2-Phenylpropan-2-ol by Asch

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37 substances in Reaxys

2016-05-12 15h:55m:27s (EST)

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2016-05-12 15h:57m:46s (EST)

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Reaxys ID 1905012 View in Reaxys

1/1 CAS Registry Number: 617-94-7 Chemical Name: 1-methyl-1-phenylethyl alcohol; 2-Phenyl-2propanol Linear Structure Formula: HOC(CH3)2C6H5 Molecular Formula: C9H12O Molecular Weight: 136.194 Type of Substance: isocyclic InChI Key: BDCFWIDZNLCTMF-UHFFFAOYSA-N Note:

Substance Label (78) Label References 1b

Nishino, Toshiki; Nishiyama, Yutaka; Sonoda, Noboru; Tetrahedron Letters; vol. 43; nb. 20; (2002); p. 3689 - 3691, View in Reaxys; Nishino, Toshiki; Nishiyama, Yutaka; Sonoda, Noboru; Bulletin of the Chemical Society of Japan; vol. 76; nb. 3; (2003); p. 635 - 641, View in Reaxys; Mochalov; Fedotov; Trofimova; Zefirov; Russian Journal of Organic Chemistry; vol. 51; nb. 9; (2015); p. 1217 - 1231; Zh. Org. Khim.; vol. 51; nb. 9; (2015); p. 1241 - 1255,15, View in Reaxys

Shirakawa, Eiji; Hironaka, Koji; Otsuka, Hidehito; Hayashi, Tamio; Chemical Communications; nb. 37; (2006); p. 3927 - 3929, View in Reaxys; Shao, Xinxin; Xu, Chunfa; Lu, Long; Shen, Qilong; Journal of Organic Chemistry; vol. 80; nb. 6; (2015); p. 3012 - 3021, View in Reaxys; Aoyama, Tadashi; Furukawa, Takuya; Hayakawa, Mamiko; Takido, Toshio; Kodomari, Mitsuo; Synlett; vol. 26; nb. 13; (2015); p. 1875 1879; Art.No: ST-2015-U0226-L, View in Reaxys

Baati; Valleix; Mioskowski; Barma; Falck; Organic letters; vol. 2; nb. 4; (2000); p. 485 - 487, View in Reaxys; Klimova; Berestneva, T. Klimova; Mendoza, J. M. Martinez; Stivalet, J. M. Mendez; Toscano; Garcia, M. Martinez; Synthetic Communications; vol. 38; nb. 14; (2008); p. 2299 - 2315, View in Reaxys; Durn-Pea, Mara Jess; Botubol-Ares, Jos Manuel; Hanson, James R.; Hernndez-Galn, Rosario; Collado, Isidro G.; European Journal of Organic Chemistry; vol. 2015; nb. 28; (2015); p. 6333 6340, View in Reaxys

Tummatorn, Jumreang; Thongsornkleeb, Charnsak; Ruchirawat, Somsak; Thongaram, Phanida; Kaewmee, Benyapa; Synthesis (Germany); vol. 46; nb. 11; (2015); Art.No: SS-2014-Z0553-PSP, View in Reaxys; Tummatorn, Jumreang; Thongsornkleeb, Charnsak; Ruchirawat, Somsak; Thongaram, Phanida; Kaewmee, Benyapa; Synthesis (Germany); vol. 47; nb. 3; (2015); p. 323 - 329; Art.No: SS-2014Z0553-PSP, View in Reaxys

2-Ph-2-PrOH

Li, Jian-Yuan; Kim, Hun Young; Oh, Kyungsoo; Organic Letters; vol. 17; nb. 5; (2015); p. 1288 - 1291, View in Reaxys

Nishiguchi, Ikuzo; Kita, Yoshio; Watanabe, Masamitsu; Ishino, Yoshio; Ohno, Toshinobu; Maekawa, Hirofumi; Synlett; nb. 7; (2000); p. 1025 - 1027, View in Reaxys; Terao, Yoshito; Wakui, Hiroyuki; Nomoto, Michiyo; Satoh, Tetsuya; Miura, Masahiro; Nomura, Masakatsu; Journal of Organic Chemistry; vol. 68; nb. 13; (2003); p. 5236 - 5243, View in Reaxys; Das, Debjit; Roy, Sujit; Advanced Synthesis and Catalysis; vol. 355; nb. 7; (2013); p. 1308 - 1314, View in Reaxys; Nakanowatari, Sachiyo; Ackermann, Lutz; Chemistry - A European Journal; vol. 20; nb. 18; (2014); p. 5409 - 5413, View in Reaxys

Thomas; Asokan; Journal of the Chemical Society. Perkin Transactions 1; nb. 20; (2001); p. 2583 - 2587, View in Reaxys; Fukui, Miho; Hoshino, Yuki; Satoh, Tetsuya; Miura, Masahiro; Tanaka, Ken; Advanced Synthesis and Catalysis; vol. 356; nb. 7; (2014); p. 1638 - 1644, View in Reaxys

Liao, Shixia; Peng, Feng; Yu, Hao; Wang, Hongjuan; Applied Catalysis A: General; vol. 478; (2014); p. 1 8, View in Reaxys

7'''

Crespi, Stefano; Ravelli, Davide; Protti, Stefano; Albini, Angelo; Fagnoni, Maurizio; Chemistry - A European Journal; vol. 20; nb. 52; (2014); p. 17572 - 17578, View in Reaxys

Kataoka, Yasutaka; Makihira, Isamu; Utsunomiya, Masaru; Tani, Kazuhide; Journal of Organic Chemistry; vol. 62; nb. 24; (1997); p. 8540 - 8543, View in Reaxys; Yu, Jun-Lai; Wang, Hui; Zou, Kai-Feng; Zhang, Jia-Rui; Gao, Xiang; Zhang, Dan-Wei; Li, Zhan-Ting; Tetrahedron; vol. 69; nb. 1; (2013); p. 310 - 315, View in Reaxys

Zawadiak, Jan; Gilner, Danuta; Mazurkiewicz, Roman; Tetrahedron Letters; vol. 40; nb. 21; (1999); p. 4059 - 4062, View in Reaxys; Sawadjoon, Supaporn; Lundstedt, Anna; Samec, Joseph S.M.; ACS Catalysis; vol. 3; nb. 4; (2013); p. 635 - 642, View in Reaxys

Fernandez Gonzalez, Davinia; Brand, Jonathan P.; Mondiere, Regis; Waser, Jerome; Advanced Synthesis and Catalysis; vol. 355; nb. 8; (2013); p. 1631 - 1639, View in Reaxys

Geer, Michael F.; Walla, Michael D.; Solntsev, Kyril M.; Strassert, Cristian A.; Shimizu, Linda S.; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5568 - 5578, View in Reaxys

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Teranishi, Satoru; Kurahashi, Takuya; Matsubara, Seijiro; Synlett; vol. 24; nb. 16; (2013); p. 2148 - 2152; Art.No: ST-2013-U0620-L, View in Reaxys

Creary, Xavier; Willis, Elizabeth D.; Gagnon, Madeleine; Journal of the American Chemical Society; vol. 127; nb. 51; (2005); p. 18114 - 18120, View in Reaxys; Fujii, Hideaki; Yamada, Takaaki; Hayashida, Kohei; Kuwada, Miki; Hamasaki, Atom; Nobuhara, Kazunori; Ozeki, Sumio; Nagase, Hiroshi; Heterocycles; vol. 85; nb. 11; (2012); p. 2685 - 2691, View in Reaxys

Sereda, Grigoriy; Rajpara, Vikul; Tetrahedron Letters; vol. 48; nb. 19; (2007); p. 3417 - 3421, View in Reaxys; Gryparis, Charis; Stratakis, Manolis; Chemical Communications (Cambridge, United Kingdom); vol. 48; nb. 87; (2012); p. 10751 - 10753,3, View in Reaxys

Baldwin, Neil J.; Nord, Anna N.; O'Donnell, Brendan D.; Mohan, Ram S.; Tetrahedron Letters; vol. 53; nb. 51; (2012); p. 6946 - 6949, View in Reaxys

DMPC

Gagarin; Mamedov; Kharlampidi; Petroleum Chemistry; vol. 42; nb. 3; (2002); p. 187 - 191, View in Reaxys; Skorokhodova; Kobotaeva; Sirotkina; Russian Journal of Applied Chemistry; vol. 78; nb. 5; (2005); p. 753 - 757, View in Reaxys; Baj, Stefan; Chrobok, Anna; International Journal of Chemical Kinetics; vol. 40; nb. 6; (2008); p. 287 - 293, View in Reaxys

Yasuda, Makoto; Yamasaki, Satoshi; Onishi, Yoshiyuki; Baba, Akio; Journal of the American Chemical Society; vol. 126; nb. 23; (2004); p. 7186 - 7187, View in Reaxys; Jadhav, Vrushali H.; Kumar, K. S. Ajish; Chaudhari, Vinod D.; Dhavale, Dilip D.; Synthetic Communications; vol. 37; nb. 8; (2007); p. 1363 - 1370, View in Reaxys; Bhati, Nishi; Sarma, Kuladip; Goswami, Amrit; Chemistry Letters; vol. 37; nb. 5; (2008); p. 496 - 497, View in Reaxys

(+/-)-18a

Machado, Luciana L.; Lemos, Telma L.G.; de Mattos, Marcos Carlos; de Oliveira, Maria da Conceicao F.; de Gonzalo, Gonzalo; Gotor-Fernandez, Vicente; Gotor, Vicente; Tetrahedron Asymmetry; vol. 19; nb. 12; (2008); p. 1418 - 1423, View in Reaxys

Saito, Takahiro; Nishimoto, Yoshihiro; Yasuda, Makoto; Baba, Akio; Journal of Organic Chemistry; vol. 71; nb. 22; (2006); p. 8516 - 8522, View in Reaxys; Baciocchi, Enrico; Del Giacco, Tiziana; Lanzalunga, Osvaldo; Mencarelli, Paolo; Procacci, Barbara; Journal of Organic Chemistry; vol. 73; nb. 15; (2008); p. 5675 - 5682, View in Reaxys

Tab 3, B, entry 1

Miyoshi, Norikazu; Matsuo, Tsuyoshi; Asaoka, Masashi; Matsui, Aki; Wada, Makoto; Chemistry Letters; vol. 36; nb. 1; (2007); p. 28 - 29, View in Reaxys

Table 2, entry 13

Dalpozzo, Renato; De Nino, Antonio; Maiuolo, Loredana; Oliverio, Manuela; Procopio, Antonio; Russo, Beatrice; Tocci, Amedeo; Australian Journal of Chemistry; vol. 60; nb. 1; (2007); p. 75 - 79, View in Reaxys

Hartung, Jens; Schneiders, Nina; Gottwald, Thomas; Tetrahedron Letters; vol. 48; nb. 34; (2007); p. 6027 - 6030, View in Reaxys

Maurya, Mannar R.; Kumar, Umesh; Manikandan; European Journal of Inorganic Chemistry; nb. 16; (2007); p. 2303 - 2314, View in Reaxys

Jana, Umasish; Maiti, Sukhendu; Biswas, Srijit; Tetrahedron Letters; vol. 48; nb. 40; (2007); p. 7160 7163, View in Reaxys

Sanz, Roberto; Martinez, Alberto; Guilarte, Veronica; Alvarez-Gutierrez, Julia M.; Rodriguez, Felix; European Journal of Organic Chemistry; nb. 28; (2007); p. 4642 - 4645, View in Reaxys

E7, alcohol

Das, Biswanath; Krishnaiah, Maddeboina; Reddy, Vtukuri Saidi; Laxminarayana, Keetha; Helvetica Chimica Acta; vol. 90; nb. 11; (2007); p. 2163 - 2166, View in Reaxys

15d

Ikeda, Hiroshi; Hoshi, Yosuke; Namai, Hayato; Tanaka, Futoshi; Goodman, Joshua L.; Mizuno, Kazuhiko; Chemistry - A European Journal; vol. 13; nb. 33; (2007); p. 9207 - 9215, View in Reaxys

Saito, Takahiro; Yasuda, Makoto; Baba, Akio; Synlett; nb. 11; (2005); p. 1737 - 1739; Art.No: U10305ST, View in Reaxys; Mukaiyama, Teruaki; Sakurai, Naoto; Ikegai, Kazuhiro; Chemistry Letters; vol. 35; nb. 10; (2006); p. 1140 - 1141, View in Reaxys

Poon, Kevin W. C.; Dudley, Gregory B.; Journal of Organic Chemistry; vol. 71; nb. 10; (2006); p. 3923 3927, View in Reaxys

Substrate,Tab.3, run 13

Pluempanupat, Wanchai; Chavasiri, Warinthorn; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6821 6823, View in Reaxys

Lomas, John S.; Adenier, Alain; Cordier, Christine; Journal of Physical Organic Chemistry; vol. 19; nb. 5; (2006); p. 295 - 307, View in Reaxys; Falck; Li, De Run; Bejot, Romain; Mioskowski, Charles; Tetrahedron Letters; vol. 47; nb. 29; (2006); p. 5111 - 5113, View in Reaxys

33a

Masutani, Kouta; Minowa, Tomofumi; Hagiwara, Yoshiaki; Mukaiyama, Teruaki; Bulletin of the Chemical Society of Japan; vol. 79; nb. 7; (2006); p. 1106 - 1117, View in Reaxys

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Stavber, Gaj; Zupan, Marko; Stavber, Stojan; Tetrahedron Letters; vol. 47; nb. 48; (2006); p. 8463 - 8466, View in Reaxys

Lykakis, Ioannis N.; Orfanopoulos, Michael; Tetrahedron Letters; vol. 45; nb. 41; (2004); p. 7645 - 7649, View in Reaxys; Baciocchi, Enrico; Del Giacco, Tiziana; Giombolini, Paolo; Lanzalunga, Osvaldo; Tetrahedron; vol. 62; nb. 27; (2006); p. 6566 - 6573, View in Reaxys

Miyake, Hideyoshi; Nakao, Yuichi; Sasaki, Mitsuru; Chemistry Letters; vol. 35; nb. 11; (2006); p. 1262 1263, View in Reaxys

Theyssen, Nils; Hou, Zhenshan; Leitner, Walter; Chemistry - A European Journal; vol. 12; nb. 12; (2006); p. 3401 - 3409, View in Reaxys

Fischer, Christian B.; Xu, Shangjie; Zipse, Hendrik; Chemistry - A European Journal; vol. 12; nb. 22; (2006); p. 5779 - 5784, View in Reaxys

10, Table 4, entry 1

Hatano, Manabu; Matsumura, Tokihiko; Ishihara, Kazuaki; Organic Letters; vol. 7; nb. 4; (2005); p. 573 576, View in Reaxys

tert-alcohol to 1e

Ikegai, Kazuhiro; Pluempanupat, Wanchai; Mukaiyama, Teruaki; Chemistry Letters; vol. 34; nb. 5; (2005); p. 638 - 639, View in Reaxys

AH, Tab.1, run 8

Sherman, Daniel; Shelkov, Rimma; Melman, Artem; Tetrahedron Letters; vol. 46; nb. 29; (2005); p. 4901 4903, View in Reaxys

alcohol from cumene

Zhang, Rui; Yu, Wing-Yiu; Che, Chi-Ming; Tetrahedron Asymmetry; vol. 16; nb. 21; (2005); p. 3520 - 3526, View in Reaxys

Wu, Jin-Ming; Kunikawa, Shigeki; Tokuyasu, Takahiro; Masuyama, Araki; Nojima, Masatomo; Kim, Hye-Sook; Wataya, Yusuke; Tetrahedron; vol. 61; nb. 42; (2005); p. 9961 - 9968, View in Reaxys

tab5, alcohol, entry3

De, Surya K.; Gibbs, Richard A.; Tetrahedron Letters; vol. 46; nb. 48; (2005); p. 8345 - 8350, View in Reaxys

Yasuda, Makoto; Saito, Takahiro; Ueba, Masako; Baba, Akio; Angewandte Chemie - International Edition; vol. 43; nb. 11; (2004); p. 1414 - 1416, View in Reaxys

Table 1, entry 24

Habibi, Mohammad H.; Farhadi, Saeid; Journal of Chemical Research; nb. 4; (2004); p. 296 - 297, View in Reaxys

alc., Tab. 2, entry 4

Hamada, Nao; Sato, Tsuneo; Synlett; nb. 10; (2004); p. 1802 - 1804, View in Reaxys

Tab. 2, entry 28

Procopio, Antonio; Dalpozzo, Renato; De Nino, Antonio; Maiuolo, Loredana; Russo, Beatrice; Sindona, Giovanni; Advanced Synthesis and Catalysis; vol. 346; nb. 12; (2004); p. 1465 - 1470, View in Reaxys

entry 18, educt

Bosco, J. W. John; Raju, B. Rama; Saikia, Anil K.; Synthetic Communications; vol. 34; nb. 15; (2004); p. 2849 - 2855, View in Reaxys

alcohol for XVI

Petkevich; Dikusar; Potkin; Kaberdin; Moiseichuk; Yuvchenko; Kurman; Russian Journal of General Chemistry; vol. 74; nb. 4; (2004); p. 586 - 593, View in Reaxys

Substrate, Tab. 1,run 10

Tamami, Bahman; Parvanak Borujeny, Kaveh; Tetrahedron Letters; vol. 45; nb. 4; (2004); p. 715 - 718, View in Reaxys

PhCMe2OH

Galli, Carlo; Gentili, Patrizia; Lanzalunga, Osvaldo; Lucarini, Marco; Pedulli, Gian Franco; Chemical Communications; nb. 20; (2004); p. 2356 - 2357, View in Reaxys

PhC(CH3)2OH

Mukaiyama, Teruaki; Kikuchi, Wataru; Shintou, Taichi; Chemistry Letters; vol. 32; nb. 3; (2003); p. 300 301, View in Reaxys

Font-Sanchis, Enrique; Aliaga, Carolina; Cornejo, Raecca; Scaiano; Organic Letters; vol. 5; nb. 9; (2003); p. 1515 - 1518, View in Reaxys

1a (tab1 run1)

Nishino, Toshiki; Nishiyama, Yutaka; Sonoda, Noboru; Chemistry Letters; vol. 32; nb. 10; (2003); p. 918 919, View in Reaxys

tab. 3, entry 18

Shintou, Taichi; Mukaiyama, Teruaki; Chemistry Letters; vol. 32; nb. 11; (2003); p. 984 - 985, View in Reaxys

Firouzabadi, Habib; Iranpoor, Naser; Hazarkhani, Hassan; Karimi, Babak; Synthetic Communications; vol. 33; nb. 21; (2003); p. 3653 - 3660, View in Reaxys

19a

Shintou, Taichi; Kikuchi, Wataru; Mukaiyama, Teruaki; Bulletin of the Chemical Society of Japan; vol. 76; nb. 8; (2003); p. 1645 - 1667, View in Reaxys

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Fukuda, Osamu; Sakaguchi, Satoshi; Ishii, Yasutaka; Advanced Synthesis and Catalysis; vol. 343; nb. 8; (2001); p. 809 - 813, View in Reaxys; Kamigaito, Masami; Nakashima, Junko; Satoh, Kotaro; Sawamoto, Mitsuo; Macromolecules; vol. 36; nb. 10; (2003); p. 3540 - 3544, View in Reaxys

R2OH, Table 1, entry 4

Kobayashi, Shu; Iimura, Shinya; Manabe, Kei; Chemistry Letters; nb. 1; (2002); p. 10 - 11, View in Reaxys

Van Stee; Leonards; Van Loon; Jan Hendriks; Struijs; Brinkman; Maas; Water Research; vol. 36; nb. 18; (2002); p. 4455 - 4470, View in Reaxys

Liang, Xifu; Bols, Mikael; Journal of the Chemical Society. Perkin Transactions 1; nb. 4; (2002); p. 503 508, View in Reaxys

Nishiwaki, Yoshiki; Sakaguchi, Satoshi; Ishii, Yasutaka; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5663 - 5668, View in Reaxys

Vedejs, Edwin; Daugulis, Olafs; Journal of Organic Chemistry; vol. 61; nb. 17; (1996); p. 5702 - 5703, View in Reaxys; Tokuyasu, Takahiro; Kunikawa, Shigeki; Masuyama, Araki; Nojima, Masatomo; Organic Letters; vol. 4; nb. 21; (2002); p. 3595 - 3598, View in Reaxys

Sawada, Daisuke; Ito, Yukishige; Tetrahedron Letters; vol. 42; nb. 13; (2001); p. 2501 - 2504, View in Reaxys

Terao; Wakui; Satoh; Miura; Nomura; Journal of the American Chemical Society; vol. 123; nb. 42; (2001); p. 10407 - 10408, View in Reaxys

Maksyuta; Suprun; Opeida; Turovskii; Russian Journal of Organic Chemistry; vol. 37; nb. 6; (2001); p. 814 - 818, View in Reaxys

DMBA

Steenken, Steen; Ramaraj, Ramasamy; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2001); p. 1613 - 1619, View in Reaxys

Pp-OH

Boyer, Bernard; Keramane, El-Mehdi; Roque, Jean-Pierre; Pavia, Andre A.; Tetrahedron Letters; vol. 41; nb. 16; (2000); p. 2891 - 2894, View in Reaxys

Grossi, Loris; Strazzari, Samantha; Journal of Organic Chemistry; vol. 65; nb. 9; (2000); p. 2748 - 2754, View in Reaxys

substrate,t.1,entry Dailey, Jennifer I.; Hays, Ryan S.; Lee, Hua; Mitchell, Randall M.; Ries, Jennifer J.; Landolt, Robert G.; 1 Husmann, Hollie H.; Lockridge, Joseph B.; Hendrickson, William H.; Journal of Organic Chemistry; vol. 65; nb. 8; (2000); p. 2568 - 2571, View in Reaxys PhC(Me)2OH

Zhulin; Lipovich; Antonovskii; Russian Journal of Physical Chemistry A; vol. 73; nb. 6; (1999); p. 883 888, View in Reaxys

XXIV

Fomenko; Korchagina; Yarovaya; Gatilov; Salakhutdinov; Ione; Barkhash; Russian Journal of Organic Chemistry; vol. 35; nb. 7; (1999); p. 1006 - 1017, View in Reaxys

ref. 12

Metallinos, Costa; Nerdinger, Sven; Snieckus, Victor; Organic Letters; vol. 1; nb. 8; (1999); p. 1183 1186, View in Reaxys

AAOL

Baldasano, Jose M.; Delgado, Rosa; Calbo, Josep; Environmental Science and Technology; vol. 32; nb. 3; (1998); p. 405 - 412, View in Reaxys

Dolenc, Darko; Plesnicar, Bozo; Journal of the American Chemical Society; vol. 119; nb. 11; (1997); p. 2628 - 2632, View in Reaxys

CumOH

Kazakov; Kabal'nova; Khursan; Shereshovets; Russian Chemical Bulletin; vol. 46; nb. 4; (1997); p. 663 671, View in Reaxys

Patent-Specific Data (5) Prophetic ComLocation in Patent References pound Page/Page column

Patent; Rohm and Haas Electronic Materials LLC; Cameron, James F.; Jain, Vipul; LaBeaume, Paul J.; Sung, Jin Wuk; Thackeray, James W.; US8945814; (2015); (B2) English, View in Reaxys Patent; Pfizer Inc; US2009/170886; (2009); (A1) English, View in Reaxys Patent; SHELL OIL COMPANY; WO2005/5350; (2005); (A2) English, View in Reaxys Patent; Daicel Chemical Industries, Ltd.; EP1413568; (2004); (A2) English, View in Reaxys

prophetic product

Patent; International Flavors and Fragrances Inc.; US4092333; (1978); (A1) English, View in Reaxys; Patent; The Goodyear Tire and Rubber Company; US4143076;

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(1979); (A1) English, View in Reaxys; Patent; International Flavors and Fragrances Inc.; US4096158; (1978); (A1) English, View in Reaxys Derivative (6) Comment (Derivative) p-Nitrobenzoat : F=133-134grad

References Brown; Peters; Journal of the American Chemical Society; vol. 99; (1977); p. 1712, View in Reaxys

Komplex mit Egorov et al.; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 169,173; ; p. 203, View in Reaxys CH3CN: IR (OHBande), Absorptionskoeffizient, Halbwertsbreite; Gleichgewichtskonstante; Bindungsenthalpie Alkohol-CH3CN; Dipolmoment; dielektrische Permeabilitaet phenyl urethane: F: 113grad

Choe; Tsutsumi; Nippon Kagaku Zasshi; vol. 81; (1960); p. 586,588; Chem.Abstr.; vol. 56; nb. 397; (1962), View in Reaxys

Phenylurethan C16H17NO2 F: 110-111grad

Maruyama et al.; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1883; Chem.Abstr.; vol. 56; nb. 3385; (1962), View in Reaxys

<α.α-DimethylKharasch,M.S. et al.; Journal of Organic Chemistry; vol. 25; (1960); p. 1000 - 1006, View in Reaxys benzylmercapto>essigsaeure: F: 69-70grad 4-nitro-benzoyl derivative (mp: 134-135 degree )

Braude; Timmons; Journal of the Chemical Society; (1950); p. 2000,2006, View in Reaxys

Melting Point (19) 1 of 19

Melting Point [°C]

32 - 34

Klimova; Berestneva, T. Klimova; Mendoza, J. M. Martinez; Stivalet, J. M. Mendez; Toscano; Garcia, M. Martinez; Synthetic Communications; vol. 38; nb. 14; (2008); p. 2299 - 2315, View in Reaxys 2 of 19

Melting Point [°C]

30 - 31

Bors, Daniel A.; Kaufman, Michael J.; Streitwieser, Andrew Jr.; Journal of the American Chemical Society; vol. 107; nb. 24; (1985); p. 6975 - 6982, View in Reaxys 3 of 19

Melting Point [°C]

Amelichev, V. A.; Saidov, G. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 1; (1981); p. 187 - 192,164 - 168, View in Reaxys 4 of 19

Melting Point [°C]

36 - 37

Stepovik; Khamylova; J. Gen. Chem. USSR (Engl. Transl.); vol. 45; (1975); p. 61,54, View in Reaxys 5 of 19

Melting Point [°C]

Dierichs; Preu; Chemische Berichte; vol. 90; (1957); p. 1208,1213, View in Reaxys; Kharasch et al.; Journal of Organic Chemistry; vol. 15; (1950); p. 775,778; Journal of Organic Chemistry; vol. 16; (1951); p. 1458,1465, View in Reaxys; Kropf et al.; Justus Liebigs Annalen der Chemie; (1974); p. 1013, View in Reaxys 6 of 19

Melting Point [°C]

30 - 32

Hadley; Halsall; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1974); p. 1334,1345, View in Reaxys 7 of 19

Melting Point [°C]

Humphris; Scott; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 831,834, View in Reaxys 8 of 19

Melting Point [°C]

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Terent'ew et al.; Neftekhimiya; vol. 1; (1962); p. 567,462, View in Reaxys; Sokolov et al.; Zhurnal Organicheskoi Khimii; vol. 8; (1972); p. 751,760, View in Reaxys 9 of 19

Melting Point [°C]

31 - 32

Solvent (Melting Point)

heptane

Kulicki; Stec; Roczniki Chemii; vol. 45; (1971); p. 601,602, View in Reaxys 10 of 19

Melting Point [°C]

35 - 37

Matsubara; Perkin; Journal of the Chemical Society; vol. 87; (1905); p. 671, View in Reaxys; Hala; Chemicky Prumysl; vol. 18; (1968); p. 412; Chem.Abstr.; vol. 69; nb. 83193; (1968), View in Reaxys 11 of 19

Melting Point [°C]

Kulicki; et al.; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 39; (1967); p. 67,71, View in Reaxys 12 of 19

Melting Point [°C]

Patent; Badische Anilin- und Soda-Fabrik A.G.; DE1275041; (1966); Chem.Abstr.; vol. 69; nb. 96208x; (1968), View in Reaxys 13 of 19

Melting Point [°C]

31 - 32

Solvent (Melting Point)

petroleum ether

Verkade,P.E. et al.; Recueil des Travaux Chimiques des Pays-Bas; vol. 82; (1963); p. 637 - 650, View in Reaxys; Alagy et al.; Bulletin de la Societe Chimique de France; (1961); p. 1309, View in Reaxys 14 of 19

Melting Point [°C]

Traynelis,V.J. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 2377 - 2383, View in Reaxys 15 of 19

Melting Point [°C]

25 - 27

Maruyama et al.; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1883; Chem.Abstr.; vol. 56; nb. 3385; (1962), View in Reaxys 16 of 19

Melting Point [°C]

34 - 35

Solvent (Melting Point)

petroleum ether

Armstrong et al.; Journal of the Chemical Society; (1950); p. 666,670, View in Reaxys 17 of 19

Melting Point [°C]

31.56

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 18 of 19

Melting Point [°C]

29 - 30

Kharasch; Cooper; Journal of Organic Chemistry; vol. 10; (1945); p. 46,48, View in Reaxys 19 of 19

Melting Point [°C]

Grignard; Annales de Chimie (Cachan, France); vol. <7> 24; (1901); p. 468; Chem. Zentralbl.; vol. 72; nb. II; (1901); p. 623, View in Reaxys; Grignard; Chem. Zentralbl.; vol. 72; nb. II; (1901); p. 623, View in Reaxys; Tissier; Grignard; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 132; (1901); p. 685, View in Reaxys Boiling Point (49) Boiling Point [°C] Pressure (Boiling Point) [Torr] 67 - 68

Comment (Boiling References Point)

0.2

202

Taha, Ahmed A.; International Journal of Chemical Kinetics; vol. 44; nb. 8; (2012); p. 514 - 523, View in Reaxys Klages; Chemische Berichte; vol. 35; (1902); p. 2649; Chemische Berichte; vol. 39; (1906); p. 2591, View in Reaxys; Patent; SUMITOMO CHEMICAL COMPANY, LIMITED; WO2008/123384; (2008); (A1) English, View in Reaxys

201

760.051

Patent; SHELL OIL COMPANY; WO2005/5350; (2005); (A2) English, View in Reaxys

0.9

Gurudutt, K. N.; Rao, L. Jagan Mohan; Rao, Sanjay; Srinivas, P.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 32; nb. 4; (1993); p. 468 - 470, View in Reaxys

7/45

2016-05-12 16:03:43

124.15

Karaseva, N. V.; Karavaeva, A. P.; Antonova, T. N.; Chabutkina, E. M.; Koshel, G. N.; J. Appl. Chem. USSR (Engl. Transl.); vol. 64; nb. 7.1; (1991); p. 1486 - 1489,1339 - 1342, View in Reaxys

Fomin et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 76,76,78, View in Reaxys; Fomin, V. A.; Ovchinnikova, Yu. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 2; (1987); p. 452 456,393 - 397, View in Reaxys

Bors, Daniel A.; Kaufman, Michael J.; Streitwieser, Andrew Jr.; Journal of the American Chemical Society; vol. 107; nb. 24; (1985); p. 6975 - 6982, View in Reaxys

68 - 70

0.3

Villenave, J. J.; Filliatre, C.; Maillard, B.; Jaouhari, R.; Bulletin des Societes Chimiques Belges; vol. 91; nb. 4; (1982); p. 301 - 310, View in Reaxys

Amelichev, V. A.; Saidov, G. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 1; (1981); p. 187 - 192,164 - 168, View in Reaxys

Kelly,D.P.; Spear,R.J.; Australian Journal of Chemistry; vol. 31; (1978); p. 1209 - 1221, View in Reaxys

Hock; Lang; Chemische Berichte; vol. 77/79; (1944); p. 257,262, View in Reaxys; Brown; Peters; Journal of the American Chemical Society; vol. 99; (1977); p. 1712, View in Reaxys

Mayeda; Journal of the American Chemical Society; vol. 97; (1975); p. 4012,4013, View in Reaxys

87 - 92

Sternerup; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 28; (1974); p. 579, View in Reaxys

88 - 89

Hadley; Halsall; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1974); p. 1334,1345, View in Reaxys

93 - 94

Walling,C.; Padwa,A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1593 - 1597, View in Reaxys; Klages; Chemische Berichte; vol. 35; (1902); p. 2649; Chemische Berichte; vol. 39; (1906); p. 2591, View in Reaxys; Chalezki; Zhurnal Obshchei Khimii; vol. 15; (1945); p. 524,525; Chem.Abstr.; (1946); p. 4696, View in Reaxys; Humphris; Scott; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 831,834, View in Reaxys

Duismann,W.; Ruechardt,C.; Chemische Berichte; vol. 106; (1973); p. 1083 - 1098, View in Reaxys

94.8 - 95.3

Takeda et al.; Nippon Kagaku Kaishi; (1972); p. 213, View in Reaxys

62 - 64

Wang,C.H.; Kingsbury,C.A.; Journal of Organic Chemistry; vol. 37; nb. 15; (1972); p. 2489 - 2494, View in Reaxys

88 - 91

Burghardt et al.; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 60; (1972); p. 3,4-7,9,10,12-17, View in Reaxys

Baliah,V.; Nadar,P.A.; Indian Journal of Chemistry; vol. 9; (1971); p. 1339 - 1341, View in Reaxys

60 - 65

Jones,L.B.; Foster,J.P.; Journal of Organic Chemistry; vol. 35; (1970); p. 1777 - 1781, View in Reaxys

Olah,G.A. et al.; Journal of the American Chemical Society; vol. 91; nb. 6; (1969); p. 1458 - 1469, View in Reaxys

218

760

Hala; Chemicky Prumysl; vol. 18; (1968); p. 412; Chem.Abstr.; vol. 69; nb. 83193; (1968), View in Reaxys

Tuzun; Yukseksik; Communications de la Faculte des Sciences de l'Universite d'Ankara, Serie B: Chimie; vol. 14; nb. 3; (1967); p. 34,35-52; Chem.Abstr.; vol. 70; nb. 67787a; (1969), View in Reaxys

98.1

760

Lesteva,T.M. et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 40; (1967); p. 1808 - 1814,1738 - 1743, View in Reaxys

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2016-05-12 16:03:43

74.5

5-6

Lesteva,T.M. et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 40; (1967); p. 1808 - 1814,1738 - 1743, View in Reaxys

0.4

Neumann et al.; Chemische Berichte; vol. 100; (1967); p. 1063, View in Reaxys

58 - 59

Koyama,K. et al.; Tetrahedron; vol. 23; (1967); p. 2665 - 2674, View in Reaxys

0.1

Patent; Badische Anilin- und Soda-Fabrik A.G.; DE1275041; (1966); Chem.Abstr.; vol. 69; nb. 96208x; (1968), View in Reaxys

83 - 84

Macdonald; Shannon; Australian Journal of Chemistry; vol. 18; (1965); p. 1009,1014, 1015, View in Reaxys

Pines; Schappell; Journal of Organic Chemistry; vol. 29; (1964); p. 1503,1507, View in Reaxys

98 - 106

Traynelis,V.J. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 2377 - 2383, View in Reaxys

74 - 75

Ishii et al.; Kogyo Kagaku Zasshi; vol. 64; (1961); p. 472; Chem.Abstr.; vol. 57; nb. 7149, View in Reaxys

Patent; Koninklijke Industrieele Maatschappij vorheen Noury + van der Lande, N.V.; BE613440; (1961); Chem.Abstr.; vol. 58; nb. 1402b; (1963), View in Reaxys

64 - 65

Alagy et al.; Bulletin de la Societe Chimique de France; (1961); p. 1309, View in Reaxys

Choe; Tsutsumi; Nippon Kagaku Zasshi; vol. 81; (1960); p. 586,588; Chem.Abstr.; vol. 56; nb. 397; (1962), View in Reaxys

71 - 72

Maruyama et al.; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1883; Chem.Abstr.; vol. 56; nb. 3385; (1962), View in Reaxys

69 - 72

Denney; Denney; Journal of the American Chemical Society; vol. 82; (1960); p. 1389,1393, View in Reaxys

74 - 90

Denney; Denney; Journal of the American Chemical Society; vol. 82; (1960); p. 1389,1393, View in Reaxys

Grace; Symons; Journal of the Chemical Society; (1959); p. 958,960, View in Reaxys

100

Ito; Tokutake; Takamine Kenkyusho Nenpo; vol. 8; (1956); p. 47,50; Chem.Abstr.; (1958); p. 397, View in Reaxys

192.63

760

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

118.68 - 143.52

47.2 - 123.8

Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2879, View in Reaxys

Petrow; Kaplan; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1947); p. 295,303; Chem.Abstr.; (1949); p. 1718, View in Reaxys

114 - 115

Matsubara; Perkin; Journal of the Chemical Society; vol. 87; (1905); p. 671, View in Reaxys

86 - 88

Boedtker; Bulletin de la Societe Chimique de France; vol. <3> 25; (1901); p. 851, View in Reaxys

89 - 90

Tissier; Grignard; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 132; (1901); p. 685, View in Reaxys

215 - 220

Decomposition.

Boedtker; Bulletin de la Societe Chimique de France; vol. <3> 25; (1901); p. 851, View in Reaxys

Refractive Index (21)

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Refractive Index

Wavelength (Refractive Index) [nm]

Temperature (Refractive Index) [°C]

References

1.5316

589

1.9

Fomin, V. A.; Ovchinnikova, Yu. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 2; (1987); p. 452 - 456,393 - 397, View in Reaxys

1.531

589

Villenave, J. J.; Filliatre, C.; Maillard, B.; Jaouhari, R.; Bulletin des Societes Chimiques Belges; vol. 91; nb. 4; (1982); p. 301 - 310, View in Reaxys

1.5315

589

Amelichev, V. A.; Saidov, G. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 1; (1981); p. 187 - 192,164 - 168, View in Reaxys

1.51159

589

House,H.O. et al.; Journal of Organic Chemistry; vol. 41; nb. 19; (1976); p. 3067 - 3076, View in Reaxys

1.5138

589

Burghardt et al.; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 60; (1972); p. 3,4-7,9,10,12-17, View in Reaxys

1.521

589

Sokolov et al.; Zhurnal Organicheskoi Khimii; vol. 8; (1972); p. 751,760, View in Reaxys

1.5318

589

18.5

Fomin et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 76,76,78, View in Reaxys

1.5143

589

Kulicki; Stec; Roczniki Chemii; vol. 45; (1971); p. 601,602, View in Reaxys

1.5102

589

Jones,L.B.; Foster,J.P.; Journal of Organic Chemistry; vol. 35; (1970); p. 1777 - 1781, View in Reaxys

1.5331

589

Kulicki; et al.; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 39; (1967); p. 67,71, View in Reaxys

1.5373

589

Koyama,K. et al.; Tetrahedron; vol. 23; (1967); p. 2665 - 2674, View in Reaxys

1.524

589

Patent; Badische Anilin- und Soda-Fabrik A.G.; DE1275041; (1966); Chem.Abstr.; vol. 69; nb. 96208x; (1968), View in Reaxys

1.5206

589

Pines; Schappell; Journal of Organic Chemistry; vol. 29; (1964); p. 1503,1507, View in Reaxys

1.5207

589

Walling,C.; Padwa,A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1593 - 1597, View in Reaxys

1.5242

589

Terent'ew et al.; Neftekhimiya; vol. 1; (1962); p. 567,462, View in Reaxys

1.5215

589

Patent; Koninklijke Industrieele Maatschappij vorheen Noury + van der Lande, N.V.; BE613440; (1961); Chem.Abstr.; vol. 58; nb. 1402b; (1963), View in Reaxys

1.5235

589

Choe; Tsutsumi; Nippon Kagaku Zasshi; vol. 81; (1960); p. 586,588; Chem.Abstr.; vol. 56; nb. 397; (1962), View in Reaxys

1.5128

589

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

1.515

589

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

1.5325

589

Petrow; Kaplan; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1947); p. 295,303; Chem.Abstr.; (1949); p. 1718, View in Reaxys

1.5314

589

18.5

Boedtker; Bulletin de la Societe Chimique de France; vol. <3> 25; (1901); p. 851, View in Reaxys

Density (7) 1 of 7

Density [g·cm-3]

0.9724

Reference Temperature [°C]

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Measurement Temperature [°C]

Kuramshin, E. M.; Molyavko, M. A.; Zlot-skii, S. S.; Rakhmankulov, D. L.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 6; (1985); p. 1393 - 1398,1242 - 1246, View in Reaxys 2 of 7

Density [g·cm-3]

0.9724

Hala; Chemicky Prumysl; vol. 18; (1968); p. 412; Chem.Abstr.; vol. 69; nb. 83193; (1968), View in Reaxys 3 of 7

Density [g·cm-3]

0.9782

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 4 of 7

Density [g·cm-3]

0.9824

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 5 of 7

Density [g·cm-3]

0.9735

Reference Temperature [°C]

Measurement Temperature [°C]

Petrow; Kaplan; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1947); p. 295,303; Chem.Abstr.; (1949); p. 1718, View in Reaxys 6 of 7

Density [g·cm-3]

0.9724

Reference Temperature [°C]

Measurement Temperature [°C]

18.5

Klages; Chemische Berichte; vol. 35; (1902); p. 2649; Chemische Berichte; vol. 39; (1906); p. 2591, View in Reaxys 7 of 7

Density [g·cm-3]

1.0177

Measurement Temperature [°C]

Boedtker; Bulletin de la Societe Chimique de France; vol. <3> 25; (1901); p. 851, View in Reaxys Adsorption (MCS) (1) 1 of 1

Description (Adsorption (MCS))

Adsorption

Kutscher et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 598,574; Chem.Abstr.; nb. 18631; (1961), View in Reaxys Association (MCS) (4) 1 of 4

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

gaseous matrix

Partner (Association (MCS))

wather; NH3

Li, S.; Bernstein, E. R.; Journal of Chemical Physics; vol. 97; nb. 10; (1992); p. 7383 - 7391, View in Reaxys

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2 of 4

Description (Association Stability constant of the complex with ... (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

zinc naphthenate

Kozlov, S. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 60; nb. 1.2; (1990); p. 175 - 180,153 - 157, View in Reaxys 3 of 4

Description (Association Spectrum of the complex (MCS)) Drago et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 2883, View in Reaxys; Drago et al.; Canadian Journal of Chemistry; vol. 47; (1969); p. 1639, View in Reaxys

4 of 4

Description (Association Further physical properties of the complex (MCS)) Kharasch,M.S. et al.; Journal of Organic Chemistry; vol. 25; (1960); p. 1000 - 1006, View in Reaxys

Azeotropes (MCS) (1) 1 of 1

Temperature (Azeotropes (MCS)) [°C]

99.2

Pressure (Azeotropes (MCS)) [Torr]

20.03

Azeotropes

phenol

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys Chromatographic Data (3) Chromatographic Location data GC (Gas chromatography)

HPLC (High performance liquid chromatography)

References Spiridon, Iuliana; Nechita, Constantin Bogdan; Niculaua, Marius; Silion, Mihaela; Armatu, Alice; Teaca, Carmen-Alice; Bodirlau, Ruxanda; Central European Journal of Chemistry; vol. 11; nb. 10; (2013); p. 1699 - 1709, View in Reaxys; Xu, Yang-Bin; Wang, Kai; Zhu, Rui-Zhi; Shou, Mao-De; Zhe, Wei; Liu, Qiang; Asian Journal of Chemistry; vol. 27; nb. 5; (2015); p. 1903 - 1906, View in Reaxys

supporting information

Tano, Tetsuro; Mieda, Kaoru; Sugimoto, Hideki; Ogura, Takashi; Itoh, Shinobu; Dalton Transactions; vol. 43; nb. 12; (2014); p. 4871 - 4877, View in Reaxys; Li, Zejiang; Xiao, Yingxia; Liu, Zhong-Quan; Chemical Communications; vol. 51; nb. 49; (2015); p. 9969 - 9971, View in Reaxys; Paria, Sayantan; Ohta, Takehiro; Morimoto, Yuma; Ogura, Takashi; Sugimoto, Hideki; Fujieda, Nobutaka; Goto, Kei; Asano, Kaori; Suzuki, Takeyuki; Itoh, Shinobu; Journal of the American Chemical Society; vol. 137; nb. 34; (2015); p. 10870 - 10873, View in Reaxys

GC (Gas chroma- supporting infortography) mation

Geer, Michael F.; Walla, Michael D.; Solntsev, Kyril M.; Strassert, Cristian A.; Shimizu, Linda S.; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5568 - 5578, View in Reaxys

Crystal Property Description (3) Colour & Other Location Properties colourless

supporting information

References Nakanowatari, Sachiyo; Ackermann, Lutz; Chemistry - A European Journal; vol. 20; nb. 18; (2014); p. 5409 - 5413, View in Reaxys

colourless

Riva; Gagliardi; Martinelli; Passarella; Vigo; Rencurosi; Tetrahedron; vol. 66; nb. 17; (2010); p. 3242 - 3247, View in Reaxys; Kamijo, Shin; Amaoka, Yuuki; Inoue, Masayuki; Synthesis; nb. 14; (2010); p. 2475 - 2489; Art.No: E27210SS, View in Reaxys

Prismen

Decomposition (1) 1 of 1

Decomposition [°C]

215 - 220

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Kuramshin, E. M.; Molyavko, M. A.; Zlot-skii, S. S.; Rakhmankulov, D. L.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 6; (1985); p. 1393 - 1398,1242 - 1246, View in Reaxys Dissociation Exponent (1) 1 of 1

Comment (Dissociation Exponent)

(pk')pK(a)

Kreshkov et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1605; ; p. 2817, View in Reaxys Electrical Data (1) 1 of 1

Description (Electrical Data)

Electrical properties

Mayeda; Journal of the American Chemical Society; vol. 97; (1975); p. 4012,4013, View in Reaxys Electrical Moment (1) 1 of 1

Description (Electrical Moment)

Dipole moment

Egorov et al.; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 169,173; ; p. 203, View in Reaxys Electrical Polarizability (1) Description (Elec- References trical Polarizability) Atom polarization

Egorov et al.; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 169,173; ; p. 203, View in Reaxys

Electrochemical Behaviour (1) Description (Elec- References trochemical Behaviour) Polarography

Mayeda,E.A. et al.; Journal of the American Chemical Society; vol. 94; nb. 19; (1972); p. 6812 - 6816, View in Reaxys

Enthalpy of Formation (2) Enthalpy of ForTemperature (Enmation [Jmol-1] thalpy of Formation) [°C]

Pressure (Enthalpy of Formation) [Torr]

References

-168100

750.06

Verevkin, Sergey P.; Journal of Chemical and Engineering Data; vol. 44; nb. 6; (1999); p. 1245 - 1251, View in Reaxys

250400

Van-Chin-Syan, Yu. Ya.; Dolbneva, T. N.; Dikii, M. A.; Cuchmarev, S. K.; Russian Journal of Physical Chemistry; vol. 58; nb. 12; (1984); p. 1783 - 1785; Zhurnal Fizicheskoi Khimii; vol. 58; (1984); p. 2937 2940, View in Reaxys

Enthalpy of Sublimation (1) Enthalpy of Subli- Temperature (En- References mation [Jmol-1] thalpy of Sublimation) [°C] 82280

298.15

Enthalpy of Vaporization (1) Enthalpy of VaTemperature (Enporization thalpy of Vapori[Jmol-1] zation) [°C] 64960

Verevkin, Sergey P.; Journal of Chemical and Engineering Data; vol. 44; nb. 6; (1999); p. 1245 - 1251, View in Reaxys References

Verevkin, Sergey P.; Journal of Chemical and Engineering Data; vol. 44; nb. 6; (1999); p. 1245 - 1251, View in Reaxys

Further Information (6) Description (Fur- References ther Information) Further information

Granzhan et al.; Journal of Applied Spectroscopy; vol. 20; (1974); p. 359,360; ; p. 473, View in Reaxys

Further information

Mamatov; Yagudaev; Journal of Applied Spectroscopy; vol. 8; (1968); p. 498; ; p. 825, View in Reaxys

Further information

Normant; Cuvigny; Bulletin de la Societe Chimique de France; (1966); p. 3344,3346, 3349, View in Reaxys

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Further information

Gronowitz,S. et al.; Acta Chemica Scandinavica (1947-1973); vol. 19; (1965); p. 1215 - 1220, View in Reaxys

Further information

Oki; Iwamura; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 1552, View in Reaxys

Further information

Williams,J.F.A.; Tetrahedron; vol. 18; (1962); p. 1487 - 1493, View in Reaxys

Gas Phase (1) Description (Gas Phase) Association in the gas phase Liquid Phase (1) Description (Liquid Phase) Self-association in solution

References Takeda et al.; Nippon Kagaku Kaishi; (1972); p. 213, View in Reaxys

References Perez-Casas, Silvia; Trejo, Luis M.; Costas, Miguel; Journal of the Chemical Society, Faraday Transactions; vol. 87; nb. 11; (1991); p. 1733 - 1738, View in Reaxys; Lomas, John S.; Adenier, Alain; Cordier, Christine; Journal of Physical Organic Chemistry; vol. 19; nb. 5; (2006); p. 295 - 307, View in Reaxys

Liquid/Vapour Systems (MCS) (6) 1 of 6

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 107 - 124.2 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 60 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

1,5-cyclooctadiene monoepoxide

Karaseva, N. V.; Karavaeva, A. P.; Antonova, T. N.; Chabutkina, E. M.; Koshel, G. N.; J. Appl. Chem. USSR (Engl. Transl.); vol. 64; nb. 7.1; (1991); p. 1486 - 1489,1339 - 1342, View in Reaxys 2 of 6

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 108.4 - 124.2 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 60 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

Cyclooctene oxide

Karaseva, N. V.; Karavaeva, A. P.; Antonova, T. N.; Chabutkina, E. M.; Koshel, G. N.; J. Appl. Chem. USSR (Engl. Transl.); vol. 64; nb. 7.1; (1991); p. 1486 - 1489,1339 - 1342, View in Reaxys 3 of 6

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 66.6 - 98.7 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 20.03 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

(R)-1,2-epoxy-7-octene

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys 4 of 6

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 66.6 - 98.7 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 20.03 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

(R)-1,2-epoxy-7-octene

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys 5 of 6

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 85.4 - 98.7 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 20.03 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

phenol

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys 6 of 6

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 85.4 - 98.7 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 20.03 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

phenol

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys Mechanical Properties (1) Description (MeReferences chanical Properties) Molar volume

Carr; Doherty; Kamlet; Taft; Melander; Horvath; Analytical Chemistry; vol. 58; nb. 13; (1986); p. 2674 2680, View in Reaxys

Molecular Deformation (1) Description (MoReferences lecular Deformation) Fundamental vibrations

Brook,A.G.; Pannell,K.H.; Journal of Organometallic Chemistry; vol. 8; (1967); p. 179 - 184, View in Reaxys

Other Thermochemical Data (1) Description (Oth- References er Thermochemical Data) Enthalpy of selfassociation

Perez-Casas, Silvia; Trejo, Luis M.; Costas, Miguel; Journal of the Chemical Society, Faraday Transactions; vol. 87; nb. 11; (1991); p. 1733 - 1738, View in Reaxys

Solubility (MCS) (2) 1 of 2

Comment (Solubility (MCS))

H2O (Tab. 2)

Afanasenkova; Burova; Malenko; Shakunova; ; vol. 46; nb. 9 Part 2; (1973); p. 2248 - 2249, View in Reaxys 2 of 2

Temperature (Solubility (MCS)) [°C]

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Solvent (Solubility (MCS))

H2O

Carter et al.; Journal of Pharmacy and Pharmacology; vol. 10; (1958); p. Spl. 149 T, 153 T, View in Reaxys Vapour Pressure (1) Comment (VaReferences pour Pressure) Equation: Karaseva, N. V.; Karavaeva, A. P.; Antonova, T. N.; Chabutkina, E. M.; Koshel, G. N.; J. Appl. Chem. lgP=7.7479-2051. USSR (Engl. Transl.); vol. 64; nb. 7.1; (1991); p. 1486 - 1489,1339 - 1342, View in Reaxys 32/(219.47+t) NMR Spectroscopy (40) 1 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- [(2)H6]acetone scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Dong, Jia Jia; Harvey, Emma C.; Faans-Mastral, Martn; Browne, Wesley R.; Feringa, Ben L.; Journal of the American Chemical Society; vol. 136; nb. 49; (2014); p. 17302 - 17307, View in Reaxys 2 of 40

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Hatano, Manabu; Ito, Orie; Suzuki, Shinji; Ishihara, Kazuaki; Journal of Organic Chemistry; vol. 75; nb. 15; (2010); p. 5008 - 5016, View in Reaxys; Xia, Qinqin; Liu, Xiaolong; Zhang, Yuejiao; Chen, Chao; Chen, Wanzhi; Organic Letters; vol. 15; nb. 13; (2013); p. 3326 - 3329, View in Reaxys 3 of 40

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Location

supporting information

Rodrigues, Catarina A.B.; De Matos, Marta Norton; Guerreiro, Bruno M.H.; Goncalves, Ana M.L.; Romao, Carlos C.; Afonso, Carlos A.M.; Tetrahedron Letters; vol. 52; nb. 22; (2011); p. 2803 - 2807, View in Reaxys; Hoshino, Yujiro; Suzuki, Kenzo; Honda, Kiyoshi; Synlett; vol. 23; nb. 16; (2012); p. 2375 - 2380; Art.No: ST-2012-U0504-L, View in Reaxys

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5 of 40

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Yamamoto, Yutaro; Hasegawa, Hiroto; Yamataka, Hiroshi; Journal of Organic Chemistry; vol. 76; nb. 11; (2011); p. 4652 - 4660, View in Reaxys 7 of 40

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Yan, Hailong; Oh, Joong-Suk; Song, Choong Eui; Organic and Biomolecular Chemistry; vol. 9; nb. 23; (2011); p. 8119 - 8121, View in Reaxys 8 of 40

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Yan, Hailong; Oh, Joong-Suk; Song, Choong Eui; Organic and Biomolecular Chemistry; vol. 9; nb. 23; (2011); p. 8119 - 8121, View in Reaxys 9 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Hatano, Manabu; Ito, Orie; Suzuki, Shinji; Ishihara, Kazuaki; Chemical Communications; vol. 46; nb. 15; (2010); p. 2674 - 2676, View in Reaxys 10 of 40

Description (NMR Spec- Chemical shifts troscopy)

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Hatano, Manabu; Ito, Orie; Suzuki, Shinji; Ishihara, Kazuaki; Chemical Communications; vol. 46; nb. 15; (2010); p. 2674 - 2676, View in Reaxys 11 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Kamijo, Shin; Amaoka, Yuuki; Inoue, Masayuki; Synthesis; nb. 14; (2010); p. 2475 - 2489; Art.No: E27210SS, View in Reaxys 12 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Kamijo, Shin; Amaoka, Yuuki; Inoue, Masayuki; Synthesis; nb. 14; (2010); p. 2475 - 2489; Art.No: E27210SS, View in Reaxys 13 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

-50

Frequency (NMR Spectroscopy) [MHz]

300

Howard, Fredrick; Sawadjoon, Supaporn; Samec, Joseph S.M.; Tetrahedron Letters; vol. 51; nb. 32; (2010); p. 4208 - 4210, View in Reaxys 14 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Zhang, Yuhua; Feng, Jianqing; Li, Chao-Jun; Journal of the American Chemical Society; vol. 130; nb. 10; (2008); p. 2900 - 2901, View in Reaxys 15 of 40

Description (NMR Spec- Chemical shifts troscopy)

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Zhang, Yuhua; Feng, Jianqing; Li, Chao-Jun; Journal of the American Chemical Society; vol. 130; nb. 10; (2008); p. 2900 - 2901, View in Reaxys 16 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Ikeda, Hiroshi; Hoshi, Yosuke; Namai, Hayato; Tanaka, Futoshi; Goodman, Joshua L.; Mizuno, Kazuhiko; Chemistry - A European Journal; vol. 13; nb. 33; (2007); p. 9207 - 9215, View in Reaxys 17 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

Miyoshi, Norikazu; Matsuo, Tsuyoshi; Wada, Makoto; European Journal of Organic Chemistry; nb. 20; (2005); p. 4253 - 4255, View in Reaxys 18 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

67.5

Tokuyasu, Takahiro; Kunikawa, Shigeki; Masuyama, Araki; Nojima, Masatomo; Organic Letters; vol. 4; nb. 21; (2002); p. 3595 - 3598, View in Reaxys 19 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

270

Tokuyasu, Takahiro; Kunikawa, Shigeki; Masuyama, Araki; Nojima, Masatomo; Organic Letters; vol. 4; nb. 21; (2002); p. 3595 - 3598, View in Reaxys 20 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

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Grossman, G.; Komber, G.; Kroshvitts, G.; Kirpichnikov, P. A.; Mukmeneva, N. A.; Pobedimskii, D. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 38; nb. 1.1; (1989); p. 26 - 32; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 1; (1989); p. 34 - 41, View in Reaxys; Faehl, Larry G.; Kice, John L.; Journal of Organic Chemistry; vol. 45; nb. 12; (1980); p. 2507 - 2509, View in Reaxys; Pryor, William A.; Castle, Laurence; Church, Daniel F.; Journal of the American Chemical Society; vol. 107; nb. 1; (1985); p. 211 - 217, View in Reaxys; Guijarro; Yus; Tetrahedron; vol. 50; nb. 11; (1994); p. 3447 - 3452, View in Reaxys; Dailey, Jennifer I.; Hays, Ryan S.; Lee, Hua; Mitchell, Randall M.; Ries, Jennifer J.; Landolt, Robert G.; Husmann, Hollie H.; Lockridge, Joseph B.; Hendrickson, William H.; Journal of Organic Chemistry; vol. 65; nb. 8; (2000); p. 2568 - 2571, View in Reaxys 21 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

270.05

Kataoka, Yasutaka; Makihira, Isamu; Utsunomiya, Masaru; Tani, Kazuhide; Journal of Organic Chemistry; vol. 62; nb. 24; (1997); p. 8540 - 8543, View in Reaxys 22 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Hayashi; Matsumoto; Ito; Tetrahedron Asymmetry; vol. 2; nb. 7; (1991); p. 601 - 612, View in Reaxys; Bors, Daniel A.; Kaufman, Michael J.; Streitwieser, Andrew Jr.; Journal of the American Chemical Society; vol. 107; nb. 24; (1985); p. 6975 - 6982, View in Reaxys; Ishii, Yasutaka; Iwahama, Takahiro; Sakaguchi, Satoshi; Nakayama, Kouichi; Nishiyama, Yutaka; Journal of Organic Chemistry; vol. 61; nb. 14; (1996); p. 4520 - 4526, View in Reaxys 23 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Servis,K.L.; Shue,F.F.; Journal of the American Chemical Society; vol. 102; (1980); p. 7233, View in Reaxys; Begtrup, Mikael; Elguero, Jose; Faure, Robert; Camps, Pelayo; Estopa, Carmen; et al.; Magnetic Resonance in Chemistry; vol. 26; (1988); p. 134 - 151, View in Reaxys; Ishii, Yasutaka; Iwahama, Takahiro; Sakaguchi, Satoshi; Nakayama, Kouichi; Nishiyama, Yutaka; Journal of Organic Chemistry; vol. 61; nb. 14; (1996); p. 4520 4526, View in Reaxys; Lomas, John S.; Journal of the Chemical Society. Perkin Transactions 2; vol. 1996; nb. 12; (1996); p. 2601 - 2609, View in Reaxys 24 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Olah,G.A.; Westerman,P.W.; Journal of the American Chemical Society; vol. 95; (1973); p. 7530 - 7531, View in Reaxys; Guijarro; Yus; Tetrahedron; vol. 50; nb. 11; (1994); p. 3447 - 3452, View in Reaxys 25 of 40

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

1H-1H

Guijarro; Yus; Tetrahedron; vol. 50; nb. 11; (1994); p. 3447 - 3452, View in Reaxys 26 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

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Solvents (NMR Spectro- CCl4 scopy) Villenave, J. J.; Filliatre, C.; Maillard, B.; Jaouhari, R.; Bulletin des Societes Chimiques Belges; vol. 91; nb. 4; (1982); p. 301 - 310, View in Reaxys; Gurudutt, K. N.; Rao, L. Jagan Mohan; Rao, Sanjay; Srinivas, P.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 32; nb. 4; (1993); p. 468 470, View in Reaxys 27 of 40

Description (NMR Spec- Linewidth of NMR absorption troscopy) Kozlov, S. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 60; nb. 1.2; (1990); p. 175 - 180,153 - 157, View in Reaxys

28 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CS2; cyclohexane-d12 scopy) Temperature (NMR Spectroscopy) [°C]

26.9

Schaefer, Ted; Sebastian, Rudy; Peeling, James; Penner, Glenn H.; Koh, Kevin; Canadian Journal of Chemistry; vol. 67; (1989); p. 1015 - 1021, View in Reaxys 30 of 40

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CS2; cyclohexane-d12 scopy) Temperature (NMR Spectroscopy) [°C]

26.9

Comment (NMR Spectroscopy)

1H-1H.

Schaefer, Ted; Sebastian, Rudy; Peeling, James; Penner, Glenn H.; Koh, Kevin; Canadian Journal of Chemistry; vol. 67; (1989); p. 1015 - 1021, View in Reaxys 31 of 40

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- acetone-d6 scopy) Pryor, William A.; Ohto, Norio; Church, Daniel F.; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p. 3614 - 3622, View in Reaxys 32 of 40

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

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Solvents (NMR Spectro- acetone-d6 scopy) Pryor, William A.; Ohto, Norio; Church, Daniel F.; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p. 3614 - 3622, View in Reaxys 33 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- acetone-d6 scopy) Pryor, William A.; Ohto, Norio; Church, Daniel F.; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p. 3614 - 3622, View in Reaxys 34 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- acetone-d6 scopy) Temperature (NMR Spectroscopy) [°C]

-73

Pryor, William A.; Ohto, Norio; Church, Daniel F.; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p. 3614 - 3622, View in Reaxys 35 of 40

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- acetone-d6 scopy) Temperature (NMR Spectroscopy) [°C]

-73

Pryor, William A.; Ohto, Norio; Church, Daniel F.; Journal of the American Chemical Society; vol. 104; nb. 21; (1982); p. 5813 - 5814, View in Reaxys 36 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CCl4 scopy) Temperature (NMR Spectroscopy) [°C]

Aganov, A. V.; Antonovskii, V. L.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 31; nb. 2; (1982); p. 247 - 250; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 2; (1982); p. 271 - 275, View in Reaxys 37 of 40

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- tetradeuteriomethanol scopy) Fuchs, Wolfram; Kalbacher, Hubert; Voelter, Wolfgang; Organic Magnetic Resonance; vol. 17; nb. 3; (1981); p. 157 - 162, View in Reaxys 38 of 40

Description (NMR Spec- NMR with shift reagents troscopy)

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Ikeda; Fukuzumi; Journal of the American Oil Chemists' Society; vol. 51; (1974); p. 340, View in Reaxys; Lycka et al.; Journal of Organometallic Chemistry; vol. 174; (1979); p. 41,43, View in Reaxys 39 of 40

Description (NMR Spec- NMR troscopy) Olah,G.A. et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 3548 - 3559, View in Reaxys; Wursthorn,K.R. et al.; Journal of the American Chemical Society; vol. 100; nb. 9; (1978); p. 2779 - 2789, View in Reaxys; Oki,M.; Iwamura,H.; Bulletin of the Chemical Society of Japan; vol. 36; (1963); p. 1 - 4, View in Reaxys; House,H.O. et al.; Journal of Organic Chemistry; vol. 41; nb. 19; (1976); p. 3067 - 3076, View in Reaxys; SolladieCavallo; Solladie; Organic Magnetic Resonance; vol. 10; (1977); p. 235, View in Reaxys; Wang; Kingsbury; Journal of Organic Chemistry; vol. 37; (1972); p. 2489,2492, View in Reaxys; Bartlett; Lahav; Israel Journal of Chemistry; vol. 10; (1972); p. 101,105, View in Reaxys; Braun et al.; Journal of Organometallic Chemistry; vol. 97; (1975); p. 429,436, View in Reaxys; Kreshkov et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1605; ; p. 2817, View in Reaxys; Ward; Mair; Analytical Chemistry; vol. 41; (1969); p. 538, View in Reaxys

40 of 40

Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

in Fluorsulfonsaeure; Fig. 8

Farnum,D.G.; Journal of the American Chemical Society; vol. 89; nb. 12; (1967); p. 2970 - 2975, View in Reaxys IR Spectroscopy (11) 1 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Comment (IR Spectroscopy)

film

Taha, Ahmed A.; International Journal of Chemical Kinetics; vol. 44; nb. 8; (2012); p. 514 - 523, View in Reaxys 2 of 11

Description (IR Spectroscopy)

Spectrum

Location

supporting information

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Miyoshi, Norikazu; Matsuo, Tsuyoshi; Wada, Makoto; European Journal of Organic Chemistry; nb. 20; (2005); p. 4253 - 4255, View in Reaxys 4 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

NaCl

Comment (IR Spectroscopy)

3374 - 544 cm**(-1)

Ishii, Yasutaka; Iwahama, Takahiro; Sakaguchi, Satoshi; Nakayama, Kouichi; Nishiyama, Yutaka; Journal of Organic Chemistry; vol. 61; nb. 14; (1996); p. 4520 - 4526, View in Reaxys 5 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3380 - 1490 cm**(-1)

Guijarro; Yus; Tetrahedron; vol. 50; nb. 11; (1994); p. 3447 - 3452, View in Reaxys 6 of 11

Description (IR Spectroscopy)

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House,H.O. et al.; Journal of Organic Chemistry; vol. 41; nb. 19; (1976); p. 3067 - 3076, View in Reaxys; Terentev; J. Anal. Chem. USSR (Engl. Transl.); vol. 24; (1969); p. 743,584, View in Reaxys; Terent'ev et al.; Journal of Applied Spectroscopy; vol. 5; (1966); p. 346,348; ; p. 463, View in Reaxys; Kirchner; Richter; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 81; (1972); p. 274, View in Reaxys; Kovner et al.; Optics and Spectroscopy; vol. 8; (1960); p. 64; ; p. 128, View in Reaxys; Ikeda; Fukuzumi; Journal of the American Oil Chemists' Society; vol. 51; (1974); p. 340, View in Reaxys 7 of 11

Description (IR Spectroscopy)

Bands

Egorov et al.; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 169,173; ; p. 203, View in Reaxys; Syper et al.; Roczniki Chemii; vol. 46; (1972); p. 849,850, 852, View in Reaxys 8 of 11

Description (IR Spectroscopy)

Spectrum

Knizek et al.; Collection of Czechoslovak Chemical Communications; vol. 29; (1964); p. 2935,2939, View in Reaxys; Oki; Iwamura; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 1552, View in Reaxys 9 of 11

Description (IR Spectroscopy)

Intensity of IR bands

Comment (IR Spectroscopy)

Intensitaet und Halbwertsbreite der OH-Valenzschwingungsbanden bei 3627 cmE-1 und 3616 cmE-1 (CCl4).

Oki; Iwamura; Bulletin of the Chemical Society of Japan; vol. 32; (1959); p. 955,958, View in Reaxys 10 of 11

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

cyclohexane

Comment (IR Spectroscopy)

1750 - 650 cm**(-1)

Philpotts; Thain; Analytical Chemistry; vol. 24; (1952); p. 638,641, View in Reaxys 11 of 11

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1750 - 650 cm**(-1)

Philpotts; Thain; Analytical Chemistry; vol. 24; (1952); p. 638,641, View in Reaxys Mass Spectrometry (11) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

gas chromatogra- supporting inforphy mass specmation trometry (GCMS); spectrum

Geer, Michael F.; Walla, Michael D.; Solntsev, Kyril M.; Strassert, Cristian A.; Shimizu, Linda S.; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5568 - 5578, View in Reaxys; Liu, Shouxin; Zhang, Qi; Li, Huiying; Yang, Yihua; Tian, Xia; Whiting, Andrew; Chemistry - A European Journal; vol. 21; nb. 27; (2015); p. 9671 9675, View in Reaxys; Wang, Bin; Lee, Yong-Min; Clmancey, Martin; Seo, Mi Sook; Sarangi, Ritimukta; Latour, Jean-Marc; Nam, Wonwoo; Journal of the American Chemical Society; vol. 138; nb. 7; (2016); p. 2426 - 2436, View in Reaxys

high resolution mass spectrometry (HRMS); photoionization; spectrum

Parshintsev, Jevgeni; Vaikkinen, Anu; Lipponen, Katriina; Vrkoslav, Vladimir; Cvaka, Josef; Kostiainen, Risto; Kotiaho, Tapio; Hartonen, Kari; Riekkola, Marja-Liisa; Kauppila, Tiina J.; Rapid Communications in Mass Spectrometry; vol. 29; nb. 13; (2015); p. 1233 - 1241, View in Reaxys

electrospray ionisation (ESI); fragmentation pattern

supporting information

liquid chromatog- supporting inforraphy mass specmation trometry (LCMS); electrospray ioni-

Rana, Sujoy; Dey, Aniruddha; Maiti, Debabrata; Chemical Communications; vol. 51; nb. 77; (2015); p. 14469 - 14472, View in Reaxys Hong, Seungwoo; Wang, Bin; Seo, Mi Sook; Lee, Yong-Min; Kim, Myoung Jin; Kim, Hyung Rok; Ogura, Takashi; Garcia-Serres, Ricardo; Clemancey, Martin; Latour, Jean-Marc; Nam, Wonwoo; Angewandte Chemie - International Edition; vol. 53; nb. 25; (2014);

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sation (ESI); IT (ion trap); spectrum

p. 6388 - 6392; Angew. Chem.; vol. 126; nb. 25; (2014); p. 6506 6510,5, View in Reaxys

EI (Electron imsupporting inforpact); GCMS mation (Gas chromatography mass spectrometry); Spectrum

Kamata, Keigo; Yamaura, Taiyo; Mizuno, Noritaka; Angewandte Chemie - International Edition; vol. 51; nb. 29; (2012); p. 7275 7278, View in Reaxys

HRMS (High resolution mass spectrometry); FAB (Fast atom bombardment); Positive secondary ions; Spectrum

supporting information

Hatano, Manabu; Ito, Orie; Suzuki, Shinji; Ishihara, Kazuaki; Chemical Communications; vol. 46; nb. 15; (2010); p. 2674 - 2676, View in Reaxys

FAB (Fast atom bombardment); HRMS (High resolution mass spectrometry); Spectrum

supporting information

Hatano, Manabu; Ito, Orie; Suzuki, Shinji; Ishihara, Kazuaki; Journal of Organic Chemistry; vol. 75; nb. 15; (2010); p. 5008 - 5016, View in Reaxys

spectrum

Guijarro; Yus; Tetrahedron; vol. 50; nb. 11; (1994); p. 3447 - 3452, View in Reaxys; Kimura; Ogata; Bulletin of the Chemical Society of Japan; vol. 56; nb. 2; (1983); p. 471 - 473, View in Reaxys; Fowley, Lissa A.; Lee, Jesse C.; Crabtree, Robert H.; Siegbahn, Per E. M.; Journal of Organometallic Chemistry; vol. 504; nb. 1-2; (1995); p. 57 - 68, View in Reaxys metastable ions; My, Nguyen kieu; Schilling, Marita; Schwarz, Helmut; Organic IKE(S) (ion kinetic Mass Spectrometry; vol. 22; (1987); p. 254 - 258, View in Reaxys energy (spectrum))

fragmentation pattern; electron impact (EI); spectrum

Teleshefsky, L. A.; Jones, B. E.; Abbey, L. E.; Bostwick, D. E.; Burgess, E. M; Moran T. F.; Organic Mass Spectrometry; vol. 17; nb. 10; (1982); p. 481 - 492, View in Reaxys House,H.O. et al.; Journal of Organic Chemistry; vol. 41; nb. 19; (1976); p. 3067 - 3076, View in Reaxys; Alberola et al.; Anales de Quimica (1968-1979); vol. 72; (1976); p. 848, View in Reaxys

UV/VIS Spectroscopy (7) 1 of 7

Description (UV/VIS Spectroscopy)

Absorption maxima

Absorption Maxima (UV/ 258 VIS) [nm] Amyes, Tina L.; Richard, John P.; Novak, Michael; Journal of the American Chemical Society; vol. 114; nb. 21; (1992); p. 8032 - 8041, View in Reaxys 2 of 7

Description (UV/VIS Spectroscopy)

UV/VIS

House,H.O. et al.; Journal of Organic Chemistry; vol. 41; nb. 19; (1976); p. 3067 - 3076, View in Reaxys 3 of 7

Description (UV/VIS Spectroscopy)

Spectrum

Olah,G.A. et al.; Journal of the American Chemical Society; vol. 88; nb. 7; (1966); p. 1488 - 1495, View in Reaxys; Mamatov; Yagudaev; Journal of Applied Spectroscopy; vol. 8; (1968); p. 498; ; p. 825, View in Reaxys; Bywater; Worsfold; Canadian Journal of Chemistry; vol. 44; (1966); p. 1671,1673, View in Reaxys 4 of 7

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

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Comment (UV/VIS Spectroscopy)

220 - 500 nm

Grace; Symons; Journal of the Chemical Society; (1959); p. 958,960, View in Reaxys; Lawruschin; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 2697,2701; engl. Ausg. S. 3005, 3008, View in Reaxys 5 of 7

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2SO4

Comment (UV/VIS Spectroscopy)

220 - 500 nm

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. trichloroacetic acid

Comment (UV/VIS Spectroscopy)

220 - 500 nm

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

220 - 280 nm

Robinson et al.; Biochemical Journal; vol. 59; (1955); p. 153,154, View in Reaxys Pharmacological Data (1) 1 of 1

Comment (Pharmacological Data)

Bioactivities present

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diene-styrene at low temp. (<=300 deg C); table Concentration in the Environment (7) 1 of 7

Media (Concentration in the Environment)

groundwater

Location

Lombardy, Italy

Contamination Concentration

105 - 200 ng/l

Method, Remarks (Concentration in the Environment)

water samples from 8 wells (upstream and downstream) collected near industrial waste landfill; title comp. analyzed using GC/MS(EI-SIM)

Benfenati; Porazzi; Bagnati; Forner; Martinez, M. Pardo; Mariani; Fanelli; Chemosphere; vol. 51; nb. 8; (2003); p. 677 - 683, View in Reaxys 2 of 7

Media (Concentration in the Environment)

leachate

Location

Lombardy, Italy

Contamination Concentration

177 - 334 μg/l

Method, Remarks (Concentration in the Environment)

leachate samples from 2 wells collected near industrial waste landfill; title comp. analyzed using GC/MS(EI-SIM)

Benfenati; Porazzi; Bagnati; Forner; Martinez, M. Pardo; Mariani; Fanelli; Chemosphere; vol. 51; nb. 8; (2003); p. 677 - 683, View in Reaxys 3 of 7

Media (Concentration in the Environment)

water

Location

Lobith, river Rhine, Netherlands

Contamination Concentration

300 ng/l

Method, Remarks (Concentration in the Environment)

non-filtered samples; August - October 1998; 80 l of sampled water solid-phase-extracted for 24 h by 150 ml of a 1:1 (v/v) XAD-4/XAD-8 polymer mixture; GC-AED (atomic emission detection)/MS analysis

Van Stee; Leonards; Van Loon; Jan Hendriks; Struijs; Brinkman; Maas; Water Research; vol. 36; nb. 18; (2002); p. 4455 - 4470, View in Reaxys 4 of 7

Media (Concentration in the Environment)

water

Location

Eijsden, river Meuse, Netherlands

Contamination Concentration

30 ng/l

Method, Remarks (Concentration in the Environment)

non-filtered samples; August - October 1998; 80 l of sampled water solid-phase-extracted for 24 h by 150 ml of a 1:1 (v/v) XAD-4/XAD-8 polymer mixture; GC-AED (atomic emission detection)/MS analysis

Van Stee; Leonards; Van Loon; Jan Hendriks; Struijs; Brinkman; Maas; Water Research; vol. 36; nb. 18; (2002); p. 4455 - 4470, View in Reaxys 5 of 7

Media (Concentration in the Environment)

water

Location

Maassluis, Netherlands

Contamination Concentration

100 ng/l

Method, Remarks (Concentration in the Environment)

non-filtered samples; August - October 1998; 80 l of sampled water solid-phase-extracted for 24 h by 150 ml of a 1:1 (v/v) XAD-4/XAD-8 polymer mixture; GC-AED (atomic emission detection)/MS analysis

Van Stee; Leonards; Van Loon; Jan Hendriks; Struijs; Brinkman; Maas; Water Research; vol. 36; nb. 18; (2002); p. 4455 - 4470, View in Reaxys

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2016-05-12 16:03:43

6 of 7

Media (Concentration in the Environment)

water

Location

Noordwijkerhout, Netherlands

Contamination Concentration

30 ng/l

Method, Remarks (Concentration in the Environment)

non-filtered samples; August - October 1998; 80 l of sampled water solid-phase-extracted for 24 h by 150 ml of a 1:1 (v/v) XAD-4/XAD-8 polymer mixture; GC-AED (atomic emission detection)/MS analysis

Van Stee; Leonards; Van Loon; Jan Hendriks; Struijs; Brinkman; Maas; Water Research; vol. 36; nb. 18; (2002); p. 4455 - 4470, View in Reaxys 7 of 7

Media (Concentration in the Environment)

air

Location

Martorell, Spain

Contamination Concentration

1.4 - 2.2 ng/l

Method, Remarks (Concentration in the Environment)

samples collected at two receptor sites: urban and suburban stations between October 1992 and July 1993, gas chromatography

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