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24 substances in Reaxys
2016-05-07 14h:12m:59s (EST)
1 substances in Reaxys
2016-05-07 14h:52m:10s (EST)
NO 2
1. Query
Search as: As drawn 2. Query
(1. Query) AND itemno in (1)
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Reaxys ID 506236 View in Reaxys
O
1/1 CAS Registry Number: 108-03-2 Chemical Name: 1-Nitropropane; Nitropropane; 1-nitropropane Linear Structure Formula: CH3(CH2)2NO2 Molecular Formula: C3H7NO2 Molecular Weight: 89.0941 Type of Substance: acyclic InChI Key: JSZOAYXJRCEYSX-UHFFFAOYSA-N Note:
N O
Substance Label (70) Label References 2c
Chen, Bang-Chi; Hynes Jr., John; Pandit, Chennagiri R.; Zhao, Rulin; Skoumbourdis, Amanda P.; Wu, Hong; Sundeen, Joseph E.; Leftheris, Katerina; Heterocycles; vol. 55; nb. 5; (2001); p. 951 - 960, View in Reaxys; Ballini, Roberto; Balsamini, Cesarino; Diamantini, Giuseppe; Savoretti, Nicoletta; Synthesis; nb. 7; (2005); p. 1055 - 1057; Art.No: Z21904SS, View in Reaxys; Petrini, Marino; Torregiani, Elisabetta; Tetrahedron Letters; vol. 47; nb. 21; (2006); p. 3501 - 3503, View in Reaxys; Kumar, R. Arun; Saidulu; Prasad, K. Rajendra; Kumar, G. Sathish; Sridhar; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 354; nb. 16; (2012); p. 2985 - 2991, View in Reaxys; He, Hai-Xiao; Yang, Wen; Du, Da-Ming; Advanced Synthesis and Catalysis; vol. 355; nb. 6; (2013); p. 1137 - 1148, View in Reaxys; Rueping, Magnus; Vila, Carlos; Bootwicha, Teerawut; ACS Catalysis; vol. 3; nb. 7; (2013); p. 1676 - 1680, View in Reaxys; Zhao, Yu; Zhang, Chenhao; Chin, Kek Foo; Pytela, Oldrich; Wei, Guo; Liu, Hongjun; Bures, Filip; Jiang, Zhiyong; RSC Advances; vol. 4; nb. 57; (2014); p. 30062 - 30067, View in Reaxys; Fioravanti, Stefania; Pelagalli, Alessia; Pellacani, Lucio; Sciubba, Fabio; Vergari, Maria Cecilia; Amino Acids; vol. 46; nb. 8; (2014); p. 1961 - 1970, View in Reaxys; Yasui, Koji; Kato, Takanari; Kojima, Kohei; Nagasawa, Kazuo; Chemical Communications; vol. 51; nb. 12; (2015); p. 2290 - 2293, View in Reaxys; Wang, Bin; Shelar, Deepak Prakash; Han, Xian-Zhu; Li, Ting-Ting; Guan, Xiangguo; Lu, Wei; Liu, Kun; Chen, Yong; Fu, Wen-Fu; Che, Chi-Ming; Chemistry - A European Journal; vol. 21; nb. 3; (2015); p. 1184 1190, View in Reaxys; Bai, Zhushuang; Ji, Ling; Ge, Zemei; Wang, Xin; Li, Runtao; Organic and Biomolecular Chemistry; vol. 13; nb. 19; (2015); p. 5363 - 5366, View in Reaxys; Yao, Qian; Wang, Zhen; Zhang, Yuheng; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming; Journal of Organic Chemistry; vol. 80; nb. 11; (2015); p. 5704 - 5712, View in Reaxys; Li, Lijun; Zhang, Sheng; Hu, Yanbin; Li, Yanan; Li, Chong; Zha, Zhenggen; Wang, Zhiyong; Chemistry - A European Journal; vol. 21; nb. 37; (2015); p. 12885 - 12888, View in Reaxys; Shelar, Deepak Prakash; Li, Ting-Ting; Chen, Yong; Fu, Wen-Fu; ChemPlusChem; vol. 80; nb. 10; (2015); p. 1541 - 1546, View in Reaxys; Mikhaylov, Andrey A.; Dilman, Alexander D.; Novikov, Roman A.; Khoroshutina, Yulia A.; Struchkova, Marina I.; Arkhipov, Dmitry E.; Nelyubina, Yulia V.; Tabolin, Andrey A.; Ioffe, Sema L.; Tetrahedron Letters; vol. 57; nb. 1; (2016); p. 11 - 14, View in Reaxys; Li, Yifei; Feng, Chengjie; Shi, Hui; Xu, Xianxiu; Organic Letters; vol. 18; nb. 2; (2016); p. 324 - 327, View in Reaxys
2
Denmark, Scott E.; Kallemeyn, Jeffrey M.; Journal of Organic Chemistry; vol. 70; nb. 7; (2005); p. 2839 2842, View in Reaxys; Gao, Na; Chen, Yan-Li; He, Yan-Hong; Guan, Zhi; RSC Advances; vol. 3; nb. 37; (2013); p. 16850 - 16856, View in Reaxys; Zhang, Wen-Qiang; Li, Qiu-Yan; Zhang, Quan; Lu, Yingqiao; Lu, Han; Wang, Wenguang; Zhao, Xinsheng; Wang, Xiao-Jun; Inorganic Chemistry; vol. 55; nb. 3; (2016); p. 1005 - 1007, View in Reaxys; Quan, Ying; Li, Qiu-Yan; Zhang, Quan; Zhang, Wen-Qiang; Lu, Han; Yu, Jun-Hao; Chen, Jian; Zhao, Xinsheng; Wang, Xiao-Jun; RSC Advances; vol. 6; nb. 29; (2016); p. 23995 23999, View in Reaxys
1
Li, Shengkun; Huang, Kexuan; Zhang, Xumu; Chemical Communications; vol. 50; nb. 64; (2014); p. 8878 - 8881, View in Reaxys; Marc, Patricia; Lynch, James; Blacker, A. John; Williams, Jonathan M. J.; Chemical Communications; vol. 52; nb. 5; (2016); p. 1013 - 1016, View in Reaxys
5
Holmquist, Melireth; Blay, Gonzalo; Pedro, Jose R.; Chemical Communications; vol. 50; nb. 66; (2014); p. 9309 - 9312, View in Reaxys; Perez, Vincent; Rabasso, Nicolas; Fadel, Antoine; European Journal of Organic Chemistry; vol. 2016; nb. 2; (2016); p. 320 - 324, View in Reaxys
16c
Andrs, Jos M.; De La Cruz, Noelia; Valle, Mara; Pedrosa, Rafael; ChemPlusChem; vol. 81; nb. 1; (2016); p. 86 - 92, View in Reaxys
5b
Weimin, Peng; Shizheng, Zhu; Guifang, Jin; Tetrahedron; vol. 57; nb. 27; (2001); p. 5781 - 5784, View in Reaxys; Handa, Shinya; Gnanadesikan, Vijay; Matsunaga, Shigeki; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 129; nb. 16; (2007); p. 4900 - 4901, View in Reaxys; Li, Lei; Zhao, Yu-Long; Wang, Qian; Lin, Tao; Liu, Qun; Organic Letters; vol. 17; nb. 2; (2015); p. 370 - 373, View in Reaxys
2b
Bi, Xihe; Dong, Dewen; Liu, Qun; Pan, Wei; Zhao, Lei; Li, Bing; Journal of the American Chemical Society; vol. 127; nb. 13; (2005); p. 4578 - 4579, View in Reaxys; Attanasi, Orazio A.; Favi, Gianfranco; Filippone, Paolino; Giorgi, Gianluca; Lillini, Samuele; Mantellini, Fabio; Perrulli, Francesca R.; Synlett; nb. 17; (2006); p. 2731 - 2734, View in Reaxys; Ogawa, Takanori; Kumagai, Naoya; Shibasaki, Masakatsu; Angewandte Chemie - International Edition; vol. 52; nb. 24; (2013); p. 6196 - 6201; Angew. Chem.; vol. 125; nb. 24; (2013); p. 6316 - 6321, View in Reaxys; Kim, Su Yeon; Kim, Ko Hoon; Lim, Jin Woo; Kim, Jae Nyoung; Bulletin of the Korean Chemical Society; vol. 36; nb. 12; (2015); p. 2932 - 2935, View in Reaxys
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3b
Yamada; Moll; Shibasaki; Synlett; nb. SPEC. ISS; (2001); p. 980 - 982, View in Reaxys; Kunetsky, Roman A.; Dilman, Alexander D.; Tsvaygboym, Konstantin P.; Ioffe, Sema L.; Strelenko, Yury A.; Tartakovsky, Vladimir A.; Synthesis; nb. 9; (2003); p. 1339 - 1346, View in Reaxys; Xu, Xuenong; Furukawa, Tomihiro; Okino, Tomotaka; Miyabe, Hideto; Takemoto, Yoshiji; Chemistry - A European Journal; vol. 12; nb. 2; (2006); p. 466 - 476, View in Reaxys; Photiadou, Anna D.; Stathakis, Christos I.; Gallos, John K.; Journal of Heterocyclic Chemistry; vol. 45; nb. 4; (2008); p. 1251 - 1253, View in Reaxys; Aksenov, Nicolai A.; Aksenov, Alexander V.; Nadein, Oleg N.; Aksenov, Dmitrii A.; Smirnov, Alexander N.; Rubin, Michael; RSC Advances; vol. 5; nb. 88; (2015); p. 71620 - 71626, View in Reaxys
2h
Reddy, Chada Raji; Kumaraswamy, Paridala; Reddy, Motatipally Damoder; Organic and Biomolecular Chemistry; vol. 10; nb. 45; (2012); p. 9052 - 9057,6, View in Reaxys; Shved, Alexander S.; Tabolin, Andrey A.; Khomutova, Yulia A.; Ioffe, Sema L.; Tetrahedron Letters; vol. 55; nb. 45; (2014); p. 6220 - 6223, View in Reaxys; Ho, Hon Eong; Ishikawa, Yoshifumi; Asao, Naoki; Yamamoto, Yoshinori; Jin, Tienan; Chemical Communications; vol. 51; nb. 64; (2015); p. 12764 - 12767, View in Reaxys
31b
Pedrosa, Rafael; Andrs, Jos M.; vila, Deisy P.; Ceballos, Miriam; Pindado, Rodrigo; Green Chemistry; vol. 17; nb. 4; (2015); p. 2217 - 2225, View in Reaxys
1i
Dey, Chandan; Lindstedt, Erik; Olofsson, Berit; Organic Letters; vol. 17; nb. 18; (2015); p. 4554 - 4557, View in Reaxys
48b
Scharnagel, Dagmar; Müller, Andreas; Prause, Felix; Eck, Martin; Goller, Jessica; Milius, Wolfgang; Breuning, Matthias; Chemistry - A European Journal; vol. 21; nb. 35; (2015); p. 12488 - 12500, View in Reaxys
7c
Wessling, Michael; Schäfer, Hans J.; Beilstein Journal of Organic Chemistry; vol. 11; (2015); p. 1163 1174, View in Reaxys
m
Romo-Prez, Adriana; Miranda, Luis D.; Garca, Abraham; Tetrahedron Letters; vol. 56; nb. 48; (2015); p. 6669 - 6673, View in Reaxys
1c
Dumestre, Paul; El Kaim, Laurent; Tetrahedron Letters; vol. 40; nb. 45; (1999); p. 7985 - 7986, View in Reaxys; Dilman, A. D.; Lyapkalo, I. M.; Ioffe, S. L.; Strelenko, Yu. A.; Tartakovsky, V. A.; Russian Chemical Bulletin; vol. 49; nb. 5; (2000); p. 874 - 878; Izvestiya Akademi Nauk, Seriya Khimicheskaya; nb. 5; (2000); p. 876 - 880, View in Reaxys; Simoneau, Christopher A.; Strohl, Alexis M.; Ganem, Bruce; Tetrahedron Letters; vol. 48; nb. 10; (2007); p. 1809 - 1811, View in Reaxys; Kumar, Akshay; Kaur, Jasneet; Chimni, Swapandeep Singh; Jassal, Amanpreet Kaur; RSC Advances; vol. 4; nb. 47; (2014); p. 24816 24819, View in Reaxys
3c
Katritzky, Alan R.; Abdel-Fattah, Ashraf A. A.; Gromova, Anna V.; Witek, Rachel; Steel, Peter J.; Journal of Organic Chemistry; vol. 70; nb. 23; (2005); p. 9211 - 9214, View in Reaxys; Sohtome, Yoshihiro; Hashimoto, Yuichi; Nagasawa, Kazuo; European Journal of Organic Chemistry; nb. 13; (2006); p. 2894 - 2897, View in Reaxys; Takada, Keisuke; Takemura, Nobuko; Cho, Kaori; Sohtome, Yoshihiro; Nagasawa, Kazuo; Tetrahedron Letters; vol. 49; nb. 10; (2008); p. 1623 - 1626, View in Reaxys; Wang, Yuanyuan; Wu, Yuetong; Wang; Dai, Liyi; Chinese Journal of Chemistry; vol. 30; nb. 8; (2012); p. 1709 - 1714, View in Reaxys; Cao, Dongdong; Chai, Zhuo; Zhang, Jiaxing; Ye, Zhengqing; Xiao, Hua; Wang, Hongyu; Chen, Jinhao; Wu, Xiaoyu; Zhao, Gang; Chemical Communications; vol. 49; nb. 53; (2013); p. 5972 5974, View in Reaxys; Yan, Hao; Wang, Yuling; Pan, Congming; Zhang, Hao; Yang, Sizhuo; Ren, Xiaoyu; Li, Jian; Huang, Guosheng; European Journal of Organic Chemistry; vol. 2014; nb. 13; (2014); p. 2754 - 2763, View in Reaxys
3
Xu, Kun; Lai, Guoyin; Zha, Zhenggen; Pan, Susu; Chen, Huanwen; Wang, Zhiyong; Chemistry - A European Journal; vol. 18; nb. 39; (2012); p. 12357 - 12362, View in Reaxys; Sadeghzadeh, Seyed Mohsen; Nasseri, Mohammad Ali; Journal of the Iranian Chemical Society; vol. 11; nb. 4; (2014); p. 1197 - 1205, View in Reaxys
6c
Kitagaki, Shinji; Ueda, Takahiro; Mukai, Chisato; Chemical Communications; vol. 49; nb. 38; (2013); p. 4030 - 4032, View in Reaxys; Wang, Bin; Liu, Yuxin; Sun, Cong; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng; Organic Letters; vol. 16; nb. 24; (2014); p. 6432 - 6435, View in Reaxys
5c
Rabasso, Nicolas; Fadel, Antoine; Tetrahedron Letters; vol. 55; nb. 44; (2014); p. 6068 - 6071, View in Reaxys
7ab
Sukhorukov, Alexey Yu.; Kapatsyna, Maria A.; Yi, Tammy Lim Ting; Park, Hyeong Ryool; Naumovich, Yana A.; Zhmurov, Petr A.; Khomutova, Yulia A.; Ioffe, Sema L.; Tartakovsky, Vladimir A.; European Journal of Organic Chemistry; vol. 2014; nb. 36; (2014); p. 8148 - 8159, View in Reaxys
4c
Uraguchi, Daisuke; Sakaki, Sawako; Ooi, Takashi; Journal of the American Chemical Society; vol. 129; nb. 41; (2007); p. 12392 - 12393, View in Reaxys; Zu, Liansuo; Xie, Hexin; Li, Hao; Wang, Jian; Wang, Wei; Advanced Synthesis and Catalysis; vol. 349; nb. 17-18; (2007); p. 2660 - 2664, View in Reaxys; Patent; Mitsui Chemicals, Inc.; National University Corporation Nagoya University; US2009/131716; (2009); (A1) English, View in Reaxys; Wang, Hong-Yu; Chai, Zhuo; Zhao, Gang; Tetrahedron; vol. 69; nb. 25; (2013); p. 5104 - 5111, View in Reaxys; Piscopo, Calogero G.; Sartori, Giovanni; Mayoral, Jose A.; La-
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nari, Daniela; Vaccaro, Luigi; Maggi, Raimondo; Synlett; vol. 24; nb. 19; (2013); p. 2596 - 2600; Art.No: ST-2013-D0688-L, View in Reaxys 35b
Kancharla, Papireddy; Reynolds, Kevin A.; Tetrahedron; vol. 69; nb. 39; (2013); p. 8375 - 8385, View in Reaxys
1c; nPrNO&2%
Quintavalla, Arianna; Lanza, Francesco; Montroni, Elisa; Lombardo, Marco; Trombini, Claudio; Journal of Organic Chemistry; vol. 78; nb. 23; (2013); p. 12049 - 12064, View in Reaxys
PrNO2
Kim, Jae Nyoung; Im, Yang Jin; Gong, Ji Hyeon; Lee, Ka Young; Tetrahedron Letters; vol. 42; nb. 25; (2001); p. 4195 - 4197, View in Reaxys; Raghavan, Sadagopan; Rajender; Chemical communications (Cambridge, England); nb. 15; (2002); p. 1572 - 1573, View in Reaxys; Klein, Guenter; Pandiaraju, Subramaniam; Reiser, Oliver; Tetrahedron Letters; vol. 43; nb. 42; (2002); p. 7503 - 7506, View in Reaxys; Boobalan, Ramalingam; Lee, Gene-Hsian; Chen, Chinpiao; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2511 - 2520, View in Reaxys
11
Zhou, Yirong; Liu, Qiang; Gong, Yuefa; Organic and Biomolecular Chemistry; vol. 10; nb. 37; (2012); p. 7618 - 7627, View in Reaxys
2a
Nishiwaki, Nagatoshi; Knudsen, Kristian Rahbek; Gothelf, Kurt V.; Jrgensen, Karl Anker; Angewandte Chemie - International Edition; vol. 40; nb. 16; (2001); p. 2992 - 2995, View in Reaxys; Ooi, Takashi; Fujioka, Shingo; Maruoka, Keiji; Journal of the American Chemical Society; vol. 126; nb. 38; (2004); p. 11790 11791, View in Reaxys; Ostrowski, Stanislaw; Wyrebek, Przemyslaw; Mikus, Agnieszka; Heterocycles; vol. 68; nb. 5; (2006); p. 885 - 888, View in Reaxys; Ballini, Roberto; Gabrielli, Serena; Palmieri, Alessandro; Synlett; nb. 15; (2007); p. 2430 - 2432, View in Reaxys; Tanaka, Seiji; Oguma, Yukinari; Tanaka, Yusuke; Echizen, Hidenori; Masu, Hyuma; Yamaguchi, Kentaro; Kishikawa, Keiki; Kohmoto, Shigeo; Yamamoto, Makoto; Tetrahedron; vol. 64; nb. 7; (2008); p. 1388 - 1396, View in Reaxys
4b
Poupart; Fazal; Goulet; Ly Thy Mar; Journal of Organic Chemistry; vol. 64; nb. 4; (1999); p. 1356 - 1361, View in Reaxys; Handa, Shinya; Nagawa, Keita; Sohtome, Yoshihiro; Matsunaga, Shigeki; Shibasaki, Masakatsu; Angewandte Chemie - International Edition; vol. 47; nb. 17; (2008); p. 3230 - 3233, View in Reaxys
6b
Zhang, Qian; Sun, Shaoguang; Hu, Jianglei; Liu, Qun; Tan, Jing; Journal of Organic Chemistry; vol. 72; nb. 1; (2007); p. 139 - 143, View in Reaxys
23H
Takemoto, Yoshiji; Miyabe, Hideto; Chimia; vol. 61; nb. 5; (2007); p. 269 - 275, View in Reaxys
EtCH2NO2
Kawakami; Suzuki; Tetrahedron Letters; vol. 40; nb. 6; (1999); p. 1157 - 1160, View in Reaxys; Caldarelli, Marina; Habermann, Joerg; Ley, Steven V.; Journal of the Chemical Society - Perkin Transactions 1; nb. 2; (1999); p. 107 - 110, View in Reaxys; Chamakh, Ahlem; M'hirsi, Mustapha; Villieras, Jean; Lebreton, Jacques; Amri, Hassen; Synthesis; nb. 2; (2000); p. 295 - 299, View in Reaxys; Park; Kurth; Chemical Communications; nb. 19; (2000); p. 1835 - 1836, View in Reaxys; Gallos, John K.; Koftis, Theocharis V.; Journal of the Chemical Society. Perkin Transactions 1; nb. 4; (2001); p. 415 - 423, View in Reaxys; Filho, Joao R. de Freitas; Cottier, Louis; Srivastava, Rajendra M.; Sinou, Denis; Synlett; nb. 9; (2003); p. 1358 1360, View in Reaxys; Lee, Anna; Kim, Woosung; Lee, Jinwoo; Hyeon, Taeghwan; Kim, B. Moon; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2595 - 2598, View in Reaxys; Chang, Yu-Wei; Yang, JingJun; Dang, Jin-Ning; Xue, Yue-Xia; Synlett; nb. 14; (2007); p. 2283 - 2285, View in Reaxys
1a
Dilman; Lyapkalo; Ioffe; Strelenko; Tartakovsky; Synthesis; nb. 10; (1999); p. 1767 - 1775, View in Reaxys; Ballini, Roberto; Fiorini, Dennis; Palmieri, Alessandro; Tetrahedron Letters; vol. 45; nb. 38; (2004); p. 7027 - 7029, View in Reaxys; Arcadi, Antonio; Bianchi, Gabriele; Inesi, Achille; Marinelli, Fabio; Rossi, Leucio; Synlett; nb. 7; (2007); p. 1031 - 1036, View in Reaxys
CH3CH2CH2NO2 Park, Kyung-Ho; Olmstead, Marilyn M.; Kurth, Mark J.; Synlett; nb. 9 SPEC. ISS.; (2003); p. 1267 - 1270, View in Reaxys; Dominguez, Rosa Maria; Herize, Armando; Rotinov, Alexandra; Alvarez-Aular, Alvaro; Visbal, Gonzalo; Chuchani, Gabriel; Journal of Physical Organic Chemistry; vol. 17; nb. 5; (2004); p. 399 408, View in Reaxys; Cecchi, Luca; De Sarlo, Francesco; Machetti, Fabrizio; Synlett; nb. 15; (2007); p. 2451 - 2453, View in Reaxys 1d
Ballini, Roberto; Bosica, Giovanna; Fiorini, Dennis; Righi, Paolo; Synthesis; nb. 5; (2002); p. 681 - 685, View in Reaxys; Ballini, Roberto; Fiorini, Dennis; Gil, Maria Victoria; Palmieri, Alessandro; Tetrahedron Letters; vol. 44; nb. 50; (2003); p. 9033 - 9034, View in Reaxys; Wang, Jian; Li, Hao; Zu, Liansuo; Jiang, Wei; Wang, Wei; Advanced Synthesis and Catalysis; vol. 348; nb. 15; (2006); p. 2047 - 2050, View in Reaxys
4 (R2=Pr)
Ballini, Roberto; Clemente, Roberto Rabanedo; Palmieri, Alessandro; Petrini, Marino; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 191 - 196, View in Reaxys
educt to 2c
Park, Da Yeon; Gowrisankar, Saravanan; Kim, Jae Nyoung; Tetrahedron Letters; vol. 47; nb. 37; (2006); p. 6641 - 6645, View in Reaxys
educt to 4m
Lu, Shao-Feng; Du, Da-Ming; Xu, Jiaxi; Zhang, Shi-Wei; Journal of the American Chemical Society; vol. 128; nb. 23; (2006); p. 7418 - 7419, View in Reaxys
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1b
Ballini, Roberto; Barboni, Luciano; Bosica, Giovanna; Journal of Organic Chemistry; vol. 65; nb. 19; (2000); p. 6261 - 6263, View in Reaxys; Ballini, Roberto; Bosica, Giovanna; Fiorini, Dennis; Tetrahedron Letters; vol. 42; nb. 48; (2001); p. 8471 - 8473, View in Reaxys; Basavaiah, Deevi; Rao, Jamjanam Srivardhana; Tetrahedron Letters; vol. 45; nb. 8; (2004); p. 1621 - 1625, View in Reaxys; Ballini, Roberto; Fiorini, Dennis; Gil, Maria Victoria; Palmieri, Alessandro; Tetrahedron; vol. 60; nb. 12; (2004); p. 2799 2804, View in Reaxys; Ogibin; Ilovaisky; Merkulova; Nikishin; Russian Chemical Bulletin; vol. 53; nb. 11; (2004); p. 2558 - 2563, View in Reaxys; Ballini, Roberto; Palmieri, Alessandro; Advanced Synthesis and Catalysis; vol. 348; nb. 10-11; (2006); p. 1154 - 1156, View in Reaxys
1, R1 = Et
Ballini, Roberto; Barboni, Luciano; Bosica, Giovanna; Filippone, Paolino; Peretti, Sabina; Tetrahedron; vol. 56; nb. 24; (2000); p. 4095 - 4099, View in Reaxys; Elmaaty, Tarek Abou; Castle, Lyle W.; Organic Letters; vol. 7; nb. 24; (2005); p. 5529 - 5530, View in Reaxys
ANC; R1=H, R2=Me
Sukhorokov, Alexey Yu.; Bliznets, Igor V.; Lesiv, Alexey V.; Khomutova, Yulija A.; Strelenko, Yuriy A.; Ioffe, Sema L.; Synthesis; nb. 7; (2005); p. 1077 - 1082; Art.No: P14804SS, View in Reaxys
3a
Ooi, Takashi; Takada, Saki; Fujioka, Shingo; Maruoka, Keiji; Organic Letters; vol. 7; nb. 23; (2005); p. 5143 - 5146, View in Reaxys
7, R1=H, R2=Et
Kawai, Kouichi; Ebata, Takuma; Kitazume, Tomoya; Journal of Fluorine Chemistry; vol. 126; nb. 6; (2005); p. 956 - 961, View in Reaxys
8b
Kisanga, Philip B.; Ilankumaran, Palanichamy; Fetterly, Brandon M.; Verkade, John G.; Journal of Organic Chemistry; vol. 67; nb. 11; (2002); p. 3555 - 3560, View in Reaxys; Janecki, Tomasz; Blaszczyk, Edyta; Studzian, Kazimierz; Janecka, Anna; Krajewska, Urszula; Rozalski, Marek; Journal of Medicinal Chemistry; vol. 48; nb. 10; (2005); p. 3516 - 3521, View in Reaxys
1e
Ballini, Roberto; Bosica, Giovanna; Fiorini, Dennis; Gil, Maria Victoria; Palmieri, Alessandro; Synthesis; nb. 4; (2004); p. 605 - 609, View in Reaxys
7b
Blaszczyk, Edyta; Krawczyk, Henryk; Janecki, Tomasz; Synlett; nb. 15; (2004); p. 2685 - 2688, View in Reaxys
educt to 13
Chavan, Subhash P.; Pasupathy; Venkatraman; Kale, Ramesh R.; Tetrahedron Letters; vol. 45; nb. 37; (2004); p. 6879 - 6882, View in Reaxys
1, R=CH3CH2
Ballini, Roberto; Bosica, Giovanna; Livi, Damiana; Palmieri, Alessandro; Maggi, Raimondo; Sartori, Giovanni; Tetrahedron Letters; vol. 44; nb. 11; (2003); p. 2271 - 2273, View in Reaxys
2 (R&3%=Me)
Chimichi, Stefano; Boccalini, Marco; Cosimelli, Barbara; Dall'Acqua, Francesco; Viola, Giampietro; Tetrahedron; vol. 59; nb. 28; (2003); p. 5215 - 5223, View in Reaxys
RCH2NO2, R=CH2CH3
Ahmed, Fahim; Donaldson, William A.; Synthetic Communications; vol. 33; nb. 15; (2003); p. 2685 - 2693, View in Reaxys
1, R = Et
Ballini, Roberto; Barboni, Luciano; Giarlo, Guido; Journal of Organic Chemistry; vol. 68; nb. 23; (2003); p. 9173 - 9176, View in Reaxys
7
O'Neil, Ian A.; Lai, Justine Y. Q.; Wynn, Duncan; Chemical Communications; nb. 1; (1999); p. 59 - 60, View in Reaxys; Vanelle, Patrice; Terme, Thierry; Giraud, Luc; Crozet, Michel P.; Tetrahedron Letters; vol. 42; nb. 3; (2001); p. 391 - 393, View in Reaxys; Banwell, Martin G.; Edwards, Alison J.; Jolliffe, Katrina A.; Smith, Jason A.; Hamel, Ernest; Verdier-Pinard, Pascal; Organic and Biomolecular Chemistry; vol. 1; nb. 2; (2003); p. 296 - 305, View in Reaxys
6a
Ballini, Roberto; Bosica, Giovanna; Mase, Aldo; Petrini, Marino; European Journal of Organic Chemistry; nb. 16; (2000); p. 2927 - 2931, View in Reaxys; Chimichi, Stefano; Boccalini, Marco; Cosimelli, Barbara; Viola, Giampietro; Vedaldi, Daniela; Dall'Acqua, Francesco; Tetrahedron Letters; vol. 43; nb. 42; (2002); p. 7473 - 7476, View in Reaxys
Tab., substr., entry 10
Chandrasekhar; Narsihmulu; Jagadeshwar; Synlett; nb. 5; (2002); p. 771 - 772, View in Reaxys
nitro compd educt El Kaim; Grimaud; Jana; Tirla; Tetrahedron Letters; vol. 43; nb. 11; (2002); p. 2037 - 2038, View in Reaxys to 1b 4
Krawczyk, Henryk; Wolf, Wojciech M.; Sliwinski, Marcin; Journal of the Chemical Society. Perkin Transactions 1; nb. 24; (2002); p. 2794 - 2798, View in Reaxys
3h
Djekou, Serge; Gellis, Armand; Maldonado, Jose; Crozet, Michel P.; Vanelle, Patrice; Heterocycles; vol. 55; nb. 3; (2001); p. 535 - 544, View in Reaxys
2, R=Et
Demicheli, Giuseppina; Maggi, Raimondo; Mazzacani, Alessandro; Righi, Paolo; Sartori, Giovanni; Bigi, Franca; Tetrahedron Letters; vol. 42; nb. 12; (2001); p. 2401 - 2403, View in Reaxys
2, R1 = C2H5
Beji, Feten; Lebreton, Jacques; Villieras, Jean; Amri, Hassen; Tetrahedron; vol. 57; nb. 50; (2001); p. 9959 - 9962, View in Reaxys
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3h/i
Ballini, Roberto; Barboni, Luciano; Bosica, Giovanna; Petrini, Marino; Synlett; nb. 3; (2000); p. 391 393, View in Reaxys
RCH2NO2, R=C2H5
Terme, Thierry; Crozet, Michel P.; Giraud, Luc; Vanelle, Patrice; Tetrahedron; vol. 56; nb. 8; (2000); p. 1097 - 1101, View in Reaxys
2z
Ballini, Roberto; Bigi, Franca; Gogni, Elena; Maggi, Raimondo; Sartori, Giovanni; Journal of Catalysis; vol. 191; nb. 2; (2000); p. 348 - 353, View in Reaxys
1, R=Et
Youn, So Won; Kim, Yong Hae; Synlett; nb. 6; (2000); p. 880 - 882, View in Reaxys
educt to 6f
Vanelle; Terme; Crozet; Tetrahedron Letters; vol. 41; nb. 33; (2000); p. 6383 - 6385, View in Reaxys
1f
Ballini, Roberto; Marcantoni, Enrico; Perella, Silvia; Journal of Organic Chemistry; vol. 64; nb. 8; (1999); p. 2954 - 2957, View in Reaxys
3f
Dumestre, Paul; El Kaim, Laurent; Gregoire, Ariane; Chemical Communications; nb. 9; (1999); p. 775 776, View in Reaxys
nitro-comp. to 12a Park, Kyung-Ho; Kurth, Mark J.; Tetrahedron Letters; vol. 40; nb. 32; (1999); p. 5841 - 5844, View in Reaxys 1;R=H,R1=C2H5
Ballini; Bosica; Petrelli; Petrini; Synthesis; nb. 7; (1999); p. 1236 - 1240, View in Reaxys
nitroalkane for 3
Lee, Shi Yong; Lee, Bum Sung; Lee, Chi-Wan; Oh, Dong Young; Synthetic Communications; vol. 29; nb. 20; (1999); p. 3621 - 3626, View in Reaxys
1j
Ballini, Roberto; Bosica, Giovanna; Parrini, Mauro; Chemistry Letters; nb. 10; (1999); p. 1105 - 1106, View in Reaxys
1c,o
Ballini, Roberto; Bosica, Giovanna; Parrini, Mauro; Tetrahedron Letters; vol. 39; nb. 43; (1998); p. 7963 7964, View in Reaxys
1-NP
Kohl; Gescher; Xenobiotica; vol. 27; nb. 8; (1997); p. 843 - 852, View in Reaxys
Patent-Specific Data (9) Prophetic ComLocation in Patent References pound Page/Page column
Patent; NOVARTIS AG; Fairhurst, Robin Alec; Furet, Pascal; Kalthoff, Frank Stephan; Lerchner, Andreas; Rueeger, Heinrich; US2014/135330; (2014); (A1) English, View in Reaxys; Patent; HOFFMANN-LA ROCHE INC.; Han, Xingchun; Javanbakht, Hassan; Jiang, Min; Liang, Chungen; Wang, Jianping; Wang, Yongguang; Wang, Zhanguo; Weikert, Robert James; Yang, Song; Zhou, Chengang; US2015/210682; (2015); (A1) English, View in Reaxys Patent; FLEXUS BIOSCIENCES, INC.; JAEN, Juan Carlos; OSIPOV, Maksim; POWERS, Jay Patrick; SHUNATONA, Hunter Paul; WALKER, James Ross; ZIBINSKY, Mikhail; (151 pag.); WO2015/188085; (2015); (A1) English, View in Reaxys Patent; Trauth, Daniel M.; Green, George D.; Swedo, Raymond J.; US2011/92750; (2011); (A1) English, View in Reaxys Patent; Manzer, Leo Ernest; US2004/192934; (2004); (A1) English, View in Reaxys Patent; Manzer, Leo Ernest; US2004/192936; (2004); (A1) English, View in Reaxys Patent; E.I. DUPONT DE NEMOURS AND COMPANY; WO2004/84633; (2004); (A1) English, View in Reaxys Patent; Chee, Gaik-Lean; Dekeyser, Mark A.; Seebold JR., Kenneth W.; Osika, Ewa Maria; Brouwer, Walter G.; Park, Sheldon B.; Lai, Hoi Kiong; US2004/266738; (2004); (A1) English, View in Reaxys Patent; Niewohner, Ulrich; Niewohner, Maria; Bauser, Marcus; Erguden, Jens-Kerim; Flubacher, Dietmar; Naab, Paul; Repp, Thorsten-Oliver; Stoltefuss, Jurgen; Burkhardt, Nils; Sewing, Andrea; Schauer, Michael; Schlemmer, Karl-Heinz; Weber, Olaf; Boyer, Stephen J.; Miglarese, Mark; Fan, Jianmei; Phillips, Barton; Raudenbush, Brian C.; Wang, Yamin; US2003/236276; (2003); (A1) English, View in Reaxys
prophetic product
Claim
Patent; Berg; Lloyd; US5425854; (1995); (A1) English, View in Reaxys; Patent; Roquette Freres; US4339387; (1982); (A1) English, View in Reaxys
Related Structure (2) Related Structure Referenced Com- References pound
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The following tau- 1-nitropropane tomers are discussed: /BRN= 1840287/
Veltwisch, Dieter; Asmus, Klaus-Dieter; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1143 - 1146, View in Reaxys Gupta; Raghavan; Indian Journal of Chemistry; vol. 9; (1971); p. 233, View in Reaxys
Derivative (9) Comment (Derivative)
References
Carbanion, Rkt.m. Shinkai et al.; Biopolymers; vol. 17; (1978); p. 2757,2758,2759, View in Reaxys 3,10-Dimethyl-8cyano-isoalloxazin (-->k2 (Tab.II), E1/2 (Tab.II)) Na-Salz: IR-, Raman-Sp.
Brookes; Jonathan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 187,188, View in Reaxys
Na-Salz: Rk. mit Feuer; Markofsky; Journal of Organic Chemistry; vol. 29; (1964); p. 935,938, View in Reaxys Essigsaeure-(2nitropropylester), W. -> 3,5-Diethylisoxazol Na-Salz: Charakteristische IRBanden
Feuer,H. et al.; Spectrochimica Acta; vol. 19; (1963); p. 431 - 434, View in Reaxys
Na-Salz: Rk. m. Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1359 - 1360, Et3OBF4, View in Reaxys CH2Cl2 (N2, 0grad, 15min) -> Propyliden-nitronsaeureethylester Na-Salz: NaC3H6NO2; Prep.: 1-Nitropropan, A., NaOEt; Nd.; IR-Sp. (1750-650 cm-1; S.1190)
Buczkowski; Urbanski; Spectrochimica Acta; vol. 18; (1962); p. 1187,1188, View in Reaxys
via conversion 1nitro-propionaldehyde phenylhydrazone (mp: 98-101 degree )
Slebodzinski; Makaruk; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III> 3; (1955); p. 377,379, View in Reaxys
via conversion 1nitro-propionaldehyde-<4-nitrophenylhydrazone> (mp: 139-140 degree )
Slebodzinski; Makaruk; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III> 3; (1955); p. 377,379, View in Reaxys
calcium salt; Further Data see Handbook (Chemical Behaviour)
Patent; Pecherer; US2346272; (1941), View in Reaxys; Patent; Comm.Solv.Corp.; US2113813; (1937), View in Reaxys; Patent; Comm.Solv.Corp.; US2113814; (1937), View in Reaxys; Lippincott; Hass; Industrial and Engineering Chemistry; vol. 31; (1939); p. 119, View in Reaxys; Patent; Purdue Res.Found.; US2113812; (1937), View in Reaxys; Johnson; Degering; Journal of Organic Chemistry; vol. 8; (1943); p. 11, View in Reaxys; Patent; Purdue Res.Found.; US2267375; (1940), View in Reaxys
Purification (1) References Kemula; Sybilski; Roczniki Chemii; vol. 38; (1964); p. 861,864, 868, View in Reaxys; Kemula; Sybilska; Acta Chimica Academiae Scientiarum Hungaricae; vol. 27; (1961); p. 137, View in Reaxys Melting Point (3) 1 of 3
Melting Point [°C]
-103.99
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 2 of 3
Melting Point [°C]
-104.56
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Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 3 of 3
Melting Point [°C]
-108
Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p. 891, View in Reaxys Boiling Point (15) Boiling Point [°C] Pressure (Boiling Point) [Torr]
References
131 - 132
Bordwell,F.G.; Bartmess,J.E.; Journal of Organic Chemistry; vol. 43; (1978); p. 3101 3107, View in Reaxys; Patent; DOW CORNING CORPORATION; WO2007/67723; (2007); (A1) English, View in Reaxys
128 - 130
Zarchi, Mohammad Ali Karimi; Zarei, Amin; Journal of the Chinese Chemical Society; vol. 52; nb. 2; (2005); p. 309 - 311, View in Reaxys
130.5
Pacholec, Frank; Butler, Hal T.; Poole, Colin F.; Analytical Chemistry; vol. 54; nb. 12; (1982); p. 1938 - 1941, View in Reaxys
79 - 81
140
Gilbert,K.E.; Borden,W.T.; Journal of Organic Chemistry; vol. 44; (1979); p. 659 - 661, View in Reaxys
130 - 132
760
Gelbard,G.; Colonna,S.; Synthesis; (1977); p. 113 - 116, View in Reaxys
132
Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys; Khan; Chemistry Letters; (1975); p. 879, View in Reaxys
128
Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys
43 - 44
25
131.6
Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p. 1284,1287, View in Reaxys Suzuki et al.; Kogyo Kagaku Zasshi; vol. 72; (1969); p. 720; Chem.Abstr.; vol. 72; nb. 33224; (1970), View in Reaxys
58 - 59
59
Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 315, View in Reaxys
58.5
59
Tal'vik; Pikhl; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 204, View in Reaxys
131
761
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys
128.2 - 128.4
732
Cass et al.; Journal of the Chemical Society; (1958); p. 958,960, View in Reaxys
131.18
760
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys
130.5 - 131.5
Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys
Refractive Index (20) Refractive Index Wavelength (Refractive Index) [nm]
Temperature (Refractive Index) [°C]
References
1.3994
589
25
Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys
1.3995
589
25
Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys
1.3996
589
23
Bordwell,F.G.; Bartmess,J.E.; Journal of Organic Chemistry; vol. 43; (1978); p. 3101 - 3107, View in Reaxys
1.399
589
25
Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys
1.4015
589
20
Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys; Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p. 1284,1287, View in Reaxys; Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p.
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315, View in Reaxys; Tal'vik; Pikhl; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 204, View in Reaxys Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys 1.405
589
20
Monfort et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 67; (1970); p. 748,749-753, View in Reaxys
1.3996
589
25
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys
1.39
589
50
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys
1.4016
589
20
Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys
1.39956
589
25
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys
1.39755
589
30
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys
1.4018
589
20
Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys
1.3982
656.3
20
Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys
1.4013
589
20
Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys
1.4064
486.1
20
Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys
1.4108
434
20
Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys
1.39787
656.3
24.3
Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys
1.40027
589
24.3
Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys
1.41104
434
24.3
Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys
Density (25) 1 of 25
Density [g·cm-3]
0.9891
Measurement Temperature [°C]
20
Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 2 of 25
Density [g·cm-3]
0.9956
Measurement Temperature [°C]
25
Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys 3 of 25
Density [g·cm-3]
0.9899
Measurement Temperature [°C]
30
Dewan, R.K.; Sharma, A.K.; Mehta, S.K.; Journal of Solution Chemistry; vol. 17; nb. 5; (1988); p. 459 - 466, View in Reaxys 4 of 25
Density [g·cm-3]
1.0009
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Measurement Temperature [°C]
19.9
Matsumoto; Suzuki; Takahashi; Saito; Bulletin of the Chemical Society of Japan; vol. 58; nb. 1; (1985); p. 1 - 4, View in Reaxys 5 of 25
Density [g·cm-3]
0.98947
Measurement Temperature [°C]
30
Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys 6 of 25
Density [g·cm-3]
0.985
Reference Temperature [°C]
4
Measurement Temperature [°C]
20
Tolstova et.al; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 907,959, View in Reaxys 7 of 25
Density [g·cm-3]
1.003
Reference Temperature [°C]
4
Measurement Temperature [°C]
20
Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p. 1284,1287, View in Reaxys 8 of 25
Density [g·cm-3]
1.017
Reference Temperature [°C]
4
Measurement Temperature [°C]
25
Monfort et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 67; (1970); p. 748,749-753, View in Reaxys 9 of 25
Density [g·cm-3]
1.0063
Reference Temperature [°C]
4
Measurement Temperature [°C]
20
Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 315, View in Reaxys 10 of 25
Density [g·cm-3]
1.0011
Reference Temperature [°C]
4
Measurement Temperature [°C]
20
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 11 of 25
Density [g·cm-3]
0.996
Reference Temperature [°C]
4
Measurement Temperature [°C]
25
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 12 of 25
Density [g·cm-3]
0.9685
Reference Temperature [°C]
4
Measurement Temperature [°C]
50
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Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 13 of 25
Density [g·cm-3]
1.00144
Reference Temperature [°C]
4
Measurement Temperature [°C]
20
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 14 of 25
Density [g·cm-3]
0.99609
Reference Temperature [°C]
4
Measurement Temperature [°C]
25
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 15 of 25
Density [g·cm-3]
0.99073
Reference Temperature [°C]
4
Measurement Temperature [°C]
30
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 16 of 25
Density [g·cm-3]
0.9955
Reference Temperature [°C]
4
Measurement Temperature [°C]
25
Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 17 of 25
Density [g·cm-3]
0.9296 - 1.0009
Reference Temperature [°C]
4
Measurement Temperature [°C]
20 - 87
Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 18 of 25
Density [g·cm-3]
0.8861 - 1.0053
Reference Temperature [°C]
4
Measurement Temperature [°C]
15.3 - 122
Friend; Hargreaves; Phil.Mag.; vol. <7>34; (1943); p. 810; Chem.Abstr.; (1944); p. 1409, View in Reaxys 19 of 25
Density [g·cm-3]
0.9957
Reference Temperature [°C]
4
Measurement Temperature [°C]
25
Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys 20 of 25
Density [g·cm-3]
1.0081
Reference Temperature [°C]
4
Measurement Temperature [°C]
24.3
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Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys 21 of 25
Density [g·cm-3]
1.0221
Measurement Temperature [°C]
4
Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 22 of 25
Density [g·cm-3]
1.0108
Measurement Temperature [°C]
15
Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 23 of 25
Density [g·cm-3]
1.0023
Measurement Temperature [°C]
25
Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 24 of 25
Density [g·cm-3]
1.099
Measurement Temperature [°C]
12
Pauwels; Chem. Zentralbl.; C.1898 I,193, View in Reaxys 25 of 25
Density [g·cm-3]
1
Measurement Temperature [°C]
16.5
Pauwels; Chem. Zentralbl.; C.1898 I,193, View in Reaxys Adsorption (MCS) (6) 1 of 6
Description (Adsorption (MCS))
Adsorption
Temperature (Adsorption (MCS)) [°C]
15
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 6
Description (Adsorption (MCS))
Further physical properties of the adsorbed molecule
Temperature (Adsorption (MCS)) [°C]
100
Partner (Adsorption (MCS))
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Armstrong, Daniel W.; He, Lingfeng; Liu, Yan-Song; Analytical Chemistry; vol. 71; nb. 17; (1999); p. 3873 - 3876, View in Reaxys 3 of 6
Description (Adsorption (MCS))
Further physical properties of the adsorbed molecule
Temperature (Adsorption (MCS)) [°C]
100
Partner (Adsorption (MCS))
1-butyl-3-methylimidazolium chloride
Armstrong, Daniel W.; He, Lingfeng; Liu, Yan-Song; Analytical Chemistry; vol. 71; nb. 17; (1999); p. 3873 - 3876, View in Reaxys 4 of 6
Description (Adsorption (MCS))
Further physical properties of the adsorbed molecule
Temperature (Adsorption (MCS)) [°C]
100
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Partner (Adsorption (MCS))
(5 percent-phenyl-methylpolysiloxane)
Armstrong, Daniel W.; He, Lingfeng; Liu, Yan-Song; Analytical Chemistry; vol. 71; nb. 17; (1999); p. 3873 - 3876, View in Reaxys 5 of 6
Description (Adsorption (MCS))
Further physical properties of the adsorbed molecule
Temperature (Adsorption (MCS)) [°C]
100
Partner (Adsorption (MCS))
2,6,10,15,19,23-hexamethyltetracosane
Armstrong, Daniel W.; He, Lingfeng; Liu, Yan-Song; Analytical Chemistry; vol. 71; nb. 17; (1999); p. 3873 - 3876, View in Reaxys 6 of 6
Description (Adsorption (MCS))
Enthalpy of adsorption
Cochrane; Rudham; Transactions of the Faraday Society; vol. 61; (1965); p. 2246,2250, View in Reaxys; Eley; Bulletin de la Societe Chimique de France; (1970); p. 3197,3199, View in Reaxys Association (MCS) (10) 1 of 10
Description (Association Association with compound (MCS)) Solvent (Association (MCS))
N,N-dimethyl-formamide
Partner (Association (MCS))
C37H20O20(8-)*16H2O*4C3H7NO*2In(3+)*2C2H8N(1+)
Xue, Yun-Shan; He, Yabing; Zhou, Lian; Chen, Fei-Jian; Xu, Yan; Du, Hong-Bin; You, Xiao-Zeng; Chen, Banglin; Journal of Materials Chemistry A; vol. 1; nb. 14; (2013); p. 4525 - 4530, View in Reaxys 2 of 10
Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]
25
Comment (Association (MCS))
film
Partner (Association (MCS))
cycloheptaamylose
Shtykov; Korenman; Rusanova; Gorin; Kalach; Pankin; Doklady Chemistry; vol. 396; nb. 4-6; (2004); p. 119 121, View in Reaxys 3 of 10
Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))
cetane
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 4 of 10
Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]
25
Partner (Association (MCS))
water
Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Carr, Peter W.; Doherty, Robert F.; Taft, Robert W.; Journal of Physical Chemistry; vol. 91; nb. 7; (1987); p. 1996 - 2004, View in Reaxys 5 of 10
Description (Association NMR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]
-80
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Partner (Association (MCS))
kryptofix 221
Schmidt, Emmanuel; Tremillon, Jean-Michel; Kintzinger, Jean-Pierre; Popov, Alexander I.; Journal of the American Chemical Society; vol. 105; nb. 26; (1983); p. 7563 - 7566, View in Reaxys 6 of 10
Description (Association Dipole moment of the complex (MCS)) Solvent (Association (MCS))
benzene
Temperature (Association (MCS)) [°C]
25
Partner (Association (MCS))
AlBr3
Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 7 of 10
Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))
benzene
Temperature (Association (MCS)) [°C]
25
Partner (Association (MCS))
AlBr3
Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 8 of 10
Description (Association Dipole moment of the complex (MCS)) Solvent (Association (MCS))
benzene
Temperature (Association (MCS)) [°C]
25
Partner (Association (MCS))
GaBr3
Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 9 of 10
Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))
benzene
Temperature (Association (MCS)) [°C]
25
Partner (Association (MCS))
GaBr3
Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 10 of 10
Description (Association Spectrum of the complex (MCS)) Corset et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 1707, View in Reaxys; Baitinger et al.; Tetrahedron; vol. 20; (1964); p. 1635,1639, View in Reaxys; Su; Hong; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1461,1464, View in Reaxys
Azeotropes (MCS) (7) 1 of 7
Temperature (Azeotropes (MCS)) [°C]
56.4
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Pressure (Azeotropes (MCS)) [Torr]
60
Azeotropes
ethylbenzene
Berg; Harrison; Montgomery; Industrial and Engineering Chemistry; vol. 38; (1946); p. 1151, View in Reaxys 2 of 7
Temperature (Azeotropes (MCS)) [°C]
91.2
Azeotropes
water
Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys 3 of 7
Azeotropes
water
Horsley; Azeotropic Data II(=Advances in Chemistry Series Nr.35)<Washington 1962>S.77, View in Reaxys 4 of 7
Azeotropes
propan-1-ol
Horsley; Azeotropic Data II(=Advances in Chemistry Series Nr.35)<Washington 1962>S.77, View in Reaxys 5 of 7
Azeotropes
butan-1-ol
Horsley; Azeotropic Data II(=Advances in Chemistry Series Nr.35)<Washington 1962>S.77, View in Reaxys 6 of 7
Azeotropes
butan-2-ol
Horsley; Azeotropic Data II(=Advances in Chemistry Series Nr.35)<Washington 1962>S.77, View in Reaxys 7 of 7
Azeotropes
isobutyl alcohol
Horsley; Azeotropic Data II(=Advances in Chemistry Series Nr.35)<Washington 1962>S.77, View in Reaxys Boundary Surface Phenomena (MCS) (1) 1 of 1
Description (Boundary Surface Phenomena (MCS))
Boundary surface phenomena
Zapior,B.; Sliwa,B.; Roczniki Chemii; vol. 39; (1965); p. 1461 - 1468, View in Reaxys Chromatographic Data (1) Chromatographic References data HPLC (High performance liquid chromatography)
Bhattacharya, Apurba; Purohit, Vikram C.; Rinaldi, Frank; Organic Process Research and Development; vol. 7; nb. 3; (2003); p. 254 - 258, View in Reaxys
Circular Dichroism (1) References Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys Compressibility (1) Description (Com- References pressibility) Isothermal compressibility
Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys
Conformation (1) Object of Investi- References gation Conformation
Stone; Maki; Journal of Chemical Physics; vol. 37; (1962); p. 1326,1329, View in Reaxys
Cross-Sections (1) Description References (Cross-Sections) Collision crosssection
Christophorou; Christodoulides; Journal of Physics B: Atomic and Molecular Physics; vol. 2; (1969); p. 71,80, View in Reaxys
Dielectric Constant (1) References Zboinski et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 85,87,91, View in Reaxys; Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys
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Dissociation Exponent (10) 1 of 10
Comment (Dissociation Exponent)
(k')K
Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3107,3108, View in Reaxys 2 of 10
Comment (Dissociation Exponent)
(pk')pK
Bordwell,F.G.; Bartmess,J.E.; Journal of Organic Chemistry; vol. 43; (1978); p. 3101 - 3107, View in Reaxys; Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3095,3096, View in Reaxys; Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3107,3108, View in Reaxys 3 of 10
Comment (Dissociation Exponent)
(pk')in waessriger Lsg.
Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys 4 of 10
Comment (Dissociation Exponent)
(pk')pK (Acn.)
Fedorov; Aksenenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1166; ; p. 2040, View in Reaxys 5 of 10
Comment (Dissociation Exponent)
(pk')pK (Tributylphosphate)
Fedorov; Aksenenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1166; ; p. 2040, View in Reaxys 6 of 10
Comment (Dissociation Exponent)
(k')Tabelle 6
Belikov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 272,275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 335, View in Reaxys 7 of 10
Comment (Dissociation Exponent)
(pk')pK(a) in DMSO
Faleev et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1970); p. 69; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1970); p. 73, View in Reaxys 8 of 10
Comment (Dissociation Exponent)
(pk')pK (DMF)
Fedorov et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 838; Zhurnal Fizicheskoi Khimii; vol. 43; (1969); p. 1508, View in Reaxys 9 of 10
Comment (Dissociation Exponent)
(pk')pK(a): 14.54
Belonkon' et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1969); p. 949,950,954; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1969); p. 1039, View in Reaxys 10 of 10
Comment (Dissociation Exponent)
(pk')in W. (Temp. nicht angegeben; spektrophotometr. ermittelt)
Nowikow et al.; Tetrahedron, Supplement; vol. 6; (1964); p. 119,128; Chem.Abstr.; nb. 14665; (1965), View in Reaxys Dynamic Viscosity (2) Dynamic Viscosi- Temperature (Dyty [P] namic Viscosity) [°C]
References
0.00798
25
Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys
0.003066 0.009253
15.3 - 122
Friend; Hargreaves; Phil.Mag.; vol. <7>34; (1943); p. 810; Chem.Abstr.; (1944); p. 1409, View in Reaxys
Electrical Data (3) 1 of 3
Description (Electrical Data)
Electrical properties
Location
supporting information
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Prakash, G. K. Surya; Wang, Fang; Ni, Chuanfa; Shen, Jingguo; Haiges, Ralf; Yudin, Andrei K.; Mathew, Thomas; Olah, George A.; Journal of the American Chemical Society; vol. 133; nb. 26; (2011); p. 9992 - 9995, View in Reaxys 2 of 3
Description (Electrical Data)
Dielectric relaxation time
Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys 3 of 3
Description (Electrical Data)
Electrical conductivity
Little; Singleterry; Journal of Physical Chemistry; vol. 68; (1964); p. 2709, View in Reaxys Electrical Moment (6) 1 of 6
Description (Electrical Moment)
Dipole moment
Moment (Electrical Moment) [D]
3.72
Temperature (Electrical Moment) [°C]
19.9
Solvent (Electrical Moment)
benzene
Balakier, Grazyna; Polish Journal of Chemistry; vol. 54; nb. 11/12; (1980); p. 2297 - 2304, View in Reaxys 2 of 6
Description (Electrical Moment)
Dipole moment
Comment (Electrical Moment)
μ
Zboinski et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 85,87,91, View in Reaxys; Polezzo; Simonetta; Chemical Physics Letters; vol. 1; (1967); p. 85, View in Reaxys; Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys 3 of 6
Description (Electrical Moment)
Dipole moment
Nelson et al.; Journal of Physical Chemistry; vol. 71; (1967); p. 2742, View in Reaxys; Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys; Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys 4 of 6
Description (Electrical Moment)
Dipole moment
Comment (Electrical Moment)
Table 1
Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys 5 of 6
Description (Electrical Moment)
Dipole moment
Moment (Electrical Moment) [D]
3.72
Wiswall; Smyth; Journal of Chemical Physics; vol. 9; (1941); p. 357, View in Reaxys 6 of 6
Description (Electrical Moment)
Dipole moment
Moment (Electrical Moment) [D]
3.57
Groves; Sugden; Journal of the Chemical Society; (1937); p. 162, View in Reaxys Electrochemical Behaviour (7) Description (Elec- Comment (Electrochemical Betrochemical Behaviour) haviour)
References
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Enthalpy of disso- Enthalpy: 11304 ciation (electrolyt- J/mol. Temperaic) / protonation ture: 24 deg C.
Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys
Thermodynamic parameters for dissociation / protonation
Arnett, Edward M.; Venkatasubramaniam, K. G.; Journal of Organic Chemistry; vol. 48; nb. 10; (1983); p. 1569 - 1578, View in Reaxys
Electrochemical properties
Glushchenko; Radaev; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 27; (1978); p. 463; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 27; (1978); p. 538, View in Reaxys
Enthalpy of disso- . ciation (electrolytic) / protonation
Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys
Kinetics of dissociation (electrolytic) / protonation
Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys
Polarography
Gupta; Raghavan; Indian Journal of Chemistry; vol. 9; (1971); p. 233, View in Reaxys; Gavioli et al.; Collection of Czechoslovak Chemical Communications; vol. 36; (1971); p. 730,733, 736, View in Reaxys
pH of aqueous solutions
gesaettigte Loesung: 4.33.
Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p. 891, View in Reaxys
Electrochemical Characteristics (13) 1 of 13
Description (Electrochemical Characteristics)
voltammetry
Solvent (Electrochemical Characteristics)
neat liquid
Temperature (Electrochemical Characteristics) [°C]
21
Caban, Karolina; Donten, Mikolaj; Stojek, Zbigniew; Journal of Physical Chemistry B; vol. 108; nb. 3; (2004); p. 1153 - 1159, View in Reaxys 2 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 1.09 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -0.96 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 3 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 2.1 cal Characteristics)
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Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.03 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 4 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 3.12 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.08 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 5 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 4.05 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.14 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 6 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 5.08 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.19 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys
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7 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 6.11 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.21 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 8 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 7.12 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.22 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 9 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 8.15 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.23 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 10 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 9.1 cal Characteristics)
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Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.23 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 11 of 13
Description (Electrochemical Characteristics)
redox potential
Solvent (Electrochemical Characteristics)
acetonitrile; methanol
pH-Value (Electrochemi- 10.05 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]
25
Comment (Electrochem- -1.24 V; Product: /BRN= 1731121/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product
N-propylhydroxylamine
Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 12 of 13
Description (Electrochemical Characteristics)
polarographic half-wave potential
Gavioli et al.; Collection of Czechoslovak Chemical Communications; vol. 36; (1971); p. 730,733, 736, View in Reaxys 13 of 13
Description (Electrochemical Characteristics)
polarographic current/voltage curve
Stewart; Bonner; Analytical Chemistry; vol. 22; (1950); p. 793, View in Reaxys; Radin; De Vries; Analytical Chemistry; vol. 24; (1952); p. 971, View in Reaxys; Bergman; James; Transactions of the Faraday Society; vol. 48; (1952); p. 956,960; Transactions of the Faraday Society; vol. 50; (1954); p. 60,63, View in Reaxys Energy Data (MCS) (18) 1 of 18
Description (Energy Data (MCS))
Heat capacity of mixtures
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
ethanol
Tanaka, Reiji; Toyama, Satoru; Journal of Chemical and Engineering Data; vol. 41; nb. 6; (1996); p. 1455 - 1458, View in Reaxys 2 of 18
Description (Energy Data (MCS))
Enthalpy of solution
Temperature (Energy Data (MCS)) [°C]
24
Partner (Energy Data (MCS))
water
Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys 3 of 18
Description (Energy Data (MCS))
Enthalpy of solution
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Temperature (Energy Data (MCS)) [°C]
24
Partner (Energy Data (MCS))
0.01 M aq. NaOH
Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys 4 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
cyclohexane
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 5 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
methanol
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 6 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
diethyl ether
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 7 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
dichloromethane
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 8 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
acetonitrile
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 9 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
H2O
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 10 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
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Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
nitromethane
Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 11 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25 - 45
Partner (Energy Data (MCS))
cyclohexane
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 12 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25 - 45
Partner (Energy Data (MCS))
tetrachloromethane
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 13 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25 - 45
Partner (Energy Data (MCS))
benzene
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 14 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Temperature (Energy Data (MCS)) [°C]
25
Partner (Energy Data (MCS))
para-xylene
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 15 of 18
Description (Energy Data (MCS))
Excess thermochemical parameter
Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys; Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys; Nicolaides; Eckert; Journal of Chemical and Engineering Data; vol. 23; (1978); p. 152,154, View in Reaxys 16 of 18
Description (Energy Data (MCS))
Enthalpy of mixing
Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys 17 of 18
Description (Energy Data (MCS))
Enthalpy of mixing
Partner (Energy Data (MCS))
chlorobenzene
Lacher; Buck; Parry; Journal of the American Chemical Society; vol. 63; (1941); p. 2423, View in Reaxys 18 of 18
Description (Energy Data (MCS))
Enthalpy of mixing
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Partner (Energy Data (MCS))
ethylene dibromide
Lacher; Buck; Parry; Journal of the American Chemical Society; vol. 63; (1941); p. 2423, View in Reaxys Enthalpy of Combustion (1) References Lebedeva; Ryadnenko; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1382; ; p. 2442, View in Reaxys Enthalpy of Formation (1) References Voelkel; Tomasik; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 25; (1977); p. 415,416, View in Reaxys; Lebedeva; Ryadnenko; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1382; ; p. 2442, View in Reaxys Enthalpy of Fusion (1) References Ljaschkewitsch; Neftekhimiya; vol. 1; (1962); p. 329,219, View in Reaxys Enthalpy of Vaporization (1) Enthalpy of VaTemperature (Enporization thalpy of Vapori[Jmol-1] zation) [°C] 42286.7
24.85
References
Miroshnichenko; Vorob'eva; Russian Journal of Physical Chemistry A; vol. 73; nb. 3; (1999); p. 349 - 355, View in Reaxys
Further Information (34) Description (Fur- References ther Information) Further information
Shinkai et al.; Biopolymers; vol. 17; (1978); p. 2757,2758,2759, View in Reaxys
Further information
Chizhov et al.; Organic Mass Spectrometry; vol. 13; (1978); p. 611,612, View in Reaxys
Further information
Voelkel; Tomasik; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 25; (1977); p. 415,416, View in Reaxys
Further information
Bakale et al.; Journal of Chemical Physics; vol. 67; (1977); p. 5788,5790, View in Reaxys
Further information
Laub; Purnell; Journal of the American Chemical Society; vol. 98; (1976); p. 30,31, View in Reaxys
Further information
Levine; Bethea; Journal of Chemical Physics; vol. 63; (1975); p. 2666,2675, View in Reaxys
Further information
Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys
Further information
Lebedeva; Ryadnenko; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1382; ; p. 2442, View in Reaxys
Further information
Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys
Further information
Chandra; Nath; Journal of Chemical Physics; vol. 51; (1969); p. 5299, View in Reaxys
Further information
Brookes; Jonathan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 187,188, View in Reaxys
Further information
Haddon; McLafferty; Analytical Chemistry; vol. 41; (1969); p. 31, View in Reaxys
Further information
Dewar et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 3590, View in Reaxys
Further information
Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2120, View in Reaxys
Further information
Nelson et al.; Journal of Physical Chemistry; vol. 71; (1967); p. 2742, View in Reaxys
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Further information
Griffith et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 533, View in Reaxys
Further information
Spokes; Benson; Journal of the American Chemical Society; vol. 89; (1967); p. 6030,6034, View in Reaxys
Further information
Perez Masia et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 1093,1094-1102, View in Reaxys
Further information
Borgardt,F.G. et al.; Journal of Organic Chemistry; vol. 31; (1966); p. 2806 - 2811, View in Reaxys
Further information
Hankinson; Thompson; Journal of Chemical and Engineering Data; vol. 10; (1965); p. 18, View in Reaxys
Further information
Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 4888,4889, View in Reaxys
Further information
Witanowski et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2569,2570, View in Reaxys
Further information
Feuer; Markofsky; Journal of Organic Chemistry; vol. 29; (1964); p. 935,938, View in Reaxys
Further information
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys
Further information
Baskov et al.; Tetrahedron; vol. 20; (1964); p. 1519,1523, View in Reaxys
Further information
Hofman et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 554,555, View in Reaxys
Further information
Geiseler; Kessler; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 571, View in Reaxys
Further information
Feuer,H. et al.; Spectrochimica Acta; vol. 19; (1963); p. 431 - 434, View in Reaxys
Further information
Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1359 - 1360, View in Reaxys
Further information
Buczkowski; Urbanski; Spectrochimica Acta; vol. 18; (1962); p. 1187,1188, 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
Piette et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4212,4213, View in Reaxys
Further information
Klimowa; SaGrodina; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1961); p. 160; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1961); p. 176, View in Reaxys
Further information
Altshuller; Cohen; Analytical Chemistry; vol. 32; (1960); p. 881, View in Reaxys
Ionization Potential (1) References Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys; Dewar et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 3590, View in Reaxys Liquid/Liquid Systems (MCS) (5) 1 of 5
Description (Liquid/ Liquid Systems (MCS))
Distribution between solvent 1 + 2
Solvent (Liquid/Liquid Systems (MCS))
gas
Temperature (Liquid/ Liquid Systems (MCS)) [°C]
39.2
Partner (Liquid/Liquid Systems (MCS))
apolane
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Weckwerth, Jeff D.; Carr, Peter W.; Vitha, Mark F.; Nasehzadeh, Asad; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3712 - 3716, View in Reaxys 2 of 5
Description (Liquid/ Liquid Systems (MCS))
Distribution between solvent 1 + 2
Partner (Liquid/Liquid Systems (MCS))
cetane; water
Abraham, Michael H.; Whiting, Gary S.; Fuchs, Richard; Chambers, Eric J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 2; (1990); p. 291 - 300, View in Reaxys 3 of 5
Description (Liquid/ Liquid Systems (MCS))
Distribution between solvent 1 + 2
Solvent (Liquid/Liquid Systems (MCS))
H2O
Partner (Liquid/Liquid Systems (MCS))
octanol
Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys 4 of 5
Description (Liquid/ Liquid Systems (MCS))
Distribution between solvent 1 + 2
Solvent (Liquid/Liquid Systems (MCS))
H2O
Temperature (Liquid/ Liquid Systems (MCS)) [°C]
25
Partner (Liquid/Liquid Systems (MCS))
oleyl alcohol
Kuehne; Bocek; Scharfenberg; Frank; European Journal of Medicinal Chemistry; vol. 16; nb. 1; (1981); p. 7 - 12, View in Reaxys 5 of 5
Description (Liquid/ Liquid Systems (MCS))
Distribution between solvent 1 + 2
Kemula; Buchowski; Teperek; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 9; (1961); p. 601, View in Reaxys; Kemula et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 12; (1964); p. 347, View in Reaxys Liquid/Vapour Systems (MCS) (17) 1 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
cetane
Dallas, Andrew J.; Carr, Peter W.; Journal of Physical Chemistry; vol. 98; nb. 18; (1994); p. 4927 - 4939, View in Reaxys 2 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
n-heptane
Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys; Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 3 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))
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Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
1-heptene
Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys 4 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
1,6--heptadiene
Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys 5 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
benzene
Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 6 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
tetrachloromethane
Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 7 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 80.4 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
chlorobenzene
Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 8 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 27.9 - 67.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
hexane
Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 9 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))
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Temperature (Liquid/ 89.6 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
toluene
Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 10 of 17
Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys
11 of 17
Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Dowell; Stewart; Phosphorus and Sulfur and the Related Elements; vol. 1; (1976); p. 135,137, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys; Monfort et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 67; (1970); p. 748,749-753, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys
12 of 17
Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys
13 of 17
Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys
14 of 17
Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
ethylene dibromide
Lacher; Hunt; Journal of the American Chemical Society; vol. 63; (1941); p. 1753,1754, View in Reaxys; Lacher; Buck; Parry; Journal of the American Chemical Society; vol. 63; (1941); p. 2423, View in Reaxys 15 of 17
Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
chlorobenzene
Lacher; Hunt; Journal of the American Chemical Society; vol. 63; (1941); p. 1753,1754, View in Reaxys; Lacher; Buck; Parry; Journal of the American Chemical Society; vol. 63; (1941); p. 2423, View in Reaxys 16 of 17
Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 120 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))
ethylene dibromide
Lacher; Hunt; Journal of the American Chemical Society; vol. 63; (1941); p. 1753,1754, View in Reaxys; Lacher; Buck; Parry; Journal of the American Chemical Society; vol. 63; (1941); p. 2423, View in Reaxys 17 of 17
Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 120 Vapour Systems (MCS)) [°C]
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Partner (Liquid/Vapour Systems (MCS))
chlorobenzene
Lacher; Hunt; Journal of the American Chemical Society; vol. 63; (1941); p. 1753,1754, View in Reaxys; Lacher; Buck; Parry; Journal of the American Chemical Society; vol. 63; (1941); p. 2423, View in Reaxys Mechanical & Physical Properties (MCS) (9) 1 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
25
Partner (Mechanical & Physical Properties (MCS))
ethanol
Tanaka, Reiji; Toyama, Satoru; Journal of Chemical and Engineering Data; vol. 41; nb. 6; (1996); p. 1455 - 1458, View in Reaxys 2 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
20
Partner (Mechanical & Physical Properties (MCS))
benzene
Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 3 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
20
Partner (Mechanical & Physical Properties (MCS))
para-xylene
Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 4 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
20
Partner (Mechanical & Physical Properties (MCS))
1,3,5-trimethyl-benzene
Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 5 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
25 - 45
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Partner (Mechanical & Physical Properties (MCS))
cyclohexane
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 6 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
25 - 45
Partner (Mechanical & Physical Properties (MCS))
tetrachloromethane
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 7 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
25 - 45
Partner (Mechanical & Physical Properties (MCS))
benzene
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 8 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
25
Partner (Mechanical & Physical Properties (MCS))
para-xylene
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys 9 of 9
Description (Mechanical & Physical Properties (MCS))
Volume change on mixing
Temperature (Mechanical & Physical Properties (MCS)) [°C]
25
Partner (Mechanical & Physical Properties (MCS))
hexane
Marsh, Kenneth N.; Allan, Warren A.; Richards, Alan E.; Journal of Chemical Thermodynamics; vol. 16; nb. 12; (1984); p. 1107 - 1120, View in Reaxys Mechanical Properties (4) Description (MeReferences chanical Properties) Molar volume
Dewan, R.K.; Sharma, A.K.; Mehta, S.K.; Journal of Solution Chemistry; vol. 17; nb. 5; (1988); p. 459 - 466, View in Reaxys; Taft; Abraham; Famini; Doherty; Abboud; Kamlet; Journal of Pharmaceutical Sciences; vol. 74; nb. 8; (1985); p. 807 - 814, View in Reaxys
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Virial coefficients of the equation of state
Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys
Compressibility
Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys
Viscosity
Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys
Optics (3) Description (Optics)
References
Magnetic circular dichroism
Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys
Rayleigh scattering
Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys
Magnetorotation
Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys; Bonnafous; Labarre; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1376, View in Reaxys
Other Thermochemical Data (6) Description (Oth- Comment (Other er Thermochemi- Thermochemical cal Data) Data)
References
Enthalpy
Eley; Bulletin de la Societe Chimique de France; (1970); p. 3197,3199, View in Reaxys; Belik; Shlyapochnikov; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 26; (1977); p. 2585; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 26; (1977); p. 2795, View in Reaxys
Thermodynamic properties
Dear et al.; Transactions of the Faraday Society; vol. 59; (1963); p. 713,717, View in Reaxys
Cryoscopic constant
Ljaschkewitsch; Neftekhimiya; vol. 1; (1962); p. 329,219, View in Reaxys
Heat of combustion at constant volume
bei 26.7grad: 481.7 kcal/mol.
Cass et al.; Journal of the Chemical Society; (1958); p. 958,960, View in Reaxys
Heat of combustion at constant volume
zu H2O (fluessig), Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, CO2(Gas) und View in Reaxys Stickstoff (Gas) bei 25grad: 481.33+-0.61 kcal/Mol.
Heat of combustion at constant volume
477.8 Cal/Mol.
Swientoslawski; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 72; (1910); p. 66; Chem. Zentralbl.; vol. 80; nb. II; (1909); p. 2144, View in Reaxys
Solubility (MCS) (4) 1 of 4
Saturation
in pure solvent
Comment (Solubility (MCS))
equation
Jain, Neera; Yalkowsky, Samuel H.; Journal of Pharmaceutical Sciences; vol. 90; nb. 2; (2001); p. 234 - 252, View in Reaxys 2 of 4
Saturation
in pure solvent
Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Carr, Peter W.; Doherty, Robert F.; Taft, Robert W.; Journal of Physical Chemistry; vol. 91; nb. 7; (1987); p. 1996 - 2004, View in Reaxys; Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys; Valvani; Yalkowsky; Roseman; Journal of Pharmaceutical Sciences; vol. 70; nb. 5; (1981); p. 502 - 507, View in Reaxys; Kamlet; Doherty; Abboud; Abraham; Taft; Journal of Pharmaceutical Sciences; vol. 75; nb. 4; (1986); p. 338 - 349, View in Reaxys 3 of 4
Temperature (Solubility (MCS)) [°C]
20
Solvent (Solubility (MCS))
H2O
v.Schickh; Angewandte Chemie; vol. 62; (1950); p. 547,554, View in Reaxys
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4 of 4
Temperature (Solubility (MCS)) [°C]
20
Solvent (Solubility (MCS))
H2O
Comment (Solubility (MCS))
9.99999E-02 ml solvent dissolves. 1.5 ml Substance.
Richardson; Schlechter; Haller; J.econ.Entomol.; vol. 36; (1943); p. 111; Chem.Abstr.; (1943); p. 4144, View in Reaxys Solution Behaviour (MCS) (6) 1 of 6
Description (Solution Behaviour (MCS))
Solubility [Henry constant]
Temperature (Solution Behaviour (MCS)) [°C]
20 - 50
Partner (Solution Behaviour (MCS))
H2O
Dohnal; Benes; Journal of Chemical and Engineering Data; vol. 44; nb. 5; (1999); p. 1097 - 1102, View in Reaxys 2 of 6
Description (Solution Behaviour (MCS))
Mutual solubility
Temperature (Solution Behaviour (MCS)) [°C]
0 - 90.5
Partner (Solution Behaviour (MCS))
H2O
Stephenson; Journal of Chemical and Engineering Data; vol. 37; nb. 1; (1992); p. 80 - 95, View in Reaxys 3 of 6
Description (Solution Behaviour (MCS))
Dissolving capacity
Temperature (Solution Behaviour (MCS)) [°C]
20
Partner (Solution Behaviour (MCS))
water
v.Schickh; Angewandte Chemie; vol. 62; (1950); p. 547,554, View in Reaxys 4 of 6
Description (Solution Behaviour (MCS))
Dissolving capacity
Partner (Solution Behaviour (MCS))
dinitrogen tetraoxide; N2O4
Fowler et al.; Journal of the American Chemical Society; vol. 69; (1947); p. 1638, View in Reaxys 5 of 6
Description (Solution Behaviour (MCS))
Dissolving capacity
Partner (Solution Behaviour (MCS))
cellulose ester
Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys; Bogin; Wampner; Industrial and Engineering Chemistry; vol. 34; (1942); p. 1093, View in Reaxys 6 of 6
Description (Solution Behaviour (MCS))
Dissolving capacity
Comment (Solution Behaviour (MCS))
100 ml 1-Nitro-propan loesen 0.5 ml Wasser.
Partner (Solution Behaviour (MCS))
water
Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p. 891, View in Reaxys Surface Tension (3) Surface Tension Temperature [g·s-2] (Surface Tension) [°C]
References
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Snead; Clever; Journal of Chemical and Engineering Data; vol. 7; (1962); p. 393, View in Reaxys 23.07 - 30.66
17.1 - 86.7
Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys
29.28
25
Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys
Transport Data (1) Description References (Transport Data) Thermal conductivity
Sakiadis; Coates; A.I.Ch.E.Journal; vol. 1; (1955); p. 275,277, View in Reaxys
Transport Phenomena (MCS) (1) 1 of 1
Description (Transport Phenomena (MCS))
Diffusion
Evanoff; Harris; Canadian Journal of Chemistry; vol. 56; (1978); p. 574, View in Reaxys Vapour Pressure (5) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]
Comment (Vapour Pressure)
References
Saunders; Spaull; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 28; (1961); p. 332,337, View in Reaxys; Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 901, View in Reaxys equation exists.
Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys
7.5
20
v.Schickh; Angewandte Chemie; vol. 62; (1950); p. 547,554, View in Reaxys
3.96 - 728.2
10 - 130
Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys
57.04 - 760
58.7 - 131.4
Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2879, View in Reaxys
NMR Spectroscopy (28) 1 of 28
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]
29.14
Frequency (NMR Spectroscopy) [MHz]
400
Location
supporting information
Li, Shengkun; Huang, Kexuan; Zhang, Xumu; Chemical Communications; vol. 50; nb. 64; (2014); p. 8878 - 8881, View in Reaxys 2 of 28
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]
31.04
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Frequency (NMR Spectroscopy) [MHz]
100
Location
supporting information
Li, Shengkun; Huang, Kexuan; Zhang, Xumu; Chemical Communications; vol. 50; nb. 64; (2014); p. 8878 - 8881, View in Reaxys 3 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]
400
Location
supporting information
Kostal, Jakub; Voutchkova, Adelina M.; Jorgensen, William L.; Organic Letters; vol. 14; nb. 1; (2012); p. 260 263, View in Reaxys 4 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
Solvents (NMR Spectro- acetone scopy) Temperature (NMR Spectroscopy) [°C]
35
Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Wejroch, Krystyna; Magnetic Resonance in Chemistry; vol. 36; nb. SPEC. ISS.; (1998); p. S85-S92, View in Reaxys 5 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
Solvents (NMR Spectro- cyclohexane scopy) Temperature (NMR Spectroscopy) [°C]
35
Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Wejroch, Krystyna; Magnetic Resonance in Chemistry; vol. 36; nb. SPEC. ISS.; (1998); p. S85-S92, View in Reaxys 6 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
15N
Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]
23.9
Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance (1969-1992); vol. 97; nb. 3; (1992); p. 568 594, View in Reaxys 7 of 28
Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]
23.9
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Comment (NMR Spectroscopy)
13C-15N, 1H-15N.
Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance (1969-1992); vol. 97; nb. 3; (1992); p. 568 594, View in Reaxys 8 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- CDCl3 scopy) Bailey, William F.; Cioffi, Eugene A.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 181 - 183, View in Reaxys 9 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- CCl4 scopy) Hsiu, Su-Lan; Takai, Hitoshi; Sasaki, Yoshio; Chemical & Pharmaceutical Bulletin; vol. 32; nb. 6; (1984); p. 2091 2099, View in Reaxys 10 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- gas scopy) Temperature (NMR Spectroscopy) [°C]
170
Hsiu, Su-Lan; Takai, Hitoshi; Sasaki, Yoshio; Chemical & Pharmaceutical Bulletin; vol. 32; nb. 6; (1984); p. 2091 2099, View in Reaxys 11 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- gas scopy) Temperature (NMR Spectroscopy) [°C]
100
Hsiu, Su-Lan; Takai, Hitoshi; Sasaki, Yoshio; Chemical & Pharmaceutical Bulletin; vol. 32; nb. 6; (1984); p. 2091 2099, View in Reaxys 12 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
Solvents (NMR Spectro- acetone scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 13 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
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Solvents (NMR Spectro- dimethylsulfoxide scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 14 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
Solvents (NMR Spectro- CCl4 scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 15 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
Solvents (NMR Spectro- neat (no solvent) scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 16 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- ClSO2F scopy) Temperature (NMR Spectroscopy) [°C]
-60
Olah, George A.; Fung, Alexander P.; Rawdah, Tarik N.; Journal of Organic Chemistry; vol. 45; nb. 21; (1980); p. 4149 - 4153, View in Reaxys 17 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Bowman, W. Russ; Golding, Bernard T.; Watson, William P.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 731 - 736, View in Reaxys 18 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- tetradeuteriomethanol scopy) Bowman, W. Russ; Golding, Bernard T.; Watson, William P.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 731 - 736, View in Reaxys 19 of 28
Description (NMR Spec- NMR troscopy) Gilbert,K.E.; Borden,W.T.; Journal of Organic Chemistry; vol. 44; (1979); p. 659 - 661, View in Reaxys; Lippmaa,E.T. et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 924 - 928; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 1006 1011, View in Reaxys; Ejchart,A.; Organic Magnetic Resonance; vol. 10; (1977); p. 263, View in Reaxys; Miyajima,G.; Nishimoto,K.; Organic Magnetic Resonance; vol. 6; (1974); p. 313, View in Reaxys; Monitz; Gutowsky; Journal of Chemical Physics; vol. 38; (1963); p. 1155,1158, View in Reaxys; Cavanaugh; Dailey; Journal of Chemi-
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cal Physics; vol. 34; (1961); p. 1099,1100, View in Reaxys; Nagy et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 639, View in Reaxys; Knunjanz et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1966); p. 1013; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1966); p. 1062, View in Reaxys; Hilbers et al.; Pure and Applied Chemistry; vol. 32; (1972); p. 197,199,202, View in Reaxys; Maciel et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 1466, View in Reaxys; Alexandrou; Jannakoudakis; Tetrahedron Letters; (1968); p. 3841, View in Reaxys 20 of 28
Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)
NMR Chemical shifts
Moniz; Poranski; jr.; Journal of Magnetic Resonance (1969-1992); vol. 11; (1973); p. 62, View in Reaxys 21 of 28
Description (NMR Spec- NMR with shift reagents troscopy) Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 21; (1973); p. 2488,2489, 2490, View in Reaxys
22 of 28
Description (NMR Spec- Chemical shifts troscopy) Baskov et al.; Tetrahedron; vol. 20; (1964); p. 1519,1523, View in Reaxys; Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2120, View in Reaxys
23 of 28
Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)
14N
Poranski; Moniz; Journal of Physical Chemistry; vol. 71; (1967); p. 1142, View in Reaxys; Herbison-Evans; Richards; Molecular Physics; vol. 8; (1964); p. 19,26, View in Reaxys 24 of 28
Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)
d. nach γ-Bestrahlung (77K) erh. Radikals
Chachaty; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 262; (1966); p. 680, View in Reaxys 25 of 28
Description (NMR Spec- Spectrum troscopy) Witanowski et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2569,2570, View in Reaxys; Hofman et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 554,555, View in Reaxys
26 of 28
Description (NMR Spec- Spin-spin coupling constants troscopy) Stone; Maki; Journal of Chemical Physics; vol. 37; (1962); p. 1326,1329, View in Reaxys
27 of 28
Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)
17O
Christ et al.; Helvetica Chimica Acta; vol. 44; (1961); p. 865, View in Reaxys 28 of 28
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
14N
Holder; Klein; Journal of Chemical Physics; vol. 23; (1955); p. 1956, View in Reaxys IR Spectroscopy (13) 1 of 13
Description (IR Spectroscopy)
Spectrum
Solvent (IR Spectroscopy)
solid
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Temperature (IR Spectroscopy) [°C]
-193.15
Shilina; Russian Journal of General Chemistry; vol. 69; nb. 11; (1999); p. 1779 - 1783, View in Reaxys 2 of 13
Description (IR Spectroscopy)
IR
Iogansen; Litovchenko; Journal of Applied Spectroscopy; vol. 2; (1965); p. 159; ; p. 243, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys; Nowikow et al.; Tetrahedron, Supplement; vol. 6; (1964); p. 119,128; Chem.Abstr.; nb. 14665; (1965), View in Reaxys; Geiseler; Kessler; Nitro Compounds., Proc. Intern. Symp.; (1964); p. 187 - 194; Chem.Abstr.; vol. 64; nb. 1928f; (1966), View in Reaxys 3 of 13
Description (IR Spectroscopy)
Bands
Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys 4 of 13
Description (IR Spectroscopy)
Spectrum
Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Buczkowski; Urbanski; Spectrochimica Acta; vol. 18; (1962); p. 1187,1188, View in Reaxys 5 of 13
Description (IR Spectroscopy)
Spectrum
Solvent (IR Spectroscopy)
paraffin
Comment (IR Spectroscopy)
5000 - 1000 cm**(-1); Suspension.
Urbanski; Roczniki Chemii; vol. 31; (1957); p. 37,45; Bulletin de l'Academie Polonaise des Sciences, Classe 3: Mathematique, Astronomie, Physique, Chimie, Geologie et Geographie; vol. 4; (1956); p. 381; Chem.Abstr.; (1957); p. 12659, View in Reaxys 6 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
5000 - 667 cm**(-1); im Dampf.
Pierson et al.; Analytical Chemistry; vol. 28; (1956); p. 1218,1222; A. P. I. Res. Project; vol. 44; nb. 1220; (1951), View in Reaxys 7 of 13
Description (IR Spectroscopy)
Bands
Comment (IR Spectroscopy)
NO2-Streckschwingungsbanden und weitere IR-Banden der Fluess..
Haszeldine; Journal of the Chemical Society; (1953); p. 2525, View in Reaxys 8 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
5000 - 455 cm**(-1); im Dampf.
Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys 9 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
5000 - 455 cm**(-1); fluess..
Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys 10 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
10000 - 667 cm**(-1)
Nielsen; Smith; Industrial and Engineering Chemistry, Analytical Edition; vol. 15; (1943); p. 610, View in Reaxys
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11 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
1818 - 1111 cm**(-1)
Barnes; Liddel; Williams; Industrial and Engineering Chemistry, Analytical Edition; vol. 15; (1943); p. 659,687, View in Reaxys 12 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
2000 - 667 cm**(-1)
Mathieu; Massignon; Annales de Physique (Paris, France); vol. <11>16; (1941); p. 10,12,13; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 212; (1941); p. 1085, View in Reaxys 13 of 13
Description (IR Spectroscopy)
Spectrum
Comment (IR Spectroscopy)
5000 - 667 cm**(-1); fluess..
A.P.I.Res.Projekt 44 Nr.1753<1956>, View in Reaxys Mass Spectrometry (10) Description (Mass Comment (Mass Spectrometry) Spectrometry)
References
Photoionization; TOFMS (Time of flight mass spectrum); Spectrum
Xie, Mingfeng; Zhou, Zhongyue; Wang, Zhandong; Chen, Dongna; Qi, Fei; International Journal of Mass Spectrometry; vol. 303; nb. 2-3; (2011); p. 137 - 146, View in Reaxys
spectrum; chemical ionization (CI)
Kadentsev; Kolotyrkina; Stomakhin; Chizhov; Shevelev; Russian Chemical Bulletin; vol. 46; nb. 6; (1997); p. 1184 - 1185, View in Reaxys
spectrum
Ross, Philip L.; Van Bramer, Scott E.; Johnston, Murray V.; Applied Spectroscopy; vol. 50; nb. 5; (1996); p. 608 - 613, View in Reaxys
chemical ionization (CI); spectrum
Kadentsev, V. I.; Kolotyrkina, N. G.; Stomakhin, A. A.; Chizhov, O. S.; Russian Chemical Bulletin; vol. 44; nb. 9; (1995); p. 1698 - 1704; Izvestiya Akademi Nauk, Seriya Khimicheskaya; nb. 9; (1995); p. 1767 - 1773, View in Reaxys
fragmentation pattern; spectrum
Hindawi, S. K.; Fokkers, R. H.; Pinkse, F. A.; Nibbering, N. M. M.; Organic Mass Spectrometry; vol. 21; (1986); p. 243 - 250, View in Reaxys
electron impact (EI)
MIKE (mass ion kinetic energy); collisional activation
Hindawi, S. K.; Fokkers, R. H.; Pinkse, F. A.; Nibbering, N. M. M.; Organic Mass Spectrometry; vol. 21; (1986); p. 243 - 250, View in Reaxys
fragmentation pattern; spectrum
collisional activation
Egsgaard; Carlsen; Elbel; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 90; nb. 4; (1986); p. 369 - 374, View in Reaxys Fileleeva et al.; Theoretical and Experimental Chemistry; vol. 11; (1975); p. 283,285, View in Reaxys; Chizhov et al.; Organic Mass Spectrometry; vol. 13; (1978); p. 611,612, View in Reaxys; Haddon; McLafferty; Analytical Chemistry; vol. 41; (1969); p. 31, View in Reaxys; Tsuda et al.; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 614, View in Reaxys
fragmentation pattern
Elektronenstoss
Collin; Bulletin de la Societe Royale des Sciences de Liege; vol. 23; (1954); p. 194 196, View in Reaxys
appearance potentials
positiver Ionen bei Fragmentierung durch Elektronenstoss.
Collin; Bulletin de la Societe Royale des Sciences de Liege; vol. 23; (1954); p. 194 196, View in Reaxys
UV/VIS Spectroscopy (6) 1 of 6
Description (UV/VIS Spectroscopy)
UV/VIS
Ungnade et al.; Journal of Physical Chemistry; vol. 68; (1964); p. 3226, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys; Belikov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science
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(English Translation); vol. 20; (1971); p. 272,275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 335, View in Reaxys 2 of 6
Description (UV/VIS Spectroscopy)
Absorption maxima
Nielsen,A.T.; Journal of Organic Chemistry; vol. 27; (1962); p. 2001 - 2006, View in Reaxys; Bonnafous; Labarre; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1376, View in Reaxys; Bayliss; Wills-Johnson; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 551,553, View in Reaxys; Nielsen; Cordes; Tetrahedron, Supplement; vol. 6; (1964); p. 235,236, View in Reaxys 3 of 6
Description (UV/VIS Spectroscopy)
Absorption maxima
Solvent (UV/VIS Spectroscopy)
ethanol
Comment (UV/VIS Spectroscopy)
UV-Absorption.
Urbanski; Tetrahedron; vol. 61; (1959); p. 1,5, View in Reaxys 4 of 6
Description (UV/VIS Spectroscopy)
Spectrum
Solvent (UV/VIS Spectroscopy)
ethanol
Urbanski; Ciecierska; Roczniki Chemii; vol. 29; (1955); p. 11,14,15; Chem.Abstr.; (1955); p. 11414, View in Reaxys 5 of 6
Description (UV/VIS Spectroscopy)
Absorption maxima
Solvent (UV/VIS Spectroscopy)
light petroleum
Comment (UV/VIS Spectroscopy)
UV-Absorption.
Haszeldine; Journal of the Chemical Society; (1953); p. 2525, View in Reaxys 6 of 6
Description (UV/VIS Spectroscopy)
Spectrum
Solvent (UV/VIS Spectroscopy)
ethanol
Comment (UV/VIS Spectroscopy)
neutrale und alkalische Loesungen.
Zelinski; Rosanow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 630, View in Reaxys; Hantzsch; Voigt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 593, View in Reaxys ESR Spectroscopy (2) 1 of 2
Description (ESR Spectroscopy)
ESR
Gilbert,B.C. et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1272 - 1279, View in Reaxys; Chachaty; Rosilio; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 777,780,783,785-788, View in Reaxys 2 of 2
Description (ESR Spectroscopy)
Spectrum
Piette et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4212,4213, View in Reaxys Raman Spectroscopy (2) Description (Ram- Comment (Raman Spectroscopy) an Spectroscopy) Spectrum
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Spectrum
fluess.
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Pharmacological Data (8) 1 of 8
Comment (Pharmacological Data)
Bioactivities present
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Effect (Pharmacological Data)
pharmacokinetics
Species or Test-System (Pharmacological Data)
nitroalkane oxidase of Streptomyces ansochromogenes
Type (Pharmacological Data)
Km
Value of Type (Pharmacological Data)
35.7 mmol/l
Li, Yanhua; Gao, Zengqiang; Hou, Haifeng; Li, Lei; Zhang, Jihui; Yang, Haihua; Dong, Yuhui; Tan, Huarong; Biochemical and Biophysical Research Communications; vol. 405; nb. 3; (2011); p. 344 - 348, View in Reaxys 3 of 8
Effect (Pharmacological Data)
binding affinity
Species or Test-System (Pharmacological Data)
recombinant nitronate monooxygenase of Hansenula mrakii
Kind of Dosing (Pharmacological Data)
title comp. administered as nitronate form dissolved in ethanol
Further Details (Pharmacological Data)
dissociation constant (Kd)
Type (Pharmacological Data)
Kd
Value of Type (Pharmacological Data)
5.3 mmol/l
Francis, Kevin; Gadda, Giovanni; Bioorganic Chemistry; vol. 37; nb. 5; (2009); p. 167 - 172, View in Reaxys 4 of 8
Effect (Pharmacological Data)
binding affinity
Species or Test-System (Pharmacological Data)
recombinant nitronate monooxygenase of Hansenula mrakii
Kind of Dosing (Pharmacological Data)
title comp. administered as nitronate form dissolved in ethanol
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Results
molecular target: nitronate monooxygenase
Francis, Kevin; Gadda, Giovanni; Bioorganic Chemistry; vol. 37; nb. 5; (2009); p. 167 - 172, View in Reaxys 5 of 8
Effect (Pharmacological Data)
genetic toxicity in vitro
Species or Test-System (Pharmacological Data)
ovine seminal vesicle cells
Concentration (Pharmacological Data)
<= 10 mmol/l
Method (Pharmacological Data)
DNA repair synthesis test; in DMEM; bromodeoxyuridine density-shift method; in the presence of FdUrd, BrdUrd and <3H>dCyd (10 μCi/ml); incubated for 18 h; radioactivity incorporated into unreplicated DNA strands measurements
Further Details (Pharmacological Data)
confluent cells preincubated with 40 μM FdUrd and 200 μM BrdUrd for 1 h; 2-3 independent experiments
Comment (Pharmacological Data)
No effect
Kreis, Patricia; Degen, Gisela H.; Andrae, Ulrich; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 413; nb. 1; (1998); p. 69 - 81, View in Reaxys 6 of 8
Effect (Pharmacological Data)
biotransformation
Species or Test-System (Pharmacological Data)
BALB/c mice hepatocytes
Sex
male
Concentration (Pharmacological Data)
5 mmol/l
Method (Pharmacological Data)
in vitro; mice weighing 20-25 g; denitrification; effect of methylene blue (50 μM)
Results
rate of nitrite formation: without methylene blue: ca. 0.5 nmol NO2(-)/min/1E6 cells, with methylene blue: ca. 1 nmol NO2(-)/min/1E6 cells
Kohl; Gescher; Xenobiotica; vol. 27; nb. 8; (1997); p. 843 - 852, View in Reaxys 7 of 8
Effect (Pharmacological Data)
enzyme; induction of
Species or Test-System (Pharmacological Data)
rat liver aryl sulfotransferase
Sex
male
Concentration (Pharmacological Data)
2 mmol/l
Exposure Period (Pharmacological Data)
90 min
Method (Pharmacological Data)
enzyme from livers of F344 rats, medium: sodium phosphate, sodium hydroxide, pH 7.0, room temperature, 30 min, saturated with guanosine 2 mM, mercaptoethanol, PAPS, mixture shaken gently, 37 deg C; 8-aminoguanosine, 8-oxoguanosine analyzed; HPLC-EC
Comment (Pharmacological Data)
No effect
Fiala; Sodum; Hussain; Rivenson; Dolan; Toxicology; vol. 99; nb. 1-2; (1995); p. 89 - 97, View in Reaxys 8 of 8
Effect (Pharmacological Data)
DNA; examination of
Species or Test-System (Pharmacological Data)
rat hepatocytes
Sex
male
Concentration (Pharmacological Data)
1E-07 - 0.001 mol/l
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Exposure Period (Pharmacological Data)
7d
Method (Pharmacological Data)
hepatocytes isolated from adult F344 rats by two-step perfusion of liver with collagenase, vehicle, DMSO, cultures incubated, 20 h, cells attached to coverslips washed, stained after exposure, 4 deg C; net nuclear grain counts calculated
Results
did not induce DNA repair at any concentrations
Fiala; Sodum; Hussain; Rivenson; Dolan; Toxicology; vol. 99; nb. 1-2; (1995); p. 89 - 97, View in Reaxys Transport and Distribution (5) 1 of 5
Type (Transport and Distribution)
partition
Media (Transport and Distribution)
air - Leonardite humic acid
Results
Leonardite humic acid/air partition coefficient, KHA,air = 2.03E3 - 2.99E3 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 5
Type (Transport and Distribution)
sorption
Media (Transport and Distribution)
air - Leonardite humic acid
Results
experimental sorption enthalpy, ΔabsHi = -45.6 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 5
Type (Transport and Distribution)
partition
Media (Transport and Distribution)
air - Leonardite humic acid
Results
Leonardite humic acid/air partition coefficient, KHA,air = 6.11E2 - 3.73E3 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)
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; 5-75 deg C; temperature dependence of partition equilibrium studied
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 5
Type (Transport and Distribution)
partition
Media (Transport and Distribution)
air-water
Results
air-water partition coefficient Kaw=2.5E-3
Method, Remarks (Transport and Distribution)
static headspace GC method
Welke, Birgit; Ettlinger, Karin; Riederer, Markus; Environmental Science and Technology; vol. 32; nb. 8; (1998); p. 1099 - 1104, View in Reaxys 5 of 5
Type (Transport and Distribution)
partition
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Media (Transport and Distribution)
air-cuticular matrix membranes of tomato fruit
Results
air-cuticular matrix membranes partition coefficient KMXa=2500
Method, Remarks (Transport and Distribution)
cuticular membranes isol. from mature tomato fruits (Lycopersicon esculentum Mill. cultivar Vendor); static headspace GC method; glass vials; 25 deg C; 3 h; exper. with relat. humid. 26-76 percent also
Welke, Birgit; Ettlinger, Karin; Riederer, Markus; Environmental Science and Technology; vol. 32; nb. 8; (1998); p. 1099 - 1104, View in Reaxys Use (3) Use Pattern
References
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Reaction modifier
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Polar aprotic solvent for preparation of silane esters
Patent; Xerox Corporation; US2006/122414; (2006); (A1) English, View in Reaxys; Patent; Xerox Corporation; EP1669362; (2006); (A1) English, View in Reaxys
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