); p. 359,361, View in Reaxys

11 of 24

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von unverduenntem Brombenzol bei Temperaturen von -20grad bis +60grad. van Eick; Poley; Appl. scient. Res.; vol. 6; (1957); p. 359,364, View in Reaxys

12 of 24

Description (Electrical Da- Dielectric strength ta) Comment (Electrical Data) bei 20grad. Musset et al.; Z. ang. Phys.; vol. 8; (1956); p. 8,10, View in Reaxys

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13 of 24

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Tetrachlormethan geloestem Brombenzol bei 24grad. Le Fevre; Sullivan; Journal of the Chemical Society; (1954); p. 2873,2876, View in Reaxys

14 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von unverduenntem Brombenzol bei Temperaturen von 1grad bis 75grad und 10 cm Wellenlaenge. Branin; Smyth; Journal of Chemical Physics; vol. 20; (1952); p. 1121,1124, View in Reaxys

15 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Loesungen in Cyclohexan bzw. in Benzol bei 20grad Wellenzahlen von 1,6 cmE-1 bis 0.606 cmE-1 bzw. von 1.60 cmE-1 bis 0.274 cmE-1. Whiffen; Transactions of the Faraday Society; vol. 46; (1950); p. 130,135, View in Reaxys

16 of 24

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Cyclohexan und in Benzol geloestem Brombenzol bei 20grad. Whiffen; Transactions of the Faraday Society; vol. 46; (1950); p. 130,135, View in Reaxys

17 of 24

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von Loesungen in Benzol. Fischer; Zeitschrift fuer Naturforschung; vol. 4 a; (1949); p. 707,716; Naturwissenschaften; vol. 43; (1956); p. 153, View in Reaxys

18 of 24

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von fluessigem Brombenzol. Hennelly; Heston; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4105, View in Reaxys

19 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von fluessigem Brombenzol im Bereich der cm-Wellen. Hennelly; Heston; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4105, View in Reaxys

20 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Loesungen in Benzol. Whiffen; Thompson; Transactions of the Faraday Society; vol. 42 A; (1946); p. 118; Chem.Abstr.; (1949); p. 6018, View in Reaxys; Powles; Transactions of the Faraday Society; vol. 44; (1948); p. 537,541, 543, View in Reaxys; Jackson; Powles; Transactions of the Faraday Society; vol. 42 A; (1946); p. 101,105, View in Reaxys

21 of 24

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Loesungen in Cyclohexan-Paraffin-Gemischen. Whiffen; Thompson; Transactions of the Faraday Society; vol. 42 A; (1946); p. 118; Chem.Abstr.; (1949); p. 6018, View in Reaxys

22 of 24

Description (Electrical Da- Dielectric strength ta) Comment (Electrical Data) des mit Stickstoff verduennten Dampfes. Charlton; Cooper; Gen. Electric Rev.; vol. 40; (1937); p. 438,440, View in Reaxys

23 of 24

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) Brombenzol zeigt bei 0grad keine elektrische Leitfaehigkeit.

81/219

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Wertyporoch; Adamus; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 31,34, 35, 40, View in Reaxys 24 of 24

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) bei 25grad. Rabinowitsch; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 119; (1926); p. 64; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 58; (1926); p. 230, View in Reaxys

Electrical Moment (61) 1 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.28

Borovikov; Makovetskii; Pivovarova; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 1; (1996); p. 33 - 38, View in Reaxys 2 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.45

Nurok, David; Kleyle, Robert M.; Hajdu, Paul; Ellsworth, Brenda; Myers, Steven S.; Brogan, Terrance M.; Lipkowitz, Kenneth B.; Glen, Robert C.; Analytical Chemistry; vol. 67; nb. 23; (1995); p. 4423 - 4430, View in Reaxys 3 of 61

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

hexane

Comment (Electrical Moment)

Dipole moment (range begins): 5.9E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 4 of 61

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

dodecane

Comment (Electrical Moment)

Dipole moment (range begins): 5.9E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 5 of 61

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

CCl4

Comment (Electrical Moment)

Dipole moment (range begins): 5.6E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 6 of 61

Description (Electrical Moment)

Dipole moment

82/219

2018-06-17 20:44:10

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

benzene

Comment (Electrical Moment)

Dipole moment (range begins): 5.8E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 7 of 61

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

dioxane

Comment (Electrical Moment)

Dipole moment (range begins): 5.7E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 8 of 61

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

pentane

Comment (Electrical Moment)

Dipole moment (range begins): 5.6E30 C*m; Dipole moment (range ends): 5.8E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 9 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.41

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

dioxane

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 10 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.42

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

CCl4

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.53

83/219

2018-06-17 20:44:10

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

benzene

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.53

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

dodecane

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.68

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

hexane

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.72

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

pentane

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.5

Temperature (Electrical Moment) [°C]

24.9

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

benzene

Kisilenko, A. A.; Zeikan', A. A.; Vdovenko, S. I.; Kukhar', V. P.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 17; nb. 7; (1981); p. 684 - 689; Khimiya Geterotsiklicheskikh Soedinenii; nb. 7; (1981); p. 927 - 931, View in Reaxys 16 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.6

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2018-06-17 20:44:10

Temperature (Electrical Moment) [°C]

24.9

Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

dioxane

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Hexan

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 18 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Cyclohexan

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 19 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in CCl4

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 20 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Benzol

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 21 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Toluol

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 22 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in CS2

Vuks; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 70; ; p. 134, View in Reaxys 23 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

E.A Mazurenko, Extraction Handbook <in Russ.>, Tekhnika, Kiev (1972) und/oder J.Hildebrand, R.Scott, The Solubility of Nonelectrolytes, New York (1950)

Petrov et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 32; (1977); p. 1487,1180,1181,1184, View in Reaxys 24 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

bei 20grad: 1.70 D

Bonnet; Barriol; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 74; (1977); p. 600,602, View in Reaxys 25 of 61

Description (Electrical Moment)

Dipole moment

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Comment (Electrical Moment)

bei 22grad: 1.72 D

Bonnet; Barriol; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 74; (1977); p. 600,602, View in Reaxys 26 of 61

Description (Electrical Moment)

Dipole moment

Dube; Parshad; Journal of Physical Chemistry; vol. 73; (1969); p. 3236, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys; Mermillod-Blardet; Mauret; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 278; (1974); p. 633, View in Reaxys; Kramer; Zeitschrift fuer Naturforschung; vol. 15a; (1960); p. 552, View in Reaxys; Hanna; Abd-El-Nour; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 246; (1971); p. 292,294, View in Reaxys; Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys; Srivastava; Crossley; Canadian Journal of Chemistry; vol. 54; (1976); p. 1418,1420, 1422, View in Reaxys; Cumper; Tetrahedron; vol. 25; (1969); p. 3131, View in Reaxys 27 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Cyclohexan u. Benzol (μ)

Srivastava; Talesara; Journal of the Indian Chemical Society; vol. 52; (1975); p. 365, View in Reaxys 28 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys 29 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ, aus McChellan: Tables of experimental dipole moments, London: W.H.Freeman and Co 1963

Khosla et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 251; (1972); p. 129,130, 135, View in Reaxys 30 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ(B), μ(Liq)

Meyyappan; Aranachalam; Journal of the Indian Chemical Society; vol. 49; (1972); p. 1047, View in Reaxys 31 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (S. 572) nach Ref. 8: J. W. Smith in 'Electric Dipol 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 32 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Tab.VI

Allinger et al.; Journal of Organic Chemistry; vol. 36; (1971); p. 2747, View in Reaxys 33 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.56

Jain; Walker; Journal of Physical Chemistry; vol. 75; (1971); p. 2942, View in Reaxys 34 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Temp.abh. v. μ, μ2 (Tab.3)

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Nigam et al.; Indian Journal of Chemistry; vol. 8; (1970); p. 908,910, View in Reaxys 35 of 61

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 36 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

π (Bzl.) bei 25grad: 2.70D

Franchini; Transactions of the Faraday Society; vol. 63; (1967); p. 2610,2613, View in Reaxys 37 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

unverd.

Vaks; Sov. Phys. Dokl. (Engl. Transl.); vol. 12; (1967); p. 801,325, View in Reaxys 38 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

π (p-Xylol) bei 15grad: 1.59D

Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys 39 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

π (p-Xylol) bei 60grad: 1.58D

Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys 40 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.58D (π; CCl4, 20grad)

Goetz et al.; Justus Liebigs Annalen der Chemie; vol. 681; (1965); p. 1,2,8, View in Reaxys 41 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

C-H Bindung (aus IR-Intensit.)

Cole; Michell; Spectrochimica Acta; vol. 20; (1964); p. 739,742, View in Reaxys 42 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.48D (π, Dioxan)

Thompson; Hallberg; Journal of Physical Chemistry; vol. 67; (1963); p. 2486, View in Reaxys 43 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ:1.55D (Bzl., 30grad)

Baliah,V.; Uma,M.; Tetrahedron; vol. 19; (1963); p. 455 - 464, View in Reaxys 44 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.73D

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Deitsch; Russian Journal of Physical Chemistry; vol. 36; (1962); p. 959; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 1777, View in Reaxys 45 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.52D

Anantakrishnan; Setu Rao; Current Science; vol. 29; (1960); p. 51, View in Reaxys 46 of 61

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.57D (π, Bzl.)

Cumper; Vogel; Journal of the Chemical Society; (1960); p. 4723,4725, View in Reaxys 47 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.7

Method (Electrical Moment)

Dielectric constant (π)

Le Fevre; Rao; Australian Journal of Chemistry; vol. 8; (1955); p. 140, View in Reaxys 48 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.51

Method (Electrical Moment)

Dielectric constant (π)

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 49 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.56

Solvent (Electrical Moment)

benzene

Hoejendahl; Phys. Z.; vol. 30; p. 394; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 1898, View in Reaxys; Hoejendahl; Nature (London, United Kingdom); vol. 117; p. 892; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 1114, View in Reaxys; Littlejohn; Smith; Journal of the Chemical Society; (1953); p. 2456,2457, View in Reaxys 50 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.54

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

benzene

Brown; De Vries; Journal of the American Chemical Society; vol. 73; (1951); p. 1811, View in Reaxys; Whiffen; Transactions of the Faraday Society; vol. 46; (1950); p. 130,135, View in Reaxys 51 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.55

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Method (Electrical Moment)

Dielectric constant (π)

Solvent (Electrical Moment)

benzene

Brown; De Vries; Journal of the American Chemical Society; vol. 73; (1951); p. 1811, View in Reaxys; Whiffen; Transactions of the Faraday Society; vol. 46; (1950); p. 130,135, View in Reaxys 52 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.55

Method (Electrical Moment)

Microwave absorption

Solvent (Electrical Moment)

cyclohexane

Whiffen; Transactions of the Faraday Society; vol. 46; (1950); p. 130,135, View in Reaxys 53 of 61

Description (Electrical Moment)

Bond moment

Cole; Thompson; Transactions of the Faraday Society; vol. 46; (1950); p. 103,107, View in Reaxys 54 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.77

Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2212,2214, View in Reaxys 55 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.58

Solvent (Electrical Moment)

dioxane

Brooks; Hobbs; Journal of the American Chemical Society; vol. 62; (1940); p. 2851,2852, View in Reaxys 56 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.53

Solvent (Electrical Moment)

benzene

Cowley; Partington; Journal of the Chemical Society; (1937); p. 130,131, View in Reaxys 57 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.53

Solvent (Electrical Moment)

CCl4

Das; Roy; Indian Journal of Physics (1926-1976); vol. 5; (1930); p. 441,459, View in Reaxys; Cowley; Partington; Journal of the Chemical Society; (1937); p. 130,131, View in Reaxys 58 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.6

Solvent (Electrical Moment)

hexane

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Sutton; Hampson; Transactions of the Faraday Society; vol. 31; (1935); p. 945,957, View in Reaxys; Cowley; Partington; Journal of the Chemical Society; (1937); p. 130,131, View in Reaxys 59 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.55

Solvent (Electrical Moment)

benzene

Le Fevre; Le Fevre; Journal of the Chemical Society; (1936); p. 1130,1136, View in Reaxys; Otto; Wenzke; Industrial and Engineering Chemistry, Analytical Edition; vol. 6; (1934); p. 187, View in Reaxys 60 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.71

Groves; Sugden; Journal of the Chemical Society; (1935); p. 971,972; Journal of the Chemical Society; (1937); p. 1992,1996, View in Reaxys 61 of 61

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.52

Solvent (Electrical Moment)

benzene

Mueller; Sack; Phys. Z.; vol. 31; (1930); p. 815,820, View in Reaxys Electrical Polarizability (2) Description (Elec- References trical Polarizability) Optical anisotropy

Unanue,A.; Bothorel,P.; Bulletin de la Societe Chimique de France; (1964); p. 573 - 578, View in Reaxys; Le Fevre; Rao; Journal of the Chemical Society; (1958); p. 1465, View in Reaxys; Canselier; Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 880,882, View in Reaxys; Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 626, View in Reaxys; Saiz et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p. 1538,1540, 1541, 1545, View in Reaxys; Aroney et al.; Australian Journal of Chemistry; vol. 18; (1965); p. 1501,1504, View in Reaxys; Lucas et al.; Molecular Physics; vol. 18; (1970); p. 505,511,513,515,519,520, View in Reaxys

Molar polarization

Canselier; Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 880,882, View in Reaxys; Mermillod-Blardet; Mauret; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 278; (1974); p. 633, View in Reaxys

Electrochemical Behaviour (4) Description (Elec- References trochemical Behaviour) Thermodynamic parameters for dissociation / protonation

Wenthold; Squires; Journal of Mass Spectrometry; vol. 30; nb. 1; (1995); p. 17 - 24, View in Reaxys

Polarography

Jakobson; Petrow; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk; vol. 7; (1965); p. 75,78, View in Reaxys; Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys; Parkanyi; Zahradnik; Collection of Czechoslovak Chemical Communications; vol. 30; (1965); p. 4287,4290, View in Reaxys

Proton affinity

Klotz; Drost; Organic Mass Spectrometry; vol. 6; (1972); p. 647,651, View in Reaxys

Electrochemical properties

van der Ziel et al.; Physical Review Letters; vol. 15; (1965); p. 190,192, View in Reaxys

Electrochemical Characteristics (18) 1 of 18

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

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Argueello, Juan E.; Penenory, Alicia B.; Journal of Organic Chemistry; vol. 68; nb. 6; (2003); p. 2362 - 2368, View in Reaxys 2 of 18

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

Budnikova; Kafiyatullina; Kargin; Sinyashin; Russian Journal of General Chemistry; vol. 71; nb. 2; (2001); p. 231 - 233, View in Reaxys 3 of 18

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Enemaerke, Rasmus J.; Christensen, Torben B.; Jensen, Henrik; Daasbjerg, Kim; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2001); p. 1620 - 1630, View in Reaxys 4 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

Potential: -2.44 V. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: 0.1 M nBu4BF4, vs. SCE

Product

bromobenzene radical anion

Pause, Laurence; Robert, Marc; Saveant, Jean-Michel; Journal of the American Chemical Society; vol. 121; nb. 30; (1999); p. 7158 - 7159, View in Reaxys 5 of 18

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

tetrahydrofuran

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-2.2 V; Product: /BRN= 7526038/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: vs. SCE

Product

bromobenzene radical anion

Galli, Carlo; Gentili, Patrizia; Acta Chemica Scandinavica; vol. 52; nb. 1; (1998); p. 67 - 76, View in Reaxys 6 of 18

Description (Electrochemical Characteristics)

redox potential

Jennings et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 719,720, 721, 722, View in Reaxys; Budnikova; Petrukhina; Kargin; Russian Journal of General Chemistry; vol. 66; nb. 10; (1996); p. 1645 - 1648, View in Reaxys 7 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Sease,J.W. et al.; Journal of the American Chemical Society; vol. 90; nb. 10; (1968); p. 2595 - 2598, View in Reaxys; O'Reilly; Elving; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 75; (1977); p. 507,509, View in Reaxys; Polievktov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 1322,1161,1163, View in Reaxys; Loutfy; Yip; Canadian Journal of Chemistry; vol. 51; (1973); p. 1881,1882, View in Reaxys; Fry; Krieger; Journal of Organic Chemistry; vol. 41; (1976); p. 54,55, View in Reaxys; Sease; Reed; Tetrahedron Letters; (1975); p. 393,394, View in Reaxys; Hussey; Diefenderfer; Journal of the American Chemical Society; vol. 89; (1967); p. 5359,5360, View in Reaxys; Lewitzka, F.; Loehmannsroeben, H.-G.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 169; nb. 2; (1990); p. 181 - 202, View in Reaxys; Rogers, Harold R.; Rogers, Randall J.; Mitchell, H. Lee; Whitesides, George M.; Journal of the American Chemical Society; vol. 102; nb. l; (1980); p. 231 - 238, View in Reaxys; Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys; Yanilkin, V. V.; Maksimyuk, N. I.; Kargin, Yu. M.; Russian Chemical Bulletin; vol. 43; nb. 6; (1994); p. 957 - 959; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 6; (1994); p. 1022 - 1024, View in Reaxys

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8 of 18

Description (Electrochemical Characteristics)

oxidation potential

Neikam et al.; Journal of the Electrochemical Society; vol. 111; (1964); p. 1190, View in Reaxys; Magdesieva, T.V.; Shishkin, V.N.; Butin, K.P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 11.1; (1991); p. 2400 - 2403,2227 - 2229, View in Reaxys; Butin, K. P.; Moiseeva, A. A.; Magdesieva, T. V.; Sergeeva, E. V.; Rozenberg, V. I.; Kharitonov, V. G.; Russian Chemical Bulletin; vol. 43; nb. 5; (1994); p. 783 - 789; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 5; (1994); p. 839 845, View in Reaxys 9 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-1.81 V; Product: /BRN= 969212/. Method: potentiometry. Description: vs Ag/AgBr

Product

benzene

Liu, Yumin; Schwartz, Jeffrey; Journal of Organic Chemistry; vol. 59; nb. 5; (1994); p. 940 - 942, View in Reaxys 10 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

24.9

Comment (Electrochemical Characteristics)

-2.7 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: polarography. Description: working electrodes: DME and HDME; reference electrodes: Ag/AgNO3; Pt sheet as the counter electrode; Bu4NClO4 as supporting electrolyte

Product

benzene

Andreoli, Roberto; Gavioli, Giovanna Battistuzzi; Borsari, Marco; Fontanesi, Claudio; Journal of the Chemical Society, Faraday Transactions; vol. 90; nb. 21; (1994); p. 3241 - 3244, View in Reaxys 11 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Temperature (Electrochemical Characteristics) [°C]

24.9

Comment (Electrochemical Characteristics)

-2.61 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: polarography. Description: working electrodes: DME and HDME; reference electrodes: Ag/AgCl, KClsat; Pt sheet as the counter electrode; Bu4NClO4 as supporting; electrolyte

Product

benzene

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

24.9

Comment (Electrochemical Characteristics)

-2.63 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: polarography. Description: working electrodes: DME and HDME; reference electrodes: Ag/AgCl, NaClsat; Pt sheet as the counter electrode; Bu4NClO4 as supporting; electrolyte

Product

benzene

Andreoli, Roberto; Gavioli, Giovanna Battistuzzi; Borsari, Marco; Fontanesi, Claudio; Journal of the Chemical Society, Faraday Transactions; vol. 90; nb. 21; (1994); p. 3241 - 3244, View in Reaxys

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13 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

ethanol

Temperature (Electrochemical Characteristics) [°C]

24.9

Comment (Electrochemical Characteristics)

-2.68 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: polarography. Description: working electrodes: DME and HDME; reference electrodes: Hg/Hg2Cl2, KClsat; Pt sheet as the counter electrode; Bu4NClO4 as supporting; electrolyte

Product

benzene

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-2.55 V; Product: /BRN= 3587306/. No. of transm. electrons: 1. Method: voltammetry. Description: Hg cathode, silver chloride electrode as reference; 0.05 M Bu4NBF4

Product

phenyl radical

Magdesieva, T.V.; Shishkin, V.N.; Butin, K.P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 11.1; (1991); p. 2403 2405,2230 - 2232, View in Reaxys 15 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-1.87 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: polarography. Description: tetraethylammonium perchlorate as supporting electrolyte

Product

benzene

Casado, Juan; Ortega, Manuel; Gallardo Iluminada; Collection of Czechoslovak Chemical Communications; vol. 54; nb. 4; (1989); p. 911 - 921, View in Reaxys 16 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-1.89 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: polarography. Description: tetraethylammonium perchlorate as supporting electrolyte, ein the presence of phenol

Product

benzene

Casado, Juan; Ortega, Manuel; Gallardo Iluminada; Collection of Czechoslovak Chemical Communications; vol. 54; nb. 4; (1989); p. 911 - 921, View in Reaxys 17 of 18

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

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Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

2.62 V; Product: /BRN= 969212/. No. of transm. electrons: 1. Method: polarography. Description: dropping mercury electrode; 0.05 M tetrabutylammonium perchlorate

Product

benzene

Butin, K. P.; Ivkina, A. A.; Shishkin, V. N.; Tanaseichuk, B. S.; Reutov, O. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 32; nb. 1; (1983); p. 82 - 88; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 1; (1983); p. 98 - 104, View in Reaxys 18 of 18

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Heyrovsky; Sorm; Forejt; Collection of Czechoslovak Chemical Communications; vol. 12; (1947); p. 16; Chem.Abstr.; (1947); p. 5402, View in Reaxys; v. Stackelberg; Stracke; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 53; (1949); p. 118,121, View in Reaxys; Lewin; Fodiman; Zhurnal Fizicheskoi Khimii; vol. 28; (1954); p. 601,605; Chem.Abstr.; (1954); p. 11218, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Jordan et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 7189, View in Reaxys

Energy Data (MCS) (34) 1 of 34

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.85

Partner (Energy Data (MCS))

fullerene-C6 0

Korobov, Mikhail V.; Mirakyan, Andrej L.; Avramenko, Natalia V.; Olofsson, Gerd; Smith, Allan L.; Ruoff, Rodney S.; Journal of Physical Chemistry B; vol. 103; nb. 8; (1999); p. 1339 - 1346, View in Reaxys 2 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 30

Partner (Energy Data (MCS))

cyclohexanone

Yang, X. N.; Zhang, J. H.; Journal of Chemical Thermodynamics; vol. 26; nb. 5; (1994); p. 449 - 456, View in Reaxys 3 of 34

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

water

Borisover, M. D.; Baitalov, F. D.; Solomonov, B. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 12.1; (1991); p. 2629 2638,2436 - 2443, View in Reaxys 4 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

130

Partner (Energy Data (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-propyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb. 3; (1989); p. 280 - 284, View in Reaxys 5 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

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Temperature (Energy Data (MCS)) [°C]

130

Partner (Energy Data (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-butyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb. 3; (1989); p. 280 - 284, View in Reaxys 6 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

130

Partner (Energy Data (MCS))

Bis(3-((4-(propoxycarbonyl)-2,3,5,6-tetrachlorobenzoyl)oxy)propyl)tetrachloroterephthalate

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb. 3; (1989); p. 280 - 284, View in Reaxys 7 of 34

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 8 of 34

Description (Energy Data (MCS))

Enthalpy of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

fluorobenzene

Otin, S.; Fernandez, J.; Veamonte, M.; Velasco, I.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 18; nb. 6; (1986); p. 571 - 574, View in Reaxys 9 of 34

Description (Energy Data (MCS))

Enthalpy of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

chlorobenzene

Otin, S.; Fernandez, J.; Veamonte, M.; Velasco, I.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 18; nb. 6; (1986); p. 571 - 574, View in Reaxys 10 of 34

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 11 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

4- methyl-2-pentanone

Jayalakshmi, T.; Reddy, Kalluru S.; Canadian Journal of Chemistry; vol. 63; (1985); p. 2824 - 2828, View in Reaxys

95/219

2018-06-17 20:44:10

12 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

4- methyl-2-pentanone

Jayalakshmi, T.; Reddy, Kalluru S.; Canadian Journal of Chemistry; vol. 63; (1985); p. 2824 - 2828, View in Reaxys 13 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

benzene

Otin, S.; Toledo, M. J.; Munoz, J.; Velasco, I.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 17; nb. 10; (1985); p. 935 - 940, View in Reaxys 14 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

toluene

Otin, S.; Toledo, M. J.; Munoz, J.; Velasco, I.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 17; nb. 10; (1985); p. 935 - 940, View in Reaxys 15 of 34

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 16 of 34

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

cyclohexane

Solomonov, B. N.; Antipin, I. S.; Novikov, V. B.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 52; nb. 12; (1982); p. 2681 - 2688,2364 - 2370, View in Reaxys 17 of 34

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 18 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

cyclohexane

Murakami, Sachio; Kimura, Fumio; Polish Journal of Chemistry; vol. 54; nb. 10; (1980); p. 2011 - 2018, View in Reaxys

96/219

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19 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

benzene

Murakami, Sachio; Kimura, Fumio; Polish Journal of Chemistry; vol. 54; nb. 10; (1980); p. 2011 - 2018, View in Reaxys 20 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

para-xylene

Murakami, Sachio; Kimura, Fumio; Polish Journal of Chemistry; vol. 54; nb. 10; (1980); p. 2011 - 2018, View in Reaxys 21 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

toluene

Murakami, Sachio; Kimura, Fumio; Polish Journal of Chemistry; vol. 54; nb. 10; (1980); p. 2011 - 2018, View in Reaxys 22 of 34

Description (Energy Data (MCS))

Excess thermochemical parameter

Nigam et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 159,160 - 162, View in Reaxys; Mahl et al.; Journal of Chemical Thermodynamics; vol. 9; (1977); p. 61,62, 63, View in Reaxys; Moerke et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 252; (1973); p. 323,325, View in Reaxys; Wilhelm et al.; Thermochimica Acta; vol. 31; (1979); p. 85,88,89, View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 77; (1973); p. 263, View in Reaxys 23 of 34

Description (Energy Data (MCS))

Enthalpy of solution

Solomonov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 2329,2113, View in Reaxys; Fuchs; Rodewald; Journal of the American Chemical Society; vol. 95; (1973); p. 5897,5898, View in Reaxys; Fuchs et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 4705, View in Reaxys; Butler et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 1153,1157,1158, View in Reaxys; Krishnan; Friedman; Journal of Physical Chemistry; vol. 75; (1971); p. 3606, View in Reaxys; Kozlova et al.; Theoretical and Experimental Chemistry; vol. 8; (1972); p. 465; ; p. 558, View in Reaxys 24 of 34

Description (Energy Data (MCS))

Thermodynamic properties of system with

Khosla et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 251; (1972); p. 129,130, 135, View in Reaxys; Moerke et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 252; (1973); p. 323,325, View in Reaxys; Langer; Parnell; Journal of Physical Chemistry; vol. 70; (1966); p. 904, View in Reaxys 25 of 34

Description (Energy Data (MCS))

Enthalpy of mixtures

Deshpande; Pandya; Transactions of the Faraday Society; vol. 63; (1967); p. 2346, View in Reaxys 26 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

Neumann; v. Weber; Journal fuer Praktische Chemie (Leipzig); vol. 19; (1963); p. 206,209, View in Reaxys 27 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

benzene

Canning; Cheesman; Journal of the Chemical Society; (1955); p. 1230,1231, View in Reaxys 28 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

97/219

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Partner (Energy Data (MCS))

toluene

Canning; Cheesman; Journal of the Chemical Society; (1955); p. 1230,1231, View in Reaxys 29 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

chlorobenzene

Kremann; Meingast; Gugl; Monatshefte fuer Chemie; vol. 35; (1914); p. 1304, View in Reaxys; Canning; Cheesman; Journal of the Chemical Society; (1955); p. 1230,1231, View in Reaxys 30 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

chloroform

Tamres; Journal of the American Chemical Society; vol. 74; (1952); p. 3375,3376, View in Reaxys 31 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

tetrachloromethane

Tamres; Journal of the American Chemical Society; vol. 74; (1952); p. 3375,3376, View in Reaxys 32 of 34

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

ethanol

Schulze; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 197; (1951); p. 105,112, View in Reaxys 33 of 34

Description (Energy Data (MCS))

Enthalpy of mixtures

Partner (Energy Data (MCS))

benzene

Biron; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 42; (1910); p. 178; Chem. Zentralbl.; vol. 81; nb. I; (1910); p. 1913, View in Reaxys 34 of 34

Description (Energy Data (MCS))

Enthalpy of mixtures

Partner (Energy Data (MCS))

chlorobenzene

Biron; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 42; (1910); p. 178; Chem. Zentralbl.; vol. 81; nb. I; (1910); p. 1913, View in Reaxys Enthalpy of Formation (1) References Holm; Journal of Organometallic Chemistry; vol. 56; (1973); p. 87,90, View in Reaxys; Williams; Bowen; Organic Mass Spectrometry; vol. 11; (1976); p. 223,224, View in Reaxys; Speranza et al.; Journal of the American Chemical Society; vol. 99; (1977); p. 5583,5588, View in Reaxys; Halliwell; Nyburg; Journal of the Chemical Society; (1960); p. 4603,4607, View in Reaxys Enthalpy of Fusion (2) Enthalpy of Fusion References [Jmol-1] 10634.5

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys

8373.6

Timmermans; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 637, View in Reaxys

Enthalpy of Vaporization (6) Enthalpy of Vapori- Temperature (Enzation [Jmol-1] thalpy of Vaporization) [°C] 43900

References

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

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38518.5

156

37932.4 37884.2

Silberman-Granowsskaja; Schugam; Zhurnal Fizicheskoi Khimii; vol. 14; (1940); p. 1004; Chem.Abstr.; (1941); p. 3867, View in Reaxys 154.8

38061.7 45509.7

Al-Dhahir, Adnan A. Karim; Swan, Idris M.; Journal of the Indian Chemical Society; vol. 59; nb. 5; (1982); p. 645 - 653, View in Reaxys

Mathews; Journal of the American Chemical Society; vol. 48; (1926); p. 572, View in Reaxys Nagornow; Rotinjanz; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 77; (1911); p. 704, View in Reaxys

Dreisbach,R.R.; Physical Properties of Chemical Compounds (= Advances in Chemistry Series Nr. 15) <Washington 1955> S. 150, View in Reaxys

Further Information (173) Description (FurReferences ther Information) Further information Korostelev et al.; Journal of Applied Spectroscopy; vol. 31; (1979); p. 1562,1564, View in Reaxys Further information Medved et al.; Organic Mass Spectrometry; vol. 14; (1979); p. 307,309, View in Reaxys Further information Leung; Harrison; Journal of the American Chemical Society; vol. 101; (1979); p. 3168,3172, View in Reaxys Further information Anisimov et al.; Chemical Physics; vol. 44; (1979); p. 367, View in Reaxys Further information Vuks; Optics and Spectroscopy; vol. 47; (1979); p. 502; Optika i Spektroskopiya; p. 907, View in Reaxys Further information Shanmugasundaram; Acta Chimica Academiae Scientiarum Hungaricae; vol. 96; (1978); p. 151,154, 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 Polumbrik; Serguchev; Theoretical and Experimental Chemistry; vol. 14; (1978); p. 104; ; p. 130, View in Reaxys Further information Lund et al.; Chemical Physics; vol. 28; (1978); p. 167,169, View in Reaxys Further information Chen et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 7243,7244, 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 O'Reilly; Elving; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 75; (1977); p. 507,509, View in Reaxys Further information Bouchoux; Organic Mass Spectrometry; vol. 12; (1977); p. 681, View in Reaxys Further information Oudar et al.; Journal of Chemical Physics; vol. 67; (1977); p. 1626,1630, View in Reaxys Further information Clark; Kolb; Journal of Organic Chemistry; vol. 42; (1977); p. 359,360, View in Reaxys Further information Korostelev et al.; Journal of Applied Spectroscopy; vol. 27; (1977); p. 1487, View in Reaxys Further information Bertucci et al.; Journal of Chemical Physics; vol. 66; (1977); p. 605,612, View in Reaxys Further information Bendig; Kreysig; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 1176, View in Reaxys Further information Uno et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 33; (1977); p. 607,610, 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 Fry; Krieger; Journal of Organic Chemistry; vol. 41; (1976); p. 54,55, View in Reaxys Further information Rouch et al.; Acta Physica Polonica, A; vol. 50; (1976); p. 503,510,512, View in Reaxys Further information Baldwin et al.; Organic Mass Spectrometry; vol. 11; (1976); p. 1181,1182, View in Reaxys Further information Klimasheva et al.; Optics and Spectroscopy; vol. 40; (1976); p. 141; ; p. 245, View in Reaxys Further information Raetsch; Patz; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 257; (1976); p. 520,522, View in Reaxys Further information Adler; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 427; (1976); p. 247,256, View in Reaxys Further information Hemminger et al.; Journal of Chemical Physics; vol. 65; (1976); p. 2798,2801, View in Reaxys Further information Levine; Bethea; Journal of Chemical Physics; vol. 63; (1975); p. 2666,2675, View in Reaxys Further information Levine; Journal of Chemical Physics; vol. 63; (1975); p. 115, View in Reaxys Further information Sease; Reed; Tetrahedron Letters; (1975); p. 393,394, View in Reaxys

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Further information Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys Further information Bertucci; Flygare; Journal of Chemical Physics; vol. 63; (1975); p. 1, View in Reaxys Further information Namiki et al.; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 3073,3076,3077, View in Reaxys Further information Bitman et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 1361,1336,1337, View in Reaxys Further information Lin et al.; Journal of Chemical Physics; vol. 60; (1974); p. 4994,4997, View in Reaxys Further information Gol'danskii et al.; Sov. Phys. Dokl. (Engl. Transl.); vol. 18; (1974); p. 316,491, View in Reaxys Further information Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys Further information Wilhelm; Journal of Chemical Physics; vol. 58; (1973); p. 3558,3559, View in Reaxys Further information Karasek et al.; Analytical Chemistry; vol. 45; (1973); p. 1210,1213, View in Reaxys Further information Streets; Ceasar; Molecular Physics; vol. 26; (1973); p. 1037,1039,1041,1050, 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 Berthelot et al.; Journal of Molecular Structure; vol. 18; (1973); p. 435,441, View in Reaxys Further information Shanmugasundaram et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 252; (1973); p. 209,210, View in Reaxys Further information Nayar; Kudchadker; Journal of Chemical and Engineering Data; vol. 18; (1973); p. 356,357, View in Reaxys Further information Korenman; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 380,394, View in Reaxys Further information Tumosa et al.; Journal of Chemical Physics; vol. 58; (1973); p. 1833, View in Reaxys Further information Keruzore; Labarre; Tetrahedron; vol. 29; (1973); p. 2925, View in Reaxys Further information Johari; Smyth; Journal of Chemical Physics; vol. 56; (1972); p. 4411,4412, View in Reaxys Further information Topp; Rentzepis; Journal of Chemical Physics; vol. 56; (1972); p. 1066,1068, View in Reaxys Further information Bock,H. et al.; Chemische Berichte; vol. 105; (1972); p. 3850 - 3864, View in Reaxys Further information Baruah; Indian Journal of Pure and Applied Physics; vol. 10; (1972); p. 75, View in Reaxys Further information Nigam; Maini; Indian Journal of Chemistry; vol. 10; (1972); p. 197, View in Reaxys Further information DULLIEN FAL; AIChE Journal; vol. 18; nb. 1; (1972); p. 62 - 70, View in Reaxys Further information Knoesel,R. et al.; Bulletin de la Societe Chimique de France; (1971); p. 4471 - 4480, View in Reaxys Further information Gregoire; Meinnel; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 272; (1971); p. 347, View in Reaxys Further information Gunn; Yamada; AIChE Journal; vol. 17; (1971); p. 1341,1342, View in Reaxys Further information Bhagvanth Rao et al.; Journal of the Indian Institute of Science; vol. 53; (1971); p. 99,103, View in Reaxys Further information Peschel; Schnorrer; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 75; (1971); p. 96,101, 104, 105, 109, View in Reaxys Further information Johnstone et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 5; (1970); p. 241, View in Reaxys Further information Johari; Goldstein; Journal of Chemical Physics; vol. 53; (1970); p. 2372,2374, View in Reaxys Further information Baker; Turner; Philosophical Transactions of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 268; (1970); p. 131,136, 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 Sergeev et al.; Optics and Spectroscopy; vol. 29; (1970); p. 63; ; p. 119, View in Reaxys Further information Myasishcheva et al.; High Energy Chemistry; vol. 4; (1970); p. 398; ; p. 447, View in Reaxys Further information Mansingh; Journal of Chemical Physics; vol. 52; (1970); p. 5896,5898, View in Reaxys Further information Csueroes et al.; Acta Chimica Academiae Scientiarum Hungaricae; vol. 63; (1970); p. 425, View in Reaxys Further information Cvitas; Molecular Physics; vol. 19; (1970); p. 297, View in Reaxys

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Further information Bobovich; Bortkevich; Journal of Applied Spectroscopy; vol. 11; (1969); p. 1312; ; p. 820, View in Reaxys Further information Bobovich; Bortkevich; Journal of Applied Spectroscopy; vol. 11; (1969); p. 1200; ; p. 662, View in Reaxys Further information Kett; Anderson; Journal of Physical Chemistry; vol. 73; (1969); p. 1268, View in Reaxys Further information Rastogi; Yadava; Journal of Chemical Physics; vol. 51; (1969); p. 2826,2827, 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 Dube; Parshad; Journal of Physical Chemistry; vol. 73; (1969); p. 3236, View in Reaxys Further information Chu; Lin; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 16; (1969); p. 56,65, View in Reaxys Further information Howe; Williams; Journal of the American Chemical Society; vol. 91; (1969); p. 7137,7141, View in Reaxys Further information Facchetti et al.; Chimica e l'Industria (Milan, Italy); vol. 51; (1969); p. 1373, View in Reaxys Further information Warman et al.; Journal of Chemical Physics; vol. 51; (1969); p. 3477, View in Reaxys Further information Steelhammer; Wentworth; Journal of Chemical Physics; vol. 51; (1969); p. 1802,1804,1809, View in Reaxys Further information Radcliffe; Steele; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 597, View in Reaxys Further information Recko; Sadowska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 17; (1969); p. 307,308, View in Reaxys Further information Ben-Reuven; Gershon; Journal of Chemical Physics; vol. 51; (1969); p. 893, View in Reaxys Further information Lecomte; Bulletin de la Societe Chimique de France; (1969); p. 2215,2224, View in Reaxys Further information Cumper; Tetrahedron; vol. 25; (1969); p. 3131, View in Reaxys Further information Nomura et al.; Tetrahedron Letters; (1969); p. 639, View in Reaxys Further information Laurent et al.; Bulletin de la Societe Chimique de France; (1969); p. 70, View in Reaxys Further information Andrieu; Mollier; Bulletin de la Societe Chimique de France; (1969); p. 831, View in Reaxys Further information Gray et al.; Journal of Chemical Physics; vol. 48; (1968); p. 1145,1148, View in Reaxys Further information Hartmann; Schmidt; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 62; (1968); p. 312, View in Reaxys Further information Persky et al.; Journal of Chemical Physics; vol. 49; (1968); p. 2347,2353, View in Reaxys Further information Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys Further information Christophorou; Stockdale; Journal of Chemical Physics; vol. 48; (1968); p. 1956,1957, View in Reaxys Further information Cantacuzene; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 516, View in Reaxys Further information Langer et al.; Journal of Physical Chemistry; vol. 72; (1968); p. 4020, View in Reaxys Further information Hanna; Abd-El-Nour; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 238; (1968); p. 161, 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 Lisitsa; Ralko; Optics and Spectroscopy; vol. 24; (1968); p. 284; ; p. 540, View in Reaxys Further information Chu; Lin; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 16; (1968); p. II-55,65, View in Reaxys Further information Huang; Sullivan; Australian Journal of Chemistry; vol. 21; (1968); p. 1721,1723, View in Reaxys Further information Kroh; Burzynska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 16; (1968); p. 509,510, View in Reaxys Further information Cercek; Journal of Physical Chemistry; vol. 72; (1968); p. 3832, View in Reaxys Further information Dumas et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 267; (1968); p. 267, View in Reaxys Further information Hansch et al.; Journal of Organic Chemistry; vol. 33; (1968); p. 347, View in Reaxys Further information Sease,J.W. et al.; Journal of the American Chemical Society; vol. 90; nb. 10; (1968); p. 2595 - 2598, View in Reaxys Further information Baker et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 22, View in Reaxys

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Further information Francis; Journal of Chemical and Engineering Data; vol. 12; (1967); p. 269,271, View in Reaxys Further information Ivekovic; Gertner; Croatica Chemica Acta; vol. 39; (1967); p. 103,105, View in Reaxys Further information BUehler; Ebert; Nature (London, United Kingdom); vol. 214; (1967); p. 1220, View in Reaxys Further information Sinha et al.; Indian Journal of Physics (1926-1976); vol. 41; (1967); p. 183,194, 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 Krishnaji; Mansingh; Journal of Chemical Physics; vol. 44; (1966); p. 1590,1592, View in Reaxys Further information Pendred et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1966); p. 1009, View in Reaxys Further information Christophorou et al.; Journal of Chemical Physics; vol. 44; (1966); p. 3506, View in Reaxys Further information Giles; Whittle; Transactions of the Faraday Society; vol. 62; (1966); p. 128, View in Reaxys Further information Christophorou et al.; Journal of Chemical Physics; vol. 45; (1966); p. 536, View in Reaxys Further information Christophorou et al.; Journal of Chemical Physics; vol. 45; (1966); p. 1081,1084, View in Reaxys Further information Winkler; Winkler; Journal of the American Chemical Society; vol. 88; (1966); p. 969,970, View in Reaxys Further information Fraser; Renaud; Journal of the American Chemical Society; vol. 88; (1966); p. 4365,4367, View in Reaxys Further information Kerr et al.; Molecular Physics; vol. 10; (1966); p. 14, View in Reaxys Further information Brown; Wirkkala; Journal of the American Chemical Society; vol. 88; (1966); p. 1453,1455, 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 Garg; Kadaba; Journal of Physical Chemistry; vol. 69; (1965); p. 674, View in Reaxys Further information Farrell; Newton; Journal of Physical Chemistry; vol. 69; (1965); p. 3506, View in Reaxys Further information Rosenthal; Dailey; Journal of Chemical Physics; vol. 43; (1965); p. 2093,2109, View in Reaxys Further information Schanel et al.; Collection of Czechoslovak Chemical Communications; vol. 30; (1965); p. 3140, 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 Griffiths; Derwish; Journal of Molecular Spectroscopy; vol. 13; (1964); p. 393,397, View in Reaxys Further information Nepras; Zahradnik; Collection of Czechoslovak Chemical Communications; vol. 29; (1964); p. 1555,1556, View in Reaxys Further information Dunken et al.; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 4; (1964); p. 312, View in Reaxys Further information Wayland; Drago; Journal of the American Chemical Society; vol. 86; (1964); p. 5240,5241, View in Reaxys Further information Maksimowa; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 102; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 197, View in Reaxys Further information Lerch; Cosandey; Helvetica Chimica Acta; vol. 47; (1964); p. 2417; Chem.Abstr.; vol. 56; nb. 9393; (1962), View in Reaxys Further information Porter; Ward; Proceedings of the Chemical Society, London; (1964); p. 288, View in Reaxys Further information Voigt; Reid; Journal of the American Chemical Society; vol. 86; (1964); p. 3930,3932, View in Reaxys Further information Voigt; Journal of the American Chemical Society; vol. 86; (1964); p. 3611,3614, View in Reaxys Further information Deverse; King; Journal of Chemical Physics; vol. 41; (1964); p. 3833,3835, View in Reaxys Further information Barriol; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 259; (1964); p. 4010, View in Reaxys Further information Stockdale; Hurst; Journal of Chemical Physics; vol. 41; (1964); p. 255, 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 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 Dullien; Transactions of the Faraday Society; vol. 59; (1963); p. 856,862, View in Reaxys

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Further information Bryce-Smith et al.; Proceedings of the Chemical Society, London; (1963); p. 219, View in Reaxys Further information Marckmann et al.; Berichte der Bunsen-Gesellschaft; vol. 67; (1963); p. 33, View in Reaxys Further information Zhokhovskii; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 1428; Zhurnal Fizicheskoi Khimii; vol. 37; (1963); p. 2635, View in Reaxys Further information Plucknett; Richards; Journal of Chemical and Engineering Data; vol. 8; (1963); p. 239, View in Reaxys Further information Read et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1778, View in Reaxys Further information Garst; Cole; Tetrahedron Letters; (1963); p. 679,681, View in Reaxys Further information Imanov; Zul'fugarzade; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 188; ; p. 366, 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 Kropp; Burton; Journal of Chemical Physics; vol. 37; (1962); p. 1742,1746, View in Reaxys Further information Tsuji et al.; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 2045, 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 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 McLafferty; Analytical Chemistry; vol. 34; (1962); p. 16,23, View in Reaxys Further information Blouri; Cerceau; Bulletin de la Societe Chimique de France; (1961); p. 791, View in Reaxys Further information Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 126, View in Reaxys Further information Amaya; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1278,1281, 1284, View in Reaxys Further information LeFevre; Steel; Chemistry and Industry (London, United Kingdom); (1961); p. 670, View in Reaxys Further information Schmid; Bellanato; Zeitschrift fuer Elektrochemie; vol. 65; (1961); p. 362, View in Reaxys Further information Hatcher; Journal of Chemical Physics; vol. 35; (1961); p. 2266, View in Reaxys Further information Everard; Swan; Proceedings of the Chemical Society, London; (1961); p. 212, View in Reaxys Further information Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 91, View in Reaxys Further information Brownstein; Canadian Journal of Chemistry; vol. 38; (1960); p. 1590,1592, View in Reaxys Further information Smith; Mortensen; Journal of Chemical Physics; vol. 32; (1960); p. 508,510, View in Reaxys Further information Bardamowa; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR; vol. 2; (1960); p. 71,72,73, 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 Halliwell; Nyburg; Journal of the Chemical Society; (1960); p. 4603,4607, View in Reaxys Further information Terpugowa; Optika i Spektroskopiya; vol. 7; (1959); p. 581,582-587; Chem.Abstr.; nb. 10496; (1960), View in Reaxys Further information Martinet; Rapport CEA-R - France, Commissariat a l'Energie Atomique; vol. 888; (1958); p. 1,20,33,45,46,60,68; Chem.Abstr.; vol. 54; nb. 12719e; (1960), View in Reaxys Heat Capacity Cp (8) Heat Capacity Cp Temperature (Heat [Jmol-1K-1] Capacity Cp) [°C] 151.63 - 167.15

Comment (Heat Capacity Cp)

9.99 - 79.99

References Goralski, Pawet; Piekarski, Henryk; Journal of Chemical and Engineering Data; vol. 52; nb. 2; (2007); p. 655 - 659, View in Reaxys Deshpande et al.; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 469,470-472, View in Reaxys; Nigam et al.; Indian Journal of Chemistry; vol. 8; (1970); p. 908,910, View in Reaxys

158.43

Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys

54.93 - 159.01

-183 - 47

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys

103/219

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145.57

Kolossowsski; Udowenko; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1027,1030; Chem. Zentralbl.; vol. 107; nb. I; (1936); p. 970, View in Reaxys

59.87 - 127.7

-172 - -41.5

Andrews; Haworth; Journal of the American Chemical Society; vol. 50; (1928); p. 3000, View in Reaxys

151.48 - 160.98

20 - 80

Williams; Daniels; Journal of the American Chemical Society; vol. 47; (1925); p. 1493, View in Reaxys Spezifische Waerme zwischen 17grad und 65grad: 0.239 cal/g.

Kremann; Meingast; Gugl; Monatshefte fuer Chemie; vol. 35; (1914); p. 1304, View in Reaxys

Heat Capacity Cv (1) References Deshpande; Bhatgadde; Australian Journal of Chemistry; vol. 24; (1971); p. 1817,1820, View in Reaxys Interatomic Distances and Angles (4) Description Comment (Interatomic Distances and Angles)

References

Electron distribution

Kanekar et al.; Proceedings - Indian Academy of Sciences, Section A; vol. 65; (1967); p. 353,356, View in Reaxys; Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 16; nb. 7; (1968); p. 1187, View in Reaxys

Interatomic distances and angles

Joliet; Berthon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 260; (1965); p. 2805, View in Reaxys; Rosenthal; Dailey; Journal of Chemical Physics; vol. 43; (1965); p. 2093,2109, View in Reaxys

Interatomic distances and angles

durch Elektronenbeugung ermittelt.

Interatomic distances and angles

roentgenographisch Schoppe; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 34; (1936); p. 461,465, 469, ermittelt. View in Reaxys

Ionization Potential (17) Ionization Potential Method (Ionization [eV] Potential)

Yuzawa; Yamaha; Bulletin of the Chemical Society of Japan; vol. 26; (1953); p. 414,416, View in Reaxys

Comment (Ionization Potential)

References

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

9.63

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

10.53

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

11.19

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

11.95

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

12.68

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

12.96

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

14.06

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

14.52

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

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15.2

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

15.66

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

16.85

Type: vertical. Higher potentials: 16.85 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

8.98

Photoionization

Watanabe; Journal of Chemical Physics; vol. 26; (1957); p. 542,543; Journal of Chemical Physics; vol. 22; (1954); p. 1564,1566, View in Reaxys; Walter, K.; Scherm, K.; Boesl, U.; Journal of Physical Chemistry; vol. 95; nb. 3; (1991); p. 1188 - 1194, View in Reaxys Type: vertical. Fujisawa, S.; Ohno, K.; Masuda, S.; Harada, Y.; Journal of the American Higher potentials: Chemical Society; vol. 108; nb. 21; (1986); p. 6505 - 6511, View in Reaxys 9.64, 10.65, 11.20, 12.00, 12.70, 12.9, 14.10, 14.50, 15.17, 15.70, 16.81 eV Johnstone et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 5; (1970); p. 241, View in Reaxys; Baker; Turner; Philosophical Transactions of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 268; (1970); p. 131,136, View in Reaxys; Walkley; Journal of Chemical Physics; vol. 33; (1960); p. 621, View in Reaxys; Pignataro et al.; Annali di Chimica (Rome, Italy); vol. 64; (1974); p. 139,141, 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; Streets; Ceasar; Molecular Physics; vol. 26; (1973); p. 1037,1039,1041,1050, View in Reaxys; Boschi; Salahub; Canadian Journal of Chemistry; vol. 52; (1974); p. 1217,1220, View in Reaxys; Yeo; Williams; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 886, View in Reaxys; Baldwin et al.; Organic Mass Spectrometry; vol. 11; (1976); p. 1181,1182, View in Reaxys; Bendig; Kreysig; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 1176, View in Reaxys; Sell; Kuppermann; Chemical Physics; vol. 33; (1978); p. 367, View in Reaxys; Momigny et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 1; (1968); p. 53,55, 56, 59, 60, 62, View in Reaxys; Crable; Kearns; Journal of Physical Chemistry; vol. 66; (1962); p. 436,437, View in Reaxys; Majer; Patrick; Transactions of the Faraday Society; vol. 58; (1962); p. 17,18, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys; Adler; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 427; (1976); p. 247,256, View in Reaxys; Baker et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 22, View in Reaxys

9.41

Electron impact

Morrison; Nicholson; Journal of Chemical Physics; vol. 20; (1952); p. 1021, View in Reaxys

8.5

Electron impact

Hartmann; Svendsen; Zeitschrift fuer Physikalische Chemie (Leipzig); <N.F.> 11 <1957> 16, 21, View in Reaxys

Kinematic Viscosity (2) Kinematic Viscosi- Temperature (Kine- Comment (Kinety [St] matic Viscosity) matic Viscosity) [°C] 25

0.00267 - 0.00681

References

Kinematic viscosity Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemis(range begins): try; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 1.0597 <unit not given>

20 - 141.5

Golik; Rawikowitsch; Zhurnal Fizicheskoi Khimii; vol. 24; (1950); p. 524,525; Chem.Abstr.; (1950); p. 8721, View in Reaxys

Liquid Phase (6)

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Description (Liquid Comment (Liquid Phase) Phase)

References

Correlation function of the liquid

Lanshina; Journal of Structural Chemistry; vol. 43; nb. 6; (2002); p. 1006 - 1010, View in Reaxys

Structure of the liquid

Schultz, E.; Bertagnolli, H.; Frahm, R.; Journal of Chemical Physics; vol. 92; nb. 1; (1990); p. 667 - 672, View in Reaxys; Bertagnolli, H.; Engelhardt, T.; Chieux, P.; Berichte der BunsenGesellschaft; vol. 92; (1988); p. 84 - 91, View in Reaxys; Bertagnolli, H.; Engelhardt, T.; Lengeler, B.; Berichte der Bunsen-Gesellschaft; vol. 91; (1987); p. 1287 - 1292, View in Reaxys; Demidov; Libov; Russian Journal of Physical Chemistry A; vol. 71; nb. 12; (1997); p. 1997 - 1999, View in Reaxys

Association in the liquid state

Bertagnolli, H.; Engelhardt, T.; Lengeler, B.; Berichte der Bunsen-Gesellschaft; vol. 91; (1987); p. 1287 - 1292, View in Reaxys; Demidov; Libov; Russian Journal of Physical Chemistry A; vol. 71; nb. 12; (1997); p. 1997 - 1999, View in Reaxys

Liquid-crystalline properties

Haloui et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 72; (1975); p. 1097, View in Reaxys

Rotational correlation time

Jackson; Simic-Glavaski; Molecular Physics; vol. 18; (1970); p. 393, View in Reaxys

Self-association in solution

von unverduenntem Trautteur; Nuovo Cimento; vol. <8> 14; (1937); p. 265, View in Reaxys fluessigen und von in Benzol geloestem Brombenzol.

Liquid/Liquid Systems (MCS) (23) 1 of 23

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Shiflett, Mark B.; Niehaus, Anne Marie S.; Yokozeki; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2090 - 2094, View in Reaxys 2 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

69.99 - 109.99

Partner (Liquid/Liquid Systems (MCS))

1-Hexadecanol; air

Xiao, Hang; Lei, Ying Duan; Wania, Frank; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p. 338 - 346, View in Reaxys 3 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

26.85

Pressure (Liquid/Liquid Systems (MCS)) [Torr]

60004.8

Partner (Liquid/Liquid Systems (MCS))

carbon dioxide

Timko, Michael T.; Nicholson, Benjamin F.; Steinfeld, Jeffrey I.; Smith, Kenneth A.; Tester, Jefferson W.; Journal of Chemical and Engineering Data; vol. 49; nb. 4; (2004); p. 768 - 778, View in Reaxys 4 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

n-heptane; dimethyl sulfoxide

Hillerich, Jens; Plenio, Herbert; Chemical Communications; nb. 24; (2003); p. 3024 - 3025, View in Reaxys 5 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS))

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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 6 of 23

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 7 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

benzene; hexane

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

Porous sol-gel silica glass

Badjic, Jovica D.; Kostic, Nenad M.; Journal of Physical Chemistry B; vol. 104; nb. 47; (2000); p. 11081 - 11087, View in Reaxys 8 of 23

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 9 of 23

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 10 of 23

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

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2018-06-17 20:44:10

Weckwerth, Jeff D.; Carr, Peter W.; Vitha, Mark F.; Nasehzadeh, Asad; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3712 - 3716, View in Reaxys 11 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

octanol; air

Hiatt, Michael H.; Analytical Chemistry; vol. 69; nb. 6; (1997); p. 1127 - 1134, View in Reaxys 12 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.9

Partner (Liquid/Liquid Systems (MCS))

2-{2-[4-(1,1,3,3-tetramethyl-butyl)-phenoxy]-ethoxy}-ethanol

Suslov, D. A.; Solomonov, B. N.; Russian Journal of Physical Chemistry; vol. 69; nb. 7; (1995); p. 1140 - 1143; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 7; (1995); p. 1264 - 1267, View in Reaxys 13 of 23

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 15 of 23

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 16 of 23

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

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2018-06-17 20:44:10

17 of 23

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 18 of 23

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 19 of 23

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

Korenman, Ya. I.; Sel'manshchuk, N. N.; Russian Journal of Physical Chemistry; vol. 56; nb. 4; (1982); p. 558 - 560; Zhurnal Fizicheskoi Khimii; vol. 56; nb. 4; (1982); p. 920 - 923, View in Reaxys 20 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

octanol

Yalkowsky; Valvani; Journal of Pharmaceutical Sciences; vol. 69; nb. 8; (1980); p. 912 - 922, View in Reaxys 21 of 23

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; Beroza; Bowman; Analytical Chemistry; vol. 38; (1966); p. 1544,1547, View in Reaxys; Niclas; Kollecker; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 16; (1976); p. 367, View in Reaxys; Sekine et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 995, View in Reaxys; Korenman et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 683,726, View in Reaxys

22 of 23

Description (Liquid/Liquid Critical solution temperature Systems (MCS)) Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys

23 of 23

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

ethanol; H2O

Partner (Liquid/Liquid Systems (MCS))

bromine

Bugarszky; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 71; (1910); p. 753,758, View in Reaxys Liquid/Solid Systems (MCS) (17) 1 of 17

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Partner (Liquid/Solid Systems (MCS))

fullerene-C6 0

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Korobov, Mikhail V.; Mirakian, Andrey L.; Avramenko, Natalia V.; Valeev, Eduard F.; Neretin, Ivan S.; Slovokhotov, Yuri L.; Smith, Allan L.; Olofsson, Gerd; Ruoff, Rodney S.; Journal of Physical Chemistry B; vol. 102; nb. 19; (1998); p. 3712 - 3717, View in Reaxys 2 of 17

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Partner (Liquid/Solid Systems (MCS))

cis-decalin

Murthy, S. S. N.; Kumar, Deepak; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 14; (1993); p. 2423 2428, View in Reaxys 3 of 17

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Temperature (Liquid/Solid Systems (MCS)) [°C]

-45.1 - -28.1

Partner (Liquid/Solid Systems (MCS))

chlorobenzene

Smith; Molecular crystals and liquid crystals; vol. 65; nb. 3-4; (1981); p. 285 - 306, View in Reaxys 4 of 17

Description (Liquid/Solid Systems (MCS))

Melting diagram

Goates et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 217,219, View in Reaxys; Moellmer et al.; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 317,318, 319, View in Reaxys 5 of 17

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Comment (Liquid/Solid Systems (MCS))

Eutektikum.

Partner (Liquid/Solid Systems (MCS))

chloroform

Reeves; Schneider; Canadian Journal of Chemistry; vol. 35; (1957); p. 251,256, View in Reaxys 6 of 17

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

benzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 7 of 17

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

fluorobenzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 8 of 17

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

chlorobenzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 9 of 17

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

iodobenzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 10 of 17

Description (Liquid/Solid Systems (MCS))

Solidification diagram

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Comment (Liquid/Solid Systems (MCS))

Eutektikum.

Partner (Liquid/Solid Systems (MCS))

aluminium bromide

Burbage; Garrett; Journal of Physical Chemistry; vol. 56; (1952); p. 730, View in Reaxys 11 of 17

Description (Liquid/Solid Systems (MCS))

Solidification points of mixtures

Partner (Liquid/Solid Systems (MCS))

(+-)-3-bromo-cycloocta-1c,5c-diene

Cope et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2510,2514, View in Reaxys 12 of 17

Description (Liquid/Solid Systems (MCS))

Eutectic

Partner (Liquid/Solid Systems (MCS))

1,3-Dichlorobenzene

Timmermans; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 632, View in Reaxys 13 of 17

Description (Liquid/Solid Systems (MCS))

Eutectic

Partner (Liquid/Solid Systems (MCS))

2-methylchlorobenzene

Timmermans; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 632, View in Reaxys 14 of 17

Description (Liquid/Solid Systems (MCS))

Eutectic

Solvent (Liquid/Solid Sys- benzene tems (MCS)) Klemm; Klemm; Schiemann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 165; (1933); p. 379,386, View in Reaxys 15 of 17

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-62.5

Partner (Liquid/Solid Systems (MCS))

fluorobenzene

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys 16 of 17

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-32.5

Partner (Liquid/Solid Systems (MCS))

antimony(III) chloride

Menschutkin; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 419,422; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 380, View in Reaxys 17 of 17

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-32

Partner (Liquid/Solid Systems (MCS))

antimony(III) bromide

Menschutkin; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 419,422; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 380, View in Reaxys Liquid/Vapour Systems (MCS) (32) 1 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

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Temperature (Liquid/ Vapour Systems (MCS)) [°C]

93.91 - 147.03

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

300.024 - 759.811

Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Artigas, Hector; Lafuente, Carlos; Cea, Pilar; Royo, Felix M.; Urieta, Jose S.; Journal of Chemical and Engineering Data; vol. 42; nb. 1; (1997); p. 132 - 136, View in Reaxys 2 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour phase diagram

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

93.91 - 147.03

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

300.024 - 759.811

Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Artigas, Hector; Lafuente, Carlos; Cea, Pilar; Royo, Felix M.; Urieta, Jose S.; Journal of Chemical and Engineering Data; vol. 42; nb. 1; (1997); p. 132 - 136, View in Reaxys 3 of 32

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

93.91 - 147.03

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

300.024 - 759.811

Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Artigas, Hector; Lafuente, Carlos; Cea, Pilar; Royo, Felix M.; Urieta, Jose S.; Journal of Chemical and Engineering Data; vol. 42; nb. 1; (1997); p. 132 - 136, View in Reaxys 4 of 32

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))

2-{2-[4-(1,1,3,3-tetramethyl-butyl)-phenoxy]-ethoxy}-ethanol

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour phase diagram

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

39.9 - 119.9

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

45003.6 - 165013

Partner (Liquid/Vapour Systems (MCS))

carbon dioxide

Walther, D.; Maurer, G.; Berichte der Bunsen-Gesellschaft; vol. 96; nb. 8; (1992); p. 981 - 988, View in Reaxys 6 of 32

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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Temperature (Liquid/ Vapour Systems (MCS)) [°C]

130

Partner (Liquid/Vapour Systems (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-propyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb. 3; (1989); p. 280 - 284, View in Reaxys 7 of 32

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

130

Partner (Liquid/Vapour Systems (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-butyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb. 3; (1989); p. 280 - 284, View in Reaxys 8 of 32

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

130

Partner (Liquid/Vapour Systems (MCS))

Bis(3-((4-(propoxycarbonyl)-2,3,5,6-tetrachlorobenzoyl)oxy)propyl)tetrachloroterephthalate

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb. 3; (1989); p. 280 - 284, View in Reaxys 9 of 32

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 10 of 32

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))

Boiling points of mixtures

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

54 - 126.8

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

300 - 700

Partner (Liquid/Vapour Systems (MCS))

butanone

Kalluru, Ramanjaneyulu; Abburi, Krishnaiah; Machiraju, Ramakrishna; Journal of Chemical & Engineering Data; vol. 33; nb. 3; (1988); p. 251 - 253, View in Reaxys

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12 of 32

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 13 of 32

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

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 32

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 15 of 32

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 16 of 32

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 17 of 32

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

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18 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Yarym-Agaev, N. L.; Kalinichenko, V. P.; Russian Journal of Physical Chemistry; vol. 55; nb. 3; (1981); p. 347 - 349; Zhurnal Fizicheskoi Khimii; vol. 55; nb. 3; (1981); p. 612 - 617, View in Reaxys 19 of 32

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Dowell; Stewart; Phosphorus and Sulfur and the Related Elements; vol. 1; (1976); p. 135,137, View in Reaxys; Langer; Purnell; Journal of Physical Chemistry; vol. 67; (1963); p. 263,265,266, View in Reaxys; Janini; Martire; Journal of Physical Chemistry; vol. 78; (1974); p. 1644,1646, View in Reaxys 20 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Moerke et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 252; (1973); p. 323,325, View in Reaxys; Hine et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 1473, View in Reaxys 21 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Bourrelly; Chevalier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 1561, View in Reaxys 22 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

250

Partner (Liquid/Vapour Systems (MCS))

cyclohexanol

Studenberg; Thomas; Pr. S. Dakota Acad.; vol. 36; (1957); p. 167,169, View in Reaxys 23 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

500

Partner (Liquid/Vapour Systems (MCS))

cyclohexanol

Studenberg; Thomas; Pr. S. Dakota Acad.; vol. 36; (1957); p. 167,169, View in Reaxys 24 of 32

Description (Liquid/ Vapour Systems (MCS))

Liquid/vapour equilibrium

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

730

Partner (Liquid/Vapour Systems (MCS))

cyclohexanol

Studenberg; Thomas; Pr. S. Dakota Acad.; vol. 36; (1957); p. 167,169, View in Reaxys 25 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Neckel, Kohler; Monatshefte fuer Chemie; vol. 87; (1956); p. 176,183, 188, 189, View in Reaxys 26 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Neckel, Kohler; Monatshefte fuer Chemie; vol. 87; (1956); p. 176,183, 188, 189, View in Reaxys 27 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Neckel, Kohler; Monatshefte fuer Chemie; vol. 87; (1956); p. 176,183, 188, 189, View in Reaxys 28 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Comment (Liquid/Vapour Systems (MCS))

und Partialdampfdruck.

Partner (Liquid/Vapour Systems (MCS))

benzene

McGlashan; Windgrove; Transactions of the Faraday Society; vol. 52; (1956); p. 470,471, View in Reaxys 29 of 32

Description (Liquid/ Vapour Systems (MCS))

Partial pressures of the components

Comment (Liquid/Vapour Systems (MCS))

von Gemischen mit Benzol bei 70grad.

Martin; Transactions of the Faraday Society; vol. 33; (1937); p. 191,195, View in Reaxys 30 of 32

Description (Liquid/ Vapour Systems (MCS))

Boiling points of mixtures

Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Young; Journal of the Chemical Society; vol. 81; (1902); p. 771,772, View in Reaxys 31 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

ethanol

Schulze; Zeitschrift fuer Physikalische Chemie (Leipzig); <N. F.> 6 <1956> 315, 319, 322, View in Reaxys 32 of 32

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

Partner (Liquid/Vapour Systems (MCS))

ethanol

Schulze; Zeitschrift fuer Physikalische Chemie (Leipzig); <N. F.> 6 <1956> 315, 319, 322, View in Reaxys Magnetic Data (1) Description (Magnetic Data)

References

116/219

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Magnetic properties Bruniquel et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 1558, View in Reaxys; Bauer et al.; Monatshefte fuer Chemie; vol. 101; (1970); p. 469,470,473, View in Reaxys Magnetic Susceptibility (2) Magnetic Suscepti- References bility [10-6cm3mol-1] Pascal; Bulletin de la Societe Chimique de France; vol. <4>5; (1909); p. 1066; Annales de Chimie (Cachan, France); vol. <8>19; (1910); p. 20, View in Reaxys; Shanmugasundaram; Acta Chimica Academiae Scientiarum Hungaricae; vol. 96; (1978); p. 151,154, View in Reaxys; Baliah; Srinivasan; Indian Journal of Chemistry; vol. 9; (1971); p. 215, View in Reaxys; Shanmugasundaram et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 252; (1973); p. 209,210, View in Reaxys; Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 1315,1316,1320, View in Reaxys; Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 179,182, View in Reaxys -82.6

Rumpf; Seguin; Bulletin de la Societe Chimique de France; (1949); p. D 366, D 368; Bulletin de la Societe Chimique de France; (1950); p. 177, View in Reaxys

Mechanical & Physical Properties (MCS) (54) 1 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

1,4-dioxane

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 2 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 3 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

toluene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 4 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

117/219

2018-06-17 20:44:10

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 5 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

1,4-dioxane; benzene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 6 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

1,4-dioxane; toluene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 7 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

1,4-dioxane; tetrachloromethane

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 8 of 54

Description (Mechanical & Physical Properties (MCS))

Ultrasonic absorption

Solvent (Mechanical & Physical Properties (MCS))

H2O

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

35 μm Supelco Amberchrom CG-1000S

Zhang, Guangming; Hua, Inez; Chemosphere; vol. 46; nb. 1; (2002); p. 59 - 66, View in Reaxys 9 of 54

Description (Mechanical & Physical Properties (MCS))

Ultrasonic absorption

Solvent (Mechanical & Physical Properties (MCS))

H2O

Temperature (Mechanical & Physical Properties (MCS)) [°C]

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Partner (Mechanical & Physical Properties (MCS))

silica particles

Zhang, Guangming; Hua, Inez; Chemosphere; vol. 46; nb. 1; (2002); p. 59 - 66, View in Reaxys 10 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 40

Partner (Mechanical & Physical Properties (MCS))

2-methyl-propan-1-ol

Artigas, Hector; Dominguez, Magdalena; Mainar, Ana M.; Lopez, M. Carmen; Royo, Felix M.; Journal of Chemical and Engineering Data; vol. 43; nb. 4; (1998); p. 580 - 584, View in Reaxys 11 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol; acetic acid butyl ester

Ramachandran, D.; Rambabu, K.; Mohankrishnan, K.; Venkateswarlu, P.; Raman, G. K.; Journal of the Indian Chemical Society; vol. 73; nb. 8; (1996); p. 385 - 390, View in Reaxys 12 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

N,N-dimethyl-formamide

Ramadevi; Rao; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 65 - 67, View in Reaxys 13 of 54

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetic acid butyl ester; 2-methoxy-ethanol

Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 128 131, View in Reaxys 14 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetic acid butyl ester; 2-methoxy-ethanol

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Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 128 131, View in Reaxys 15 of 54

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

2-methoxy-ethanol

Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 135, View in Reaxys 16 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

2-methoxy-ethanol

Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 135, View in Reaxys 17 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetrahydrofuran

Naorem, Homendra; Suri, S. K.; Canadian Journal of Chemistry; vol. 67; (1989); p. 1672 - 1676, View in Reaxys 18 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

furan

Naorem, Homendra; Suri, S. K.; Canadian Journal of Chemistry; vol. 67; (1989); p. 1672 - 1676, View in Reaxys 19 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

furfural

Naorem, Homendra; Suri, S. K.; Canadian Journal of Chemistry; vol. 67; (1989); p. 1672 - 1676, View in Reaxys

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20 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

(2-furyl)methyl alcohol

Naorem, Homendra; Suri, S. K.; Canadian Journal of Chemistry; vol. 67; (1989); p. 1672 - 1676, View in Reaxys 21 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

1-methyl-pyrrolidin-2-one

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

cyclohexane

Aminabhavi, T. M.; Jayadevappa, E. S.; Prasad, B. R.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 22; nb. 3; (1983); p. 231 - 233, View in Reaxys; Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Halligudi, S. B.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 27; nb. 4; (1988); p. 303 - 307, View in Reaxys 23 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

ethyl acetate

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

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H.; Halligudi, S. B.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 27; nb. 4; (1988); p. 303 - 307, View in Reaxys 25 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Muddapur, M. V.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 26; nb. 2; (1987); p. 106 - 109, View in Reaxys 26 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

Bromoform

Aminabhavi, T M; Manjeshwar, L S; Balundgi, R H; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 26; nb. 8; (1987); p. 641 - 647, View in Reaxys 27 of 54

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetonitrile

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 28 of 54

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

dimethyl sulfoxide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 29 of 54

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

N,N-dimethyl-formamide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys

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30 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

ethyl acetate

Ukponmwan; Greenhalgh; Peters; Journal of Chemical and Engineering Data; vol. 29; nb. 4; (1984); p. 482 - 483, View in Reaxys 31 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetic acid butyl ester

Ukponmwan; Greenhalgh; Peters; Journal of Chemical and Engineering Data; vol. 29; nb. 4; (1984); p. 482 - 483, View in Reaxys 32 of 54

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

chlorobenzene

Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 16; nb. 11; (1984); p. 1031 - 1036, View in Reaxys 33 of 54

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

CCl4

Shahidi, Fereidoon; Canadian Journal of Chemistry; vol. 61; (1983); p. 1414 - 1416, View in Reaxys 34 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

hexane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 35 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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2018-06-17 20:44:10

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

n-heptane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 36 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

nonane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 37 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

decane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 38 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

dodecane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 39 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetradecane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 40 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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2018-06-17 20:44:10

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

Hexadecane

Inglese, Americo; Dell'Atti, Angelo; Castagnolo, Maurizio; Giglio, Angelo De; Journal of Chemical Thermodynamics; vol. 15; nb. 3; (1983); p. 253 - 258, View in Reaxys 41 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 14; nb. 6; (1982); p. 577 - 584, View in Reaxys 43 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

cyclohexylamine

Raju, G. Dharma; Swamy, G. Narayana; Raman, G.K.; Journal of Solution Chemistry; vol. 10; nb. 1; (1981); p. 79 - 82, View in Reaxys 44 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Saraiya; Winnick; Journal of Chemical Physics; vol. 49; (1968); p. 1447, View in Reaxys; Nigam; Singh; Transactions of the Faraday Society; vol. 65; (1969); p. 950,956, View in Reaxys; Schmack; Bittrich; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 730, View in Reaxys; Mahl et al.; Journal of Chemical Thermodynamics; vol. 3; (1971); p. 363,364, View in Reaxys; Nigam et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 159,160 - 162, View in Reaxys; Mahl et al.; Journal of Chemical Thermodynamics; vol. 9; (1977); p. 61,62, 63, View in Reaxys; Oswal et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 17; (1979); p. 605, View in Reaxys; Deshpande et al.; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 469,470-472, View in Reaxys; Fried et al.; Bulletin of the Chemical Society of Japan; vol. 50; (1977); p. 497, View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 77; (1973); p. 263, View in Reaxys 45 of 54

Description (Mechanical & Physical Properties (MCS))

Virial coefficients

Khosla et al.; Indian Journal of Chemistry; vol. 10; (1972); p. 1098, View in Reaxys

125/219

2018-06-17 20:44:10

46 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Luzkii et al.; Zhurnal Obshchei Khimii; vol. 28; (1958); p. 2386,2390; engl. Ausg. S. 2423, 2427, View in Reaxys 47 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Luzkii et al.; Zhurnal Obshchei Khimii; vol. 28; (1958); p. 2386,2390; engl. Ausg. S. 2423, 2427, View in Reaxys 48 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

cyclohexane

Kohler,Rott; Monatshefte fuer Chemie; vol. 85; (1954); p. 703,11, View in Reaxys 49 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

cyclohexane

Kohler,Rott; Monatshefte fuer Chemie; vol. 85; (1954); p. 703,11, View in Reaxys 50 of 54

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Partner (Mechanical & Physical Properties (MCS))

acetic acid

Gay; Annales de Physique (Paris, France); vol. <9> 6; (1916); p. 51; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 152; (1911); p. 519, View in Reaxys 51 of 54

Description (Mechanical & Physical Properties (MCS))

PVT Relationship

Temperature (Mechanical & Physical Properties (MCS)) [°C]

126/219

2018-06-17 20:44:10

Partner (Mechanical & Physical Properties (MCS))

water; methanol

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys 52 of 54

Description (Mechanical & Physical Properties (MCS))

PVT Relationship

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

water; ethanol

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys 53 of 54

Description (Mechanical & Physical Properties (MCS))

PVT Relationship

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

water; propan-1-ol

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys 54 of 54

Description (Mechanical & Physical Properties (MCS))

PVT Relationship

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

water; acetone

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys Mechanical Properties (5) Description (MeReferences chanical Properties) Molar volume

Petrov et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 32; (1977); p. 1487,1180,1181,1184, View in Reaxys; Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 75; (1972); p. 68, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys; Narbutt; Siekierski; Roczniki Chemii; vol. 48; (1974); p. 1777,1781, View in Reaxys; Miller et al.; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 417,418, 419, View in Reaxys; Haase et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 30; (1975); p. 916, View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 77; (1973); p. 263, 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; Jayalakshmi, T.; Reddy, Kalluru S.; Canadian Journal of Chemistry; vol. 63; (1985); p. 2824 - 2828, View in Reaxys; Reddy, K. Subramanyam; Journal of Chemical & Engineering Data; vol. 31; nb. 2; (1986); p. 238 - 240, View in Reaxys; Taft; Abraham; Famini; Doherty; Abboud; Kamlet; Journal of Pharmaceutical Sciences; vol. 74; nb. 8; (1985); p. 807 - 814, View in Reaxys

Specific volume

Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 14; nb. 6; (1982); p. 577 - 584, View in Reaxys

Viscosity

Tourky et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 216; (1961); p. 176,177, 181, 182, View in Reaxys; Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Foote; Denny; Journal of the American Chemical Society; vol. 93; (1971); p. 5168, View in Reaxys; Dubrowskii; Afonina; J. Gen. Chem. USSR (Engl. Transl.); vol. 36; (1966); p. 1875,1868, View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 75; (1972); p. 68, View in Reaxys; Ertl; Dullien; AIChE Journal; vol. 19; (1973); p. 1215,1218, View in Reaxys; Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys; Wellek et al.; AIChE Journal; vol. 12; (1966); p. 854,857, View in Reaxys; Shukla; Saxena; Zeitschrift fuer Physikalische Chem-

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ie (Muenchen, Germany); vol. 83; (1973); p. 205, View in Reaxys; Honda; Sasada; Japanese Journal of Applied Physics; vol. 16; (1977); p. 1775,1776-1778, View in Reaxys; Nigam; Singh; Indian Journal of Chemistry; vol. 9; (1971); p. 691, View in Reaxys; Haase et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 30; (1975); p. 916, View in Reaxys; Lang et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 75; (1979); p. 349,350, View in Reaxys Compressibility

Deshpande et al.; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 469,470-472, View in Reaxys; Bobyl et al.; Sov. Phys. J. (Engl. Transl.); vol. 6; (1965); p. 48,30, View in Reaxys

Internal pressure

Pillai; Suryanarayana; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 13; (1965); p. 639, View in Reaxys; Suryanarayana; Govindaswamy; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 20; (1961); p. 563, View in Reaxys

Molecular Deformation (2) Description (MoReferences lecular Deformation) Fundamental vibra- Plyler; Allen; Tidwell; Journal of Research of the National Bureau of Standards (United States); vol. 58; (1957); p. tions 255,256, 260, View in Reaxys; Plyler; Discussions of the Faraday Society; vol. 9; (1950); p. 100,102, View in Reaxys; Whiffen; Journal of the Chemical Society; (1956); p. 1350, View in Reaxys; Kakiuchi; Nippon Kagaku Zasshi; vol. 80; (1959); p. 28,30; Chem.Abstr.; (1959); p. 7763, View in Reaxys; Wyss et al.; Spectrochimica Acta; vol. 20; (1964); p. 573,575, View in Reaxys; Cole; Michell; Spectrochimica Acta; vol. 20; (1964); p. 739,742, View in Reaxys; Slepoukhine, A. Yu.; Kostyuchenko, L. S.; Udovenja, V. A.; Journal of Molecular Structure; vol. 349; (1995); p. 207 - 210, View in Reaxys Force constants

Optics (21) Description (Optics)

Becher; Hoefler; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 1703,1705, View in Reaxys; Korostelev et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1538; ; p. 2682, View in Reaxys Comment (Optics)

References

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; Abdel-Azim, Abdel-Azim A.; Munk, Petr; Journal of Physical Chemistry; vol. 91; nb. 14; (1987); p. 3910 - 3914, View in Reaxys; Lanshina; Journal of Structural Chemistry; vol. 43; nb. 6; (2002); p. 1006 - 1010, View in Reaxys

Iso-and anisotropic components of Rayleigh scattering

Lanshina; Journal of Structural Chemistry; vol. 43; nb. 6; (2002); p. 1006 - 1010, View in Reaxys

Rayleigh scattering

Zamir et al.; Journal of Chemical Physics; vol. 55; (1971); p. 3397,3400, View in Reaxys; Gershon et al.; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 316, View in Reaxys; Shakhparonov; Doklady Physical Chemistry; vol. 136-141; (1961); p. 189; Doklady Akademii Nauk SSSR; vol. 136; (1961); p. 1162, View in Reaxys; Dardy et al.; Journal of Chemical Physics; vol. 59; (1973); p. 4491, View in Reaxys; Jackson; Simic-Glavaski; Molecular Physics; vol. 18; (1970); p. 393, View in Reaxys; Abdel-Azim, Abdel-Azim A.; Munk, Petr; Journal of Physical Chemistry; vol. 91; nb. 14; (1987); p. 3910 - 3914, View in Reaxys; Friedman, J. S.; She, C. Y.; Journal of Chemical Physics; vol. 99; nb. 7; (1993); p. 4960 - 4969, View in Reaxys

Diffraction

Cumper; Vogel; Journal of the Chemical Society; (1960); p. 4723,4725, View in Reaxys; Shapiro et al.; Physical Review Letters; vol. 19; (1967); p. 1093, View in Reaxys; Almenningen, A.; Brunvoll, J.; Popik, M. V.; Sokolkov, S. V.; Vilkov, L. V.; Samdal, S.; Journal of Molecular Structure; vol. 127; (1985); p. 85 - 94, View in Reaxys; Bertagnolli, H.; Engelhardt, T.; Lengeler, B.; Berichte der Bunsen-Gesellschaft; vol. 91; (1987); p. 1287 - 1292, View in Reaxys

Linear dichroism

Jede, F.; Stratmann, A. W.; Schrader, B.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 140; (1986); p. 297 - 302, View in Reaxys

Electric birefringence (Kerr effect)

Okabayashi; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1010,1012, View in Reaxys; Topp; Rentzepis; Journal of Chemical Physics; vol. 56; (1972); p. 1066,1068, View in Reaxys; Proutiere; Camail; Molecular Physics; vol. 29; (1975); p. 1473,1477-1479, View in Reaxys; Saiz et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p. 1538,1540, 1541, 1545, View in Reaxys; Blaszczak; Acta Physica Polonica, A; vol. 49; (1976); p. 515,517, View in Reaxys; Patz, R.; Raetzsch, M.T.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 265; nb. 3; (1984); p. 467 - 473, View in Reaxys

Magnetic birefringence (CottonMouton effect)

Goldet; Annales de Physique (Paris, France); vol. <11> 10; (1938); p. 103,156, View in Reaxys; Raman; Krishnan; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 113; (1927); p. 518; Chem. Zentralbl.; vol. 98; nb. I; (1927); p. 1127, View in Reaxys; Szivessy; Zeitschrift fuer Physik; vol. 18; p. 102; Chem. Zentralbl.; vol. 95; nb. I; (1924); p. 2567, View in Reaxys; Cotton; Mouton; Annales de Chimie (Cachan, France);

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vol. <8> 19; (1910); p. 175; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, 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; Vul'fson, S. G.; Nikolaev, V. F.; Vereshchagin, A. N.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 32; nb. 10; (1983); p. 2073 - 2078; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 10; (1983); p. 2296 - 2301, View in Reaxys Magnetorotation

Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys; Haberditzl; Koeppel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 691, View in Reaxys; Murthy; Naidu; Current Science; vol. 48; (1979); p. 292, View in Reaxys

Optical properties

Uchida; Japanese Journal of Applied Physics; vol. 7; (1968); p. 1259,1262, 1263, View in Reaxys; Proutiere; Camail; Molecular Physics; vol. 29; (1975); p. 1473,1477-1479, View in Reaxys

Magnetic circular dichroism

Shieh et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 1031,1035, 1036, View in Reaxys; Foss; McCarville; Journal of the American Chemical Society; vol. 89; (1967); p. 30, View in Reaxys

Diffraction

Beugung von Roentgen-Strahlen in gasfoermigem Brombenzol.

Mechanical birefringence

Schoppe; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 34; (1936); p. 461,465, 469, View in Reaxys

Vorlaender; Fischer; Chemische Berichte; vol. 65; (1932); p. 1756,1759, View in Reaxys; Vorlaender; Specht; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 178; (1936); p. 93,108, View in Reaxys

Electric birefringence (Kerr effect)

von Loesungen in Tetrachlormethan.

Otterbein; Phys. Z.; vol. 35; (1934); p. 249,264, View in Reaxys

Magnetic birefringence (CottonMouton effect)

von Gemischen mit Tetrachlormethan.

Chinchalkar; Indian Journal of Physics (1926-1976); vol. 7; (1932); p. 499,515; Chem. Zentralbl.; vol. 104; nb. II; (1933); p. 2799, View in Reaxys

Magnetic birefringence (CottonMouton effect)

von Gemischen mit Cyclohexan.

Chinchalkar; Indian Journal of Physics (1926-1976); vol. 7; (1932); p. 499,515; Chem. Zentralbl.; vol. 104; nb. II; (1933); p. 2799, View in Reaxys

Diffraction

Beugung von Roentgen-Strahlen in fluessigem Brombenzol.

Ishino; Tanaka; Tsuji; Memoirs of the College of Science, Kyoto Imperial University; vol. <A> 13; (1930); p. 1,14, View in Reaxys

Magnetic birefringence (CottonMouton effect)

zwischen 4.7grad und 54.7grad.

Szivessy; Annalen der Physik (Weinheim, Germany); vol. <4> 68; (1922); p. 150; Zeitschrift fuer Physik; vol. 18; p. 102; Chem. Zentralbl.; vol. 95; nb. I; (1924); p. 2567, View in Reaxys

Electric birefringence (Kerr effect)

zwischen -20grad und 100grad.

Bergholm; Annalen der Physik (Weinheim, Germany); vol. <4>65; (1921); p. 137, View in Reaxys

Electric birefringence (Kerr effect)

zwischen 0grad und Bergholm; Annalen der Physik (Weinheim, Germany); vol. <4> 51; (1916); p. 424, 50grad. View in Reaxys

Electric birefringence (Kerr effect)

bei 20grad.

Leiser; Abh. Dtsch. Bunsen-Ges.; nb. 4; (1910); p. 69; Chem. Zentralbl.; vol. 82; nb. I; (1911); p. 622, View in Reaxys

Electric birefringence (Kerr effect)

Brombenzol zeigt positive elektrische Doppelbrechung.

Schmidt,W.; Ann. d. Physik; vol. <4> 7; (1902); p. 163, View in Reaxys

Other Thermochemical Data (8) Description (Other Comment (Other Thermochemical Thermochemical Data) Data)

References

Gibbs free energy

Schuurmann; Environmental Toxicology and Chemistry; vol. 14; nb. 12; (1995); p. 2067 - 2076, View in Reaxys

Thermodynamic properties

Lias; Ausloos; Journal of the American Chemical Society; vol. 100; (1978); p. 6027,6033, View in Reaxys; Pac et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 1169,1171, View in Reaxys; Bloor; Canadian Journal of Chemistry; vol. 39; (1961); p. 2256,2259, View in Reaxys; Hanna; Abd-El-Nour; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 246; (1971); p. 292,294, View in Reaxys; Dhillon; Monatshefte fuer Chemie; vol. 110; (1979); p. 847, View in Reaxys; Butler; Lielmezs; Journal of Chemical and Engineering Data; vol. 14;

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(1969); p. 335,336, View in Reaxys; Langer; Purnell; Journal of Physical Chemistry; vol. 67; (1963); p. 263,265,266, View in Reaxys; Majer; Patrick; Transactions of the Faraday Society; vol. 58; (1962); p. 17,18, View in Reaxys; Wilhelm; Battino; Journal of Chemical Physics; vol. 55; (1971); p. 4012,4014, View in Reaxys; Stevenson; Journal of Molecular Spectroscopy; vol. 15; (1965); p. 220,232, View in Reaxys; Wadsoe; Acta Chemica Scandinavica (1947-1973); vol. 22; (1968); p. 2438, View in Reaxys Enthalpy

Lias; Ausloos; Journal of the American Chemical Society; vol. 100; (1978); p. 6027,6033, View in Reaxys; Krishnan; Friedman; Journal of Physical Chemistry; vol. 73; (1969); p. 1572, View in Reaxys; Holm; Journal of Organometallic Chemistry; vol. 56; (1973); p. 87,90, View in Reaxys; Langer; Purnell; Journal of Physical Chemistry; vol. 67; (1963); p. 263,265,266, View in Reaxys; Srivastava; Crossley; Canadian Journal of Chemistry; vol. 54; (1976); p. 1418,1420, 1422, View in Reaxys

Entropy

Langer; Purnell; Journal of Physical Chemistry; vol. 67; (1963); p. 263,265,266, View in Reaxys; Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys

Heat of combustion 4737 cal/g. at constant volume

Smith; Sunner; Svedberg-Festschr. <Uppsala 1944> S. 352, 366, 367, View in Reaxys; Smith; Bjellerup; Acta Chemica Scandinavica (1947-1973); vol. 1; (1947); p. 566,569, View in Reaxys

Cryoscopic constant

Bury; Jenkins; Journal of the Chemical Society; (1934); p. 688,690, 695, View in Reaxys

in Benzol.

Heat of combustion 4757 cal/g. at constant volume

Kablukow; Perelman; Doklady Akademii Nauk SSSR; (1930); p. 519; Zhurnal Obshchei Khimii; vol. 1; (1931); p. 1249,1256; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 23, View in Reaxys

Cryoscopic constant

Dreisbach,R.R.; Physical Properties of Chemical Compounds (= Advances in Chemistry Series Nr. 15) <Washington 1955> S. 150, View in Reaxys

Partition octan-1-ol/water (MCS) (6) 1 of 6

log POW

2.9

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys 2 of 6

log POW

3.12

Temperature (Partition octan-1-ol/water (MCS)) [°C]

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 3 of 6

log POW

3.14

Temperature (Partition octan-1-ol/water (MCS)) [°C]

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 4 of 6

log POW

3.25

Temperature (Partition octan-1-ol/water (MCS)) [°C]

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 5 of 6

log POW

3.29

Temperature (Partition octan-1-ol/water (MCS)) [°C]

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 6 of 6

log POW

3.09

Temperature (Partition octan-1-ol/water (MCS)) [°C]

Ruelle, Paul; Kesselring, Ulrich W.; Journal of Pharmaceutical Sciences; vol. 87; nb. 8; (1998); p. 1015 - 1024, View in Reaxys Self-diffusion (1) References

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Ertl; Dullien; AIChE Journal; vol. 19; (1973); p. 1215,1218, View in Reaxys; Haase et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 30; (1975); p. 1084, View in Reaxys Solubility (MCS) (21) 1 of 21

Solubility [g·l-1]

0.197

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

water

Potier, Jonathan; Menuel, Stephane; Rousseau, Jolanta; Tumkevicius, Sigitas; Hapiot, Frederic; Monflier, Eric; Applied Catalysis A: General; vol. 479; (2014); p. 1 - 8, View in Reaxys 2 of 21

Saturation

in pure solvent

Comment (Solubility (MCS))

high pressure. Object(s) of Study: pressure dependence. Object(s) of Study: temperature dependence

Leeke, Gary A.; Santos, Regina C.; Seville, Jonathan; Al-Duri, Bushra; Lee, Connie K.Y.; Holmes, Andrew B.; Journal of Chemical and Engineering Data; vol. 49; nb. 1; (2004); p. 48 - 52, View in Reaxys 3 of 21

Saturation

in pure solvent

Comment (Solubility (MCS))

equation

Ruelle, Paul; Kesselring, Ulrich W.; Journal of Pharmaceutical Sciences; vol. 87; nb. 8; (1998); p. 998 - 1014, View in Reaxys; Jain, Neera; Yalkowsky, Samuel H.; Journal of Pharmaceutical Sciences; vol. 90; nb. 2; (2001); p. 234 - 252, View in Reaxys 4 of 21

Solubility [g·l-1]

0.278

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

temperature dependence

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 5 of 21

Solubility [g·l-1]

0.2745

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

temperature dependence

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 6 of 21

Solubility [g·l-1]

0.384

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

temperature dependence

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 7 of 21

Solubility [g·l-1]

0.368

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Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

temperature dependence

Finizio, Antonio; Di Guardo, Antonio; Chemosphere; vol. 45; nb. 6-7; (2001); p. 1063 - 1070, View in Reaxys 8 of 21

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

Solubility 2.82E-3 mol/l

Sanemasa, Isao; Wu, Ji-Shi; Toda, Kei; Bulletin of the Chemical Society of Japan; vol. 70; nb. 2; (1997); p. 365 - 369, View in Reaxys 9 of 21

Saturation

in pure solvent

Valvani; Yalkowsky; Roseman; Journal of Pharmaceutical Sciences; vol. 70; nb. 5; (1981); p. 502 - 507, View in Reaxys; Yalkowsky; Valvani; Journal of Pharmaceutical Sciences; vol. 69; nb. 8; (1980); p. 912 - 922, View in Reaxys 10 of 21

Comment (Solubility (MCS))

in H20

Nelson; Smit; South African Journal of Chemistry; vol. 31; (1978); p. 76, View in Reaxys 11 of 21

Comment (Solubility (MCS))

in Wasser

Vesala; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 28; (1974); p. 839,841, View in Reaxys 12 of 21

Comment (Solubility (MCS))

Loesl.Parameter

Narbutt; Siekierski; Roczniki Chemii; vol. 48; (1974); p. 1777,1781, View in Reaxys 13 of 21

Comment (Solubility (MCS))

W. bei 35grad: 2.92*1E-3 mol/l

Hine et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 1473, View in Reaxys 14 of 21

Comment (Solubility (MCS))

Decalin bei 35grad: ?

Hine et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 1473, View in Reaxys 15 of 21

Comment (Solubility (MCS))

in 1E4 ml C6H5Br loesen sich bei 25grad: 4.1 ml W. (mit HTO durch Scintillationszahlung)

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys 16 of 21

Comment (Solubility (MCS))

in 1E4 ml C6H5Br loesen sich bei 30grad: 4.7 ml W. (mit HTO durch Scintillationszahlung)

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys 17 of 21

Comment (Solubility (MCS))

in 1E4 ml C6H5Br loesen sich bei 35grad: 5.3 ml W. (mit HTO durch Scintillationszahlung)

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys 18 of 21

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

aq. AgNO3

Andrews; Keefer; Journal of the American Chemical Society; vol. 72; (1950); p. 3113, View in Reaxys

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19 of 21

Solubility [g·l-1]

0.41

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

bromobenzene

Andrews; Keefer; Journal of the American Chemical Society; vol. 72; (1950); p. 3113, View in Reaxys 20 of 21

Solubility [g·l-1]

0.446

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

bromobenzene

Andrews; Keefer; Journal of the American Chemical Society; vol. 72; (1950); p. 3113, View in Reaxys 21 of 21

Solubility [g·l-1]

0.446

Saturation

in solution

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

van Arkel; Vles; Recueil des Travaux Chimiques des Pays-Bas; vol. 55; (1936); p. 407,408, View in Reaxys; Gross; Saylor; Journal of the American Chemical Society; vol. 53; (1931); p. 1744,1750, View in Reaxys Solution Behaviour (MCS) (33) 1 of 33

Description (Solution Behaviour (MCS))

Solubility [Ostwald absorption coefficient]

Solvent (Solution Behaviour (MCS))

aq. NH3

Temperature (Solution Be- 29.85 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

air

Goergenyi, Miklos; Dewulf, Jo; Van Langenhove, Herman; Kiraly, Zoltan; Chemosphere; vol. 59; nb. 8; (2005); p. 1083 1090, View in Reaxys 2 of 33

Description (Solution Behaviour (MCS))

Solubility [Ostwald absorption coefficient]

Solvent (Solution Behaviour (MCS))

H2O

Temperature (Solution Be- 29.85 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

air

Goergenyi, Miklos; Dewulf, Jo; Van Langenhove, Herman; Kiraly, Zoltan; Chemosphere; vol. 59; nb. 8; (2005); p. 1083 1090, View in Reaxys 3 of 33

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

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4 of 33

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 33

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 33

Description (Solution Behaviour (MCS))

Solubilizing

Solvent (Solution Behaviour (MCS))

H2O

Temperature (Solution Be- 24.9 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

2-{2-[4-(1,1,3,3-tetramethyl-butyl)-phenoxy]-ethoxy}-ethanol

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

sodium dodecyl-sulfate

Muijselaar, Pim G. H. M.; Claessens, Henk A.; Cramers, Carel A.; Analytical Chemistry; vol. 66; nb. 5; (1994); p. 635 644, View in Reaxys 8 of 33

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

Makitra, R. G.; Pirig, Ya. N.; Politanskaya, T. I.; J. Appl. Chem. USSR (Engl. Transl.); vol. 54; nb. 1; (1981); p. 54 - 58,47 51, View in Reaxys 9 of 33

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

Makitra, R. G.; Pirig, Ya. N.; Politanskaya, T. I.; J. Appl. Chem. USSR (Engl. Transl.); vol. 54; nb. 1; (1981); p. 54 - 58,47 51, View in Reaxys 10 of 33

Description (Solution Behaviour (MCS))

Mutual solubility

Goozner; Labes; Molecular crystals and liquid crystals; vol. 56; nb. 3; (1979); p. 75 - 81, View in Reaxys 11 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys; Naumenko et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 42; (1969); p. 2522,2376, View in Reaxys

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12 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 0 - 44 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

hydrogenchloride

Gerrard et al.; Journal of Applied Chemistry; vol. 9; (1959); p. 89,91, View in Reaxys 13 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

helium

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 14 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

neon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 15 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

argon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 16 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

krypton

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 17 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

xenon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys

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18 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

xenon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 19 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 55 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

xenon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 20 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water

Wing; Johnston; Journal of the American Chemical Society; vol. 79; (1957); p. 864, View in Reaxys 21 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Solvent (Solution Behaviour (MCS))

heptane

Temperature (Solution Be- -78.5 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

hydrogenchloride

Brown; Brady; Journal of the American Chemical Society; vol. 74; (1952); p. 3570,3575, View in Reaxys 22 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Solvent (Solution Behaviour (MCS))

toluene

Temperature (Solution Be- -78.5 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

hydrogenchloride

Brown; Brady; Journal of the American Chemical Society; vol. 74; (1952); p. 3570,3575, View in Reaxys 23 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 20 - 67 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water

Staveley; Jeffes; Moy; Transactions of the Faraday Society; vol. 39; (1943); p. 5,8, View in Reaxys 24 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 32 haviour (MCS)) [°C]

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Partner (Solution Behaviour (MCS))

Dichlorofluoromethane

Copley; Zellhoefer; Marvel; Journal of the American Chemical Society; vol. 61; (1939); p. 3551, View in Reaxys 25 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 32 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

Dichlorodifluoromethane

Copley; Zellhoefer; Marvel; Journal of the American Chemical Society; vol. 61; (1939); p. 3551, View in Reaxys 26 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 32 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

trichlorofluoromethane

Copley; Zellhoefer; Marvel; Journal of the American Chemical Society; vol. 61; (1939); p. 3551, View in Reaxys 27 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

ammonia

Bell; Journal of the Chemical Society; (1931); p. 1376, View in Reaxys 28 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

hydrogenchloride

Bell; Journal of the Chemical Society; (1931); p. 1376, View in Reaxys 29 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

hydrogen sulfide

Bell; Journal of the Chemical Society; (1931); p. 1376, View in Reaxys 30 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

2-hydroxynitrobenzene

Sidgwick; Spurrell; Davies; Journal of the Chemical Society; vol. 107; (1915); p. 1213, View in Reaxys 31 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

4-nitro-phenol

Sidgwick; Spurrell; Davies; Journal of the Chemical Society; vol. 107; (1915); p. 1213, View in Reaxys 32 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

4-nitrobenzyl chloride

v. Halban; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 144, View in Reaxys 33 of 33

Description (Solution Behaviour (MCS))

Dissolving capacity

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Comment (Solution Behaviour (MCS))

bei verschiedenen Temperaturen und Drucken.

Partner (Solution Behaviour (MCS))

carbon dioxide

Sander; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 535, View in Reaxys Sound Properties (18) Description (Sound Comment (Sound Properties) Properties) Velocity of sound

References

temperature deMutalik, Venkatesh; Manjeshwar, Lata S.; Sairam, Malladi; Aminabhavi, Tejraj M.; Journal pendence. Object(s) of Chemical Thermodynamics; vol. 38; nb. 8; (2006); p. 1062 - 1071, View in Reaxys of Study: in the presence of additives

Velocity of sound

Padmini et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 1404,1405, View in Reaxys; Deshpande et al.; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 469,470-472, View in Reaxys; Takagi, Toshiharu; Teranishi, Hiroshi; Journal of Chemical Thermodynamics; vol. 16; nb. 11; (1984); p. 1031 - 1036, View in Reaxys; Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 - 135, View in Reaxys

Ultrasonic properties

Khabibullaev et al.; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 944, View in Reaxys; Langguth et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 495, View in Reaxys; Plass; Berichte der Bunsen-Gesellschaft; vol. 74; (1970); p. 343,344-346, View in Reaxys; Beste; Berichte der Bunsen-Gesellschaft; vol. 79; (1975); p. 54, View in Reaxys; Wratschko, Kohler; Monatshefte fuer Chemie; vol. 93; (1962); p. 374,376, View in Reaxys; Lucas et al.; Molecular Physics; vol. 18; (1970); p. 505,511,513,515,519,520, View in Reaxys

Sound absorption

Khabibullaev et al.; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 3; (1971); p. 66; ; p. 337, View in Reaxys

Velocity of sound

in fluessigem Brombenzol bei Temperaturen von 20grad.

Dshioew; Trudy Stalinirsk. pedagog. Inst.; vol. 7; (1959); p. 1,7; Chem.Abstr.; vol. 56; (1962); p. 13565, View in Reaxys

Sound absorption

bei Temperaturen von 21grad.

Parthasarathy et al.; Naturwissenschaften; Nuovo Cimento; vol. <10> 10; (1958); p. 483,111,115,117, View in Reaxys

Sound absorption

bei Temperaturen von 25grad.

Heasell; Lamb; Pr. phys. Soc. London; vol. 69; (1956); p. 869,874, View in Reaxys

Velocity of sound

in fluessigem Brombenzol bei Temperaturen von -30grad bis +45grad.

Awdus; Prim. Ultraakust. Issled. Vescestva; nb. 1; (1955); p. 43,49, 56; Chem.Abstr.; (1958); p. 822, View in Reaxys

Velocity of sound

in fluessigem Brombenzol bei Temperaturen von -20grad bis +20grad.

Belinskaja; Uc. Zap. Moskovsk. oblast. pedagog. Inst.; vol. 33; (1955); p. 221,238; Chem.Abstr.; (1958); p. 821, View in Reaxys

Sound absorption

bei Temperaturen von -26grad bis +47grad.

Koschkin; Prim. Ultraakust. Issled. Vescestva; nb. 1; (1955); p. 101,128; Chem.Abstr.; (1959); p. 20998, View in Reaxys

Velocity of sound

in fluessigem Brombenzol bei Temperaturen von 15grad und bei 25grad.

Collins; Navidi; Journal of Chemical Physics; vol. 22; (1954); p. 1254, View in Reaxys

Velocity of sound

in fluessigem Brombenzol bei Temperaturen von 22grad.

Parthasarathy; Bakhshi; Indian Journal of Physics (1926-1976); vol. 27; (1953); p. 73, View in Reaxys

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Sound absorption

bei Temperaturen von 20grad.

Parthasarathy et al.; Journal de Physique et le Radium; vol. <8> 14; (1953); p. 541,545; Nuovo Cimento; vol. <9> 10; (1953); p. 264,266, View in Reaxys

Sound absorption

bei Temperaturen von -22grad bis +40grad.

Sette; Ricerca Scientifica; vol. 22; (1952); p. 706,708, View in Reaxys

Velocity of sound

im Temperaturbereich von 0grad (1234 m/sec) bis 60grad (1047 m/ sec).

Lagemann; McMillan; Woolf; Journal of Chemical Physics; vol. 17; (1949); p. 370, View in Reaxys

Velocity of sound

in Brombenzol bei 20grad: 1170 m/ sec.

Lagemann; Evans; McMillan; Journal of the American Chemical Society; vol. 70; (1948); p. 2997, View in Reaxys

Velocity of sound

im Temperatubereich von 32.5grad (1166 m/sec) bis 120grad (88o m/ sec).

Suryaprakasam; Proceedings - Indian Academy of Sciences, Section A; vol. <A> 12; (1941); p. 341,348, View in Reaxys

Velocity of sound

bei 28grad: 1134 m/sec.

Parthasarathy; Proceedings - Indian Academy of Sciences, Section A; vol. <A> 3; (1936); p. 519,520, View in Reaxys

Space Group (2) Space Group

References Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys

Biswas; Acta Crystallographica; vol. 11; (1958); p. 882, View in Reaxys

Static Dielectric Constant (6) Static Dielectric Temperature (Static References Constant Dielectric Constant) [°C] Jahn; Moeller; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 13; (1894); p. 393, View in Reaxys; Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Magee; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 3093,3098, 3099, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys 5.506

Osipow; Panina; Zhurnal Fizicheskoi Khimii; vol. 32; (1958); p. 2287,2288, 2289; Chem.Abstr.; (1959); p. 11920, View in Reaxys

5.31

Musset et al.; Z. ang. Phys.; vol. 8; (1956); p. 8,10, View in Reaxys

5.391

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

5.74 - 4.96

1 - 55

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

5.308

Dreisbach,R.R.; Physical Properties of Chemical Compounds (= Advances in Chemistry Series Nr. 15) <Washington 1955> S. 150, View in Reaxys

Surface Tension (15) Surface Tension Temperature (Sur[g·s-2] face Tension) [°C] 28.66 - 35.8

Comment (Surface Tension)

20 - 80

References Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 126, View in Reaxys; Agarwal et al.; Journal of Chemical and Engineering Data; vol. 24; (1979); p. 181,182, View in Reaxys; Nigam; Maini; Indian Journal of Chemistry; vol. 9; (1971); p. 855, View in Reaxys; Wellek et al.; AIChE Journal; vol. 12; (1966); p. 854,857, View in Reaxys; Mahl et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 249; (1972); p. 337, View in Reaxys; Roedel; Lunkenheimer; Tenside; vol. 15; (1978); p. 135,139, View in Reaxys; Korenman; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 380,394, View in Reaxys

28.16

86.5

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

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2018-06-17 20:44:10

30.81

62.5

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

33.97

41.2

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

35.97

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

36.3

Picon; Mangeot; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 212; (1941); p. 189, View in Reaxys

35.09

Hennaut-Roland; Lek; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 183, View in Reaxys

36.34

Hennaut-Roland; Lek; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 183, View in Reaxys

36.93

Hennaut-Roland; Lek; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 183, View in Reaxys

35.75

Harkins; Jordan; Journal of the American Chemical Society; vol. 52; (1930); p. 1751,1760, View in Reaxys at:20-60 degreeC.

Postowski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 61; (1929); p. 721; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 427, View in Reaxys

22.5 - 37.92

15 - 150

Sugden; Journal of the Chemical Society; vol. 125; (1924); p. 1173, View in Reaxys

21.1 - 42.2

-17.5 - 153

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 155, View in Reaxys

31 - 37.25

13 - 70

Kremann; Meingast; Monatshefte fuer Chemie; vol. 35; (1914); p. 1360, View in Reaxys; Morgan; Daghlian; Journal of the American Chemical Society; vol. 33; (1911); p. 675; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 173, View in Reaxys

Transition Point(s) of Liquid Modification(s) (1) References Hayler; Goldstein; Journal of Chemical Physics; vol. 66; (1977); p. 4736,4741, View in Reaxys Transport Data (1) Description (Trans- References port Data) Thermal conductiv- Frontas'ew et al.; Zhurnal Fizicheskoi Khimii; vol. 20; (1946); p. 91,100; Chem.Abstr.; (1946); p. 4284, ity View in Reaxys; Filippow; Vestnik Moskovskogo Universiteta; vol. 9; nb. 12; (1954); p. 45; Chem.Abstr.; (1955); p. 15430, View in Reaxys; Riedel; Ch. Ing. Tech.; vol. 23; (1951); p. 321,323, View in Reaxys; Riedel; Mitt. Kaeltetechn. Inst.; nb. 2; (1948); p. 3,23, View in Reaxys; Kleiman et al.; Mendeleev Chemistry Journal; vol. 18; nb. 5; (1973); p. 139; ; p. 595, View in Reaxys; Guseinov et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 116; ; p. 212, View in Reaxys Transport Phenomena (MCS) (75) 1 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

1,4-dioxane

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 2 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

benzene

140/219

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Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 3 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

toluene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 4 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

tetrachloromethane

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 5 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

1,4-dioxane; benzene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 6 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

1,4-dioxane; toluene

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 7 of 75

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

1,4-dioxane; tetrachloromethane

Varshney, Surabhl; Singh, Mukhtar; Journal of Chemical and Engineering Data; vol. 51; nb. 3; (2006); p. 1136 - 1140, View in Reaxys 8 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

octanol

Gabler, Toralf; Paschke, Albrecht; Schueuermann, Gerrit; Journal of Chemical and Engineering Data; vol. 43; nb. 3; (1998); p. 413 - 416, View in Reaxys 9 of 75

Description (Transport Phenomena (MCS))

Viscosity

141/219

2018-06-17 20:44:10

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

2-methyl-propan-1-ol

Artigas, Hector; Dominguez, Magdalena; Mainar, Ana M.; Lopez, M. Carmen; Royo, Felix M.; Journal of Chemical and Engineering Data; vol. 43; nb. 4; (1998); p. 580 - 584, View in Reaxys 10 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

diethyl ether; benzene

Temperature (Transport Phenomena (MCS)) [°C]

19.85

Partner (Transport Phenomena (MCS))

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 12; (1998); p. 1876 - 1877, View in Reaxys 11 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

tetrahydrofuran

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 12 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

TETRAHYDROPYRANE

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 13 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

2-methyltetrahydrofuran

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 14 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25 - 40

Partner (Transport Phenomena (MCS))

2,5-dimethyltetrahydrofuran

Rodriguez; Lafuente; Lopez; Royo; Urieta; Journal of Solution Chemistry; vol. 26; nb. 2; (1997); p. 207 - 215, View in Reaxys 15 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

water

142/219

2018-06-17 20:44:10

Gabler, Toralf; Paschke, Albrecht; Schueuermann, Gerrit; Journal of Chemical and Engineering Data; vol. 41; nb. 1; (1996); p. 33 - 36, View in Reaxys 16 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 40

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Ramadevi; Venkatesu; Rao; Journal of Chemical and Engineering Data; vol. 41; nb. 3; (1996); p. 479 - 481, View in Reaxys 17 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

2-methoxy-ethanol

Krishnan; Rambabu; Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 40; nb. 1; (1995); p. 132 135, View in Reaxys 18 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25 - 70

Partner (Transport Phenomena (MCS))

in tetrafluoroethylene-propylene copolymeric sheets

Aminabhavi, Tejraj M.; Phayde, Hemant T. S.; Journal of Chemical & Engineering Data; vol. 39; nb. 3; (1994); p. 517 - 521, View in Reaxys 19 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

acetonitrile

Fiedel; Schwelger; Lucas; Journal of Chemical and Engineering Data; vol. 36; nb. 2; (1991); p. 169 - 170, View in Reaxys 20 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

hexane

Fiedel; Schwelger; Lucas; Journal of Chemical and Engineering Data; vol. 36; nb. 2; (1991); p. 169 - 170, View in Reaxys 21 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

ethanol

Fiedel; Schwelger; Lucas; Journal of Chemical and Engineering Data; vol. 36; nb. 2; (1991); p. 169 - 170, View in Reaxys 22 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 60

Partner (Transport Phenomena (MCS))

toluene; octanol

143/219

2018-06-17 20:44:10

Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 35; nb. 1; (1990); p. 93 - 97, View in Reaxys 23 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 60

Partner (Transport Phenomena (MCS))

octanol; hexan-1-ol

Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 35; nb. 1; (1990); p. 93 - 97, View in Reaxys 24 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 60

Partner (Transport Phenomena (MCS))

toluene

Singh, R. P.; Sinha, C. P.; Das, J. C.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 2; (1990); p. 419 - 426, View in Reaxys 25 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

tetrachloromethane

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 26 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 60

Partner (Transport Phenomena (MCS))

toluene; ethylbenzene

Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 34; nb. 3; (1989); p. 335 - 338, View in Reaxys 27 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 60

Partner (Transport Phenomena (MCS))

ethylbenzene; hexan-1-ol

Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 34; nb. 3; (1989); p. 335 - 338, View in Reaxys 28 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30 - 60

Partner (Transport Phenomena (MCS))

toluene; hexan-1-ol

Singh; Sinha; Das; Ghosh; Journal of Chemical and Engineering Data; vol. 34; nb. 3; (1989); p. 335 - 338, View in Reaxys 29 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

Bromoform

144/219

2018-06-17 20:44:10

Manjeshwar; Aminabhavi; Journal of Chemical and Engineering Data; vol. 33; nb. 2; (1988); p. 184 - 185, View in Reaxys 30 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

tetrachloromethane

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys 31 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

Bromoform

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys 32 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

tetrachloromethane

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 33 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

Bromoform

Aminabhavi, T M; Manjeshwar, L S; Balundgi, R H; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 26; nb. 8; (1987); p. 641 - 647, View in Reaxys 34 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

199.9

Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

Ashraf, S. M.; Srivastava, R.; Hussain, Asghar; Journal of Chemical & Engineering Data; vol. 31; nb. 1; (1986); p. 100 - 102, View in Reaxys 35 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

chlorobenzene

Aminabhavi, T. M.; Balundgi, R. H.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 267; nb. 5; (1986); p. 1021 - 1024, View in Reaxys; Aminabhavi, T. M.; Jayadevappa, E. S.; Prasad, B. R.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 22; nb. 3; (1983); p. 231 - 233, View in Reaxys

145/219

2018-06-17 20:44:10

36 of 75

Description (Transport Phenomena (MCS))

Thermal diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

chlorobenzene; toluene

Rowley, R. L.; Hall, M. D.; Journal of Chemical Physics; vol. 85; nb. 6; (1986); p. 3550 - 3555, View in Reaxys 37 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 38 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 39 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

acetonitrile

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 40 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

acetonitrile

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 41 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 42 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys

146/219

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43 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

258

Partner (Transport Phenomena (MCS))

(12)C5(13)CH5Br

Rutherford, W. M.; Journal of Chemical Physics; vol. 81; nb. 12.II; (1984); p. 6136 - 6139, View in Reaxys 44 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25 - 35

Partner (Transport Phenomena (MCS))

chlorobenzene; toluene

Platt, G.; Vongvanich, T.; Fowler, G.; Rowley, R. L.; Journal of Chemical Physics; vol. 77; nb. 4; (1982); p. 2121 - 2129, View in Reaxys 45 of 75

Description (Transport Phenomena (MCS))

Diffusion

Lusis; Ratcliff; AIChE Journal; vol. 17; (1971); p. 1492,1493, View in Reaxys; Fuller et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 3679, View in Reaxys; Kamal; Canjar; AIChE Journal; vol. 8; (1962); p. 329,331-332, View in Reaxys; Smith; Kollmansberger; Journal of Physical Chemistry; vol. 69; (1965); p. 4159, View in Reaxys; Haase et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 30; (1975); p. 1084, View in Reaxys 46 of 75

Description (Transport Phenomena (MCS))

Thermal diffusion

Gulari et al.; AIChE Journal; vol. 19; (1973); p. 1196,1201, View in Reaxys; Rastogi; Yadava; Journal of Chemical Physics; vol. 52; (1970); p. 2791, View in Reaxys 47 of 75

Description (Transport Phenomena (MCS))

Viscosity

Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 75; (1972); p. 68, View in Reaxys; Deitsch; Russian Journal of Physical Chemistry; vol. 36; (1962); p. 959; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 1777, View in Reaxys; Pospechow; Trudy Odesskogo Sel'skokhozyaistvennogo Instituta; vol. 9; (1957); p. 59,60-70; Chem.Abstr.; vol. 54; nb. 10482; (1960), View in Reaxys 48 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

benzene

Miller; Carman; Transactions of the Faraday Society; vol. 55; (1959); p. 1831,1835,1836, View in Reaxys 49 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

chlorobenzene

Caldwell; Babb; Journal of Physical Chemistry; vol. 60; (1956); p. 51,53, View in Reaxys 50 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

chlorobenzene

Caldwell; Babb; Journal of Physical Chemistry; vol. 60; (1956); p. 51,53, View in Reaxys

147/219

2018-06-17 20:44:10

51 of 75

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

chlorobenzene

Caldwell; Babb; Journal of Physical Chemistry; vol. 60; (1956); p. 51,53, View in Reaxys 52 of 75

Description (Transport Phenomena (MCS))

Thermal diffusion

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

carbon disulfide

Rutherford; Drickamer; Journal of Chemical Physics; vol. 22; (1954); p. 1157,1161, View in Reaxys 53 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

benzene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 54 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

toluene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 55 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

1,3,5-trimethyl-benzene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 56 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

ethylbenzene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 57 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

m-xylene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 58 of 75

Description (Transport Phenomena (MCS))

Diffusion

148/219

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Solvent (Transport Phenomena (MCS))

1-isopropyl-4-methyl-benzene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 59 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

cyclohexane

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 60 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

cyclohexene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 61 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

decahydronaphthalene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 62 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

1,2,3,4-tetrahydro-naphthalene

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 63 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

dioxane

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 64 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

hexane

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 65 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

diethyl ether

149/219

2018-06-17 20:44:10

Temperature (Transport Phenomena (MCS)) [°C]

7.5

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 66 of 75

Description (Transport Phenomena (MCS))

Diffusion

Partner (Transport Phenomena (MCS))

Davis, H. S.; Crandall, G. P.; Journal of the American Chemical Society; vol. 52; (1930); p. 3757 - 3785, View in Reaxys; vol. O: MVol.3; 58, page 482 - 484 ; (from Gmelin), View in Reaxys 67 of 75

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

benzene

Yajnik et al.; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 312, View in Reaxys 68 of 75

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

toluene

Yajnik et al.; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 312, View in Reaxys 69 of 75

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

chlorobenzene

Kremann; Gugl; Meingast; Monatshefte fuer Chemie; vol. 35; (1914); p. 1381, View in Reaxys; Unkowskaja; Wolowa; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 57; (1925); p. 109,120; Chem. Zentralbl.; vol. 97; nb. I; (1926); p. 2646, View in Reaxys 70 of 75

Description (Transport Phenomena (MCS))

Diffusion

Partner (Transport Phenomena (MCS))

iodine

Miller; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 106; (1924); p. 740, View in Reaxys 71 of 75

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

benzene

Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys 72 of 75

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

acetone

Ssachanow; Rjachowski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 47; (1915); p. 129; Chem. Zentralbl.; vol. 87; nb. I; (1916); p. 729, View in Reaxys 73 of 75

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

chloroform

150/219

2018-06-17 20:44:10

Ssachanow; Rjachowski; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 86; (1914); p. 534; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 46; (1914); p. 84, View in Reaxys 74 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

methanol

Thovert; Annales de Physique (Paris, France); vol. <9>2; (1914); p. 417; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 150; (1910); p. 270, View in Reaxys 75 of 75

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

benzene

Thovert; Annales de Physique (Paris, France); vol. <9>2; (1914); p. 417; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 150; (1910); p. 270, View in Reaxys Vapour Pressure (16) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

References Khosla et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 251; (1972); p. 129,130, 135, View in Reaxys; Hine et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 1473, View in Reaxys

43.62

McGlashan; Windgrove; Transactions of the Faraday Society; vol. 52; (1956); p. 470,471, View in Reaxys

66.17

McGlashan; Windgrove; Transactions of the Faraday Society; vol. 52; (1956); p. 470,471, View in Reaxys

0.053

-30

Riding et al.; Transactions of the Faraday Society; vol. 52; (1956); p. 1354,1362, View in Reaxys

0.158

-19.7

Riding et al.; Transactions of the Faraday Society; vol. 52; (1956); p. 1354,1362, View in Reaxys

0.175

-17.4

Riding et al.; Transactions of the Faraday Society; vol. 52; (1956); p. 1354,1362, View in Reaxys

3.1

Kohler,Rott; Monatshefte fuer Chemie; vol. 85; (1954); p. 703,11, View in Reaxys

23 - 725.2

56.1 - 154.2

Dreyer et al.; Journal fuer Praktische Chemie (Leipzig); vol. <4> 1; (1954); p. 324,326, View in Reaxys

47.16 - 507.5

71.8 - 140.7

Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2879, View in Reaxys

0.011 - 0.139

-21.9 - 0.3

Silberman-Granowsskaja; Schugam; Zhurnal Fizicheskoi Khimii; vol. 14; (1940); p. 1004; Chem.Abstr.; (1941); p. 3867, View in Reaxys

0.901

26.1

Silberman-Granowsskaja; Schugam; Zhurnal Fizicheskoi Khimii; vol. 14; (1940); p. 1004; Chem.Abstr.; (1941); p. 3867, View in Reaxys

289.1 - 2347.4

121.6 - 206

Zmaczynski; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 27; (1930); p. 514; Chem. Zentralbl.; vol. 102; nb. I; (1931); p. 1319, View in Reaxys; Zmaczynski; Rocniki Chem.; vol. 13; (1933); p. 181,189, View in Reaxys

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

130

Rabcewicz-Zubkowski; Roczniki Chemii; vol. 12; (1932); p. 163; Chem. Zentralbl.; vol. 103; nb. II; (1932); p. 2299, View in Reaxys

-25.1 - -15.1

Muendel; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 85; (1913); p. 454, View in Reaxys

30 - 270

Young; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 425, View in Reaxys

0.162 - 0.349

NMR Spectroscopy (53) 1 of 53

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

tetrahydrofuran-d8

151/219

2018-06-17 20:44:10

Location

supporting information

Koch, Alexander; Wirgenings, Marino; Krieck, Sven; Görls, Helmar; Pohnert, Georg; Westerhausen, Matthias; Organometallics; vol. 36; nb. 20; (2017); p. 3981 - 3986, View in Reaxys 2 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Li, Bai; Gao, Linfeng; Bian, Fengling; Yu, Wei; Tetrahedron Letters; vol. 54; nb. 9; (2013); p. 1063 - 1066, View in Reaxys 3 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Li, Bai; Gao, Linfeng; Bian, Fengling; Yu, Wei; Tetrahedron Letters; vol. 54; nb. 9; (2013); p. 1063 - 1066, View in Reaxys 4 of 53

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Huang, Chang-Cang; Liu, Jian-Jun; Chen, Yong; Lin, Mei-Jin; Chemical Communications; vol. 49; nb. 98; (2013); p. 11512 - 11514, View in Reaxys 5 of 53

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 6 of 53

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

152/219

2018-06-17 20:44:10

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Seo, Sangwon; Taylor, John B.; Greaney, Michael F.; Chemical Communications; vol. 48; nb. 66; (2012); p. 8270 - 8272, View in Reaxys 7 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 50.32 scopy) [MHz] Termaten, Arjan; Van der Sluis, Marcel; Bickelhaupt, Friedrich; European Journal of Organic Chemistry; nb. 11; (2003); p. 2049 - 2055, View in Reaxys 8 of 53

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

nematic phase

Celebre; Castiglione; Longeri; Emsley; Journal of Magnetic Resonance - Series A; vol. 121; nb. 2; (1996); p. 139 - 146, View in Reaxys; Carravetta; Castiglione; De Luca; Edgar; Emsley; Farrant; Foord; Lindon; Longeri; Palke; Turner; Journal of magnetic resonance (San Diego, Calif. : 1997); vol. 135; nb. 2; (1998); p. 298 - 309, View in Reaxys 9 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

nematic phase

Carravetta; Castiglione; De Luca; Edgar; Emsley; Farrant; Foord; Lindon; Longeri; Palke; Turner; Journal of magnetic resonance (San Diego, Calif. : 1997); vol. 135; nb. 2; (1998); p. 298 - 309, View in Reaxys 10 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Breuer, W.; Frohn, H. J.; Journal of Fluorine Chemistry; vol. 47; nb. 2; (1990); p. 301 - 315, View in Reaxys 11 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CCl4

Temperature (NMR Spectroscopy) [°C]

27 - 30

Biekofsky, Rodolfo R.; Pomilio, Alicia B.; Contreras, Ruben H.; Kowalewski, Dora G. de; Facelli, Julio C.; Magnetic Resonance in Chemistry; vol. 27; nb. 2; (1989); p. 158 - 161, View in Reaxys 12 of 53

Description (NMR Spectroscopy)

Chemical shifts

153/219

2018-06-17 20:44:10

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 13 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

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; Takeuchi, Yoshito; Furuyama, Hideichi; Fukushi, Sachio; Fujiwara, Shizuo; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1985); p. 175 - 178, 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 14 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

nitromethane

Contreras, R. H.; Ferraro, M. B.; Kowalewski, D. G. de; Diaz, L.; Magnetic Resonance in Chemistry; vol. 23; nb. 5; (1985); p. 296 - 300, View in Reaxys 15 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CH2Cl2

Temperature (NMR Spectroscopy) [°C]

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 16 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

24.9

Fung; Kong; Journal of the American Chemical Society; vol. 106; nb. 21; (1984); p. 6193 - 6196, View in Reaxys 17 of 53

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 18 of 53

Description (NMR Spectroscopy)

Chemical shifts

154/219

2018-06-17 20:44:10

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 19 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Bailey, William F.; Cioffi, Eugene A.; Wiberg, Kenneth B.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4219 4225, View in Reaxys 20 of 53

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 21 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

in DMSO-d(6)

Gould et al.; Journal of Magnetic Resonance (1969-1992); vol. 34; (1979); p. 37,39, View in Reaxys 22 of 53

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 23 of 53

Description (NMR Spectroscopy)

NMR

Huegel,H.M. et al.; Australian Journal of Chemistry; vol. 32; (1979); p. 1511 - 1519, View in Reaxys; Llabres,G. et al.; Canadian Journal of Chemistry; vol. 56; (1978); p. 2008 - 2012, View in Reaxys; Martin,R.H. et al.; Tetrahedron; vol. 30; (1974); p. 179 - 185, View in Reaxys; Tarpley,A.R.; Goldstein,J.H.; Journal of Physical Chemistry; vol. 76; (1972); p. 515, 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; Daineko et al.; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 2536,2555,2558,2559, View in Reaxys; Freymann et al.; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 3; (1962); p. 1222, View in Reaxys; Freymann; Archives des Sciences; vol. 12; (1959); p. 207; Chem.Abstr.; nb. 11705; (1960), View in Reaxys; Takai et al.; Chemical and Pharmaceutical Bulletin; vol. 26; (1978); p. 1303,1306, View in Reaxys; Castellano; Sun; Journal of the American Chemical Society; vol. 88; (1966); p. 4742, View in Reaxys; Hruska et al.; Canadian Journal of Chemistry; vol. 43; (1965); p. 2392,2393, View in Reaxys; Yamada et al.; Journal of the American Chemical Society; vol. 99; (1977); p. 3572,3573, View in Reaxys; Powles; Figgins; Molecular Physics; vol. 13; (1967); p. 253, View in Reaxys; Heimanek et al.; Journal of the Chemical Society, Chemical Communications; (1977); p. 561, View in Reaxys; Miyajima et al.; Chemical and Pharmaceutical Bulletin; vol. 19; (1971); p. 2301,2305, View in Reaxys; Breitmaier et al.; Tetrahedron; vol. 29; (1973); p. 2485,2486,2488, View in Reaxys; Norton; Tetrahedron; vol. 33; (1977); p. 2577,2579, 2580, View in Reaxys; Hinton; Layton; Organic Magnetic Resonance; vol. 4; (1972); p. 448, 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; Nelson et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 3089,3090, View in Reaxys; Glukhikh; Voronkov; Doklady Physical Chemistry; vol. 244-249; (1979); p. 744, View in Reaxys; Hinton; Layton; Organic Magnetic Resonance; vol. 4; (1972); p. 353,355, View in Reaxys; Coulson; Journal of the American Chemical Society; vol. 98; (1976); p. 3111,3112, View in Reaxys; Jacobsen; Schaumburg; Journal of Magnetic Resonance (1969-1992); vol. 28; (1977); p. 1,6, 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,

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2018-06-17 20:44:10

View in Reaxys; Spiesecke; Schneider; Journal of Chemical Physics; vol. 35; (1961); p. 731,732,733, View in Reaxys; Robinson; Savitzky; Journal of Magnetic Resonance (1969-1992); vol. 2; (1970); p. 269, View in Reaxys; Lynch; Canadian Journal of Chemistry; vol. 55; (1977); p. 541,543, View in Reaxys; Domazetis et al.; Journal of Organometallic Chemistry; vol. 141; (1977); p. 57,58,63, View in Reaxys; Sandhu; Journal of the American Chemical Society; vol. 97; (1975); p. 6284, View in Reaxys; Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 1090, View in Reaxys; Read et al.; Tetrahedron Letters; (1968); p. 1215, View in Reaxys; Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2137, View in Reaxys; Martin et al.; Journal of Organometallic Chemistry; vol. 11; (1968); p. 177, View in Reaxys; Castellano et al.; Tetrahedron Letters; (1967); p. 4635, View in Reaxys 24 of 53

Description (NMR Spectroscopy)

Spin-spin coupling constants

Page; Molecular Physics; vol. 13; (1967); p. 523, View in Reaxys; Tarpley Jr.; Goldstein; Journal of Physical Chemistry; vol. 75; (1971); p. 421,425, View in Reaxys; Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys; Womble; Savitsky; Journal of Magnetic Resonance (1969-1992); vol. 4; (1971); p. 226, View in Reaxys; Read; Goldstein; Journal of Molecular Spectroscopy; vol. 23; (1967); p. 179,181,186, View in Reaxys; Ernst et al.; Journal of Magnetic Resonance (1969-1992); vol. 25; (1977); p. 123,126,128, View in Reaxys 25 of 53

Description (NMR Spectroscopy)

Spin-lattice relaxation time (T1)

Mitchell; Eisner; Journal of Chemical Physics; vol. 34; (1961); p. 651,653, View in Reaxys; Norton; Tetrahedron; vol. 33; (1977); p. 2577,2579, 2580, View in Reaxys; Levy; Journal of the Chemical Society, Chemical Communications; (1972); p. 352, View in Reaxys; Powles; Neak; Proceedings of the Physical Society, London; vol. 78; (1961); p. 377,378-390; Chem.Abstr.; nb. 1082; (1962), View in Reaxys; Levy et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 1527,1530, View in Reaxys; Parkhurst et al.; Journal of Chemical Physics; vol. 55; (1971); p. 1368, View in Reaxys 26 of 53

Description (NMR Spectroscopy)

NOE

Levy et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 1527,1530, View in Reaxys 27 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

bei Zusatz von Di-tert.-butylnitroxid-Radikal

Morishima et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 4812,4814, View in Reaxys 28 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-Kontakt-Shift m. Di-t-butyl-nitroxid

Morishima et al.; Chemical Physics Letters; vol. 14; (1972); p. 372, View in Reaxys 29 of 53

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 30 of 53

Description (NMR Spectroscopy)

NMR in liquid-crystal phase

Haloui; Canet; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 275; (1972); p. 447, View in Reaxys 31 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Tarpley Jr.; Goldstein; Journal of Physical Chemistry; vol. 75; (1971); p. 421,425, View in Reaxys 32 of 53

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

156/219

2018-06-17 20:44:10

33 of 53

Description (NMR Spectroscopy)

Chemical shifts

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys 34 of 53

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; Read; Goldstein; Journal of Molecular Spectroscopy; vol. 23; (1967); p. 179,181,186, View in Reaxys 35 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Lsgm.-Verschieb. durch Stosskomplexbldg. mit Lsgm.

Ledaal; Tetrahedron Letters; (1968); p. 1683, View in Reaxys 36 of 53

Description (NMR Spectroscopy)

Spectrum

Martin; Martin; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 256; (1963); p. 5099, View in Reaxys; Read; Goldstein; Journal of Molecular Spectroscopy; vol. 23; (1967); p. 179,181,186, View in Reaxys 37 of 53

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

Aromatizitaet (aus Linienverschieb. in PMR-Spektrum)

Dhingra et al.; Proceedings - Indian Academy of Sciences, Section A; vol. 65; (1967); p. 203,205, View in Reaxys 38 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Beziehung zwischen NMR-Verschiebungen u. π-Elektronendichte

Kanekar et al.; Proceedings - Indian Academy of Sciences, Section A; vol. 65; (1967); p. 353,356, View in Reaxys 39 of 53

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

CCl4

Goetz et al.; Justus Liebigs Annalen der Chemie; vol. 681; (1965); p. 1,2,8, View in Reaxys; Ohnishi; Kawazoe; Chemical and Pharmaceutical Bulletin; vol. 12; (1964); p. 938,940, View in Reaxys 40 of 53

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

Diskussion

Savitsky et al.; Journal of Physical Chemistry; vol. 69; (1965); p. 1425, View in Reaxys 41 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

Schaefer et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 2969,2971, View in Reaxys; Savitsky et al.; Journal of Physical Chemistry; vol. 69; (1965); p. 1425, View in Reaxys 42 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

bezogen auf Bzl.

Savitsky et al.; Journal of Physical Chemistry; vol. 69; (1965); p. 1425, View in Reaxys

157/219

2018-06-17 20:44:10

43 of 53

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

Trifluoressigsaeure

Ohnishi; Kawazoe; Chemical and Pharmaceutical Bulletin; vol. 12; (1964); p. 938,940, View in Reaxys 44 of 53

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

ortho- u. meta-Wasserstoff

Schaefer et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 2969,2971, View in Reaxys 45 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

benzene

Charton-Koechlin; Leroy; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 56; (1959); p. 850,852, View in Reaxys 46 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

ethanol

Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 47 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

acetone

Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 48 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

acetonitrile

Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 49 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dioxane

Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 50 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

158/219

2018-06-17 20:44:10

Solvents (NMR Spectroscopy)

CCl4

Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 51 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CS2

Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 52 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

cyclohexane

Shimizu et al.; Bulletin of the Chemical Society of Japan; vol. 32; (1959); p. 419, View in Reaxys; Diehl; Graenacher; Helvetica Physica Acta; vol. 32; (1959); p. 288,292, View in Reaxys 53 of 53

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

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 (37) 1 of 37

Description (IR Spectroscopy)

Bands

Temperature (IR Spectroscopy) [°C]

19.85 - 549.85

Chien, Yi-Chi; Paul Wang; Lin, Kuen-Song; Huang; Yang; Chemosphere; vol. 40; nb. 4; (2000); p. 383 - 387, View in Reaxys 2 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

solid

Comment (IR Spectroscopy)

1511 - 686 cm**(-1)

Slepoukhine, A. Yu.; Kostyuchenko, L. S.; Udovenja, V. A.; Journal of Molecular Structure; vol. 349; (1995); p. 207 - 210, View in Reaxys 3 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

1476 - 519 cm**(-1)

Slepoukhine, A. Yu.; Kostyuchenko, L. S.; Udovenja, V. A.; Journal of Molecular Structure; vol. 349; (1995); p. 207 - 210, View in Reaxys 4 of 37

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

1500 - 600 cm**(-1)

159/219

2018-06-17 20:44:10

Koeser, Heinz J.K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 6; (1984); p. 547 562, View in Reaxys 5 of 37

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

1500 - 600 cm**(-1)

Koeser, Heinz J.K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 6; (1984); p. 547 562, View in Reaxys 6 of 37

Description (IR Spectroscopy)

Reflection spectrum

Koeser, Heinz J.K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 6; (1984); p. 547 562, View in Reaxys 7 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

8785 cm**(-1)

Gough, Kathleen M.; Henry, Bryan R.; Journal of Physical Chemistry; vol. 87; nb. 18; (1983); p. 3433 - 3441, View in Reaxys 8 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

Comment (IR Spectroscopy)

1600 - 200 cm**(-1)

Kivinen, Antti; Ovaska, Martti; Raesaenen, Markku; Journal of Molecular Structure; vol. 95; (1982); p. 141 - 150, View in Reaxys 9 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

4000 - 200 cm**(-1)

Kivinen, Antti; Ovaska, Martti; Raesaenen, Markku; Journal of Molecular Structure; vol. 95; (1982); p. 141 - 150, View in Reaxys 10 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

solid

Temperature (IR Spectroscopy) [°C]

-196.2

Comment (IR Spectroscopy)

500 - 400 cm**(-1)

Kivinen, Antti; Ovaska, Martti; Raesaenen, Markku; Journal of Molecular Structure; vol. 95; (1982); p. 141 - 150, View in Reaxys 11 of 37

Description (IR Spectroscopy)

Polarization of IR bands

Kivinen, Antti; Ovaska, Martti; Raesaenen, Markku; Journal of Molecular Structure; vol. 95; (1982); p. 141 - 150, View in Reaxys 12 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

decahydronaphthalene

Temperature (IR Spectroscopy) [°C]

19.9

160/219

2018-06-17 20:44:10

Comment (IR Spectroscopy)

23 cm**(-1)

Reid, Colin J.; Evans, Myron; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 733 - 738, View in Reaxys 13 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Temperature (IR Spectroscopy) [°C]

19.9

Comment (IR Spectroscopy)

25 cm**(-1)

Reid, Colin J.; Evans, Myron; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 733 - 738, View in Reaxys 14 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

19.9

Comment (IR Spectroscopy)

30 cm**(-1)

Reid, Colin J.; Evans, Myron; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 733 - 738, View in Reaxys 15 of 37

Description (IR Spectroscopy)

Bands

Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Brown et al.; Spectrochimica Acta; vol. 21; (1965); p. 659, View in Reaxys; Saffioti; LeCalve; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 28; (1972); p. 1435, 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; Mierzecki; Acta Physica Polonica; vol. 25; (1964); p. 797,808, View in Reaxys; Reid; Chemical Physics Letters; vol. 66; (1979); p. 517,520, View in Reaxys; Fruwert et al.; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 11; (1971); p. 396, View in Reaxys 16 of 37

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; Brownlee et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 557,559, View in Reaxys; Freymann et al.; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 3; (1962); p. 1222, View in Reaxys; Chekunov et al.; Journal of Applied Spectroscopy; vol. 17; (1972); p. 1489; ; p. 898, View in Reaxys; McDevitt; Fateley; Journal of Molecular Structure; vol. 5; (1970); p. 477,484, View in Reaxys; Constant et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 1022, View in Reaxys; Martin; Martin; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 256; (1963); p. 5099, View in Reaxys; Banerjee et al.; Journal of the Indian Chemical Society; vol. 56; (1979); p. 518, View in Reaxys; Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Wright; Nature; vol. 209; nb. 5023; (1966); p. 571 - 572, View in Reaxys; Larsson; Folkesson; Chemica Scripta; vol. 9; (1976); p. 148, View in Reaxys; Vincent-Geisse; Lecomte; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 1; (1962); p. 104,107, View in Reaxys; Jain; Walker; Journal of Physical Chemistry; vol. 75; (1971); p. 2942, View in Reaxys; Lisitsa; Khalimonova; Optics and Spectroscopy; vol. 11; (1961); p. 97; ; p. 185, View in Reaxys; Lisitsa; Khalimonova; Optics and Spectroscopy; vol. 11; (1961); p. 179; ; p. 332, 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; Lisitsa et al.; Optics and Spectroscopy; vol. 28; (1970); p. 128; ; p. 235, View in Reaxys; Mamatov; Yagudaev; Journal of Applied Spectroscopy; vol. 8; (1968); p. 498; ; p. 825, View in Reaxys; Sirkar et al.; Indian Journal of Physics (1926-1976); vol. 38; (1964); p. 610,620, View in Reaxys; Chekunov; Polyakova; Journal of Applied Spectroscopy; vol. 10; (1969); p. 523; ; p. 784, View in Reaxys; Horak; Vitek; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1107,1109-1116, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 32; (1972); p. 280; ; p. 535, View in Reaxys; Delorme et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 261; (1965); p. 3331, 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; Streitwieser Jr.; Klein; Journal of the American Chemical Society; vol. 86; (1964); p. 5170,5172, View in Reaxys; Benson et al.; Canadian Journal of Chemistry; vol. 50; (1972); p. 2610, View in Reaxys; Khalimonova; Optics and Spectroscopy; vol. 13; (1962); p.

161/219

2018-06-17 20:44:10

447; ; p. 791, View in Reaxys; Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys 17 of 37

Description (IR Spectroscopy)

Spectrum

Krueger; Mettee; Canadian Journal of Chemistry; vol. 42; (1964); p. 288,289, View in Reaxys; Wyss et al.; Spectrochimica Acta; vol. 20; (1964); p. 573,575, 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; Korostelev et al.; Journal of Applied Spectroscopy; vol. 27; (1977); p. 1487, View in Reaxys; Hindle et al.; Journal of Chemical Physics; vol. 62; (1975); p. 3230, View in Reaxys; Bortkevich; Bobovich; Journal of Applied Spectroscopy; vol. 7; (1967); p. 518; ; p. 767, View in Reaxys; Uno et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 33; (1977); p. 607,610, View in Reaxys; Wiberley et al.; Analytical Chemistry; vol. 32; (1960); p. 217,219, View in Reaxys; Mansingh; Journal of Chemical Physics; vol. 52; (1970); p. 5896,5898, View in Reaxys; Griffiths; Thompson; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 298; (1967); p. 51,54, View in Reaxys; Nesmejanow et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1964); p. 574,576; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1964); p. 613, View in Reaxys; Lebas; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 59; (1962); p. 1072,1073, View in Reaxys; Lisitsa; Chalimonowa; Optika i Spektroskopiya; vol. 11; (1961); p. 185,186-191; Chem.Abstr.; nb. 25469; (1961), View in Reaxys; Harrah et al.; Spectrochimica Acta; vol. 18; (1962); p. 21,29, View in Reaxys; Fleming et al.; Molecular Physics; vol. 19; (1970); p. 853,856, View in Reaxys; Andrieu; Mollier; Bulletin de la Societe Chimique de France; (1969); p. 831, View in Reaxys 18 of 37

Description (IR Spectroscopy)

Fine structure of IR bands

Davies et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p. 1071,1074, View in Reaxys 19 of 37

Description (IR Spectroscopy)

Intensity of IR bands

Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Tunitsyn et al.; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 1,2, 5, View in Reaxys; Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Brownlee; Journal of the American Chemical Society; vol. 87; (1965); p. 3260,3261, View in Reaxys; Cameron et al.; Journal of Chemical Physics; vol. 56; (1972); p. 4717, View in Reaxys 20 of 37

Description (IR Spectroscopy)

Intensity of IR bands

Comment (IR Spectroscopy)

im Bereich von 1600 cmE-1 bis 1000 cmE-1.

Katritzky; Lagowski; Journal of the Chemical Society; (1958); p. 4155,4158, View in Reaxys 21 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

714 - 417 cm**(-1)

Plyler; Allen; Tidwell; Journal of Research of the National Bureau of Standards (United States); vol. 58; (1957); p. 255,256, 260, View in Reaxys; A.P.I. Res. Project 44 Nr. 1289, 1290 <1952>, View in Reaxys 22 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 667 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3333 - 667 cm**(-1)

Josien; Lebas; Bulletin de la Societe Chimique de France; (1956); p. 53, View in Reaxys 24 of 37

Description (IR Spectroscopy)

Intensity of IR bands

162/219

2018-06-17 20:44:10

Comment (IR Spectroscopy)

im Bereich von 1069 cmE-1 bis 1021 cmE-1.

Randle; Whiffen; Transactions of the Faraday Society; vol. 52; (1956); p. 9,10, View in Reaxys 25 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

714 - 263 cm**(-1)

Plyler; Discussions of the Faraday Society; vol. 9; (1950); p. 100,102, View in Reaxys 26 of 37

Description (IR Spectroscopy)

Intensity of IR bands

Comment (IR Spectroscopy)

C-H-Deformationsschwingungsbande bei 739 cmE-1.

Cole; Thompson; Transactions of the Faraday Society; vol. 46; (1950); p. 103,107, View in Reaxys 27 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

741 cm**(-1); Absorption der Fluessigkeit.

Bell; Thompson; Vago; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 192; (1948); p. 498,505, View in Reaxys 28 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

833 - 588 cm**(-1)

Mortimer; Blodgett; Daniels; Journal of the American Chemical Society; vol. 69; (1947); p. 823, View in Reaxys 29 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1429 - 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 30 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

10000 - 6250 cm**(-1); Absorption der Fluessigkeit.

Freymann; Naherniac; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 197; (1933); p. 829; Journal de Physique et le Radium; vol. <7> 5; (1934); p. 75,77, View in Reaxys; Freymann; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 194; (1932); p. 1471; Annales de Physique (Paris, France); vol. <10> 20; (1933); p. 243,289, View in Reaxys; Suhrmann; Klein; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 50; (1941); p. 35; Atti X. Congr. int. Chim. Rom 1938; vol. Bd.; p. 2 S. 525, 529, View in Reaxys; Barchewitz; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 203; (1936); p. 930; Annales de Physique (Paris, France); vol. <11> 11; (1939); p. 261,337, 340, View in Reaxys 31 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

500 - 222 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 32 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 769 cm**(-1)

Plum; Journal of Chemical Physics; vol. 5; (1937); p. 174, View in Reaxys

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33 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

12500 - 1250 cm**(-1)

Battista; Nuovo Cimento; vol. 14; (1937); p. 343,348, View in Reaxys; Daugherty; Physical Review; vol. <2> 34; (1929); p. 1549,1552, View in Reaxys 34 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

3226 - 2857 cm**(-1); Absorption der Fluessigkeit.

Barnes; Physical Review; vol. <2> 35; (1930); p. 1524,1529, View in Reaxys 35 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 667 cm**(-1); fluessiges Brombenzol.

Barnes; Nature (London, United Kingdom); vol. 124; p. 300; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 2016, View in Reaxys; Coblentz,W. W.; Investigations of infra-red spectra <Washington> 1905, S. 240, View in Reaxys 36 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

von Brombenzol-Dampf.

Henri; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 177; (1923); p. 1039, View in Reaxys; Purvis; Pr. Cambridge phil. Soc.; vol. 21; p. 563; Chem. Zentralbl.; vol. 94; nb. III; (1923); p. 979, View in Reaxys 37 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CS2

Comment (IR Spectroscopy)

5000 - 667 cm**(-1)

A.P.I. Res. Project 44 Nr. 1289 <1952>, View in Reaxys Mass Spectrometry (22) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

spectrum

Paragraph 0129

Patent; Duksan NeoluxCo., Ltd.; PARK, JUNG GUEN; LEE, SON HEE; PARK, HYUNG GUEN; JO, HAY MIN; LEE, DAE WON; PARK, SUNG JAY; (38 pag.); KR2015/49004; (2015); (A) Korean, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

supporting information

Li, Yaming; Qi, Zisong; Wang, Huifeng; Fu, Xinmei; Duan, Chunying; Journal of Organic Chemistry; vol. 77; nb. 4; (2012); p. 2053 - 2057, View in Reaxys

EI (Electron impact); Spectrum

Yao, Shengjun; Zhang, Xiang; Zhou, Jing; Qian, Rong; Xu, Zhe; Fang, Fang; Wei, Yuanlong; Wang, Cuihong; Yuan, Shuai; Guo, Yinlong; Journal of Mass Spectrometry; vol. 44; nb. 1; (2009); p. 32 - 39, View in Reaxys

spectrum; time-offlight mass spectra (TOFMS)

Kadi; Davidsson; Tarnovsky; Rasmusson; Akesson; Chemical Physics Letters; vol. 350; nb. 1-2; (2001); p. 93 - 98, View in Reaxys

collision-induced dissociation

Holman, Robert W.; Eary, Todd; Whittle, Ed; Gross, Michael L.; Journal of the Chemical Society. Perkin Transactions 2; nb. 10; (1998); p. 2187 2193, View in Reaxys

spectrum

Crow; Bjorseth; Knapp; Bennett; Analytical Chemistry; vol. 53; nb. 4; (1981); p. 619 - 625, View in Reaxys; Sack, Thomas M.; Gross, Michael L.; Analytical Chemistry; vol. 55; (1983); p. 2419 - 2421, View in Reaxys; Hywei Evans; Pretorlus, Warren; Ebdon, Les; Rowland, Steve; Analytical Chemistry; vol. 66; nb. 20; (1994); p. 3400 - 3407, View in Reaxys;

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Matsumoto, Junichi; Lin, Cheng-Huang; Imasaka, Totaro; Analytical Chemistry; vol. 69; nb. 22; (1997); p. 4524 - 4529, View in Reaxys spectrum; chemical ionization (CI)

Daishima, Shigeki; Iida, Yoshio; Kanda, Fujihiro; Organic Mass Spectrometry; vol. 26; nb. 5; (1991); p. 486 - 492, View in Reaxys; Vairamani, M.; Organic Mass Spectrometry; vol. 28; nb. 12; (1993); p. 1498 - 1503, View in Reaxys

fragmentation pattern; spectrum

IKE(S) (ion kinetic energy (spectrum))

Lorquet, J. C.; Leyh, B.; Organic Mass Spectrometry; vol. 28; nb. 10; (1993); p. 1225 - 1228, View in Reaxys

spectrum; chemical ionization (CI)

collisional activation

Stone, John A.; Organic Mass Spectrometry; vol. 28; nb. 10; (1993); p. 1119 - 1123, View in Reaxys

laser desorption

Wilkerson Jr., Charles W.; Reilly, James P.; Analytical Chemistry; vol. 62; nb. 17; (1990); p. 1804 - 1808, View in Reaxys

electron impact (EI); spectrum fragmentation pattern; chemical ionization (CI)

McIver, Robert T.; Hunter, Richard L.; Baykut, Goekhan; Analytical Chemistry; vol. 61; nb. 5; (1989); p. 489 - 491, View in Reaxys collisional activation

fragmentation pattern spectrum

Blom, Karl; Munson, Burnaby; Organic Mass Spectrometry; vol. 22; (1987); p. 727 - 735, View in Reaxys Bowers, William D.; Delbert, Sherri-Sue; McIver, Robert T.; Analytical Chemistry; vol. 58; (1986); p. 969 - 972, View in Reaxys

collisional activation; charge exchange with positive ions

negative ion spectroscopy

Kingston, E. E.; Beynon, J. H.; Ast, T.; Flammang, R.; Maquestiau, A.; Organic Mass Spectrometry; vol. 20; nb. 9; (1985); p. 546 - 555, View in Reaxys Crow; Bjorseth; Knapp; Bennett; Analytical Chemistry; vol. 53; nb. 4; (1981); p. 619 - 625, View in Reaxys; Olthoff, James K.; Tossell, John A.; Moore, John H.; Journal of Chemical Physics; vol. 83; nb. 11; (1985); p. 5627 - 5634, View in Reaxys

MIKE (mass ion ki- Hass, Ronald J.; Tondeur, Y.; Voyksner, R. D.; Analytical Chemistry; vol. netic energy) 55; nb. 2; (1983); p. 295 - 297, View in Reaxys spectrum

field ionization

Sokolov, V. V.; Grishin, N. N.; Petrov, A. A.; Journal of Organic Chemistry USSR (English Translation); vol. 18; (1982); p. 1586 - 1591; Zhurnal Organicheskoi Khimii; vol. 18; nb. 9; (1982); p. 1813 - 1819, View in Reaxys

chemical ionization (CI)

Crow; Bjorseth; Knapp; Bennett; Analytical Chemistry; vol. 53; nb. 4; (1981); p. 619 - 625, View in Reaxys

fragmentation pattern; chemical ionization (CI); spectrum

Luijten, W. C. M. M.; Onkenhout, W.; Thuijl, J. van; Organic Mass Spectrometry; vol. 15; nb. 7; (1980); p. 329 - 330, View in Reaxys

Johnstone; Mellon; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 68; (1972); p. 1209, View in Reaxys; Bouchoux; Organic Mass Spectrometry; vol. 12; (1977); p. 681, View in Reaxys; Compton et al.; Physics Letters; vol. 23; (1966); p. 656, View in Reaxys; Leung et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 2479,2480, View in Reaxys; Medved et al.; Organic Mass Spectrometry; vol. 14; (1979); p. 307,309, View in Reaxys; Yu; Field; Organic Mass Spectrometry; vol. 8; (1974); p. 267,273, View in Reaxys; Howe; Williams; Journal of the American Chemical Society; vol. 91; (1969); p. 7137,7141, View in Reaxys; Leung; Harrison; Journal of the American Chemical Society; vol. 101; (1979); p. 3168,3172, View in Reaxys; Martinsen; Buttrill; Organic Mass Spectrometry; vol. 11; (1976); p. 762,767, View in Reaxys; Leung; Harrison; Canadian Journal of Chemistry; vol. 54; (1976); p. 3439,3441,3443, View in Reaxys; Rosenberg et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 11; (1973); p. 433,442, 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; Facchetti et al.; Chimica e l'Industria (Milan, Italy); vol. 51; (1969); p. 1373, View in Reaxys; Howe; Williams; Organic Mass Spectrometry; vol. 2; (1969); p. 1141, View in Reaxys; McLafferty; Analytical Chemistry; vol. 34; (1962); p. 16,23, View in Reaxys; Kurz; Hage; Journal of Organic Chemistry; vol. 42; (1977); p. 4080, View in Reaxys; Momigny; Memoires

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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; Stapleton et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 1219,1220, View in Reaxys; Williams et al.; Journal of the American Chemical Society; vol. 90; (1968); p. 6759, View in Reaxys; Bentley et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 3978, View in Reaxys appearance potentials fragmentation pattern

Yeo; Williams; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 886, View in Reaxys; Majer; Patrick; Transactions of the Faraday Society; vol. 58; (1962); p. 17,18, View in Reaxys durch Elektronenstoss

Momigny; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 144,166; Ann. Soc. scient. Bruxelles; vol. # 71; (1957); p. 66, View in Reaxys

UV/VIS Spectroscopy (25) 1 of 25

Description (UV/VIS Spectroscopy)

Absorption spectrum

Absorption Maxima (UV/ VIS) [nm]

210; 261

Log epsilon

3.9; 2.28

Patent; Gao, Xiaolian; US6965040; (2005); (B1) English, View in Reaxys 2 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

solid matrix

Comment (UV/VIS Spectroscopy)

270 - 300 nm; Remark: T=77 K, in glycerol

Okutsu, Tetsuo; Kageyama, Teruyoshi; Kounose, Naomi; Tsuchiya, Jun; Hiratsuka, Hiroshi; Chemical Physics Letters; vol. 299; nb. 6; (1999); p. 597 - 602, View in Reaxys 3 of 25

Description (UV/VIS Spectroscopy)

Absorption spectrum

Comment (UV/VIS Spectroscopy)

Remark: multiphoton-ionization; supersonic molecular beam; diagram

Boesl; Zimmermann; Weickhardt; Lenoir; Schramm; Kettrup; Schlag; Chemosphere; vol. 29; nb. 7; (1994); p. 1429 1440, View in Reaxys 4 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methanol; H2O

Absorption Maxima (UV/ VIS) [nm]

228; 255

Selavka; Jiao; Krull; Sheih; Yu; Wolf; Analytical Chemistry; vol. 60; nb. 3; (1988); p. 250 - 254, View in Reaxys 5 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

261.6

Prabhumirashi, L. S.; Kutty, D. K. Narayanan; Bhide, Anjali S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 39; nb. 7; (1983); p. 663 - 668, View in Reaxys 6 of 25

Description (UV/VIS Spectroscopy)

UV/VIS

Cohen; Takahashi; Journal of the American Chemical Society; vol. 95; (1973); p. 443,444, View in Reaxys; Shorygin et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 555,556; ; p. 1057, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Swain et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 783,787, View in Reaxys; Walkley; Journal of Chemical Physics; vol. 33; (1960); p. 621,

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View in Reaxys; Deich; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 975,891, View in Reaxys; Brett; Gold; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 1437, View in Reaxys; Diedrich et al.; Canadian Journal of Chemistry; vol. 50; (1972); p. 1743,1747, View in Reaxys; Miskevitch; Gutorova; Sov. Prog. Chem. (Engl. Transl.); vol. 39; nb. 1; (1973); p. 82,80, View in Reaxys; McLachlan; McCarthy; Journal of the American Chemical Society; vol. 84; (1962); p. 2519, View in Reaxys; Hine et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 1473, View in Reaxys; Weigang; Dahl; Journal of Chemical Physics; vol. 34; (1961); p. 1848, View in Reaxys; Prakash; Singh; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 512, View in Reaxys; Vodar; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 255; (1960); p. 44,45, View in Reaxys; Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys; Dunbar et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 6506,6507,6508, View in Reaxys 7 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Buehler; Funk; Journal of Physical Chemistry; vol. 79; (1975); p. 2098,2101-2103, View in Reaxys; Jordan et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 7189, View in Reaxys; Lisitsa; Ralko; Optics and Spectroscopy; vol. 24; (1968); p. 284; ; p. 540, View in Reaxys; Baruah; Indian Journal of Pure and Applied Physics; vol. 10; (1972); p. 75, View in Reaxys; Galashin et al.; Doklady Physical Chemistry; vol. 219; (1974); p. 1092; ; p. 636, View in Reaxys; Prakash; Singh; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 512, View in Reaxys; Kimura; Nagakura; Molecular Physics; vol. 9; (1965); p. 117,120, View in Reaxys; Das; Basu; Spectrochimica Acta; vol. 17; (1961); p. 897,898, View in Reaxys; Forbes; Canadian Journal of Chemistry; vol. 39; (1961); p. 1131,1135, View in Reaxys; Perkampus; Vollbrecht; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 2173, 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 8 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Kastha; Bag; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 1661, View in Reaxys; Bossy et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 1099, View in Reaxys; Vesala; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 28; (1974); p. 839,841, View in Reaxys; Forbes; Canadian Journal of Chemistry; vol. 39; (1961); p. 1131,1135, View in Reaxys; Nigam et al.; Indian Journal of Chemistry; vol. 8; (1970); p. 908,910, View in Reaxys 9 of 25

Description (UV/VIS Spectroscopy)

Band anisotropy

Schachparonow; Russian Journal of Physical Chemistry; vol. 36; (1962); p. 1089; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 2030, View in Reaxys 10 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

213.5

Burawoy; Tetrahedron; vol. 2; (1958); p. 122,131, View in Reaxys 11 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane

Absorption Maxima (UV/ VIS) [nm]

216

Burawoy; Tetrahedron; vol. 2; (1958); p. 122,131, View in Reaxys 12 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

2,2,4-trimethyl-pentane

Comment (UV/VIS Spectroscopy)

220 - 360 nm

Tscheschko et al.; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 328; engl. Ausg. S. 365, View in Reaxys 13 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

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Comment (UV/VIS Spectroscopy)

(0,0-Uebergang) von dampffoermigem Brombenzol.

Absorption Maxima (UV/ VIS) [nm]

270.3; 272.26

Ferguson; Journal of Chemical Physics; vol. 24; (1956); p. 1263, View in Reaxys 14 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Comment (UV/VIS Spectroscopy)

(0,0-Uebergang) von in Isooctan geloestem Brombenzol.

Absorption Maxima (UV/ VIS) [nm]

270.3; 272.26

Ferguson; Journal of Chemical Physics; vol. 24; (1956); p. 1263, View in Reaxys 15 of 25

Description (UV/VIS Spectroscopy)

Singlet-triplet band

Comment (UV/VIS Spectroscopy)

von in Methylcyclohexan geloestem Brombenzol bei 323 nm und bei Raumtemperatur.

McClure et al.; Journal of Chemical Physics; vol. 22; (1954); p. 255,257, View in Reaxys 16 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Ley; v. Engelhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 33, View in Reaxys; Purvis; Journal of the Chemical Society; vol. 99; (1911); p. 824, View in Reaxys; Bowden; Braude; Journal of the Chemical Society; (1952); p. 1068,1070, View in Reaxys 17 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

245 - 280 nm

Robertson; Matsen; Journal of the American Chemical Society; vol. 72; (1950); p. 5250, View in Reaxys 18 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

250 - 280 nm; von kristallinem Brombenzol bei Temperaturen von 100 K bis 230 K.

Kanda; Tsujikawa; Sci. Rep. Res. Inst. Tohoku Univ.; vol. <A> 2; (1950); p. 1,4, View in Reaxys 19 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2O

Doub; Vandenbelt; Journal of the American Chemical Society; vol. 69; (1947); p. 2714,2717, View in Reaxys 20 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

des Dampfes im fernen UV (110-210 mμ).

Price; Walsh; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 191; (1947); p. 22,29, 30, View in Reaxys 21 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

Dampf.

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Lang,L.; Absorption Spectra in the Ultraviolet and Visible Region, 2. Aufl. Bd. 1 <Budapest 1961> S. 375-377, View in Reaxys; Asagoe; Ikemoto; Pr. phys. math. Soc. Japan; vol. <3> 22; (1940); p. 685, View in Reaxys; Masaki; Bulletin of the Chemical Society of Japan; vol. 11; (1936); p. 346, View in Reaxys 22 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Conrad-Billroth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 25; (1934); p. 139,150, View in Reaxys; Klingstedt; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 20; (1933); p. 125,126, View in Reaxys 23 of 25

Description (UV/VIS Spectroscopy)

Absorption maxima

Comment (UV/VIS Spectroscopy)

π-Strahlen.

Fournier; Guillot; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 196; (1933); p. 698, View in Reaxys 24 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

des Dampfes.

Witte; Chem. Zentralbl.; vol. 86; nb. II; (1915); p. 223, View in Reaxys; Purvis; Journal of the Chemical Society; vol. 99; (1911); p. 824, View in Reaxys 25 of 25

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

der Fluessigkeit.

Purvis; Journal of the Chemical Society; vol. 99; (1911); p. 824, View in Reaxys ESR Spectroscopy (3) 1 of 3

Description (ESR Spectro- ESR-hyperfine coupling constants scopy) Solvents (ESR Spectrosco- CCl3F py) Comment (ESR Spectroscopy)

81Br.

Maj, Paul; Hasegawa, Akinori; Symons, Martyn C. R.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 79; (1983); p. 1931 - 1938, View in Reaxys 2 of 3

Description (ESR Spectro- g-factor scopy) Maj, Paul; Hasegawa, Akinori; Symons, Martyn C. R.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 79; (1983); p. 1931 - 1938, View in Reaxys

3 of 3

Description (ESR Spectro- ESR scopy) Noda et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 2882, View in Reaxys

NQR Spectroscopy (3) Description (NQR Nucleus (NQR Spectroscopy) Spectroscopy) Nuclear quadrupole resonance

References Vega; Israel Journal of Chemistry; vol. 16; (1977); p. 213,214, View in Reaxys; Alymov et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 39; nb. 12; (1975); p. 7; ; p. 2457, View in Reaxys; Rangacharyulu; Premaswarup; Indian Journal of Pure and Applied Physics; vol. 13; (1975); p. 302,303, View in Reaxys; Jacobsen; Schaumburg; Journal of Magnetic Resonance (1969-1992); vol. 28; (1977); p. 1,6, View in Reaxys; Petukhov, S. A.; Bryukhova, E. V.; Semin, G. K.; Biguslavskii, A. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; nb. 7; (1984); p. 1389 - 1394; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 7; (1984); p. 1511 1517, View in Reaxys; Semin; Petukhov; Bryukhova; Russian Journal of Physical Chemistry A; vol. 72; nb. 3; (1998); p. 420 - 424, View in Reaxys

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Nuclear quadrupole coupling constants

Rosenthal; Dailey; Journal of Chemical Physics; vol. 43; (1965); p. 2093,2109, View in Reaxys; Jacobsen; Schaumburg; Journal of Magnetic Resonance (1969-1992); vol. 28; (1977); p. 1,6, View in Reaxys

Nuclear quadrupole 81Br coupling constants

Bersohn; Journal of Chemical Physics; vol. 22; (1954); p. 2078,2083, View in Reaxys

Rotational Spectroscopy (2) Description (Rota- References tional Spectroscopy) Microwave spectrum

Bak; Knudsen; Madsen; Physical Review; vol. <2>75; (1949); p. 1622; Chem.Abstr.; (1949); p. 5310, View in Reaxys; Rosenthal; Dailey; Journal of Chemical Physics; vol. 43; (1965); p. 2093,2109, View in Reaxys; Hanna; Abd-ElNour; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 246; (1971); p. 292,294, View in Reaxys; Almenningen, A.; Brunvoll, J.; Popik, M. V.; Sokolkov, S. V.; Vilkov, L. V.; Samdal, S.; Journal of Molecular Structure; vol. 127; (1985); p. 85 - 94, View in Reaxys

Stark effect

Bonnet; Barriol; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 74; (1977); p. 600,602, View in Reaxys; Farag; Bohn; Journal of Chemical Physics; vol. 62; (1975); p. 3946,3948, View in Reaxys

Raman Spectroscopy (12) Description (Ram- Comment (Raman an Spectroscopy) Spectroscopy) Bands

CCl4

Raman intensities

Bands

References 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 Vorobeva; Timonin; Optics and Spectroscopy; vol. 35; (1973); p. 619; ; p. 1065, View in Reaxys; Sidorov et al.; Optics and Spectroscopy; vol. 19; (1965); p. 116; ; p. 206, 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

acetone

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

Spectrum

Kohlrausch; Monatshefte fuer Chemie; vol. 76; (1947); p. 231,240, View in Reaxys; Kohlrausch; Wittek; Monatshefte fuer Chemie; vol. 74; (1943); p. 1,13, View in Reaxys; Kahovec; Reitz; Monatshefte fuer Chemie; vol. 69; (1936); p. 363,373, View in Reaxys; Kohlrausch; Pongratz; Monatshefte fuer Chemie; vol. 63; (1933); p. 427,437, View in Reaxys; Murray; Andrews; Journal of Chemical Physics; vol. 1; (1933); p. 406,408, 411, View in Reaxys; Cleeton; Dufford; Physical Review; vol. <2> 37; (1931); p. 362,369, View in Reaxys; Bhagavantam; Venkateswaran; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 127; (1930); p. 360,370, View in Reaxys; Wittek; Monatshefte fuer Chemie; vol. 73; (1941); p. 231,240; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 52; (1942); p. 315,318, View in Reaxys; Fujioka; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 11; (1929); p. 205,212, 218, View in Reaxys; Bobovich; Bortkevich; Journal of Applied Spectroscopy; vol. 9; (1965); p. 750; ; p. 144, View in Reaxys; Berezin et al.; Journal of Applied Spectroscopy; vol. 4; (1966); p. 257,259; ; p. 351, 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; Ito et al.; Journal of Chemical Physics; vol. 69; (1978); p. 606, View in Reaxys; Clark; Mc Caffery; Journal of Physical Chemistry; vol. 81; (1977); p. 1918,1922, View in Reaxys; Kuwae; Machida; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 34; (1978); p. 785,787,788, View in Reaxys; Lund et al.; Chemical Physics; vol. 28; (1978); p. 167,169, View in Reaxys; Meneely et al.; Journal of Molecular Spectroscopy; vol. 39; (1971); p. 73,76, View in Reaxys; Venkateswarlu; Radhakrishnan; Spectrochimica Acta; vol. 18; (1962); p. 1433,1438,1439, View in Reaxys; Dumas et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 267; (1968); p. 267, View in Reaxys

Raman

Lippincott; et al.; Spectrochimica Acta; vol. 22; (1966); p. 1493,1495, View in Reaxys; Brutan et al.; Sov. Phys. J. (Engl. Transl.); vol. 10; nb. 2; (1967); p. 150,80, View in Reaxys; Nevzorov; Sechkarev; Sov. Phys. J. (Engl. Transl.); vol. 14; nb. 2; (1971); p. 75,199, View in Reaxys; Sechkarev; Dvorovenko; Sov. Phys. J. (Engl. Transl.); vol. 9; nb. 2; (1966); p. 7,1, View in Reaxys; Sechkaryov; Optics and Spectroscopy; vol. 19; (1965); p. 401; ; p. 721, View in Reaxys; ElSayed et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p.

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227, View in Reaxys; Orlovich; Journal of Applied Spectroscopy; vol. 23; nb. 2; (1975); p. 1040 1042, View in Reaxys; Saiz et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p. 1538,1540, 1541, 1545, View in Reaxys; Shredova et al.; Optics and Spectroscopy; vol. 31; (1971); p. 385; ; p. 719, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 34; (1973); p. 716; ; p. 1230, View in Reaxys; Bobovich; Bortkevich; Optics and Spectroscopy; vol. 24; (1968); p. 238; Opt.Spectrosk.; p. 456, View in Reaxys; Shapiro et al.; Physical Review Letters; vol. 19; (1967); p. 1093, View in Reaxys; Lallemand; Bloembergen; Physical Review Letters; vol. 15; (1965); p. 1008, View in Reaxys; Horak; Vitek; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1107,1109-1116, View in Reaxys; Colles; Griffiths; Journal of Chemical Physics; vol. 56; (1972); p. 3384, View in Reaxys; Sechkarev; Dvorovenko; Sov. Phys. J. (Engl. Transl.); vol. 1; (1965); p. 13,7,10, View in Reaxys Bands

Kondilenko et al.; Optics and Spectroscopy; vol. 28; (1970); p. 367; ; p. 680, View in Reaxys; Sidorov et al.; Optics and Spectroscopy; vol. 19; (1965); p. 116; ; p. 206, View in Reaxys

Degree of depolarization of Raman bands

Venkateswaran; Phil. Mag.; vol. <7> 15; (1933); p. 263,273, View in Reaxys; Cabannes; Rousset; Annales de Physique (Paris, France); vol. <10> 19; (1933); p. 229,262, View in Reaxys; Sidorov et al.; Optics and Spectroscopy; vol. 19; (1965); p. 116; ; p. 206, View in Reaxys

Spectrum

von kristallinem Brombenzol bei -180grad

Spectrum

von einer festen Kastha; Indian Journal of Physics (1926-1976); vol. 31; (1957); p. 635, View in Reaxys Loesung von Brombenzol in Aethanol bei -180grad

Spectrum

von fluessigem Brombenzol

Michel; Duyckaerts; Spectrochimica Acta; vol. 8; (1956); p. 356,368, View in Reaxys

Spectrum

von kristallinem Brombenzol bei -180grad und bei -60grad

Biswas; Indian Journal of Physics (1926-1976); vol. 29; (1955); p. 503,510, 511, 515, View in Reaxys

Bands

von fluessigem Brombenzol

Biswas; Indian Journal of Physics (1926-1976); vol. 29; (1955); p. 503,510, 511, 515, View in Reaxys

Kastha; Indian Journal of Physics (1926-1976); vol. 31; (1957); p. 635, View in Reaxys

Luminescence Spectroscopy (5) Description (Lumi- References nescence Spectroscopy) Luminescence lifetime

Brocklehurst et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 1793,1796, View in Reaxys; Stegeman; Stoicheff; Physical Review A: Atomic, Molecular, and Optical Physics; vol. 7; (1973); p. 3-1160,1170,1171,1173,1176, View in Reaxys; Ito et al.; Journal of Chemical Physics; vol. 69; (1978); p. 606, View in Reaxys; Plass; Berichte der Bunsen-Gesellschaft; vol. 74; (1970); p. 343,344-346, View in Reaxys; Perkampus; Vollbrecht; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 2173, View in Reaxys; Wilkerson Jr., Charles W.; Reilly, James P.; Analytical Chemistry; vol. 62; nb. 17; (1990); p. 1804 - 1808, View in Reaxys; Okutsu, Tetsuo; Kageyama, Teruyoshi; Kounose, Naomi; Tsuchiya, Jun; Hiratsuka, Hiroshi; Chemical Physics Letters; vol. 299; nb. 6; (1999); p. 597 - 602, View in Reaxys

Luminescence quantum yield

Okutsu, Tetsuo; Kageyama, Teruyoshi; Kounose, Naomi; Tsuchiya, Jun; Hiratsuka, Hiroshi; Chemical Physics Letters; vol. 299; nb. 6; (1999); p. 597 - 602, View in Reaxys

Lasing properties

Lallemand; Bloembergen; Physical Review Letters; vol. 15; (1965); p. 1008, 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

Ogawa et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 1063,1064, View in Reaxys

Luminescence quenching

Cosandey; Lerch; Helvetica Chimica Acta; vol. 50; (1967); p. 2215, View in Reaxys

Fluorescence Spectroscopy (5) Description (Fluo- Solvent (Fluoresrescence Spectrocence Spectroscoscopy) py)

Comment (Fluores- References cence Spectroscopy)

Fluorescence

Pac et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 1169,1171, View in Reaxys; Harriman; Rockett; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1974); p. 217, View in Reaxys; Perkampus; Vollbrecht; Spectrochimica

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Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 2173, View in Reaxys Maxima

von kristallinem Brombenzol bei -180grad.

Spectrum

bei Bestrahlung mit Newcomer; Journal of the American Chemical Society; vol. 42; (1920); p. Roentgenstrahlen. 2002, View in Reaxys

Spectrum

ethanol

Biswas; Indian Journal of Physics (1926-1976); vol. 29; (1955); p. 503,510, 511, 515, View in Reaxys

Ley; v. Engelhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 33, View in Reaxys

Maxima

Im Ultraviolett.

Ley; v. Engelhardt; Chemische Berichte; vol. 41; (1908); p. 2991, View in Reaxys

Phosphorescence Spectroscopy (4) Description (Phos- Solvent (Phosphorphorescence Spec- escence Spectrotroscopy) scopy)

Comment (Phosphorescence Spectroscopy)

References

Wavelength for Spectrum: 350 700 nm

Okutsu, Tetsuo; Kageyama, Teruyoshi; Kounose, Naomi; Tsuchiya, Jun; Hiratsuka, Hiroshi; Chemical Physics Letters; vol. 299; nb. 6; (1999); p. 597 - 602, View in Reaxys

Spectrum

solid matrix

Phosphorescence

Perkampus; Vollbrecht; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 2173, View in Reaxys

Maxima

2-methyl-butane

bei -196grad.

McClure; Journal of Chemical Physics; vol. 17; (1949); p. 905,910, View in Reaxys

Maxima

ethanol; diethyl ether

bei -196grad.

McClure; Journal of Chemical Physics; vol. 17; (1949); p. 905,910, View in Reaxys

Other Spectroscopic Methods (2) Description (Other References Spectroscopic Methods) Photoelectron spec- Johnstone; Mellon; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 68; trum (1972); p. 1209, View in Reaxys; Pignataro et al.; Annali di Chimica (Rome, Italy); vol. 64; (1974); p. 139,141, View in Reaxys; Cvitas; Klasinc; Croatica Chemica Acta; vol. 50; (1977); p. 291, View in Reaxys; Marschner; Tetrahedron; vol. 31; (1975); p. 2303,2307, View in Reaxys; Sell; Kuppermann; Chemical Physics; vol. 33; (1978); p. 367, View in Reaxys; Baer et al.; Journal of Chemical Physics; vol. 64; (1976); p. 2460, View in Reaxys; Momigny et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 1; (1968); p. 53,55, 56, 59, 60, 62, View in Reaxys; Dunbar et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 6506,6507,6508, View in Reaxys; Walter, K.; Scherm, K.; Boesl, U.; Journal of Physical Chemistry; vol. 95; nb. 3; (1991); p. 1188 - 1194, View in Reaxys; Mizugai, Yoshihiro; Katayama, Mikio; Journal of the American Chemical Society; vol. 102; nb. 21; (1980); p. 6424 6426, View in Reaxys; Fujisawa, S.; Ohno, K.; Masuda, S.; Harada, Y.; Journal of the American Chemical Society; vol. 108; nb. 21; (1986); p. 6505 - 6511, View in Reaxys; Nolan, G. S.; Saethre, L. J.; Siggel, M. R.; Thomas, T. D.; Ungier, L.; Journal of the American Chemical Society; vol. 107; nb. 23; (1985); p. 6463 - 6467, View in Reaxys; Olthoff, James K.; Tossell, John A.; Moore, John H.; Journal of Chemical Physics; vol. 83; nb. 11; (1985); p. 5627 - 5634, View in Reaxys ESCA

Larsson; Folkesson; Chemica Scripta; vol. 9; (1976); p. 148, View in Reaxys

Concentration in the Environment (2) 1 of 2

Media (Concentration in the Environment)

atmospheric particulate matter

Location

Lanzhou city, Gansu Province, Northwest of China

Contamination Concentration

5.74 pg/l air

Method, Remarks (Concentration in the Environment)

average conc.; total suspended particulate matter acquired from the Lanyuan hotel; 6 air samples collected in March 2003 during 24 h periods; flow rate: 0.8 m3/min; GC-MS and GC-FID analyses; triplicate measurements

Gao; Zhou; Ma; Chen; Hu; Bulletin of Environmental Contamination and Toxicology; vol. 72; nb. 5; (2004); p. 923 - 930, View in Reaxys 2 of 2

Media (Concentration in the Environment)

drinking water

Location

Mexico

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Contamination Concentration

> 0.3 μg/l

Method, Remarks (Concentration in the Environment)

48 sampling sites from five Mexican cities; September - October; analysis using GC-MS system coupled with a purge-and-trap sampler; analysis according to U.S. EPA, 1991 and APHA, AWWA, WEF, 1992

Gelover, Silvia; Bandala, Erick R.; Leal-Ascencio, Teresa; Perez, Sixto; Martinez, Evaristo; Environmental Toxicology; vol. 15; nb. 2; (2000); p. 131 - 139, View in Reaxys Transport and Distribution (7) 1 of 7

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 2.68E3 - 6.16E3 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 2 of 7

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - Leonardite humic acid

Results

experimental sorption enthalpy, ΔabsHi = -45.0 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 3 of 7

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 6.26E2 - 3.45E3 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 4 of 7

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - snow

Results

log Ki snow surface/air (m3/m2): -3.80; 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 5 of 7

Type (Transport and Distribution)

sorption

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Media (Transport and Distribution)

air-soil

Results

log of sorption constant (Ksa): log Ksa = 2.81, 2.49 and 2.28 at relative humidity of 50, 70 and 90 percent, resp.; table, diagrams

Method, Remarks (Transport and Distribution)

dynamic sorption experiment; brown Mediterranean soil (Sicily): 3.31 percent sand, 21.90 percent silt, 75.00 percent clay, pH 5.9, specific surface area 15.86 m2/g; at 15 deg C, gas-phase relative humidity of 50, 70 and 90 percent; sorption constant determined by inverse GC

Goss, Kai-Uwe; Buschmann, Johanna; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 13; (2004); p. 3667 - 3673, View in Reaxys 6 of 7

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air-soil

Results

log of sorption constant (Ksa): log Ksa = 2.15, 1.69 and 1.30 at relative humidity of 50, 70 and 90 percent, resp.; table, diagrams

Method, Remarks (Transport and Distribution)

dynamic sorption experiment; soil (loess sample, Iowa) texture: 7.1 percent sand, 75.6 percent silt, 17.4 percent clay, pH 8.34, specific surface area 15.86 m2/g; at 15 deg C, gas-phase relative humidity of 50, 70 and 90 percent; sorption constant determined by inverse GC

Goss, Kai-Uwe; Buschmann, Johanna; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 13; (2004); p. 3667 - 3673, View in Reaxys 7 of 7

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air-water

Results

air-water partition coefficient: KAW = 0.08

Method, Remarks (Transport and Distribution)

water: conductivity = 165-170 μOhms, hardness = 75-85 mg CaCO3/l, alkalinity = 80-90 mg CaCO3/l, oxygen conc. = 8.8 ppm, pH = 8.8, 21 deg C

De Wolf, Watze; Lieder, Paul H.; Chemosphere; vol. 36; nb. 8; (1998); p. 1713 - 1724, View in Reaxys Bioaccumulation, Biomagnification and Biomonitoring (1) 1 of 1

Species (Bioaccumulation, Pimephales promelas, fathead minnows Biomagnification and Biomonitoring) Concentration (Bioaccumulation, Biomagnification and Biomonitoring)

28 μmol/l

Temperature (Bioaccumulation, Biomagnification and Biomonitoring) [°C]

21 - 22

Bioconcentration Factor (BCF)

168

Accumulation Rate Constant

26.2 - 31.7 per hour

Elimination Rate Constant

0.15 - 0.185 per hour

Method, Remarks (Bioac- female fish, 1.45-4.71 g b. wt.; water conductivity, 165-17o μOhms, hardness, 75-85 mg CaCO3/l, cumulation, Biomagnifica- alkalinity, 80-90 mg CaCO3/l, oxygen conc., 8.8 ppm, pH, 8.8 tion and Biomonitoring) De Wolf, Watze; Lieder, Paul H.; Chemosphere; vol. 36; nb. 8; (1998); p. 1713 - 1724, View in Reaxys Biodegradation (1) 1 of 1

Type (Biodegradation)

anaerobic

Inoculum

estuarine sediment slurry

Half-life Time (Biodegradation)

115 d

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Method, Remarks (Biodegradation)

sulfate-reducing sediment samples were collected at the mouth of Tsurumi River, Japan, in 1992; in screw-top test-tubes; GC/MS analysis; first-order reaction rate constant: k=0.0060 day-1

Susarla, Sridhar; Yonezawa, Yoshitaka; Masunaga, Shigeki; Water Research; vol. 32; nb. 3; (1998); p. 639 - 648, View in Reaxys Abiotic Degradation, Hydrolysis (1) 1 of 1

Type (Abiotic Degradation, Hydrolysis)

sonication

Concentration (Abiotic Degradation, Hydrolysis)

0.5 mmol/l

Temperature (Abiotic Deg- 22 radation, Hydrolysis) [°C] Rate Constant

0.034 - 0.044 min-

Method, Remarks (Abiotic title comp. in H2O sonicated at 20 kHz up to 120 min; with/without 0.05 - 10 g/l particles of silica Degradation, Hydrolysis) (10 nm - 15 μm) or organic resin (35 μm); by GC and UV-VIS analysed; solid particles slightly decreased decomposition rate of title comp. (plot) Zhang, Guangming; Hua, Inez; Chemosphere; vol. 46; nb. 1; (2002); p. 59 - 66, View in Reaxys Oxygen Demand (1) 1 of 1

Type (Oxygen Demand)

COD/ThOD

Related to

Substance

Ratio BOD5/COD

0.7

Method, Remarks (Oxygen Demand)

ThOD: theoretical oxygen demand; COD determined according to Standard Methods (1976) using MilliQ water and potassium dichromate; ThOD is the stoichiometric amount of oxygen required to oxidize a compound to end product

Baker, James R.; Milke, Mark W.; Mihelcic, James R.; Water Research; vol. 33; nb. 2; (1999); p. 327 - 334, View in Reaxys Use (7) Laboratory Use and Use Pattern Handling Solvent in pigment preparation

References Patent; Clariant International Ltd.; US7384472; (2008); (B2) English, View in Reaxys

organic additive for Patent; Samsung Electro-Mechanics Co., Ltd.; EP1820802; (2007); (A1) English, an insulating com- View in Reaxys position for a liquid lens preparation of orga- Patent; COUNCIL OF SCIENTIFIC and INDUSTRIAL RESEARCH; WO2005/61423; nomettalic reagents (2005); (A1) English, View in Reaxys such as phenyl magnesium bromide, phenyl lithium and diphenyl zinc etc. substrate for iodina- Patent; MITSUBISHI GAS CHEMICAL COMPANY, INC.; EP1595862; (2005); (A1) Engtion lish, 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

Ausgangsstoff bei Herstellung von Phenylbromsilan

Jost et al.; Chemicky Prumysl; vol. 15; (1965); p. 521, View in Reaxys

Isolation from Natural Product (1) Isolation from Nat- References ural Product

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gaster of green ant Oecophylla smaragdina

Peerzada, N.; Pakkiyaretnam, T.; Renaud, S.; Agricultural and Biological Chemistry; vol. 54; nb. 12; (1990); p. 3335 - 3336, View in Reaxys

Quantum Chemical Calculations (1) Calculated Proper- Method (Quantum ties Chemical Calculations) Electronic energy levels

Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Location

References

supporting informa- Park, In-Hyeok; Medishetty, Raghavender; Kim, Ja-Yeon; Lee, Shim tion Sung; Vittal, Jagadese J.; Angewandte Chemie - International Edition; vol. 53; nb. 22; (2014); p. 5591 - 5595; Angew.Chem.Int.Ed; vol. 126; nb. 22; (2014); p. 5697 - 5701,5, View in Reaxys

Medchem (129) 1 of 129

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : |antibody monoclonal Target : Wistar rat, strain Bor:WISWBioassay : 3 rats, 12-14 weeks old; dosed title comp.; killed; sampled kidney; prepared kidney sections; determined morphological alterations by immunohistochemical staining; intensity of immunoreaction evaluated semiquantitatively

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mmol/kg

Substance Route of Adm.

oral administration

Qualitative Results

Grade 2, slight; title comp. increased number of positively reacting tubules in cross section; P2 segment contain abundant π2μ positive structures of varying morphology; occasionally observed leakage of lysosomes

Measurement Parameter

qualitative

Hildebrand; Hartmann; Popp; Bomhard; Archives of Toxicology; vol. 71; nb. 6; (1997); p. 351 - 359, View in Reaxys 2 of 129

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : |enzyme; examination of Bioassay : controls: untreated mice; *: signif. different from control 2-3 months old mice were treated with title comp.; mice were killed 24 h after the last dose; liver was removed; changes in π-aminolevulinate dehydratase (ALA-D, EC 4.2.1.24) and synthase (ALA-S, EC 2.3.1.37) activ. in liver homogenates were measured

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

changes in ALA-S activities, ca. percent of control (dose title comp., mg/kg/d): 65* (35, 3.5 percent ALD), 70* (65, 7 percent ALD), 100* (95, 10.5 percent ALD), 110* (160, 18 percent ALD); presented as graph; no effect on ALA-D activity

Measurement Parameter

qualitative

Szymanska; Bruchajzer; Sporny; Piotrowski; Bulletin of Environmental Contamination and Toxicology; vol. 61; nb. 1; (1998); p. 22 - 30, View in Reaxys 3 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

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Bioassay Details

Target : BALB'c mouseBioassay : controls: untreated mice and sunflower oil, 10 ml/kg/d; *: signif. different from control 2-3 months old mice were treated with title comp.; mice were killed 24 h after the last dose; liver was removed; liver/total body wt. ratios were determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

title comp. signif. increased liver/total body wt. ratio only at 160 mg/kg/d (18 percent ALD); presented as graph

Measurement Parameter

qualitative

Szymanska; Bruchajzer; Sporny; Piotrowski; Bulletin of Environmental Contamination and Toxicology; vol. 61; nb. 1; (1998); p. 22 - 30, View in Reaxys 4 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : BALB'c mouseBioassay : controls: untreated mice and sunflower oil, 10 ml/kg/d; effect title comp. on necrotic changes of hepatocytes was evaluated by changes in ALT and π-GT activities 2-3 months old mice were treated with title comp.; mice were killed 24 h after the last dose; blood was taken; serum was assayed for ALT (alanine aminotransferase, EC 2.6.1.2) and π-GT (π-glutamyltransferase, EC 2.3.2.2) activities

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Szymanska; Bruchajzer; Sporny; Piotrowski; Bulletin of Environmental Contamination and Toxicology; vol. 61; nb. 1; (1998); p. 22 - 30, View in Reaxys 5 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : BALB'c mouseBioassay : controls: untreated mice and sunflower oil, 10 ml/kg/d; GSH: reduced glutathione; MDA: malondialdehyde; *: signif. different from control 2-3 months old mice were treated with title comp.; mice were killed 24 h after the last dose; liver was removed; conc. of GSH and MDA in liver homogenates were measured

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

conc. in untreated/oil control/35 (3.5 percent ALD)/65 (7 percent ALD)/95 (10.5 percent ALD)/160 (18 percent ALD) mg/kg/d title comp. treated mice: ca. 11.5/11/11.5/12.5/15*/15* (GSH), 150/160/125*/130/129/130 (MDA); presented as graphs

Measurement Parameter

qualitative

Szymanska; Bruchajzer; Sporny; Piotrowski; Bulletin of Environmental Contamination and Toxicology; vol. 61; nb. 1; (1998); p. 22 - 30, View in Reaxys 6 of 129

Substance Effect

Toxic : Acute

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : BALB'c mouseBioassay : controls: untreated mice and sunflower oil, 10 ml/kg/d 2-3 months old mice were treated with title comp.; mice were killed 24 h after the last dose; liver was

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removed; liver histology was evaluated using light microscopy; ranging the relation of steatosis: 1 (no change) - 4 (steatosis of all lobular zones) Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Szymanska; Bruchajzer; Sporny; Piotrowski; Bulletin of Environmental Contamination and Toxicology; vol. 61; nb. 1; (1998); p. 22 - 30, View in Reaxys 7 of 129

Substance Effect

Toxic : Acute

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : BALB'c mouseBioassay : 2-3 months old mice; ALD (approximate lethal dose) was determined by the method of Deichman-Le Blanc

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

Unit

mg/kg

Quantitative value

900

Szymanska; Bruchajzer; Sporny; Piotrowski; Bulletin of Environmental Contamination and Toxicology; vol. 61; nb. 1; (1998); p. 22 - 30, View in Reaxys 8 of 129

Substance Effect

Cytotoxic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Cell/tumor cell: proliferation/viability/growth

Bioassay Details

Target : hepatocytes from Sprague-Dawley rat liverBioassay : viability by trypan blue exclusion test; LC50 at 2h adult rats (250-300 g); freshly isolated hepatocytes; preincubated for 30 min in Krebs-Henseleit bicarbonate buffer with desferoxamine (500 μM)

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

LC50

Unit

Quantitative value

Measurement pX

2.52

Anari; Khan; Liu; O'Brien; Chemical Research in Toxicology; vol. 8; nb. 8; (1995); p. 997 - 1004, View in Reaxys 9 of 129

Substance Effect

Cytotoxic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Cell/tumor cell: proliferation/viability/growth

Bioassay Details

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

LC50

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Unit

Quantitative value

0.5

Measurement pX

3.3

Anari; Khan; Liu; O'Brien; Chemical Research in Toxicology; vol. 8; nb. 8; (1995); p. 997 - 1004, View in Reaxys 10 of 129

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; examination of Bioassay : pretreated rats with sodium phenobarbital, i.p., 100 mg/kg/d for 4 d; in suplem. Dulbecco's modified Eagles medium (DMEM); calcul. enzyme release; compared to control; GSH: reduced glutathione; GSSG: glutathione disulphide; NPSH: non-protein sulphydryl in vitro; in liver slices; in 24-well plates; added title comp.; with or without AGE (aged garlic extract); incubated at 37 deg C; assayed in slices NPSH content by Beutler, total glutathione (GSH and GSSG) using the DTNB-GSSG reductase recycling method

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

title comp. caused ca. 80 percent depletion of NPSH and total depletion of GSH; AGE conc.-dependently prevented effect of title comp.; presented as graph

Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 126; nb. 3; (1998); p. 213 - 222, View in Reaxys 11 of 129

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; examination of Bioassay : pretreated rats with sodium phenobarbital, i.p., 100 mg/kg/d for 4 d; slices preincubated for 30 min; in suplem. Dulbecco's modified Eagles medium (DMEM); compared to control; ECOD: 7-ethoxycoumarin O-deethylase; PROD: 7-pentoxyresorufin O-depentylase in vitro; in liver microsomes; in 24-well plates; added title comp.; with or without AGE (aged garlic extract); incubated at 0 deg C; with or without phenobarbital induction; assayed ECOD and PROD activities fluorimetrically

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

title comp. induced EROD and PROD activities by ca. 6- and 30-fold, respect., in phenobarbital induced microsomes; AGE conc.-dependently inhibited effect of title comp.; at 5 percent AGE remained >50 percent title comp.-induced activities

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Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 126; nb. 3; (1998); p. 213 - 222, View in Reaxys 12 of 129

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : pretreated rats with sodium phenobarbital, i.p., 100 mg/kg/d for 4 days; in suplem. Dulbecco's modified Eagles medium (DMEM); calculated enzyme release; compared to control; LDH: lactate dehydrogenase; ALT: alanine aminotransferase in vitro; in liver slices; in 24-well plates; added title comp.; with or without AGE (aged garlic extract); incubated at 37 deg C; assayed in culture medium and slices homogenates activity of LDH and ALT using NAD+ - linked reactions

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

title comp. increased 4-fold LDH and 2-fold ALT release from slices; AGE conc.-dependently prevented title comp.-induced ALT and LDH leakage; 5 percent AGE restored LDH and ALT leakage to control levels; presented as graph

Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 126; nb. 3; (1998); p. 213 - 222, View in Reaxys 13 of 129

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : pretreated rats with sodium phenobarbital, i.p., 100 mg/kg/d for 4 days; slices preincubated for 30 min before experiment; in suplem. Dulbecco's modified Eagles medium (DMEM); compared to control in vitro; in liver slices; in 24-well plates; added title comp.; with or without AGE (aged garlic extract); incubated at 37 deg C; measured ATP content in supernatant by firefly luciferase enzyme assay by Holm-Hansen

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

title comp. produced a dramatic decrease of slice ATP content; AGE partially but not signif. prevented title comp.-induced ATP loss from slices; presented as graph

Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 126; nb. 3; (1998); p. 213 - 222, View in Reaxys 14 of 129

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : pretreated rats with sodium phenobarbital, i.p., 100 mg/kg/d for 4 days; slices preincubated for 30 min before experiment; in suplem. Dulbecco's modified Eagles medium (DMEM); compared to control in vitro; in liver slices; in 24-well plates; added title comp.; with or without 1-5 percent AGE (aged garlic extract); incubated at 37 deg C; measured K(+) level in supernatant using a Jenway model PFP7 flame photometer

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

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Substance Name

177578

Substance Dose

1 mM

Qualitative Results

title comp. produced a rapid loss of slice K(+); slice K(+) <20 percent of that in freshly prepared slices; AGE partially and conc.-dependently prevented title comp.-induced loss of K(+); presented as graph

Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 126; nb. 3; (1998); p. 213 - 222, View in Reaxys 15 of 129

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : pretreated rats with sodium phenobarbital, i.p., 100 mg/kg/d for 4 days; slices preincubated for 30 min before experiment; in suplem. Dulbecco's modified Eagles medium (DMEM); compared to control; TBARS: thiobarbituric acid reacting substances in vitro; in liver slices; in 24-well plates; added title comp.; with or without 1-5 percent AGE (aged garlic extract); incubated at 37 deg C; measured TBARS formation in the culture medium spectrophotometrically

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

title comp. stimulated TBARS formation by ca. 5-fold; 1 percent AGE restored TBARS formation to control values; presented as graph

Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 126; nb. 3; (1998); p. 213 - 222, View in Reaxys 16 of 129

17 of 129

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : |enzyme; induction of Bioassay : blood collection; CYP1A1 induction in peripheral blood lymphocytes; SDS-PAGE and Western blot analysis

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

157 mg/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

CYP1A1 induction (3.9 fold) in lymphocytes was observed

Measurement Parameter

qualitative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |biotransformation Target : human hypatocytesBioassay : cells were cultured in 5 ml Waymouth MB752/1 medium; density, 0.6 x 106 cells/ml; humidified atmosphere, 5 percent CO2 and 95 percent air; temperature, 37 deg C human hypatocytes from post-mortem liver tissue; exposure to test chemical after 2 or 24 h pre-incubation; 4 or 24 h exposure

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Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.500000 mM

Qualitative Results

formation of 2-, 3-, and 4-bromophenols was observed in hepatocyte cultures; amounts of BrP increased with both exposure time and substrate concentration

Measurement Parameter

qualitative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |biotransformation Target : monkey hypatocytesBioassay : cells were cultured in 5 ml Waymouth MB752/1 medium; density, 0.6 x 106 cells/ml; humidified atmosphere, 5 percent CO2 and 95 percent air; temperature, 37 deg C cynomolgus monkey hypatocytes from animals which served as kidney donors for polimyelitis vavvine production; exposure to test chemical after 2 or 24 h preincubation; 4 or 24 h exposure; influence of SFK-525A was studied in separate experiments

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.500000 mM

Qualitative Results

formation of 2-, 3-, and 4-bromophenols was observed in hepatocyte cultures; amounts of BrP increased with both exposure time and substrate concentration

Measurement Parameter

qualitative

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : human hypatocytesBioassay : cells were cultured in 5 ml Waymouth MB752/1 medium; density, 0.6 x 106 cells/ml; humidified atmosphere, 5 percent CO2 and 95 percent air; temperature, 37 deg C human hypatocytes from post-mortem liver tissue; exposure to test chemical after 2 or 24 h pre-incubation; 4 or 24 h exposure

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.500000 mM

Qualitative Results

loss of cell viability; GSH depletion; the degree of the observed effects was not influenced by the duration of pre-incubation and/or exposure periods

Measurement Parameter

qualitative

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : monkey hypatocytesBioassay : cells were cultured in 5 ml Waymouth MB752/1 medium; density, 0.6 x 106 cells/ml; humidified atmosphere, 5 percent CO2 and 95 percent air; temperature, 37 deg C cynomolgus monkey hypatocytes from animals which served as kidney donors for polimyelitis vavvine production; exposure to test chemical after 2 or 24 h pre-incubation; 4 or 24 h exposure

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.500000 mM

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Qualitative Results

loss of cell viability; GSH depletion; the degree of the observed effects was not influenced by the duration of pre-incubation and/or exposure periods

Measurement Parameter

qualitative

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : Effect of Hepatotoxins on the Viability of HepG2 Cells The activity of two toxins was studied first on HepG2 cells-bromobenzene (BB) and CCl4. Cells were challenged with the toxins at different concentration levels. Precipitate formation was observed when BB was diluted with media prior to

Biological Species/NCBI ID

human

Cells/Cell Lines

Hep-G2 cell line

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

at concentration of 20 nM test compound, cells showed no viability while at lower concentrations the toxic effect was inconsistent

Measurement Parameter

qualitative

Patent; SOUTH DAKOTA STATE UNIVERSITY; US2007/49538; (2007); (A1) English, View in Reaxys 22 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

induces liver injury measured by increase of the plasma concentration of π1-acid glycoprotein (AGP) (no effect on the plasma albumin concentration) (rats)

Measurement Parameter

qualitative

Sugihara; Furuno; Kita; Murakami; Yata; Chemical and Pharmaceutical Bulletin; vol. 40; nb. 9; (1992); p. 2516 - 2519, View in Reaxys 23 of 129

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : human liver-derived HepG2 cellsBioassay : cells culturing as monolayers in DME supplemented with 10 percent v/v foetal calf serum at 37 deg C in 5 percent CO2/95 percent air; title comp. as 1 M stock solution in DMSO diluted to 0.2 mM with DMEM before addition to the incubation medium title comp. incubating with HepG2 cells; viability assessment

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

10 mM

Qualitative Results

marked cytotoxic effect; cell viability 44.6 percent of control

Measurement Parameter

qualitative

Thabrew, M. Ira; Hughes, Robin D.; Mcfarlane, Ian G.; Journal of Pharmacy and Pharmacology; vol. 49; nb. 11; (1997); p. 1132 - 1135, View in Reaxys 24 of 129

Substance Effect

Nephrotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

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Bioassay Details

Target : Swiss OF1 (Iffa-Credo) mouseBioassay : mice of 23-25 g; estimation of nephrotoxicity according to the damage of renal proximal tubules title comp. administered to mice pretreated or nonpretreated (30 min before) with periodate oxidized adenosine (ADOX); mice were sacrificed 2, 4, 6, 8, and 24 h after adminisration; kidney isolation; light microscopy

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

500 mg/kg

Substance Route of Adm.

oral administration

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Morel; Ban; Hettich; Huguet; Journal of Applied Toxicology; vol. 19; nb. 1; (1999); p. 47 - 54, View in Reaxys 25 of 129

Substance Effect

Apoptotic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Apoptosis

Bioassay Details

Target : gonadal (RTG-2) cells of Oncorhynchus mykiss, rainbow troutBioassay : control: untreated cells cells incubated with title comp. for 24 h and 48 h at 20 deg C; cells subjected to in situ hybridization (TUNEL) to detect induction of apoptosis

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

presence of pyknotic nuclei and apoptosis were observed in title comp.-treated cells

Measurement Parameter

qualitative

Zurita, Jorge L.; Jos, Angeles; Peso, Ana del; Salguero, Manuel; Lopez-Artiguez, Miguel; Repetto, Guillermo; Food and Chemical Toxicology; vol. 45; nb. 4; (2007); p. 575 - 584, View in Reaxys 26 of 129

Substance Effect

Apoptotic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Apoptosis

Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : control: untreated cells cells (ATCC no. CRL-2406) exposed to title comp. for 24-72 h at 30 deg C; subjected to in situ hybridization (TUNEL) to detect induction of apoptosis

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

presence of pyknotic nuclei and apoptosis were observed in title comp.-treated cells

Measurement Parameter

qualitative

Substance Effect

Cytotoxic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Cell/tumor cell: proliferation/viability/growth

Bioassay Details

Target : gonadal (RTG-2) cells of Oncorhynchus mykiss, rainbow troutBioassay : control: untreated cells; G6PDH leakage was marker of cell death cells incubated with title comp. for 24 h or 48 h at 20 deg C; G6PDH (glucose-6-phosphate dehydrogenase) content in culture medium determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

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Quantitative value

2.32 - 2.45

Measurement pX

2.63

Substance Effect

Cytotoxic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Cell/tumor cell: proliferation/viability/growth

Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : G6PDH was marker of cell death; control: untreated cells cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; G6PDH (glucose-6-phosphate dehydrogenase) activity in culture medium was determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

2.43 - 2.58

Measurement pX

2.61

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |metabolic Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : control: untreated cells cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; metallothionein content in cells detd. using Cadmium/haemoglobin affinity assay

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Qualitative Results

slight increase in metallothionein content in cells was observed after 24 h of title comp. exposure; table, fig.

Measurement Parameter

qualitative

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 activity; effect onBioassay : control: untreated cells cells incubated with title comp. for 24 h at 20 deg C; ethoxyresorufin-O-deethylase activity in cells determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

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Qualitative Results

slight increase in ethoxyresorufin-O-deethylase was detected in cells after 24 h of title comp. exposure, with a maximum level of induction with 1.85 mM; table, fig.

Measurement Parameter

qualitative

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 activity; effect onBioassay : control: untreated cells cells incubated with title comp. for 24 h or 48 h at 20 deg C; succinate dehydrogenase activity in cells determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

2.54 - 2.7

Measurement pX

2.6

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 activity; increase ofBioassay : cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; G6PDH (glucose-6-phosphate dehydrogenase) activity in cells determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.54 - 2.58

Measurement pX

2.81

Target Name

enzyme

Target Synonyms

enzyme

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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 activity; increase ofBioassay : cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; succinate dehydrogenase activity determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.55 - 1.59

Measurement pX

2.81

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 activity; increase ofBioassay : control: untreated cells cells incubated with title comp. for 24 h or 48 h at 20 deg C; glucose-6-phosphate dehydrogenase (G6PDH) enzyme activity in cells determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

2.5 - 2.54

Measurement pX

2.6

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)

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Bioassay Details

Effect : enzyme activity; induction ofBioassay : control: untreated cells cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; ethoxyresorufin-O-deethylase (EROD) activity in cells determined

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.54

Measurement pX

2.81

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : control: untreated cells cells (ATCC no. CRL-2406) exposed to title comp. for 24 h at 30 deg C; stained with Mayer's hematoxylin and eosin or neutral red; morphological changes evaluated under microscope

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

1 mM title comp. caused loss of cells, cytoplasmic vesicles, hydropic degeneration of cytoplasm; 1.5 mM title comp. caused decrease in no. of cells, hydropic degeneration of cytoplasm, presence of pyknotic nuclei and condensed cytoplasm; fig.

Measurement Parameter

qualitative

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : gonadal (RTG-2) cells of Oncorhynchus mykiss, rainbow troutBioassay : control: untreated cells; HDC: hydropic degeneration of cytoplasm cells incubated with title comp. for 24 h and 48 h at 20 deg C; stained with Mayer's hematoxylin and eosin or neutral red; cell morphological changes examined

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

NOAEC

Unit

Quantitative value

1.1

Measurement pX

2.96

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : HD: hydropic degeneration of cytoplasm; control: untreated cells cells (ATCC no. CRL-2406) exposed to title

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comp. for 72 h at 30 deg C; stained with Mayer's hematoxylin and eosin; morphological changes evaluated under microscope Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Measurement Parameter

NOAEC

Unit

Quantitative value

Measurement pX

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.58 - 1.77

Measurement pX

2.8

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : gonadal (RTG-2) cells of Oncorhynchus mykiss, rainbow troutBioassay : control: untreated cells cells incubated with title comp. for 24 h or 48 h at 20 deg C; lysosomal uptake of neutral red dye determined; lysosomal function evaluated and expressed as uptake in relative form to the protein content of culture

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.93 - 2.04

Measurement pX

2.71

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Target : gonadal (RTG-2) cells of Oncorhynchus mykiss, rainbow troutBioassay : control: untreated cells cells incubated with title comp. for 24 h or 48 h at 20 deg C; MTS tetrazolium reduction assay performed

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

2.07 - 2.2

Measurement pX

2.68

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : gonadal (RTG-2) cells of Oncorhynchus mykiss, rainbow troutBioassay : control: untreated cells cells incubated with title comp. for 24 h or 48 h at 20 deg C; total cellular protein content was quantified in situ, using Coomassie brilliant blue G-250

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.7 - 1.85

Measurement pX

2.77

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; lysosomal uptake of neutral dye determined; lysosomal function expressed as uptake in relative form to the protein content of culture

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.61 - 1.79

Measurement pX

2.79

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : control: untreated cells cells (ATCC no. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; lysosomal uptake of neutral red dye was evaluated

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.57 - 1.58

Measurement pX

2.8

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.69 - 1.7

Measurement pX

2.77

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : hepatocellular carcinoma PLHC-1 cells of Poeciliopsis lucidaBioassay : control: untreated cells cells (ATCC No. CRL-2406) incubated with title comp. for 24, 48 or 72 h at 30 deg C; total cellular protein content was quantified in situ, using Coomassie brilliant blue G-250

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

1.57 - 1.59

Measurement pX

2.8

Substance Effect

Phytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Chlorella vulgaris var viridisBioassay : control: without title comp. algae culture in exponential growth were exposed to title comp. for 24, 48 or 72 h at 22 deg C under water-saturated

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sterile atmosphere contg. 5% CO2 and cold light source of 8000 lux; absorbance measured at 450 nm; algae proliferation detd. Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

NOAEC

Unit

Quantitative value

1.6

Measurement pX

2.8

Substance Effect

Phytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Chlorella vulgaris var viridisBioassay : control: without title comp. algae culture in exponential growth were exposed to title comp. for 24, 48 or 72 h at 22 deg C under water-saturated sterile atmosphere contg. 5% CO2 and cold light source of 8000 lux; absorbance measured at 450 nm; algae proliferation detd.

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

2.18 - 2.35

Measurement pX

2.66

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : control: without title comp. neonates of test system were maintained at 20 deg C in presence of title comp. for 24-72 h; acute toxicity immobilization tests were performed in standard reference water according to OECD Guideline 202 (2004)

Biological Species/NCBI ID

Daphnia magna

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.0100000 mM

Measurement Parameter

NOAEC

Unit

Quantitative value

0.06

Measurement pX

4.22

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Biological Species/NCBI ID

Daphnia magna

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.0100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

0.09 - 0.11

Measurement pX

4.05

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : control: without title comp. bacteria incubated with title comp. for 5 or 15 min at 15 deg C; bioluminescence inhibition was evaluated

Biological Species/NCBI ID

Aliivibrio fischeri

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.0100000 mM

Measurement Parameter

NOAEC

Unit

Quantitative value

0.02

Measurement pX

4.7

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : control: without title comp. bacteria incubated with title comp. for 5 or 15 min at 15 deg C; bioluminescence inhibition was evaluated

Biological Species/NCBI ID

Aliivibrio fischeri

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

0.0100000 mM

Measurement Parameter

EC50

Unit

Quantitative value

0.04

Measurement pX

4.4

Zurita, Jorge L.; Jos, Angeles; Peso, Ana del; Salguero, Manuel; Lopez-Artiguez, Miguel; Repetto, Guillermo; Food and Chemical Toxicology; vol. 45; nb. 4; (2007); p. 575 - 584, View in Reaxys

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53 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic sorption experiment; brown Mediterranean soil (Sicily): 3.31 percent sand, 21.90 percent silt, 75.00 percent clay, pH 5.9, specific surface area 15.86 m2/g; at 15 deg C, gasphase relative humidity of 50, 70 and 90 percent; sorption constant determined by inverse GC

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

sorption log of sorption constant (Ksa): log Ksa = 2.81, 2.49 and 2.28 at relative humidity of 50, 70 and 90 percent, resp.; table, diagrams

Measurement Parameter

qualitative

Goss, Kai-Uwe; Buschmann, Johanna; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 13; (2004); p. 3667 - 3673, View in Reaxys 54 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic sorption experiment; soil (loess sample, Iowa) texture: 7.1 percent sand, 75.6 percent silt, 17.4 percent clay, pH 8.34, specific surface area 15.86 m2/g; at 15 deg C, gas-phase relative humidity of 50, 70 and 90 percent; sorption constant determined by inverse GC

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

sorption log of sorption constant (Ksa): log Ksa = 2.15, 1.69 and 1.30 at relative humidity of 50, 70 and 90 percent, resp.; table, diagrams

Measurement Parameter

qualitative

Goss, Kai-Uwe; Buschmann, Johanna; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 13; (2004); p. 3667 - 3673, View in Reaxys 55 of 129

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

Km (Michaelis constant)

Unit

Quantitative value

0.41

Measurement pX

3.39

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

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57 of 129

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

Vmax

Unit

nmol/min/mg protein

Quantitative value

6.4

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

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Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

CLint

Unit

µL/min/mg protein

Quantitative value

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

Km (Michaelis constant)

Unit

Quantitative value

0.3

Measurement pX

3.52

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

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60 of 129

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

Km (Michaelis constant)

Unit

Quantitative value

0.8

Measurement pX

3.1

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

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62 of 129

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

Vmax

Unit

nmol/min/mg protein

Quantitative value

1.8

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

Vmax

Unit

nmol/min/mg protein

Quantitative value

6.3

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

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63 of 129

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

CLint

Unit

µL/min/mg protein

Quantitative value

2.2

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1236661View in Reaxys

Substance Name

Bromobenzene

Substance Dose

0.300000 mM

Measurement Parameter

CLint

Unit

µL/min/mg protein

Quantitative value

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Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : C57BL6J miceBioassay : mice, 3-4 month old, vehicle, corn oil, mice killed by decapitation, blood collected, plasma separated, liver removed, homogenized, plasma sorbitol dehydrogenase (SDH) activity, blood urea nitrogen (BUN), non-protein sulfhydryl levels determination

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

250 mg/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

showed significant hepatocellular damage, plasma SDH activity elevated, NPSH levels decreased, did not elevate BUN levels

Measurement Parameter

qualitative

Manautou, Jose E.; Silva, Vanessa M.; Hennig, Gayle E.; Whiteley, Herbert E.; Toxicology; vol. 127; nb. 1-3; (1998); p. 1 10, View in Reaxys 65 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : water: conductivity = 165-170 μOhms, hardness = 75-85 mg CaCO3/l, alkalinity = 80-90 mg CaCO3/l, oxygen conc. = 8.8 ppm, pH = 8.8, 21 deg C

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

partition air-water partition coefficient: KAW = 0.08

Measurement Parameter

qualitative

De Wolf, Watze; Lieder, Paul H.; Chemosphere; vol. 36; nb. 8; (1998); p. 1713 - 1724, View in Reaxys 66 of 129

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : bacteria, T3 mutation, 20 deg C, pH 7.0; vehicle either π-cyclodextrin or H2O; bioluminescence measurement

Biological Species/NCBI ID

Photobacterium phosphoreum

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

pEC50

Unit

Quantitative value

3 - 3.87

Measurement pX

3.87

Song, Wen-lu; Huang, Qing-guo; Wang, Lian-sheng; Chemosphere; vol. 38; nb. 4; (1999); p. 693 - 698, View in Reaxys

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67 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Bioassay : mice, 6 wks old, 23 deg C, vehicle, olive oil, mice killed, blood collected, serum alanine aminotransferase (ALT) activity determination

Biological Species/NCBI ID

mouse

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

2.50000 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

ALT activity, 53.0-2530 Karmen unit/ml (14.7-15.8 in control)

Measurement Parameter

qualitative

Mizutani, Tamio; Miyamoto, Yoko; Toxicology Letters; vol. 105; nb. 1; (1999); p. 25 - 30, View in Reaxys 68 of 129

Substance Effect

Toxic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Cell/tumor cell: proliferation/viability/growth

Bioassay Details

Effect : growth inhibitionTarget : Saccharomyces cerevisiae, eucaryotic yeastBioassay : minimum inhibition zone concentration (Cmiz); temp. 29 deg C; incubation time: overnight; agar plate; title comp. in DMSO-glycerol solvent

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

log 1/Cmiz: 1.40 (Cmiz in mM/l)

Measurement Parameter

qualitative

Liao; Wang; He; Yang; Bulletin of Environmental Contamination and Toxicology; vol. 56; nb. 3; (1996); p. 460 - 466, View in Reaxys 69 of 129

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : bioluminescence inhibitionBioassay : 20 deg C Microtox test

Biological Species/NCBI ID

Photobacterium phosphoreum

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

-Log EC 50: 3.78 (mol/l)

Measurement Parameter

qualitative

Huang; Kong; Wang; Bulletin of Environmental Contamination and Toxicology; vol. 56; nb. 5; (1996); p. 758 - 765, View in Reaxys 70 of 129

Substance Effect

Toxic : Acute

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Carassias auratusBioassay : temp. 20 deg C; DO 8.2 mg/l; pH 7.5; hardness as CaCO3 110 mg/l fishes ca. 3.5 g weight, 4.0 cm length; semi-static method (water renewal at each 12 h); OECD, 1984; no fed during the exposure

Substance RN

1236661View in Reaxys

Substance Name

177578

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Qualitative Results

lg 1/LC 50: 4.19 (mol/l)

Measurement Parameter

qualitative

Liu; Wang; Chen; Li; Yu; Bulletin of Environmental Contamination and Toxicology; vol. 57; nb. 3; (1996); p. 421 - 425, View in Reaxys 71 of 129

Substance Effect

Oxidative Stress

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : human hepatoma cell HepG2Bioassay : control experiment; dsDNA = double-stranded DNA; determination of 8-hydroxy-2'-deoxyguanosine (8-OH-dGu) formation cell preincubation with 100 μM buthionine sulfoximine for 48 h; 37 deg C; measurement of lipid peroxidation as thiobarbituric acid-reactive substances (TBARS) released into medium; DNA damage determin. as remaining dsDNA level

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

significant increase of TBARS level; significant decrease of remaining dsDNA; no 8-OH-dGu formation

Measurement Parameter

qualitative

Wang, Yong-Fa; Hu, Miao-Lin; Food and Chemical Toxicology; vol. 38; nb. 5; (2000); p. 451 - 458, View in Reaxys 72 of 129

Substance Effect

Oxidative Stress

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Sprague-Dawley rat liver slicesBioassay : control experiment; 8-OH-dGu = 8-hydroxy-2'deoxyguanosine; FADU = fluorometric analysis of alkaline DNA unwinding exposure in serum bottle; 37 deg C; measurement of lipid peroxidation as thiobarbituric acid-reactive substances (TBARS) released into medium; DNA isolation from nuclei; DNA damage determin. as 8-OH-dGU level by HPLC, DNA strand breakage by FADU method

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

increase of lipid peroxidation (increased TBARS level); no DNA damage (no formation of 8-OHdGu)

Measurement Parameter

qualitative

Wang, Yong-Fa; Hu, Miao-Lin; Food and Chemical Toxicology; vol. 38; nb. 5; (2000); p. 451 - 458, View in Reaxys 73 of 129

Substance Effect

Oxidative Stress

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Sprague-Dawley rat liver slicesBioassay : 37 deg C; control experiment; GSH = glutathione; TBARS = thiobarbituric acid-reactive substances; 8-OH-dGu = 8-hydroxy-2'-deoxyguanosine; FADU = fluorometric analysis of alkaline DNA unwinding GSH-depleted liver slices from rats injected with DEM (i. p.); slice exposure in serum bottle; measurement of lipid peroxidation as TBARS released into medium; DNA isolation for damage determin. as 8-OH-dGU level by HPLC, DNA strand breakage by FADU

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

significant increase of lipid peroxidation (increased TBARS level); significant DNA damage (increased 8-OH-dGu level)

Measurement Parameter

qualitative

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Wang, Yong-Fa; Hu, Miao-Lin; Food and Chemical Toxicology; vol. 38; nb. 5; (2000); p. 451 - 458, View in Reaxys 74 of 129

Substance Effect

Oxidative Stress

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : human hepatoma cell HepG2Bioassay : control experiment; FADU = fluorometric analysis of alkaline DNA unwinding; calculation of double-stranded DNA (dsDNA) incubation at 37 deg C; measurement of lipid peroxidation as thiobarbituric acid-reactive substances (TBARS) released into medium; determination of DNA strand breakage by FADU method

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Wang, Yong-Fa; Hu, Miao-Lin; Food and Chemical Toxicology; vol. 38; nb. 5; (2000); p. 451 - 458, View in Reaxys 75 of 129

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : mitochondrial injuryTarget : Swiss CD-1 mouseBioassay : ALT = alanine aminotransferase mice weighing 25-35 g; killed at various time intervals; blood collect.; plasma ALT activ.; mitochondria isol.; O2 consumption of isol. mitochondria meas.; total glutathione, mitochondrial and cytosolic protein content determ.

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

2 mg/g

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

mitochondrial and cytosolic glutathione reduced to 41-48 percent and to 28-64 percent of control at 3-4 h and 1-2 post-dosing, resp.; state 3 respir. reduced to 16 percent at 4 h; complex II state 3 and 4 respir. reduced by 48-57 percent at 4 h; plasma

Measurement Parameter

qualitative

Wong, Simon G.W.; Card, Jeffrey W.; Racz, William J.; Toxicology Letters; vol. 116; nb. 3; (2000); p. 171 - 181, View in Reaxys 76 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Wistar rat cut liver slicesBioassay : rats, 200-300 g b. wt., 22 deg C, treated with phenobarbital sodium i.p. injection 100 mg/kg, precision-cut-liver slices and microsomes prepared, placed in 24-well plastic plate, incubated 37 deg C

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

1 mM

Qualitative Results

toxicity indicated by decreased K(1+), adenosine triphosphate and glutathione content of slices, increased release of alanine aminotransferase and lactate dehydrogenase into medium, increased formation of thiobarbituric acid reacting substances

Measurement Parameter

qualitative

Wang, Bo Han; Zuzel, Katherine A.; Rahman, Khalid; Billington, David; Toxicology; vol. 132; nb. 2-3; (1999); p. 215 225, View in Reaxys 77 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

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Bioassay Name

In vivo Measurement

Bioassay Details

Target : IMP:wist ratBioassay : ALA-U = urinary 5-aminolevulinic acid rats weighing 180-220 g; urine collect. after 7-28 d; anal. for ALA-U and porphyrins; heme oxygenase activity; killed 24 h after last dose; hewpatic microsomes prepared; heme oxygenase and enzyme activity in serum and hepatocytes

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

3 mg/kg

Substance Route of Adm.

intragastric administration

Qualitative Results

ALA-U excretion increased; coproporphyrins excretion increased at 75 mg/kg; no signif. effect on plasma or liver enzyme activity

Measurement Parameter

qualitative

Szymanska, Jadwiga A.; Piotrowski, Jerzy K.; Chemosphere; vol. 41; nb. 10; (2000); p. 1689 - 1696, View in Reaxys 78 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Bioassay : rats weighing 160-190 g; with and without treatm. with taurolithocholic acid (20 μmol/ kg); bile collected from cannulated common bile tract; rats killed 48 h after dosing; histol. exam. of liver

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

600 mg/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

decrease in bile flow; severe necrosis of perivenous (zone 3) hepatocytes; no effect of title comp. on taurolithocholic acid-induced cholestasis; no effect on biliary excretion of total bile acids after admin. of taurolithocholic acid

Measurement Parameter

qualitative

Mottino, Aldo; Tuchweber, Beatriz; Plaa, Gabriel L.; Yousef, Ibrahim M.; Toxicology Letters; vol. 116; nb. 1-2; (2000); p. 69 - 77, View in Reaxys 79 of 129

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Tetrahymena pyriformis GL-C, protozoaBioassay : controls: 1) no title comp., no T. pyriformis; 2) inoculated with T. pyriformis without title comp. population growth impairment testing; 40-h TETRATOX assay; population density quantitated spectrophotometrically at 540 nm

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

pGI50

Quantitative value

0.75

Schultz, T. Wayne; Chemical Research in Toxicology; vol. 12; nb. 12; (1999); p. 1262 - 1267, View in Reaxys 80 of 129

Substance Effect

Teratogenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : FETAX: frog embryo teratogenesis assay-Xenopus; determinations of 96-h LC50 and EC50 concentrations by Litchfield-Wilcoxon probit analysis, teratogenic index (TI=LC50:EC50) and minimum concentration to inhibit growth (MCIG) exposure of embryos to various concentra-

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tions of title comp. with/without exogenous metabolic activation system (MAS, aroclor 1254-induced rat liver microsomes) in FETAX solution (pH 7.0) at 23 deg C for 96 h Biological Species/NCBI ID

Xenopus

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

LC50, EC50 and MCIG values were 2800.0, 280.0 and >500.0 mg/l for title comp. and 300.0, 240.0 and 100.0 mg/l for title comp. + MAS, respectively; teratological responses presented in table

Measurement Parameter

qualitative

Fort, Douglas J.; Propst, Timothy L.; Stover, Enos L.; Teratogenesis Carcinogenesis and Mutagenesis; vol. 16; nb. 6; (1996); p. 307 - 315, View in Reaxys 81 of 129

Substance Effect

Teratogenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : FETAX: frog embryo teratogenesis assay-Xenopus; MAS pretreated with CHO to modulate epoxide hydrolase activity; determinations of 96-h LC50 and EC50 concentrations, teratogenic index (TI=LC50:EC50) and minimum concentration to inhibit growth (MCIG) exposure of embryos to various concentrations of title comp. with exogenous metabolic activation system (MAS, aroclor 1254-induced rat liver microsomes) inhibited by cyclohexene oxide (CHO-inhibited MAS) in FETAX solution (pH 7.0) at 23 deg C for 96 h

Biological Species/NCBI ID

Xenopus

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

LC50, EC50 and MCIG values were 150.0, 100.0 and 50.0 mg/l, respectively; teratological responses presented in table

Measurement Parameter

qualitative

Fort, Douglas J.; Propst, Timothy L.; Stover, Enos L.; Teratogenesis Carcinogenesis and Mutagenesis; vol. 16; nb. 6; (1996); p. 307 - 315, View in Reaxys 82 of 129

Substance Effect

Teratogenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : FETAX: frog embryo teratogenesis assay-Xenopus; MAS pretreated with CO to modulate P-450 activity; determinations of 96-h LC50 and EC50 concentrations, teratogenic index (TI=LC50:EC50) and minimum concentration to inhibit growth (MCIG) exposure of embryos to various concentrations of title comp. with exogenous metabolic activation system (MAS, aroclor 1254-induced rat liver microsomes) inhibited by carbon monoxide (CO-inhibited MAS) in FETAX solution (pH 7.0) at 23 deg C for 96 h

Biological Species/NCBI ID

Xenopus

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

LC50, EC50 and MCIG values were 1050.0, 400.0 and 300.0 mg/l, respectively; teratological responses presented in table

Measurement Parameter

qualitative

Fort, Douglas J.; Propst, Timothy L.; Stover, Enos L.; Teratogenesis Carcinogenesis and Mutagenesis; vol. 16; nb. 6; (1996); p. 307 - 315, View in Reaxys 83 of 129

Substance Effect

Teratogenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Bioassay : FETAX: frog embryo teratogenesis assay-Xenopus; MAS pretreated with DM to modulate glutathione conjugation; determinations of 96-h LC50 and EC50 concentrations, teratogenic index (TI=LC50:EC50) and minimum concentration to inhibit growth (MCIG) exposure of embryos to various concentrations of title comp. with exogenous metabolic activation system (MAS, aroclor 1254-induced rat liver microsomes) inhibited by diethyl maleate (DM-inhibited MAS) in FETAX solution (pH 7.0) at 23 deg C for 96 h

Biological Species/NCBI ID

Xenopus

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

LC50, EC50 and MCIG values were 100.0, 80.0 and 50.0 mg/l, respectively; teratological responses presented in table

Measurement Parameter

qualitative

Fort, Douglas J.; Propst, Timothy L.; Stover, Enos L.; Teratogenesis Carcinogenesis and Mutagenesis; vol. 16; nb. 6; (1996); p. 307 - 315, View in Reaxys 84 of 129

Substance Effect

Carcinogenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : substance inducing a reproducible and dose dependent increase in micronucleus frequency regarded as positive Syrian hamster embryo (SHE) micronucleus test in vitro; in DMSO solution; incubated for 18 h; 2000 cells counted microscopically from each coverslip, number of cells with micronuclei was determined

Biological Species/NCBI ID

Syrian hamster

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

also correlation with literature data for carcinogenicity No effect

Measurement Parameter

qualitative

Friedberg; Henning; Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis; vol. 289; nb. 1; (1993); p. 47 - 53, View in Reaxys 85 of 129

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : |enzyme; induction of Bioassay : serum ALT activ. determ. colorim. using 2,4-dibitrophenylhydrazine; π-GT activ. determ. accord. to 'Monotest 10 π-GT neu'from Boehringer-Mannheim outbred mice weigh. 23-30 g; kill. by cervical dislocat.; blood collect. from heart; alanine aminotransferase (ALT) and L-π-glutamyl-transferase (π-GT) activ. in serum

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

200 mg/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

30-120-fold increase in ALT activity; observ. 24-48 h following admin. of test comp.; increased πGT activity

Measurement Parameter

qualitative

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Szymanska, Jadwiga A.; Archives of Toxicology; vol. 72; nb. 2; (1997); p. 97 - 103, View in Reaxys 86 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : Imp Balb/cJ miceBioassay : outbred mice weigh. 23-30 g; kill. by cervical dislocat.; liver histopathology; glutathione and malondialdehyde (MDA) levels

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

200 mg/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

haemorrhagic or coagulative necrosis in liver central lobular zone; necrosis occur. only during first 48 h; GSH cont. decreas. by 80-90 percent between 2 and 12 h; 5-6-fold increas. level of MDA

Measurement Parameter

qualitative

Szymanska, Jadwiga A.; Archives of Toxicology; vol. 72; nb. 2; (1997); p. 97 - 103, View in Reaxys 87 of 129

Substance Effect

Toxic : Acute

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Target : Imp Balb/cJ miceBioassay : ALD=approximate lethal dose outbred mice weigh. 23-30 g; ALD values determ. accord. to Deichman-Le Blanc method

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

Unit

mg/kg

Quantitative value

900

Szymanska, Jadwiga A.; Archives of Toxicology; vol. 72; nb. 2; (1997); p. 97 - 103, View in Reaxys 88 of 129

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Spirostomum ambiguumBioassay : 24-well microplates as test containers; Spirotox biotest; pH = 7.4; 3 replicates; incubated in the dark at 25 deg C; test responses: morphological changes

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

pEC50

Quantitative value

0.29

Nalcz-Jawecki; Sawicki; Archives of Environmental Contamination and Toxicology; vol. 42; nb. 4; (2002); p. 389 - 395, View in Reaxys 89 of 129

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Spirostomum ambiguumBioassay : 24-well microplates as test containers; Spirotox biotest; pH = 7.4; 3 replicates; incubated in the dark at 25 deg C; lethal responses: spherical deformation and autolysis

Substance RN

1236661View in Reaxys

Substance Name

177578

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Measurement Parameter

pLC50

Quantitative value

0.365

Nalcz-Jawecki; Sawicki; Archives of Environmental Contamination and Toxicology; vol. 42; nb. 4; (2002); p. 389 - 395, View in Reaxys 90 of 129

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : |metabolic/pathway Target : Sprague-Dawley ratsBioassay : aq. hydrolysate filtered, and extracted with ether, concentrated, metabolites separated by HPLC; identification of metabolites by MS analysis; comparison with authentic samples rats pretreated with phenobarbital, 50 mg/kg for 3 d, on the 4th d (14C)title comp. injected i.p.; 4 h later rats killed livers removed, proteins precipitated from microsomes, separated and submitted in 6 M HCl soln. to acidic hydrolysis (reflux, 24 h),

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

2.50000 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

qualitative

Qualitative value

Bambal; Hanzlik; Chemical Research in Toxicology; vol. 8; nb. 5; (1995); p. 729 - 735, View in Reaxys 91 of 129

Substance Effect

Antibiotic

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Name

Cell/tumor cell: proliferation/viability/growth

Bioassay Details

Target : P. phosphoreum, marine bacteriumBioassay : bacteria cultured at 20 deg C in yeast-tryptone-salts-glycerol broth for 12-14 h T3 mutation; aq. solution; exposed for 15 min; decrease in light emission from the bacteria determined; EC50 - concentration required to reduce light emission by 50 percent; correlated with C18-EmporeTM disk/water partition coefficient

Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

pEC50

Unit

Quantitative value

3.77

Measurement pX

3.77

Lin, Zhifen; Yu, Hongxia; Wei, Dongbin; Wang, Gehui; Feng, Jianfang; Wang, Liansheng; Chemosphere; vol. 46; nb. 2; (2002); p. 305 - 310, View in Reaxys 92 of 129

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

1236661View in Reaxys

Substance Name

177578

Qualitative Results

sorption log Ki snow surface/air (m3/m2): -3.80; 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 93 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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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

1236661View in Reaxys

Substance Name

177578

Qualitative Results

partition Leonardite humic acid/air partition coefficient, KHA,air = 2.68E3 - 6.16E3 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 94 of 129

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

1236661View in Reaxys

Substance Name

177578

Qualitative Results

sorption experimental sorption enthalpy, ΔabsHi = -45.0 kJ/mol

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 95 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

partition Leonardite humic acid/air partition coefficient, KHA,air = 6.26E2 - 3.45E3 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 96 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : cells were cultured in Williams' E, Modified Earle's or Dulbecco's media for 3, 7, or 10 days prior to exposure; effect of diethylmaleate pretreatment on the viability; role of GSH

Cells/Cell Lines

Hep-G2 cell line

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

2.50000 mM

Qualitative Results

effect of medium and period in culture on toxicity; highest toxicity at 7 days for cells cultured in Williams' E (0 percent viable cells at 180 min) and Modified Earle's (ca. 20 percent viable cells) media; ca. 40 percent cell viability at 10 days in

Measurement Parameter

qualitative

Duthie; Melvin; Burke; Xenobiotica; vol. 24; nb. 3; (1994); p. 265 - 279, View in Reaxys

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97 of 129

Substance Effect

Oxidative Stress

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Bioassay : reduced glutathione peroxidase activity (GPx) in cytosol, aspartate (AST) and alanine (ALT) aminotransferases activities in plasma were determined; microsomal lipid peroxidation was evaluated in different systems in vivo; 150-g rats starved 12 h before and sacrificed 19 h after title comp. administration; microsomal and cytosol fractions of liver prepared; reduced glutathione (GSH) contents in liver

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

700 mg/kg

Substance Route of Adm.

intragastric administration

Qualitative Results

caused increase in microsomal lipid peroxidation in liver, significant rise in GPx activity accompanied by distinct GSH depletion, significant increase in AST and ALT aminotransferases activities

Measurement Parameter

qualitative

Jodynis-Liebert, Jadwiga; Murias, Marek; Bloszyk, Elzbieta; Planta Medica; vol. 65; nb. 4; (1999); p. 320 - 324, View in Reaxys 98 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |metabolic Bioassay : BB=bromobenzene; analysis: by phosphorimaging of stained blots, N-terminal sequence analysis; P=protein; H=hydrolase; C=carboxylesterase Acclimated rats (180 g) were phenobarbital-induced and killed; separated liver microsomal protein was incubated with <14C>BB and NADPH-generating system; pH 7.4; 90 min; 37 deg C; recovered microsomes fractionated; SDS-PAGE; analysis

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Qualitative Results

57- and 59-kDa separated Ps (major P band) were identified as rat liver microsomal C isozymes (3fold more abundant H A and H B) (E.C.3.1.1.1); another prominent band: 70-kDa; thesePs may be targets for metabolites which contribute in the hepatotoxicity

Measurement Parameter

qualitative

Rombach, Elizabeth M.; Hanzlik, Robert P.; Chemical Research in Toxicology; vol. 11; nb. 3; (1998); p. 178 - 184, View in Reaxys 99 of 129

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 : BB=bromobenzene; hydrolysis of 1-naphthylacetate and pnitrophenylacetate Acclimated rats (180 g) were phenobarbital-induced and killed; liver microsomes incubated with BB and NADPH-generating system; the microsomes reisolated by centrifugation; evaluation their ability (and control microsomes) to catalyse the hydrolysis;

Biological Species/NCBI ID

rat

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Substance RN

1236661View in Reaxys

Substance Name

177578

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Rombach, Elizabeth M.; Hanzlik, Robert P.; Chemical Research in Toxicology; vol. 11; nb. 3; (1998); p. 178 - 184, View in Reaxys 100 of 129

Substance Effect

Hepatotoxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Bioassay : phenobarbital-pretreated (3 d ip inject. of 80 mg/kg) rats (150-180 g); housed at 12 h light/dark cycle; food and water ad lib.; killed 4 h after treatm.; further investigation on mechanism of action which proteins are involved in effect of title comp. liver homogenates fractionated by differential ultracentrifugation; proteins separated by two-dimensional electrophoresis and analyzed for radioactiv. after transblotting by phosphorimaging; scintillation counting; Bradford assay; MALDI-TOF MS analysis

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

2 mM

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

highest spec. radiolabeling (6.1 nmol equiv 14C/mg of protein) observed in particulate fraction (P25) sedimented at 2500g from a 6000g supernatant fraction; more than 20 radiolab. protein spots observed in blots; peptide mass maps obtained for 17 spots

Measurement Parameter

qualitative

Koen, Yakov M.; Hanzlik, Robert P.; Chemical Research in Toxicology; vol. 15; nb. 5; (2002); p. 699 - 706, View in Reaxys 101 of 129

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : gene expression; effect onBioassay : 24 h after single title comp. administration total RNA from liver extracted, cDNA synthesized and labeled by Cy3 and Cy5 fluorophores; differentially expressed genes determined by hybridization with microarray slides containing 3000 rat genes

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

5 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

title comp. sign. (>2-fold) increased/decreased expression of 32/17 genes, resp.; part of them functionally joined to drug metabolism, glutathione metabolism, oxidative stress, acute phase response, protein synthesis and degradation groups (tables)

Measurement Parameter

qualitative

Heijne, Wilbert H.M.; Stierum, Rob H.; Slijper, Monique; Van Bladeren, Peter J.; Van Ommen, Ben; Biochemical Pharmacology; vol. 65; nb. 5; (2003); p. 857 - 875, View in Reaxys 102 of 129

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : glutathione content; decrease ofBioassay : GSH: reduced glutathione; GSSG: oxidised glutathione 24 h after single title comp. administration GSH+GSSG and GSSG levels in liver determined using 5,5'dithiobis-2-nitrobenzoic acid; absorbance at 405 nm measured

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Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

5 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

title comp. decreased GSH+GSSG level by 27-fold from ca. 21 to 0.8 μmol/g; low level of GSSG relative to GSH observed in title comp.-treated animals (figure)

Measurement Parameter

qualitative

Heijne, Wilbert H.M.; Stierum, Rob H.; Slijper, Monique; Van Bladeren, Peter J.; Van Ommen, Ben; Biochemical Pharmacology; vol. 65; nb. 5; (2003); p. 857 - 875, View in Reaxys 103 of 129

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : protein expression; effect onBioassay : MALDI-TOF: matrix assisted laser desorption ionisation-time of flight; NANO-ESI-MS/MS: nano-electrospray ionisation tandem mass spectrometry 24 h after single title comp. administration proteins from liver extracted, separated by two dimensional gel electrophoresis, silver stained and identified by MALDI-TOF- or NANO-ESI-MS/MS mass spectrometry

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

5 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

23 differentially expressed proteins (11 up- and 12 down-regulated significantly) found in livers of title comp.-treated rats; decrease in average size of proteins observed (figures)

Measurement Parameter

qualitative

Heijne, Wilbert H.M.; Stierum, Rob H.; Slijper, Monique; Van Bladeren, Peter J.; Van Ommen, Ben; Biochemical Pharmacology; vol. 65; nb. 5; (2003); p. 857 - 875, View in Reaxys 104 of 129

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : |enzyme; induction of Bioassay : 24 h after single title comp. administration liver cytosolic fraction prepared; glutathione-S-transferase (GST) activity determined using 1-chloro-2,4-dinitrobenzene as substrate

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

5 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

title comp. significantly increased GST acivity by ca. 1.4-fold

Measurement Parameter

qualitative

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Heijne, Wilbert H.M.; Stierum, Rob H.; Slijper, Monique; Van Bladeren, Peter J.; Van Ommen, Ben; Biochemical Pharmacology; vol. 65; nb. 5; (2003); p. 857 - 875, View in Reaxys 105 of 129

Substance Effect

Toxic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Bioassay : 24 h after single title comp. administration body and liver weights measured

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

5 mmol/kg

Substance Route of Adm.

intraperitoneal administration

Qualitative Results

title comp. decreased body weight of treated rats by 7 percent and had no significant effect on liver weight

Measurement Parameter

qualitative

Heijne, Wilbert H.M.; Stierum, Rob H.; Slijper, Monique; Van Bladeren, Peter J.; Van Ommen, Ben; Biochemical Pharmacology; vol. 65; nb. 5; (2003); p. 857 - 875, View in Reaxys 106 of 129

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : gene expression; effect onBioassay : data used to determine signature profile for oxidant stress-associated hepatotoxicity in a training set of compounds by applying methods of multivariate analysis 7-week-old rats treated with title comp., 24 h later killed and liver removed; RNA extracted from tissue homogenate, gene expression signature obtained by cDNA microarray using 3434 genes

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Name

177578

Substance Dose

900 mg/kg

Qualitative Results

number of genes which expression was found to be changed (induced or repressed) 1.5-fold: 506.3, 2-fold: 202, 4-fold: 26.3; set of 100 genes chosen that responded significantly different to oxidant stressors/reactive metabolites

Measurement Parameter

qualitative

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

rat

Substance RN

1236661View 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

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108 of 129

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

rat

Substance RN

1236661View in Reaxys

Substance Route of Adm.

oral administration

Measurement Parameter

qualitative

Measurement Object

Area under plasma concentration

Qualitative value

Not Published

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

rat

Substance RN

1236661View 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

rat

Substance RN

1236661View in Reaxys

Measurement Parameter

pKi

Unit

Qualitative value

Quantitative value

0.78

Deviation

0.45

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

In vitro lethal concentration against phenobarbital induced rat hepatocytes at 2 hours incubation with compound dissolved in DMSO

Biological Species/NCBI ID

rat

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Cells/Cell Lines

liver cell

Substance RN

1236661View in Reaxys

Measurement Parameter

LC50

Unit

Qualitative value

Quantitative value

0.6

Deviation

0.03

Measurement pX

3.22

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p. 165 - 174, View in Reaxys 112 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal concentration against human hepatocytes upon incubation for 2 h with compound dissolved in DMSO

Biological Species/NCBI ID

human

Cells/Cell Lines

liver cell

Substance RN

1236661View in Reaxys

Measurement Parameter

LC50

Unit

µM

Qualitative value

Quantitative value

1150

Deviation

115

Measurement pX

2.94

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p. 165 - 174, View in Reaxys 113 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal concentration against rat hepatocytes upon incubation for 2 h with compound dissolved in DMSO

Biological Species/NCBI ID

rat

Cells/Cell Lines

liver cell

Substance RN

1236661View in Reaxys

Measurement Parameter

LC50

Unit

µM

Qualitative value

Quantitative value

750

Deviation

Measurement pX

3.12

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p. 165 - 174, View in Reaxys 114 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal concentration against phenobarbital induced rat hepatocytes upon incubation for 2 h with compound dissolved in DMSO

Biological Species/NCBI ID

rat

Cells/Cell Lines

liver cell

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Substance RN

1236661View in Reaxys

Measurement Parameter

LC50

Unit

µM

Qualitative value

Quantitative value

600

Deviation

Measurement pX

3.22

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p. 165 - 174, View in Reaxys 115 of 129

Bioassay Category

Pharmacokinetic

Bioassay Details

In vivo concentration of the compound dissolved in DMSO required to cause liver toxicity determined by visible centrilobular necrosis at 24 h in phenobarbitol induced rat

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Measurement Parameter

concentration (parameters)

Unit

mmol/kg

Qualitative value

Quantitative value

1.51

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p. 165 - 174, View in Reaxys 116 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Acute toxicity of the compound determined as pLC50 against Pimephales promelas (fathead minnow)

Biological Species/NCBI ID

Pimephales promelas

Substance RN

1236661View in Reaxys

Measurement Parameter

pLC50

Quantitative value

3.94

Measurement pX

3.94

Khadikar, Padmakar V; Mather, Keshav C; Singh, Shalini; Phadnis, Anjani; Shrivastava, Anjali; Mandaloi, Manorama; Bioorganic and medicinal chemistry; vol. 10; nb. 6; (2002); p. 1761 - 1766, View in Reaxys 117 of 129

Substance Action on Target

Inhibitor

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Toxicity of the compound determined as pIC50 against Daphnia magna at 24h

Biological Species/NCBI ID

Daphnia magna

Substance RN

1236661View in Reaxys

Measurement Parameter

pIC50

Quantitative value

4.4

Measurement pX

4.4

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Negative logarithmic effective concentration required to inhibition of bioluminesence to Vibrio fischeri

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Biological Species/NCBI ID

Aliivibrio fischeri

Substance RN

1236661View in Reaxys

Measurement Parameter

pEC50

Measurement Object

Negative logarithmic effective concentration

Quantitative value

3.88

Measurement pX

3.88

Khadikar; Phadnis, Anjani; Shrivastava, Anjali; Bioorganic and Medicinal Chemistry; vol. 10; nb. 4; (2002); p. 1181 - 1188, View in Reaxys 119 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Toxicity of the compound determined as pEC50 against Vibrio fischeri after 15 min exposure

Biological Species/NCBI ID

Aliivibrio fischeri

Substance RN

1236661View in Reaxys

Measurement Parameter

pEC50

Quantitative value

3.78

Measurement pX

3.78

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Intraperitoneal lethal dose

Biological Species/NCBI ID

mouse

Substance RN

1236661View in Reaxys

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

Quantitative value

1000

Material Safety Data Sheet, View in Reaxys 121 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Subcutaneous lethal dose

Biological Species/NCBI ID

mouse

Substance RN

1236661View in Reaxys

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

Quantitative value

2000

Material Safety Data Sheet, View in Reaxys 122 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Oral lethal dose

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Measurement Parameter

LD50

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Unit

mg/kg

Qualitative value

Quantitative value

2699

Material Safety Data Sheet, View in Reaxys 123 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Inhalation lethal concentration;Inhalation

Biological Species/NCBI ID

rat

Substance RN

1236661View in Reaxys

Substance Route of Adm.

inhalational administration

Measurement Parameter

qualitative

Qualitative value

Not Published

Quantitative value

20400

Material Safety Data Sheet, View in Reaxys 124 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Acute aquatic toxicity of the compound to Pimephales promelas

Biological Species/NCBI ID

Pimephales promelas

Substance RN

1236661View in Reaxys

Measurement Parameter

pLC50

Quantitative value

3.89

Measurement pX

3.89

Gonzalez, Maykel Perez; Helguera, Aliuska Morales; Cabrera, Miguel Angel; Bioorganic and Medicinal Chemistry; vol. 13; nb. 5; (2005); p. 1775 - 1781, View in Reaxys 125 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Minimal toxicity dose in Hep G2 cells determined using Alamar Blue

Biological Species/NCBI ID

human

Substance RN

1236661View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Schoonen, Willem G.E.J.; De Roos, Jeroen A.D.M.; Westerink, Walter M.A.; Debiton, Eric; Toxicology in Vitro; vol. 19; nb. 4; (2005); p. 491 - 503, View in Reaxys 126 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Minimal toxicity dose in Hep G2 cells determined using Hoechst 33342

Biological Species/NCBI ID

human

Substance RN

1236661View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Schoonen, Willem G.E.J.; De Roos, Jeroen A.D.M.; Westerink, Walter M.A.; Debiton, Eric; Toxicology in Vitro; vol. 19; nb. 4; (2005); p. 491 - 503, View in Reaxys 127 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal concentration of compound against Pimephales promelas

Biological Species/NCBI ID

Pimephales promelas

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Substance RN

1236661View in Reaxys

Unit

Measurement Object

Lethal concentration

Qualitative value

Quantitative value

0.94

Environmental toxicology and chemistry / SETAC; vol. 16; nb. 6; (1997); p. 1311 - 1317, View in Reaxys 128 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Minimal toxicity dose in Hep G2 cells determined using ATP-Lite

Biological Species/NCBI ID

human

Substance RN

1236661View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Schoonen, Willem G.E.J.; De Roos, Jeroen A.D.M.; Westerink, Walter M.A.; Debiton, Eric; Toxicology in Vitro; vol. 19; nb. 4; (2005); p. 491 - 503, View in Reaxys 129 of 129

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Minimal toxicity dose in Hep G2 cells determined using Cyto-Lite

Biological Species/NCBI ID

human

Substance RN

1236661View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Schoonen, Willem G.E.J.; De Roos, Jeroen A.D.M.; Westerink, Walter M.A.; Debiton, Eric; Toxicology in Vitro; vol. 19; nb. 4; (2005); p. 491 - 503, View in Reaxys

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