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Structure
Structure/Compound Data Chemical Name: 2-methyl-1,4-benzoquinone Reaxys Registry Number: 471387
CAS Registry Number: 553-97-9 Type of Substance: isocyclic Molecular Formula: C7H6O2
Linear Structure Formula: C6H3CH3O2
Molecular Weight: 122.123
InChI Key: VTWDKFNVVLAELH-UHFFFAOYSA-N
1
N° of preparations All Preps | All Reactions 127 prep out of 823 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-methyl-1,4-benzoquinone, 2-Methyl-1,4-benzoquinone, Methylbenzoquinone Identification Substance Label (59) Label
Reference
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Available Data
N° of ref.
Identification Physical Data (155) Spectra (115) Bioactivity (80) Other Data (73)
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2B
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1b
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2a
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E
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mBQ
Bell, Jeffrey G.; Green, James R.; Wang, Jichang
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6a
Wang, Dawei; Ge, Bingyang; Du, Liyong; Miao, Hongyan; Ding, Yuqiang
Synlett, 2014 , vol. 25, # 20 art. no. ST-2014-W0606-L, p. 2895 - 2898 Title/Abstract Full Text View citing articles Show Details
q2c
Hall, Gabriel B.; Chen, Jinzhu; Mebi, Charles A.; Okumura, Noriko; Swenson, Matthew T.; Ossowski, Stephanie E.; Zakai, Uzma I.; Nichol, Gary S.; Lichtenberger, Dennis L.; Evans, Dennis H.; Glass, Richard S.
Organometallics, 2013 , vol. 32, # 21 p. 6605 - 6612 Title/Abstract Full Text View citing articles Show Details
IXc
Mironov; Shul'Ts; Shakirov; Kharitonov; Tolstikov
Russian Journal of Organic Chemistry, 2012 , vol. 48, # 6 p. 840 - 850
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2d
Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
Chemistry Letters, 2008 , vol. 37, # 3 p. 360 - 361 Title/Abstract Full Text View citing articles Show Details
dienophile run5
Kaper, Helena; Antonietti, Markus; Goettmann, Frederic
Tetrahedron Letters, 2008 , vol. 49, # 29-30 p. 4546 - 4549 Title/Abstract Full Text View citing articles Show Details
4a
Ganga; Suresh; Varma, R. Luxmi
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2008 , vol. 47, # 7 p. 1071 - 1079 Title/Abstract Full Text View citing articles Show Details
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9b
Mal, Dipakranjan; Ray, Sutapa; Sharma, Indrajeet
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MBQN
Jakober, Chris A.; Riddle, Sarah G.; Robert, Michael A.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.
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11
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Zhou, Guanglian; Zheng, Deping; Da, Shijun; Xie, Zhixiang; Li, Ying
Tetrahedron Letters, 2006 , vol. 47, # 20 p. 3349 - 3352 Title/Abstract Full Text View citing articles Show Details
MeBQ
Goerner, Helmut
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Goerner, Helmut
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Watanabe, Hiroto; Hiraoka, Ryota; Senna, Mamoru
Tetrahedron Letters, 2006 , vol. 47, # 26 p. 4481 - 4484 Title/Abstract Full Text View citing articles Show Details
2e
Zhang, Hai-Bo; Liu, Li; Chen, Yong-Jun; Wang, Dong; Li, Chao-Jun
Advanced Synthesis and Catalysis, 2006 , vol. 348, # 1-2 p. 229 - 235 Title/Abstract Full Text View citing articles Show Details
2f
Chen, Chao; Xi, Chanjuan; Ai, Zhezhe; Hong, Xiaoyin
Organic Letters, 2006 , vol. 8, # 18 p. 4055 - 4058 Title/Abstract Full Text View citing articles Show Details
1, R1=R2=H, R3=Me
Algi, Fatih; Balci, Metin
Synthetic Communications, 2006 , vol. 36, # 16 p. 2293 - 2297 Title/Abstract Full Text View citing articles Show Details
8
Scheepers, Brent A.; Klein, Rosalyn; Davies-Coleman, Michael T.
Tetrahedron Letters, 2006 , vol. 47, # 47 p. 8243 - 8246 Title/Abstract Full Text View citing articles Show Details
13
Kim, MeeKyoung; Wiemer, David F.
Tetrahedron Letters, 2005 , vol. 46, # 44 p. 7583 - 7587 Title/Abstract Full Text View citing articles Show Details
2i
Yadav; Reddy; Swamy
Synthesis, 2004 , # 1 p. 106 - 110 Title/Abstract Full Text View citing articles Show Details
1c,d
Yadav; Reddy; Swamy; Ramireddy
Synthesis, 2004 , # 11 p. 1849 - 1853 Title/Abstract Full Text View citing articles Show Details
1h
Yadav; Reddy, B. V. Subba; Swamy; Rao, K. Raghavender
Tetrahedron Letters, 2004 , vol. 45, # 31 p. 6037 - 6039 Title/Abstract Full Text View citing articles Show Details
Tab. 2, prod., entry 2
Singh, Vasundhara; Sapehiyia, Varinder; Kad, Goverdhan L.
Synthesis, 2003 , # 2 p. 198 - 200 Title/Abstract Full Text View citing articles Show Details
2, R''=Me
Yadav; Reddy; Kondaji
Synthesis, 2003 , # 7 p. 1100 - 1104 Title/Abstract Full Text View citing articles Show Details
Me-Q
Fukuzumi, Shunichi; Nishimine, Mari; Ohkubo, Kei; Tkachenko, Nikolai V.; Lemmetyinen, Helge
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6b
Board of Supervisors of Louisiana State University; Agricultural and Mechanical College
Patent: US6653311 B1, 2003 ; Title/Abstract Full Text Show Details
30
Ling, Taotao; Poupon, Erwan; Rueden, Erik J.; Kim, Sun H.; Theodorakis, Emmanuel A.
Journal of the American Chemical Society, 2002 , vol. 124, # 41 p. 12261 - 12267 Title/Abstract Full Text View citing articles Show Details
1a
Nunes, Ruth Leandro; Bieber, Lothar Wilhelm
Tetrahedron Letters, 2001 , vol. 42, # 2 p. 219 - 221 Title/Abstract Full Text View citing articles Show Details
6c
Ficht, Simon; Muelbaier, Marcel; Giannis, Athanassios
Tetrahedron, 2001 , vol. 57, # 23 p. 4863 - 4866 Title/Abstract Full Text View citing articles Show Details
2c
Tohma, Hirofumi; Morioka, Hironori; Harayama, Yu; Hashizume, Miki; Kita, Yasuyuki
Tetrahedron Letters, 2001 , vol. 42, # 39 p. 6899 - 6902 Title/Abstract Full Text View citing articles Show Details
19
Barun; Chakrabarti; Ila; Junjappa
Journal of Organic Chemistry, 2001 , vol. 66, # 12 p. 4457 - 4461 Title/Abstract Full Text View citing articles Show Details
4 (run b)
Ketcha, Daniel M.; Wilson, Lawrence J.; Portlock, David E.
Tetrahedron Letters, 2000 , vol. 41, # 33 p. 6253 - 6257 Title/Abstract Full Text View citing articles Show Details
Tab.2, quinone, entry 1
Nair; Vinod
Synthesis, 2000 , # 12 p. 1713 - 1718 Title/Abstract Full Text View citing articles Show Details
2,R1=Me,R2=R3=R4=H
Eguchi, Tadashi; Kanai, Shinobu; Kakinuma, Katsumi; Okazaki, Tadayasu; Mizoue, Kazutoshi
Chemical and Pharmaceutical Bulletin, 2000 , vol. 48, # 10 p. 1470 - 1473 Title/Abstract Full Text View citing articles Show Details
TQ
Jenner, Gerard; Salem, Ridha Ben
New Journal of Chemistry, 2000 , vol. 24, # 4 p. 203 - 207 Title/Abstract Full Text View citing articles Show Details
7
Saladino, Raffaele; Neri, Veronica; Mincione, Enrico; Marini, Stefano; Coletta, Massimiliano; Fiorucci, Chiara; Filippone, Paolino
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 4 p. 581 - 586 Title/Abstract Full Text View citing articles Show Details
Q2
Roginsky, Vitaly; Barsukova, Tatyana
Journal of the Chemical Society. Perkin Transactions 2, 2000 , # 7 p. 1575 - 1582 Title/Abstract Full Text View citing articles Show Details
Q2
Roginsky, Vitaly A.; Pisarenko, Leonid M.; Bors, Wolf; Michel, Christa
Journal of the Chemical Society. Perkin Transactions 2, 1999 , # 4 p. 871 - 876 Title/Abstract Full Text View citing articles Show Details
5c,d
Mahalingam, Rathinam J.; Selvam, Parsuraman
Chemistry Letters, 1999 , # 6 p. 455 - 456 Title/Abstract Full Text View citing articles Show Details
2-methyl-1,4-BQ
Kumagai, Yoshito; Nakajima, Hiromi; Midorikawa, Kazumi; Homma-Takeda, Shino; Shimojo, Nobuhiro
Chemical Research in Toxicology, 1998 , vol. 11, # 6 p. 608 - 613 Title/Abstract Full Text View citing articles Show Details
2-MBQ
Bramble; Boardman; Bevan; Dietrich
Environmental Toxicology and Chemistry, 1994 , vol. 13, # 2 p. 307 - 316 Title/Abstract Full Text View citing articles Show Details
Patent-Specific Data (5) Prophetic Compound
Related Markush Structure (RN)
Location in Patent
Reference
29502132
NOVOZYMES, INC.; Quinlan, Jason; Xu, Feng; Sweeney, Matthew
Patent: US9273335 B2, 2016 ; Title/Abstract Full Text Show Details
11331685
Board of Supervisors of Louisiana State University; Agricultural and Mechanical College
Patent: US6653311 B1, 2003 ; Title/Abstract Full Text Show Details
11331641
Garnett, Inc.
Patent: US6340468 B1, 2002 ; Title/Abstract Full Text Show Details
prophetic product
Claim
Canadian Patents and Development Limited
Patent: US4158822 A1, 1979 ; Title/Abstract Full Text Show Details
L'Oreal
Patent: US5180400 A1, 1993 ; Title/Abstract Full Text Show Details
prophetic product
Bayer Aktiengesellschaft
Patent: US4621138 A1, 1986 ; Title/Abstract Full Text Show Details
Bayer Aktiengesellschaft
Patent: US5138054 A1, 1992 ; Title/Abstract Full Text Show Details
Derivative (32) Comment (Derivative)
Reference
Semichinon-radikal: NMR-Kopplungskonstanten
Sharma,S.C.; Torssell,K.
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1978 , vol. 32, p. 347 - 353 Full Text View citing articles Show Details
Bis-2.4-dinitrophenylhydrazon : F: 235-236grad , gelb
Birch et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (19721999), 1976 , p. 898,903 Full Text Show Details
π-Komplexe m. aromat. C6-C8-Kohlenwasserstoffen: K (aus GLC)
Bratchikov et al.
Russian Journal of Physical Chemistry, 1976 , vol. 50, p. 333 p. 563 Full Text Show Details
H-Brueckenkomplex mit Cyclohexanol: E, ΔH (aus IR /ν(O-H)/ in CCl4 u.Iogansen-Formel)
Zaitsev; Trankvillitskaya
Russian Journal of Physical Chemistry, 1974 , vol. 48, p. 963 p. 1621 Full Text Show Details
H-Brueckenkomplex mit p-t-Butylphenol: E, ΔH (aus IR /ν(O-H)/ in CCl4 u.Iogansen-Formel)
Zaitsev; Trankvillitskaya
Russian Journal of Physical Chemistry, 1974 , vol. 48, p. 963 p. 1621 Full Text Show Details
Komplexe m. Phosphinen
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Komplex m. Trimethylphosphin; UV, VIS
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Komplex m. Triphenylphosphin; UV, VIS
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Komplex m. Tri-p-tolylphosphin; UV, VIS
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Komplex m. Phenyldimethylphosphin; UV, VIS
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Verb. mit 3,4-Benzpyren: F: 66-68grad
Laskowski
Analytical Chemistry, 1966 , vol. 38, p. 1188,1193 Chem.Abstr., 1961 , # 607 Full Text Show Details
Verb. mit 1,2,5,6-Dibenzanthracen: F: 102-105grad
Laskowski
Analytical Chemistry, 1966 , vol. 38, p. 1188,1193 Chem.Abstr., 1961 , # 607 Full Text Show Details
Addukt mit Triphenylphosphin: B.: aus den Komponenten, Ae.; F: 159-161grad (Me.-Ae.) (Zers.); IR-Abs. (Nujol, KBr): l.c.S. 2209
Beg; Siddiqui
Tetrahedron, 1966 , vol. 22, p. 2203,2211 Full Text Show Details
Addukt mit Trimethyl-phosphin: B.: aus den Komponenten, Ae.; F: 175-178grad (Me.-Ae.) (Zers.); IR-Abs. (Nujol, KBr): l.c.S. 2208
Beg; Siddiqui
Tetrahedron, 1966 , vol. 22, p. 2203,2211 Full Text Show Details
Addukt mit Tris-p-tolylphosphin: B.: aus den Komponenten, Ae.; F: 255-260grad (Zers.) (Me.-Ae.); IR-Abs. (Nujol, KBr): l.c.S. 2209
Beg; Siddiqui
Tetrahedron, 1966 , vol. 22, p. 2203,2211 Full Text Show Details
Addukt mit Phenyldimethylphosphin: B.: aus den Komponenten, Ae.; F: 234-236grad (Me.-Ae.) (Zers.); IR-Abs. (Nujol, KBr): l.c.S. 2208
Beg; Siddiqui
Tetrahedron, 1966 , vol. 22, p. 2203,2211 Full Text Show Details
Pyren-Komplex C16H10*C7H6O2: F: 111grad
Turcsanyi; Tudos
Acta Chimica Academiae Scientiarum Hungaricae, 1965 , vol. 43, p. 63,65 Full Text Show Details
Komplex mit Pyren, C7H6O2*C16H10: Charge-Transfer-Bande
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Komplex mit Naphthalin, C7H6O2*C10H8: Charge-Transfer-Bande
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Komplex mit Anthracen, C7H6O2*C14H10: Charge-Transfer-Bande
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
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Reference
Komplex mit Triphenylen, C7H6O2*C18H12: Charge-Transfer-Bande
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Komplex mit Hexamethylbenzol, C7H6O2*C12H18: Charge-Transfer-Bande
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Komplex mit Hexamethylbenzol, C7H6O2*C12H18: Charge-Transfer-Maximum
Peover
Transactions of the Faraday Society, 1964 , vol. 60, p. 479 Full Text View citing articles Show Details
Komplex mit 1,2-Dimethyl-indol, C7H6O2*C10H11N: Charge-Transfer-Maximum (CH2Cl2)
Foster; Hanson
Transactions of the Faraday Society, 1964 , vol. 60, p. 2189,2193 Full Text Show Details
Komplex mit Hexamethylbenzol, C7H6O2*C12H18: Charge-Transfer-Maximum (Cyclohexan)
Foster; Hanson
Transactions of the Faraday Society, 1964 ,
vol. 60, p. 2189,2193 Full Text Show Details
Komplex mit 2-Methyl-indol, C7H6O2*C9H9N: Charge-Transfer-Maximum (CH2Cl2)
Foster; Hanson
Transactions of the Faraday Society, 1964 , vol. 60, p. 2189,2193 Full Text Show Details
Komplex mit 3-Methyl-indol, C7H6O2*C9H9N: Charge-Transfer-Maximum (CH2Cl2)
Foster; Hanson
Transactions of the Faraday Society, 1964 , vol. 60, p. 2189,2193 Full Text Show Details
Charge-Transfer-Komplex mit Hexamethyl-benzol in CCl4: Assoziationskonst.; Bildungsenthalpie; Abs.-Max. (CCl4)
Hammond
Journal of the Chemical Society, 1964 , p. 471,473, 475 Full Text Show Details
Charge-Transfer-Komplex mit Hexamethylbenzol, xC7H6O2*yC12H18: λ(max) (in Cyclohexan): 399nm
Foster; Thomson
Transactions of the Faraday Society, 1963 , vol. 59, p. 296,298 Full Text Show Details
Charge-Transfer-Komplex mit N,N,N',N'-Tetramethyl-p-phenylendiamin, xC7H6O2*yC10H16N2: Absorption im sichtbaren Bereich 400 - 700 nm des festen Komplexes, λ(max): 619 nm; Charge-Transfer-Uebergang in Cyclohexan, λ(max) (S. 299)
Foster; Thomson
Transactions of the Faraday Society, 1963 , vol. 59, p. 296,298 Full Text Show Details
CT-Komplex mit Pyren: Abs.-Max. i. Lsg. (Dichlormethan)
Peover
Transactions of the Faraday Society, 1962 , vol. 58, p. 1656,1657 Full Text Show Details
2,4-Dinitro-phenylhydrazon: UV-Max: 204 u. 408 mμ
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1961 , vol. 16, p. 810 Full Text Show Details
Purification (1) Reference McKillop; Young
Synthetic Communications, 1977 , vol. 7, p. 467,470 Full Text Show Details
Physical Data Melting Point (28) Melting Point
Solvent (Melting Point)
70 - 75 °C
supporting information
Yoshida, Ryota; Isozaki, Katsuhiro; Yokoi, Tomoya; Yasuda, Nobuhiro; Sadakane, Koichiro; Iwamoto, Takahiro; Takaya, Hikaru; Nakamura, Masaharu
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 31 p. 7468 - 7479 Title/Abstract Full Text View citing articles Show Details
68 - 69 °C
supporting information
Sasane, Kulbhushan A.; Telvekar, Vikas N.
Synthetic Communications, 2014 , vol. 44, # 4 p. 468 - 473 Title/Abstract Full Text View citing articles Show Details
65 - 68 °C
Uliana, Marciana P.; Servilha, Bruno M.; Alexopoulos, Olga; De Oliveira, Kleber T.; Tormena, Cludio F.; Ferreira, Marco A.B.; Brocksom, Timothy J.
Tetrahedron, 2014 , vol. 70, # 39 p. 6963 - 6973 Title/Abstract Full Text View citing articles Show Details
72 - 73 °C
Hadjila, Dokari; Mohamed, Hammadi
Asian Journal of Chemistry, 2013 , vol. 25, # 11 p. 6112 - 6116 Title/Abstract Full Text View citing articles Show Details
70 °C
toluene hexane
Derikvand, Fatemeh; Bigi, Franca; Maggi, Raimondo; Piscopo, Calogero Giancarlo; Sartori, Giovanni
Journal of Catalysis, 2010 , vol. 271, # 1 p. 99 - 103 Title/Abstract Full Text View citing articles Show Details
68 - 69 °C
supporting information
Zagulyaeva, Aleksandra A.; Banek, Christopher T.; Yusubov, Mekhman S.; Zhdankin, Viktor V.
Organic Letters, 2010 , vol. 12, # 20 p. 4644 - 4647
Location
Comment (Melting Point)
Reference
Title/Abstract Full Text View citing articles Show Details
69 °C
Khansole, Sandeep V.; Patwari, Shivaji B.; Vibhute, Yeshwant B.
Journal of the Indian Chemical Society, 2009 , vol. 86, # 12 p. 1343 - 1346 Title/Abstract Full Text View citing articles Show Details
69 °C
Carstanjen
Journal fuer Praktische Chemie (Leipzig), 1881 , vol. <2> 23, p. 423,425 Full Text Show Details
Ali
Pakistan Journal of Scientific and Industrial Research, 1968 , vol. 11, p. 9,10 Full Text Show Details
Nallaiah, C.; Strickson, J. A.
Tetrahedron, 1986 , vol. 42, # 14 p. 4083 - 4088 Title/Abstract Full Text View citing articles Show Details
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
72 - 73 °C
Villemin, Didier; Hammadi, Mohamed; Hachemi, Messaoud
Synthetic Communications, 2002 , vol. 32, # 10 p. 1501 - 1515 Title/Abstract Full Text View citing articles Show Details
68 - 69 °C
ethyl acetate
Saladino, Raffaele; Neri, Veronica; Mincione, Enrico; Marini, Stefano; Coletta, Massimiliano; Fiorucci, Chiara; Filippone, Paolino
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 4 p. 581 - 586 Title/Abstract Full Text View citing articles Show Details
67 - 69 °C
Hashemi, Mohammed M.; Beni, Yousef A.
Journal of Chemical Research - Part S, 1999 , # 11 p. 672 - 673 Title/Abstract Full Text View citing articles Show Details
67 °C
Nietzki
Chemische Berichte, 1877 , vol. 10, p. 835 Justus Liebigs Annalen der Chemie, 1882 , vol. 215, p. 160 Full Text Show Details
Suresh; Skaria, Sunny; Ponrathnam
Synthetic Communications, 1996 , vol. 26, # 11 p. 2113 - 2117 Title/Abstract Full Text View citing articles Show Details
68 - 69 °C
Clark
American Chemical Journal, 1892 , vol. 14, p. 571 Full Text Show Details
Underwood; Walsh
Journal of the American Chemical Society, 1936 , vol. 58, p. 646 Organic Syntheses, 1943 , vol. Coll. Vol. II, p. 553 Full Text View citing articles Show Details
Smith; Irwin
Journal of the American Chemical Society, 1941 , vol. 63, p. 1036,1040 Full Text Show Details
Nilsson et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1973 , p. 2337,2338 Full Text Show Details
McKillop; Ray
Synthesis, 1977 , p. 847 Full Text Show Details
Barnish, Ian T.; Gibson, Martin S.
Journal of Chemical Research, Miniprint, 1992 , # 7 p. 1740 - 1757 Title/Abstract Full Text Show Details
76 °C
Method: subl. sample
Turchaninov, V. K.; Gorshkov, A. G.; Petrushenko, K. B.; Vokin, A. I.; Skvortsova, G. G.
Journal of Organic Chemistry USSR (English Translation), 1984 , vol. 20, # 5 p. 986 - 990 Zhurnal Organicheskoi Khimii, 1984 , vol. 20, # 5 p. 1084 - 1089 Title/Abstract Full Text Show Details
71 °C
diethyl ether
Varma, R. G.; Yadav, R. L.
Journal of the Indian Chemical Society, 1983 , vol. 60, p. 554 - 556 Title/Abstract Full Text Show Details
67 °C
Method: subl. sample
Kurov, G. N.; Svyatkina, L. I.; Skvortsova, G. G.; Naumova, I. P.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 10 p. 1969 1972 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 10 p. 2235 - 2238 Title/Abstract Full Text View citing articles Show Details
68 °C
Malesani, Giorgio; Galiano, Fabio; Ferlin, Maria Grazia; Masiero, Sergio
Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 563 - 569 Title/Abstract Full Text Show Details
66.5 67 °C
Jacobsen
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1979 , p. 569 Full Text Show Details
66 - 67 °C
McKillop,A. et al.
Tetrahedron, 1970 , vol. 26, p. 4031 - 4039 Full Text View citing articles Show Details
Horak,V.; Manning,W.B.
Journal of Organic Chemistry, 1979 , vol. 44, # 1 p. 120 - 123 Full Text View citing articles Show Details
Dezina et al.
Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk, 1979 , vol. 2, p. 84,88 Chem.Abstr., 1979 , vol. 91, # 56554 Full Text Show Details
71 °C
Yamada,Y.; Hosaka,K.
Synthesis, 1977 , p. 53 - 54 Full Text View citing articles Show Details
Hide facts Melting Point
Solvent (Melting Point)
Reference
65 - 66.5 °C
Jacob 3rd.; Callery; Shulgin; Castagnoli Jr.
The Journal of organic chemistry, 1976 , vol. 41, # 22 p. 3627 - 3629 Title/Abstract Full Text View citing articles Show Details
64 - 65 °C
Rao et al.
Journal of Organic Chemistry, 1975 , vol. 40, p. 2548 Full Text View citing articles Show Details
66 °C
Maruyama et al.
Bulletin of the Chemical Society of Japan, 1973 , vol. 46, p. 2470,2474 Full Text Show Details
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
67 - 68 °C
Noelting; Baumann
Chemische Berichte, 1885 , vol. 18, p. 1152 Full Text Show Details
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
65.5 - 66.5 °C
Balogh,V. et al.
Journal of Organic Chemistry, 1971 , vol. 36, # 10 p. 1339 - 1341 Full Text View citing articles Show Details
67.3 - 67.8 °C
Kumanotani et al.
Bulletin of the Chemical Society of Japan, 1968 , vol. 41, p. 2118,2120 Full Text Show Details
67 - 68 °C
petroleum ether
Hecker,E.; Meyer,E.
Chemische Berichte, 1964 , vol. 97, p. 1926 - 1939 Full Text View citing articles Show Details
Jalyowiczor
Roczniki Chemii, 1968 , vol. 42, p. 355 Full Text Show Details
68 - 69 °C
ethanol
Hammond
Journal of the Chemical Society, 1964 , p. 471,473, 475 Full Text Show Details
Refractive Index (2) Refractive Index
Wavelength (Refractive Index)
Temperature (Refractive Index)
Reference
1.5049
656.3 nm
77.9 °C
v.Auwers
Chemische Berichte, 1927 , vol. 60, p. 2138 Full Text Show Details
1.5111
587.6 nm
77.9 °C
v.Auwers
Chemische Berichte, 1927 , vol. 60, p. 2138 Full Text Show Details
Density (3)
Density
Reference Temperature
Measurement Temperature
Reference
1.2 g·cm-3
4 °C
25 °C
Borovikov; Sivachek; Makovetskii; Novikov
Russian Journal of General Chemistry, 1997 , vol. 67, # 6 p. 936 - 941 Title/Abstract Full Text View citing articles Show Details
1.083 g·cm-3
4 °C
77.9 °C
v.Auwers
Chemische Berichte, 1927 , vol. 60, p. 2138 Full Text Show Details
1.034 - 1.081 g·cm-3
4 °C
75.5 - 127.5 °C
Garner; Sugden
Journal of the Chemical Society, 1927 , p. 2881 Full Text View citing articles Show Details
Association (MCS) (14) Partner (Association (MCS))
Solvent (Association (MCS))
UV/VIS spectrum of the complex
cresol
UV/VIS spectrum of the complex
Description (Association (MCS))
Temperature (Association (MCS))
Comment (Association (MCS))
neat (no solvent)
Watanabe, Hiroto; Hiraoka, Ryota; Senna, Mamoru
Tetrahedron Letters, 2006 , vol. 47, # 26 p. 4481 - 4484 Title/Abstract Full Text View citing articles Show Details
phenol; dimethyl sulfoxide
CCl4
Kalnin'sh; Bursian
Russian Journal of Physical Chemistry A, 1996 , vol. 70, # 12 p. 2048 - 2053 Title/Abstract Full Text View citing articles Show Details
Stability constant of the complex with ...
5,15-cis-bis(2-hydroxy-1naphthyl)octaethylporphyrin
CDCl3
-30.1 - 24.9 °C
Aoyama, Yasuhiro; Asakawa, Masumi; Matsui, Yuichi; Ogoshi, Hisanobu
Journal of the American Chemical Society, 1991 , vol. 113, # 16 p. 6233 - 6240 Title/Abstract Full Text View citing articles Show Details
Enthalpy of association
5,15-cis-bis(2-hydroxy-1naphthyl)octaethylporphyrin
CDCl3
Aoyama, Yasuhiro; Asakawa, Masumi; Matsui, Yuichi; Ogoshi, Hisanobu
Journal of the American Chemical Society, 1991 , vol. 113, # 16 p. 6233 - 6240 Title/Abstract Full Text View citing articles Show Details
Further physical properties of the complex
5,15-cis-bis(2-hydroxy-1naphthyl)octaethylporphyrin
CDCl3
Aoyama, Yasuhiro; Asakawa, Masumi; Matsui, Yuichi; Ogoshi, Hisanobu
Journal of the American Chemical Society, 1991 , vol. 113, # 16 p. 6233 - 6240 Title/Abstract Full Text View citing articles Show Details
UV/VIS spectrum of the complex
10,10'-dimethyl-9,10,9',10'tetrahydro-[9,9']biacridinyl
benzene
Colter, Allan K.; Lai, Charles C.; Parsons, A. Gregg; Ramsay, N. Bruce; Saito, Gunzi
Canadian Journal of Chemistry, 1985 , vol. 63, p. 445 - 451 Title/Abstract Full Text Show Details
UV/VIS spectrum of the complex
9,10-dihydro-10-methylacridine
benzene
Colter, Allan K.; Lai, Charles C.; Parsons, A. Gregg; Ramsay, N. Bruce; Saito, Gunzi
Canadian Journal of Chemistry, 1985 , vol. 63, p. 445 - 451 Title/Abstract Full Text Show Details
UV/VIS spectrum of the complex
pyrene
benzene
Colter, Allan K.; Lai, Charles C.; Parsons, A. Gregg; Ramsay, N. Bruce; Saito, Gunzi
Canadian Journal of Chemistry, 1985 , vol. 63, p. 445 - 451 Title/Abstract Full Text Show Details
Further physical properties of the complex
10H-phenothiazine
CH2Cl2
Turchaninov, V. K.; Gorshkov, A. G.; Petrushenko, K. B.; Vokin, A. I.; Skvortsova, G. G.
Journal of Organic Chemistry USSR (English Translation), 1984 , vol. 20, # 5 p. 986 - 990 Zhurnal Organicheskoi Khimii, 1984 , vol. 20, # 5 p. 1084 - 1089 Title/Abstract Full Text Show Details
Further physical properties of the complex
10H-phenothiazine
CH2Cl2
-10 °C
Turchaninov, V. K.; Gorshkov, A. G.; Petrushenko, K. B.; Vokin, A. I.; Skvortsova, G. G.
Journal of Organic Chemistry USSR (English Translation), 1984 , vol. 20, # 5 p. 986 - 990 Zhurnal Organicheskoi Khimii, 1984 , vol. 20, # 5 p. 1084 - 1089 Title/Abstract Full Text Show Details
UV/VIS spectrum of the
ethylthioporphyrin
Mataga, Noboru; Karen, Akiya; Okada, Tadashi
Reference
complex
Journal of the American Chemical Society, 1984 , vol. 106, # 8 p. 2442 - 2443 Title/Abstract Full Text View citing articles Show Details
Further physical properties of the complex
C90H104N4O36
dimethylformamide glycerol
-73.1 °C
Ratio of solvents: 1:1
Gonzalez, Monica C.; McIntosh, Alan R.; Bolton, James R.; Weedon, Alan C.
Journal of the Chemical Society, Chemical Communications, 1984 , # 17 p. 1138 - 1140 Title/Abstract Full Text View citing articles Show Details
Association with compound
Fritzsche
Zeitschrift fuer Physikalische Chemie (Muenchen, Germany), 1964 , vol. 43, p. 154 Full Text Show Details
Zaitsev; Trankvillitskaya
Journal of Applied Spectroscopy, 1973 , vol. 18, p. 332 p. 449 Full Text View citing articles Show Details
Spectrum of the complex
Foster; Hanson
Biochimica et Biophysica Acta, 1966 , vol. 112, p. 482,484 Full Text Show Details
Chromatographic Data (1) Chromatographic data
Reference
LC (Liquid chromatography)
Wang, Shaomang; Li, Dinglong; Sun, Cheng; Yang, Shaogui; Guan, Yuan; He, Huan
Journal of Molecular Catalysis A: Chemical, 2014 , vol. 383-384, p. 128 - 136 Title/Abstract Full Text View citing articles Show Details
Crystal Phase (2) Description (Crystal Phase)
Reference
Crystal structure determination
Trommsdorf et al.
Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1970 , vol. 271, p. 45 Full Text Show Details
Interplanar spacing
Neumann; Gould
Analytical Chemistry, 1953 , vol. 25, p. 751,755 Full Text Show Details
Crystal Property Description (9) Colour & Other Properties
Location
Reference
yellow
supporting information
Yoshida, Ryota; Isozaki, Katsuhiro; Yokoi, Tomoya; Yasuda, Nobuhiro; Sadakane, Koichiro; Iwamoto, Takahiro; Takaya, Hikaru; Nakamura, Masaharu
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 31 p. 7468 - 7479 Title/Abstract Full Text View citing articles Show Details
yellow
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
orange
supporting information
Wang, Dawei; Ge, Bingyang; Du, Liyong; Miao, Hongyan; Ding, Yuqiang
Synlett, 2014 , vol. 25, # 20 art. no. ST-2014-W0606-L, p. 2895 - 2898 Title/Abstract Full Text View citing articles Show Details
brown
Hadjila, Dokari; Mohamed, Hammadi
Asian Journal of Chemistry, 2013 , vol. 25, # 11 p. 6112 - 6116 Title/Abstract Full Text View citing articles Show Details
brown
Villemin, Didier; Hammadi, Mohamed; Hachemi, Messaoud
Synthetic Communications, 2002 , vol. 32, # 10 p. 1501 - 1515 Title/Abstract Full Text View citing articles Show Details
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
yellow
supporting information
Zagulyaeva, Aleksandra A.; Banek, Christopher T.; Yusubov, Mekhman S.; Zhdankin, Viktor V.
Organic Letters, 2010 , vol. 12, # 20 p. 4644 - 4647 Title/Abstract Full Text View citing articles Show Details
Hu, Peng; Huang, Shijun; Xu, Jing; Shi, Zhang-Jie; Su, Weiping
Angewandte Chemie - International Edition, 2011 , vol. 50, # 42 p. 9926 - 9930
Title/Abstract Full Text View citing articles Show Details
Singh, Prabhpreet; Lamanna, Giuseppe; Menard-Moyon, Cecilia; Toma, Francesca Maria; Magnano, Elena; Bondino, Federica; Prato, Maurizio; Verma, Sandeep; Bianco, Alberto
Angewandte Chemie - International Edition, 2011 , vol. 50, # 42 p. 9893 - 9897 Title/Abstract Full Text View citing articles Show Details
yellow
Ling, Taotao; Poupon, Erwan; Rueden, Erik J.; Kim, Sun H.; Theodorakis, Emmanuel A.
Journal of the American Chemical Society, 2002 , vol. 124, # 41 p. 12261 - 12267 Title/Abstract Full Text View citing articles Show Details
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Maloney, David J.; Hecht, Sidney M.
Organic Letters, 2005 , vol. 7, # 19 p. 4297 - 4300 Title/Abstract Full Text View citing articles Show Details
Yakura, Takayuki; Omoto, Masanori; Yamauchi; Tian, Yuan; Ozono, Ayaka
Tetrahedron, 2010 , vol. 66, # 31 p. 5833 - 5840 Title/Abstract Full Text View citing articles Show Details
Amemiya, Takashi; Wang, Jichang
Journal of Physical Chemistry A, 2010 , vol. 114, # 51 p. 13347 - 13352 Title/Abstract Full Text View citing articles Show Details
yellow - orange
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
yellow - purple
Hashemi, Mohammed M.; Beni, Yousef A.
Journal of Chemical Research - Part S, 1999 , # 11 p. 672 - 673 Title/Abstract Full Text View citing articles Show Details
Hashemi, Mohammed M.; Karimi-Jaberi, Zahed; Eftekhari-Sis, Bagher
Journal of Chemical Research, 2005 , # 3 p. 160 - 161 Title/Abstract Full Text View citing articles Show Details
Dissociation Exponent (1) Comment (Dissociation Exponent)
Reference
(pk')Radikal: pK(a)
Rao; Hayon
Analytical Chemistry, 1976 , vol. 48, p. 564,565 Full Text Show Details
Electrical Data (1) Description (Electrical Data)
Reference
Piezoelectricity
Koptzik
Izvestiya Akademii Nauk SSSR, Seriya Fizicheskaya, 1956 , vol. 20, p. 219,222; engl. Ausg. S. 201 Chem.Abstr., 1956 , p. 11742 Full Text View citing articles Show Details
Electrical Moment (3) Description (Electrical Moment)
Moment (Electrical Moment)
Temperature (Electrical Moment)
Method (Electrical Moment)
Solvent (Electrical Moment)
Dipole moment
0.98 D
25 °C
Borovikov; Sivachek; Makovetskii; Novikov
Russian Journal of General Chemistry, 1997 , vol. 67, # 6 p. 936 - 941 Title/Abstract Full Text View citing articles Show Details
Dipole moment
1.03 D
25 °C
Dielectric constant (ε)
benzene
Gur'yanova, E. N.; Muravlyanskii, D. V.; Romm, I. P.; Sviridov, B. D.; Shifrina, R. R.
J. Gen. Chem. USSR (Engl. Transl.), 1984 , vol. 54, # 4 p. 817 824,725 - 731 Title/Abstract Full Text Show Details
Dipole moment
1.17 D
25 °C
Dielectric constant (ε)
1,3,5-trimethyl-benzene
Gur'yanova, E. N.; Muravlyanskii, D. V.; Romm, I. P.; Sviridov, B. D.; Shifrina, R. R.
J. Gen. Chem. USSR (Engl. Transl.), 1984 , vol. 54, # 4 p. 817 824,725 - 731 Title/Abstract Full Text Show Details
Electrochemical Behaviour (2) Description (Electrochemical Behaviour)
Reference
Polarography
Lindsey,A.S. et al.
Journal of the Chemical Society, 1962 , p. 4558 - 4569
Reference
Full Text View citing articles Show Details
Takamura; Hayakawa
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1971 , vol. 31, p. 225 Full Text View citing articles Show Details
Takamura; Takamura
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1968 , vol. 18, p. 159 Full Text View citing articles Show Details
Arai; Onozuka
Nippon Kagaku Kaishi, 1978 , p. 997,998 Full Text Show Details
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Takamura; Takamura
Transactions of the Faraday Society, 1965 , vol. 61, p. 1270 Full Text View citing articles Show Details
Peover
Journal of the Chemical Society, 1962 , p. 4540,4543 Full Text Show Details
Zuman
Collection of Czechoslovak Chemical Communications, 1962 , vol. 27, p. 2035,2048 Full Text Show Details
Takamura
Bulletin of the Chemical Society of Japan, 1963 , vol. 36, p. 1053 Full Text Show Details
Berg; Gollmick
Collection of Czechoslovak Chemical Communications, 1965 , vol. 30, p. 4192,4196 Full Text Show Details
Ryba et al.
Collection of Czechoslovak Chemical Communications, 1968 , vol. 33, p. 26 Full Text Show Details
Pettersson
Acta Chemica Scandinavica (1947-1973), 1964 , vol. 18, p. 1428,1429 Full Text Show Details
Electrochemical properties
Electrochemical Characteristics (44) Description (Electrochemical Characteristics)
Solvent (Electrochemical Characteristics)
pH-Value (Electrochemical Characteristics)
Temperature (Electrochemical Characteristics)
Product XRN (Electrochemical Characteristics)
Product
Location
cyclovoltammetry
benzonitrile
24.84 °C
Other electrode; potential diagram; 0.10 M tetra-nbutylammonium hexafluorophosphate
El-Khouly, Mohamed E.; El-Kemary, Maged A.; Fukuzumi, Shunichi
Journal of Photochemistry and Photobiology A: Chemistry, 2015 , vol. 302, p. 11 - 16 Title/Abstract Full Text View citing articles Show Details
cyclovoltammetry
3.82
25 °C
supporting information
Saturated silver chloride electrode; potential diagram; 0.20 mol dm-3 Na2SO4
Jozsa, Eva; Purgel, Mihaly; Bihari, Marianna; Feher, Peter Pal; Sustyak, Gabor; Varnagy, Balazs; Kiss, Virag; Lado, Eszter; Osz, Katalin
Saturated silver chloride electrode; potential diagram; 0.20 mol dm-3 Na2SO4
Jozsa, Eva; Purgel, Mihaly; Bihari, Marianna; Feher, Peter Pal; Sustyak, Gabor; Varnagy, Balazs; Kiss, Virag; Lado, Eszter; Osz, Katalin
Saturated silver chloride electrode; potential diagram; 0.20 mol dm-3 Na2SO4
Jozsa, Eva; Purgel, Mihaly; Bihari, Marianna; Feher, Peter Pal; Sustyak, Gabor; Varnagy, Balazs; Kiss, Virag; Lado, Eszter; Osz, Katalin
Saturated silver chloride electrode; potential diagram; 0.20 mol dm-3 Na2SO4
Jozsa, Eva; Purgel, Mihaly; Bihari, Marianna; Feher, Peter Pal; Sustyak, Gabor; Varnagy, Balazs; Kiss, Virag; Lado, Eszter; Osz, Katalin
cyclovoltammetry
cyclovoltammetry
cyclovoltammetry
3.97
4.19
5.77
25 °C
25 °C
25 °C
supporting information
supporting information
supporting information
Comment (Electrochemical Characteristics)
Reference
New Journal of Chemistry, 2014 , vol. 38, # 2 p. 588 - 597 Title/Abstract Full Text View citing articles Show Details
New Journal of Chemistry, 2014 , vol. 38, # 2 p. 588 - 597 Title/Abstract Full Text View citing articles Show Details
New Journal of Chemistry, 2014 , vol. 38, # 2 p. 588 - 597 Title/Abstract Full Text View citing articles Show Details
New Journal of Chemistry, 2014 , vol. 38, # 2 p. 588 - 597
Title/Abstract Full Text View citing articles Show Details
cyclovoltammetry
dichloromethane
1873156
2-methyl-1,4benzoquinone radical anion
transmitted electrons -1; Standard potential; -1.041 V; Ferrocene/ferrocenium; 0.10 M tetrabutylammonium hexafluorophosphate
Hall, Gabriel B.; Chen, Jinzhu; Mebi, Charles A.; Okumura, Noriko; Swenson, Matthew T.; Ossowski, Stephanie E.; Zakai, Uzma I.; Nichol, Gary S.; Lichtenberger, Dennis L.; Evans, Dennis H.; Glass, Richard S.
Organometallics, 2013 , vol. 32, # 21 p. 6605 6612 Title/Abstract Full Text View citing articles Show Details
Electrochemical characteristics given
Nikitina, Viktoriya A.; Nazmutdinov, Renat R.; Tsirlina, Galina A.
Journal of Physical Chemistry B, 2011 , vol. 115, # 4 p. 668 - 677 Title/Abstract Full Text View citing articles Show Details
reduction potential
H2O
7-9
23 °C
Cape, Jonathan L.; Bowman, Michael K.; Kramer, David M.
Phytochemistry, 2006 , vol. 67, # 16 p. 1781 1788 Title/Abstract Full Text View citing articles Show Details
reduction potential
various solvent(s)
7
24.85 °C
Fukuzumi, Shunichi; Nishimine, Mari; Ohkubo, Kei; Tkachenko, Nikolai V.; Lemmetyinen, Helge
Journal of Physical Chemistry B, 2003 , vol. 107, # 45 p. 12511 - 12518 Title/Abstract Full Text View citing articles Show Details
reduction potential
benzonitrile
D'Souza; Deviprasad
Journal of Organic Chemistry, 2001 , vol. 66, # 13 p. 4601 - 4609 Title/Abstract Full Text View citing articles Show Details
polarographic halfwave potential
Flaig,W. et al.
Justus Liebigs Annalen der Chemie, 1968 , vol. 719, p. 96 - 111 Full Text View citing articles Show Details
Ryba et al.
Collection of Czechoslovak Chemical Communications, 1968 , vol. 33, p. 26 Full Text Show Details
Kurov, G. N.; Svyatkina, L. I.; Skvortsova, G. G.; Naumova, I. P.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 10 p. 1969 1972 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 10 p. 2235 - 2238 Title/Abstract Full Text View citing articles Show Details
Sviridov, B. D.; Nikolaeva, T. D.; Venderina, V. F.; Zhdanov, S. I.
J. Gen. Chem. USSR (Engl. Transl.), 1985 , vol. 55, # 4 p. 821 - 824,732 - 734 Title/Abstract Full Text Show Details
Kazak; Chudaeva; Rodionova; Trofimov
Russian Journal of Applied Chemistry, 1996 , vol. 69, # 1 p. 52 - 56 Title/Abstract Full Text View citing articles Show Details
redox potential
benzonitrile various solvent(s)
5927556
methyl-pbenzoquinone radical anion
-0.56 V Product: /BRN= 5927556/. Method: cyclovoltammetry. Description: platinum button or glassy carbon electrode as the working electrode, platinum wire as the counter electrode, saturated calomel electrode as the
D'Souza, Francis
Journal of the American Chemical Society, 1996 , vol. 118, # 4 p. 923 - 924 Title/Abstract Full Text View citing articles Show Details
reference electrode oxidation potential
aq. phosphate buffer
7.4
Shumakovich; Yaropolov; Dubova; Antonova; Bachurin
Doklady Chemistry, 1996 , vol. 348, # 4-6 p. 149 - 152 Title/Abstract Full Text View citing articles Show Details
reduction potential
aq. phosphate buffer
7.4
Shumakovich; Yaropolov; Dubova; Antonova; Bachurin
Doklady Chemistry, 1996 , vol. 348, # 4-6 p. 149 - 152 Title/Abstract Full Text View citing articles Show Details
redox potential
Flaig,W. et al.
Justus Liebigs Annalen der Chemie, 1968 , vol. 719, p. 96 - 111 Full Text View citing articles Show Details
Peover
Transactions of the Faraday Society, 1964 , vol. 60, p. 479 Full Text View citing articles Show Details
Markow et al.
Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk, 1968 , vol. 3, p. 36,37 Chem.Abstr., 1969 , vol. 70, # 6864 Full Text Show Details
Moriconi et al.
Journal of Organic Chemistry, 1962 , vol. 27, p. 2772,2774, 2775 Full Text View citing articles Show Details
Fasman et al..
Doklady Physical Chemistry, 1964 , vol. 154156, p. 298 Doklady Akademii Nauk SSSR, 1964 , vol. 155, p. 434 Full Text Show Details
Tanner, Dennis D.; Deonarian, Natasha; Kharrat, Abdelmajid
Canadian Journal of Chemistry, 1989 , vol. 67, p. 171 - 175 Title/Abstract Full Text Show Details
Wilford, J. H.; Archer, M. D.; Bolton, J. R.; Ho, T.-F.; Schmidt, J. A.; Weedon, A. C.
Journal of Physical Chemistry, 1985 , vol. 89, # 25 p. 5395 - 5398 Title/Abstract Full Text View citing articles Show Details
Okubo, Masao; Tsutsumi, Toshiki; Matsuo, Koji
Bulletin of the Chemical Society of Japan, 1987 , vol. 60, p. 2085 - 2090 Title/Abstract Full Text Show Details
Matsuo, Koji; Shiraki, Ryuji; Okubo, Masao
Journal of Physical Organic Chemistry, 1994 , vol. 7, # 10 p. 567 - 577 Title/Abstract Full Text Show Details
Reynolds, Christopher A.; King, Paul M.; Richards, W. Graham
Journal of the Chemical Society, Chemical Communications, 1988 , # 21 p. 1434 - 1436 Title/Abstract Full Text View citing articles Show Details
redox potential
H2O
4.5
2041489
2methylbenzene1,4-diol
0.47 V Product: /BRN= 2041489/. No. of transm. electrons: 2 Method: potentiometry. Description: vs. NHE
Raju, K. Vijaya; Raju, G. Bangar; Yadav, M. Rajasekhar
Indian Journal of Chemistry, Section A: Inorganic, Bio-inorganic, Physical, Theoretical & Analytical Chemistry, 1993 , vol. 32, # 11 p. 1012 - 1014 Title/Abstract Full Text Show Details
redox potential
CH2Cl2
1873156
2-methyl-1,4benzoquinone radical anion
-0.39 V Product: /BRN= 4134590/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: Working electrode: Pt, reference electrode:
Aumueller, Alexander; Huenig, Siegfried
Liebigs Annalen der Chemie, 1986 , # 1 p. 165 176 Title/Abstract Full Text Show Details
Ag/AgCl/CH3CN, supporting electrolyte: Bu4NBF4 polarographic halfwave potential
aq. NaOH
2041489
2methylbenzene1,4-diol
-0.23 V Product: /BRN= 2041489/. No. of transm. electrons: 2. Method: cyclovoltammetry. Description: hangingmercurydrop electrode (working,) calomel electrode (reference); 0.1M NaOH-solution
Suga, Kosaku; Aoyagui, Shigeru
Bulletin of the Chemical Society of Japan, 1986 , vol. 59, # 6 p. 1937 - 1940 Title/Abstract Full Text Show Details
redox potential
acetonitrile
24.9 °C
6015810
C7H6O2(2)*Mg(2+)
0.32 V Product: /BRN= 6015810/. No. of transm. electrons: 2. Method: cyclovoltammetry. Description: potentiostatgalvanostat, microelectrode, NaCl/calomel reference electrode, in presence of Mg2+
Fukuzumi, Shunichi; Nishizawa, Nobuaki; Tanaka, Toshio
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (19721999), 1985 , p. 371 - 378 Title/Abstract Full Text View citing articles Show Details
redox potential
acetonitrile
24.9 °C
6015810
C7H6O2(2)*Mg(2+)
0.1 V Product: /BRN= 6015810/. No. of transm. electrons: 2. Method: cyclovoltammetry. Description: potentiostatgalvanostat, platinum microelectrode, NaCl/calomel reference electrode, in presence of Mg(2+) ion
Fukuzumi, Shunichi; Nishizawa, Nobuaki; Tanaka, Toshio
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (19721999), 1985 , p. 371 - 378 Title/Abstract Full Text View citing articles Show Details
Product
Comment (Electrochemical Characteristics)
Reference
Show next 20
Hide facts
Description (Electrochemical Characteristics)
Solvent (Electrochemical Characteristics)
Temperature (Electrochemical Characteristics)
Product XRN (Electrochemical Characteristics)
redox potential
H2O HCl
28 °C
2041489
2methylbenzene1,4-diol
0.59 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 0.5M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O HCl
28 °C
2041489
2methylbenzene1,4-diol
0.61 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 1.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O HCl
28 °C
2041489
2methylbenzene1,4-diol
0.64 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 3.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O HCl
28 °C
2041489
2methylbenzene1,4-diol
0.66 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 5.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O HCl
28 °C
2041489
2methylbenzene1,4-diol
0.68 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 7.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O
28 °C
2041489
2-
0.69 V
Murty, N. Krishna; Murty, Peri M. Dakshina
HCl
methylbenzene1,4-diol
Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 9.0M
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O H2SO4
28 °C
2041489
2methylbenzene1,4-diol
0.59 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 0.5M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O H2SO4
28 °C
2041489
2methylbenzene1,4-diol
0.6 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 1.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O H2SO4
28 °C
2041489
2methylbenzene1,4-diol
0.64 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 3.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O H2SO4
28 °C
2041489
2methylbenzene1,4-diol
0.65 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 5.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O H2SO4
28 °C
2041489
2methylbenzene1,4-diol
0.67 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 7.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.52 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 0.5M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.53 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 1.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.54 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 3.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.57 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 5.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.59 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 7.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.61 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 9.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene1,4-diol
0.63 V Product: /BRN= 2041489/. Method: potentiometry. Description: versus NHE; acidity 11.0M
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
redox potential
H2O acetic acid
28 °C
2041489
2methylbenzene-
0.64 V Product: /BRN= 2041489/. Method: potentiometry.
Murty, N. Krishna; Murty, Peri M. Dakshina
Indian Journal of Chemistry, Section A: Inorganic,
1,4-diol
Description: versus NHE; acidity 12.5M
Physical, Theoretical & Analytical, 1982 , vol. 21, # 7 p. 756 - 757 Title/Abstract Full Text Show Details
polarographic halfwave potential
acetonitrile
20 °C
1873156
2-methyl-1,4benzoquinone radical anion
-0.51 V Product: /BRN= 1873156/. No. of transm. electrons: 1. Method: pulse polarography. Description: saturated calomel electrode, tetraethylammonium perchlorate supporting electrolyte, differential technique
Bruce, Malcolm; Heatley, Frank; Ryles, Roderick G.; Scrivens, James H.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (19721999), 1980 , p. 860 - 866 Title/Abstract Full Text View citing articles Show Details
redox potential
in wss.-aethanol. HCl.
Bobrowa
Zhurnal Fizicheskoi Khimii, 1952 , vol. 26, p. 822,832 Chem.Abstr., 1952 , p. 10961 Full Text Show Details
polarographic current/voltage curve
Smith et al.
Journal of the American Chemical Society, 1941 , vol. 63, p. 1018,1019 Journal of the American Chemical Society, 1942 , vol. 64, p. 447,448 Full Text View citing articles Show Details
Page; Robinson
Journal of the Chemical Society, 1943 , p. 133 Full Text Show Details
Stromberg; Reinus
Zhurnal Obshchei Khimii, 1946 , vol. 16, p. 1431,1437 Chem.Abstr., 1947 , p. 5479 Full Text Show Details
redox potential
des Systems Methyl-benzochinon-(1.4)/2-Methylhydrochinon.
Hunter; Kvalnes
Journal of the American Chemical Society, 1932 , vol. 54, p. 2869,2874 Full Text Show Details
Kvalnes
Journal of the American Chemical Society, 1934 , vol. 56, p. 670 Full Text View citing articles Show Details
redox potential
des Systems Toluchinon/p-Xylohydrochinon in 0,1 nSchwefelsaeure bei 25,4grad.
Biilmann; Jensen; Pedersen
Journal of the Chemical Society, 1925 , vol. 127, p. 207 Full Text Show Details
Electron Binding (1) Description (Electron Binding)
Reference
Electron affinity
Chen; Wentworth
Journal of Chemical Physics, 1975 , vol. 63, p. 3183,3189 Full Text Show Details
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Tanner, Dennis D.; Deonarian, Natasha; Kharrat, Abdelmajid
Canadian Journal of Chemistry, 1989 , vol. 67, p. 171 - 175 Title/Abstract Full Text Show Details
Kurov, G. N.; Svyatkina, L. I.; Skvortsova, G. G.; Naumova, I. P.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 10 p. 1969 - 1972 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 10 p. 2235 - 2238 Title/Abstract Full Text View citing articles Show Details
Grimsrud, Eric P.; Caldwell, Gary; Chowdhury, Swapan; Kebarle, Paul
Journal of the American Chemical Society, 1985 , vol. 107, # 16 p. 4627 - 4634 Title/Abstract Full Text View citing articles Show Details
Heinis, Thomas; Chowdhury, Swapan; Scott, Susannah L.; Kebarle, Paul
Journal of the American Chemical Society, 1988 , vol. 110, # 2 p. 400 - 407 Title/Abstract Full Text View citing articles Show Details
Energy Data (MCS) (1) Description (Energy Data (MCS))
Partner (Energy Data (MCS))
Solvent (Energy Data (MCS))
Temperature (Energy Data (MCS))
Enthalpy of mixing
GaCl3
benzene
25 °C
Reference Gur'yanova, E. N.; Muravlyanskii, D. V.; Romm, I. P.; Sviridov, B. D.; Shifrina, R. R.
J. Gen. Chem. USSR (Engl. Transl.), 1984 , vol. 54, # 4 p. 817 - 824,725 - 731 Title/Abstract Full Text Show Details
Enthalpy of Combustion (1) Enthalpy of Combustion
Reference
-3.37162E+06 Jmol-1
Valeur
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1897 , vol. 125, p. 872 Annales de Chimie (Cachan, France), 1900 , vol. <7> 21, p. 478 Full Text Show Details
Further Information (31) Description (Further Information)
Reference
Further information
Beitz; Miller
Journal de Chimie Physique et de Physico-Chimie Biologique, 1979 , vol. 71, p. 4579 Full Text View citing articles Show Details
Further information
Sharma; Torssell
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1978 , vol. 32, p. 347,350 Full Text Show Details
Further information
Maquestian et al.
Organic Mass Spectrometry, 1977 , vol. 12, p. 631,633 Full Text Show Details
Further information
Merienne-Lafore
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1977 , vol. 33, p. 453 Full Text View citing articles Show Details
Further information
Bratchikov et al.
Russian Journal of Physical Chemistry, 1976 , vol. 50, p. 333 p. 563 Full Text Show Details
Further information
van't Hof; Schmidt
Chemical Physics Letters, 1975 , vol. 36, p. 457 Full Text View citing articles Show Details
Further information
Zaitsev; Trankvillitskaya
Russian Journal of Physical Chemistry, 1974 , vol. 48, p. 963 p. 1621 Full Text Show Details
Further information
Potapov; Sorokin
High Energy Chemistry, 1971 , vol. 5, p. 435 p. 487 Full Text Show Details
Further information
Koyanagi et al.
Journal of Molecular Spectroscopy, 1970 , vol. 34, p. 450,453 Full Text Show Details
Further information
McKillop et al.
Angewandte Chemie, 1970 , vol. 82, p. 84 Full Text Show Details
Further information
Dalton; Teitei
Australian Journal of Chemistry, 1969 , vol. 22, p. 1525,1529 Full Text Show Details
Further information
Gonikberg et al.
Doklady Chemistry, 1969 , vol. 185, p. 276 Dokl. Akad. Nauk SSSR Ser. Khim., 1969 , vol. 185, p. 828 Full Text Show Details
Further information
Govil
Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical, 1967 , p. 1420 Full Text Show Details
Further information
Shannon et al.
Chemical Communications (London), 1966 , p. 478 Full Text View citing articles Show Details
Further information
Aplin; Pike
Chemistry and Industry (London, United Kingdom), 1966 , p. 2009 Full Text Show Details
Further information
Meinwald et al.
Journal of the American Chemical Society, 1966 , vol. 88, p. 1590 Full Text View citing articles Show Details
Further information
Laskowski
Analytical Chemistry, 1966 , vol. 38, p. 1188,1193 Chem.Abstr., 1961 , # 607 Full Text Show Details
Further information
Monti
Journal of Organic Chemistry, 1966 , vol. 31, p. 2669,2671 Full Text Show Details
Further information
Beg; Siddiqui
Tetrahedron, 1966 , vol. 22, p. 2203,2211 Full Text Show Details
Further information
Bowie et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1966 , p. 335,336 Full Text Show Details
Hide facts Description (Further Information)
Reference
Further information
Jones; Murrell
Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical, 1966 , p. 1421 Full Text View citing articles Show Details
Further information
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Further information
Turcsanyi; Tudos
Acta Chimica Academiae Scientiarum Hungaricae, 1965 , vol. 43, p. 63,65 Full Text Show Details
Further information
Peover
Transactions of the Faraday Society, 1964 , vol. 60, p. 479 Full Text View citing articles Show Details
Further information
Foster; Hanson
Transactions of the Faraday Society, 1964 , vol. 60, p. 2189,2193 Full Text Show Details
Further information
Bryce-Smith; Gilbert
Proceedings of the Chemical Society, London, 1964 , p. 87 Full Text Show Details
Further information
Berg; Kramarczyk
Berichte der Bunsen-Gesellschaft, 1964 , vol. 68, p. 296 Full Text Show Details
Further information
Foster; Thomson
Transactions of the Faraday Society, 1963 , vol. 59, p. 296,298 Full Text Show Details
Further information
Peover
Transactions of the Faraday Society, 1962 , vol. 58, p. 1656,1657 Full Text Show Details
Further information
Kuboyama
Bulletin of the Chemical Society of Japan, 1962 , vol. 35, p. 295 Full Text Show Details
Further information
Barbier
Journal of Chromatography, 1959 , vol. 2, p. 649 Full Text View citing articles Show Details
Ionization Potential (2) Ionization Potential
Method (Ionization Potential)
Comment (Ionization Potential)
Reference
9.8 eV
PE
Higher potentials: 10.17eV, 10.37eV, 10.85ev
Gleiter, Rolf; Schaefer, Wolfgang; Staab, Heinz A.
Chemische Berichte, 1988 , vol. 121, p. 1257 - 1264 Title/Abstract Full Text Show Details
Dougherty,D. et al.
Journal of the American Chemical Society, 1978 , vol. 100, p. 5597 - 5603 Full Text View citing articles Show Details
Potapov; Sorokin
High Energy Chemistry, 1971 , vol. 5, p. 435 p. 487 Full Text Show Details
Liquid/Liquid Systems (MCS) (1) Description (Liquid/Liquid Systems (MCS))
Partner (Liquid/Liquid Systems (MCS))
Reference
Distribution between solvent 1 + 2
1-octanol/water
Moret, Ed E.; Boer, Mark de; Hilbers, Hans W.; Tollenaere, Jan P.; Janssen, Lambert H. M.; et al.
J. Med. Chem., 1996 , vol. 39, # 3 p. 720 - 728 Title/Abstract Full Text View citing articles Show Details
Liquid/Solid Systems (MCS) (1) Description (Liquid/Solid Systems (MCS))
Reference
Eutectic
Laskowski
Analytical Chemistry, 1960 , vol. 32, p. 1171,1173 Full Text Show Details
Molecular Deformation (1) Description (Molecular Deformation)
Reference
Fundamental vibrations
Merienne-Lafore
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1976 , vol. 32, p. 1235,1237,1238 Full Text View citing articles Show Details
Other Thermochemical Data (2) Description (Other Thermochemical Data)
Comment (Other Thermochemical Data)
Reference
Heat of combustion at constant volume
803,3 kcal/Mol.
Valeur
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1897 , vol. 125, p. 872 Annales de Chimie (Cachan, France), 1900 , vol. <7> 21, p. 478 Full Text Show Details
Swietoslawski; Starczewska
Journal de Chimie Physique et de Physico-Chimie Biologique, 1926 , vol. 23, p. 822 Full Text Show Details
Heat of combustion at constant volume
805.0 kcal/Mol.
Valeur
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1897 , vol. 125, p. 872 Annales de Chimie (Cachan, France), 1900 , vol. <7> 21, p. 478 Full Text Show Details
Partition octan-1-ol/water (MCS) (2) Partition Constant POW
log POW
Reference
13.9
Kumagai, Yoshito; Nakajima, Hiromi; Midorikawa, Kazumi; Homma-Takeda, Shino; Shimojo, Nobuhiro
Chemical Research in Toxicology, 1998 , vol. 11, # 6 p. 608 - 613 Title/Abstract Full Text View citing articles Show Details
0.72
Schultz; Sinks; Cronin
Aquatic Toxicology, 1997 , vol. 39, # 3-4 p. 267 - 278 Title/Abstract Full Text View citing articles Show Details
Solubility (MCS) (1) Comment (Solubility (MCS))
Reference
water soluble
Jozsa, Eva; Purgel, Mihaly; Bihari, Marianna; Feher, Peter Pal; Sustyak, Gabor; Varnagy, Balazs; Kiss, Virag; Lado, Eszter; Osz, Katalin
New Journal of Chemistry, 2014 , vol. 38, # 2 p. 588 - 597 Title/Abstract Full Text View citing articles Show Details
Surface Tension (1) Surface Tension
Temperature (Surface Tension)
Reference
27.63 - 33.86 g·s-2
76.5 - 131 °C
Garner; Sugden
Journal of the Chemical Society, 1927 , p. 2881 Full Text View citing articles Show Details
Spectra NMR Spectroscopy (46) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Temperature (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts Spectrum
1H
chloroform-d1
Chemical shifts Spectrum
13C
chloroform-d1
Chemical shifts Spectrum
1H
Chemical shifts Spectrum
Location
Reference
392 MHz
supporting information
Yoshida, Ryota; Isozaki, Katsuhiro; Yokoi, Tomoya; Yasuda, Nobuhiro; Sadakane, Koichiro; Iwamoto, Takahiro; Takaya, Hikaru; Nakamura, Masaharu
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 31 p. 7468 - 7479 Title/Abstract Full Text View citing articles Show Details
98.5 MHz
supporting information
Yoshida, Ryota; Isozaki, Katsuhiro; Yokoi, Tomoya; Yasuda, Nobuhiro; Sadakane, Koichiro; Iwamoto, Takahiro; Takaya, Hikaru; Nakamura, Masaharu
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 31 p. 7468 - 7479 Title/Abstract Full Text View citing articles Show Details
chloroform-d1
400 MHz
supporting information
Wang, Dawei; Ge, Bingyang; Ju, Anqi; Zhou, Yucheng; Xu, Chongying; Ding, Yuqiang
Journal of Organometallic Chemistry, 2015 , vol. 780, p. 30 - 33 Title/Abstract Full Text View citing articles Show Details
Wang, Dawei; Ge, Bingyang; Du, Liyong; Miao, Hongyan; Ding, Yuqiang
Synlett, 2014 , vol. 25, # 20 art. no. ST-2014-W0606-L, p. 2895 - 2898 Title/Abstract Full Text View citing articles Show Details
1H
chloroform-d1
26.84 °C
300 MHz
supporting information
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
13C
chloroform-d1
26.84 °C
75 MHz
supporting information
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
Khansole, Sandeep V.; Patwari, Shivaji B.; Vibhute, Yeshwant B.
Journal of the Indian Chemical Society, 2009 , vol. 86, # 12 p. 1343 - 1346 Title/Abstract Full Text View citing articles Show Details
Bell, Jeffrey G.; Green, James R.; Wang, Jichang
Journal of Physical Chemistry A, 2014 , vol. 118, # 42 p. 9795 - 9800 Title/Abstract Full Text View citing articles Show Details
Spectrum
1H
water-d2
25 °C
400 MHz
supporting information
Jozsa, Eva; Purgel, Mihaly; Bihari, Marianna; Feher, Peter Pal; Sustyak, Gabor; Varnagy, Balazs; Kiss, Virag; Lado, Eszter; Osz, Katalin
New Journal of Chemistry, 2014 , vol. 38, # 2 p. 588 - 597 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
60 MHz
supporting information
Sasane, Kulbhushan A.; Telvekar, Vikas N.
Synthetic Communications, 2014 , vol. 44, # 4 p. 468 - 473 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
250 MHz
Hadjila, Dokari; Mohamed, Hammadi
Asian Journal of Chemistry, 2013 , vol. 25, # 11 p. 6112 - 6116 Title/Abstract Full Text View citing articles Show Details
COSY (Correlation Spectroscopy)
1H 1H
chloroform-d1
400.1 MHz
supporting information
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
HSQC (Heteronuclear Single Quantum Coherence)
1H 13C
supporting information
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
1H
chloroform-d1
400.1 MHz
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
13C
chloroform-d1
100.6 MHz
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
270 MHz
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
chloroform-d1
68 MHz
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
300 MHz
supporting information
Singh, Prabhpreet; Lamanna, Giuseppe; Menard-Moyon, Cecilia; Toma, Francesca Maria; Magnano, Elena; Bondino, Federica; Prato, Maurizio; Verma, Sandeep; Bianco, Alberto
Angewandte Chemie - International Edition, 2011 , vol. 50, # 42 p. 9893 - 9897 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
1H
chloroform-d1
300 MHz
supporting information
Zagulyaeva, Aleksandra A.; Banek, Christopher T.; Yusubov, Mekhman S.; Zhdankin, Viktor V.
Organic Letters, 2010 , vol. 12, # 20 p. 4644 - 4647 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
500 MHz
supporting information
Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
Angewandte Chemie - International Edition, 2008 , vol. 47, # 42 p. 8093 - 8095 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
chloroform-d1
125 MHz
supporting information
Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
Angewandte Chemie - International Edition, 2008 , vol. 47, # 42 p. 8093 - 8095 Title/Abstract Full Text View citing articles Show Details
Show next 20
Hide facts
Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Temperature (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Comment (NMR Spectroscopy)
Chemical shifts
1H
CDCl3
200 MHz
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Mal, Dipakranjan; Ray, Sutapa; Sharma, Indrajeet
Journal of Organic Chemistry, 2007 , vol. 72, # 13 p. 4981 - 4984 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
300 MHz
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
75 MHz
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
Hiranuma Hidetoshi; Miller, Sidney I.
Journal of Organic Chemistry, 1982 , vol. 47, # 26 p. 5083 - 5088 Title/Abstract Full Text View citing articles Show Details
Pratt, Daniel V.; Ruan, Fuqiang; Hopkins, Paul B.
Journal of Organic Chemistry, 1987 , vol. 52, # 22 p. 5053 - 5055 Title/Abstract Full Text View citing articles Show Details
Aversa, M. C.; Giannetto, P.; Saija, A.
Magnetic Resonance in Chemistry, 1985 , vol. 23, # 5 p. 322 - 326 Title/Abstract Full Text Show Details
Hashemi, Mohammed M.; Karimi-Jaberi, Zahed; Eftekhari-Sis, Bagher
Journal of Chemical Research, 2005 , # 3 p. 160 - 161 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
50 MHz
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Reference
Chemical shifts
1H
CDCl3
250 MHz
Villemin, Didier; Hammadi, Mohamed; Hachemi, Messaoud
Synthetic Communications, 2002 , vol. 32, # 10 p. 1501 - 1515 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
400 MHz
Ling, Taotao; Poupon, Erwan; Rueden, Erik J.; Kim, Sun H.; Theodorakis, Emmanuel A.
Journal of the American Chemical Society, 2002 , vol. 124, # 41 p. 12261 - 12267 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
Chudek, John A.; Foster, Roy; Reid, Francis J.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984 , # 2 p. 287 - 292 Title/Abstract Full Text View citing articles Show Details
Ling, Taotao; Poupon, Erwan; Rueden, Erik J.; Kim, Sun H.; Theodorakis, Emmanuel A.
Journal of the American Chemical Society, 2002 , vol. 124, # 41 p. 12261 - 12267 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
tetradeuteriomethanol
250 MHz
Ficht, Simon; Muelbaier, Marcel; Giannis, Athanassios
Tetrahedron, 2001 , vol. 57, # 23 p. 4863 - 4866 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
80 MHz
Hashemi, Mohammed M.; Beni, Yousef A.
Journal of Chemical Research - Part S, 1999 , # 11 p. 672 - 673 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
Gready, Jill E.; Hata, Kazumi; Sternhell, Sever; Tansey, Charles W.
Australian Journal of Chemistry, 1990 , vol. 43, # 3 p. 593 - 600 Title/Abstract Full Text Show Details
Suresh; Skaria, Sunny; Ponrathnam
Synthetic Communications, 1996 , vol. 26, # 11 p. 2113 - 2117 Title/Abstract Full Text View citing articles Show Details
CIDNP
Hutchinson et al.
Molecular Physics, 1975 , vol. 29, p. 1767 Full Text Show Details
Meng, Q.; Yamakage, Y.; Maeda, K.; Azumi, T.
Zeitschrift fuer Physikalische Chemie (Muenchen, Germany), 1993 , vol. 180, # 1/2 p. 95 - 110 Title/Abstract Full Text Show Details
Chemical shifts
1H
CDCl3 CCl4
Meng, Q.; Yamakage, Y.; Maeda, K.; Azumi, T.
Zeitschrift fuer Physikalische Chemie (Muenchen, Germany), 1993 , vol. 180, # 1/2 p. 95 - 110 Title/Abstract Full Text Show Details
Chemical shifts
1H
CD3CN
Binstead, Robert A.; McGuire, Mark E.; Dovletoglou, Angelos; Seok, Won K.; Roecker, Lee E.; Meyer, Thomas J.
Journal of the American Chemical Society, 1992 , vol. 114, # 1 p. 173 186 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
trifluoroacetic acid
Barnish, Ian T.; Gibson, Martin S.
Journal of Chemical Research, Miniprint, 1992 , # 7 p. 1740 - 1757 Title/Abstract Full Text Show Details
Spin-spin coupling constants
trifluoroacetic acid
1H-1H.
Barnish, Ian T.; Gibson, Martin S.
Journal of Chemical Research, Miniprint, 1992 , # 7 p. 1740 - 1757 Title/Abstract Full Text Show Details
Chemical shifts
17O
acetonitrile
75 °C
Boykin, D. W.; Baumstark, A. L.; Mehdizadeh, A.; Venkatramanan, M. K.
Magnetic Resonance in Chemistry, 1990 , vol. 28, p. 305 - 310 Title/Abstract Full Text Show Details
Spin-spin coupling constants
1H-1H
Gready, Jill E.; Hata, Kazumi; Sternhell, Sever; Tansey, Charles W.
Australian Journal of Chemistry, 1990 , vol. 43, # 3 p. 593 - 600 Title/Abstract Full Text Show Details
Spin-spin coupling constants
CDCl3
1H-1H
Hiranuma Hidetoshi; Miller, Sidney I.
Journal of Organic Chemistry, 1982 , vol. 47, # 26 p. 5083 - 5088 Title/Abstract Full Text View citing articles Show Details
Pratt, Daniel V.; Ruan, Fuqiang; Hopkins, Paul B.
Journal of Organic Chemistry, 1987 , vol. 52, # 22 p. 5053 - 5055 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
acetone-d6
Malesani, Giorgio; Galiano, Fabio; Ferlin, Maria Grazia; Masiero, Sergio
Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 563 - 569 Title/Abstract Full Text Show Details
Fischer, Alfred; Henderson, George N.
Synthesis, 1985 , # 6/7 p. 641 - 643 Title/Abstract Full Text Show Details
Spin-spin coupling constants
acetone-d6
1H-1H
Fischer, Alfred; Henderson, George N.
Synthesis, 1985 , # 6/7 p. 641 - 643 Title/Abstract Full Text Show Details
NMR with shift reagents
Aversa, M. C.; Giannetto, P.; Saija, A.
Magnetic Resonance in Chemistry, 1985 , vol. 23, # 5 p. 322 - 326 Title/Abstract Full Text Show Details
NMR
Yamada,Y.; Hosaka,K.
Synthesis, 1977 , p. 53 - 54 Full Text View citing articles Show Details
Berger,S.; Rieker,A.
Tetrahedron, 1972 , vol. 28, p. 3123 Full Text View citing articles Show Details
Nilsson et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and BioOrganic Chemistry (1972-1999), 1973 , p. 2337,2338 Full Text Show Details
Norris; Sternhell
Australian Journal of Chemistry, 1966 , vol. 19, p. 617,625 Full Text Show Details
Kato; Mizushima; Kurata; Fujimaki
Agricultural and Biological Chemistry, 1973 , vol. 37, # 11 p. 2677 - 2678 Title/Abstract Full Text View citing articles Show Details
Minematsu et al.
Journal of Organometallic Chemistry, 1975 , vol. 91, p. 389,390 Full Text Show Details
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
Chemical shifts
Deuterochlf.
Bowie et al.
Tetrahedron, 1966 , vol. 22, p. 1771,1772 Full Text Show Details
Chemical shifts
Bzl.
Bowie et al.
Tetrahedron, 1966 , vol. 22, p. 1771,1772 Full Text Show Details
Chemical shifts
NMR-Abs.
Wagner et al.
Tetrahedron Letters, 1965 , p. 4233,4236 Full Text Show Details
IR Spectroscopy (21) Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Location
Bands
neat (no solvent, solid phase)
supporting information
Yoshida, Ryota; Isozaki, Katsuhiro; Yokoi, Tomoya; Yasuda, Nobuhiro; Sadakane, Koichiro; Iwamoto, Takahiro; Takaya, Hikaru; Nakamura, Masaharu
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 31 p. 7468 - 7479 Title/Abstract Full Text View citing articles Show Details
Bands
film
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
Bands
potassium bromide
supporting information
Sasane, Kulbhushan A.; Telvekar, Vikas N.
Synthetic Communications, 2014 , vol. 44, # 4 p. 468 - 473 Title/Abstract Full Text View citing articles Show Details
Bands
potassium bromide
Khansole, Sandeep V.; Patwari, Shivaji B.; Vibhute, Yeshwant B.
Journal of the Indian Chemical Society, 2009 , vol. 86, # 12 p. 1343 - 1346 Title/Abstract Full Text View citing articles Show Details
Hadjila, Dokari; Mohamed, Hammadi
Asian Journal of Chemistry, 2013 , vol. 25, # 11 p. 6112 - 6116 Title/Abstract Full Text View citing articles Show Details
Bands
neat liquid
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka;
Comment (IR Spectroscopy)
Reference
Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Bands
film
Ling, Taotao; Poupon, Erwan; Rueden, Erik J.; Kim, Sun H.; Theodorakis, Emmanuel A.
Journal of the American Chemical Society, 2002 , vol. 124, # 41 p. 12261 - 12267 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Spectrum
KBr
Hashemi, Mohammed M.; Karimi-Jaberi, Zahed; Eftekhari-Sis, Bagher
Journal of Chemical Research, 2005 , # 3 p. 160 - 161 Title/Abstract Full Text View citing articles Show Details
Bands
CHCl3
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Bands
KBr
Hashemi, Mohammed M.; Beni, Yousef A.
Journal of Chemical Research - Part S, 1999 , # 11 p. 672 - 673 Title/Abstract Full Text View citing articles Show Details
Villemin, Didier; Hammadi, Mohamed; Hachemi, Messaoud
Synthetic Communications, 2002 , vol. 32, # 10 p. 1501 - 1515 Title/Abstract Full Text View citing articles Show Details
Bands
2860 - 1590 cm**(-1)
Suresh; Skaria, Sunny; Ponrathnam
Synthetic Communications, 1996 , vol. 26, # 11 p. 2113 - 2117 Title/Abstract Full Text View citing articles Show Details
Bands
acetonitrile
1662 cm**(-1)
Binstead, Robert A.; McGuire, Mark E.; Dovletoglou, Angelos; Seok, Won K.; Roecker, Lee E.; Meyer, Thomas J.
Bands
CHCl3
1658 cm**(-1)
Pratt, Daniel V.; Ruan, Fuqiang; Hopkins, Paul B.
Journal of Organic Chemistry, 1987 , vol. 52, # 22 p. 5053 - 5055 Title/Abstract Full Text View citing articles Show Details
Spectrum
CCl4
170 - 40 cm**(-1)
Trommsdorff, H. P.; Wiersma, D. A.; Zelsmann, H. R.
Journal of Chemical Physics, 1985 , vol. 82, # 1 p. 48 - 52 Title/Abstract Full Text View citing articles Show Details
Spectrum
gas
170 - 40 cm**(-1)
Trommsdorff, H. P.; Wiersma, D. A.; Zelsmann, H. R.
Journal of Chemical Physics, 1985 , vol. 82, # 1 p. 48 - 52 Title/Abstract Full Text View citing articles Show Details
Bands
CCl4
1663 - 1661 cm**(-1)
Meyerson, Matthew L.
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1985 , vol. 41, # 11 p. 1263 - 1268 Title/Abstract Full Text View citing articles Show Details
Fine structure of IR bands
Meyerson, Matthew L.
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1985 , vol. 41, # 11 p. 1263 - 1268 Title/Abstract Full Text View citing articles Show Details
Bands
KBr
1660 cm**(-1)
Hiranuma Hidetoshi; Miller, Sidney I.
Journal of Organic Chemistry, 1982 , vol. 47, # 26 p. 5083 - 5088 Title/Abstract Full Text View citing articles Show Details
IR
Yamada,Y.; Hosaka,K.
Synthesis, 1977 , p. 53 - 54 Full Text View citing articles Show Details
Hunt et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1967 , p. 791,795 Full Text Show Details
Zaitsev; Trankvillitskaya
Journal of Applied Spectroscopy, 1973 , vol. 18, p. 332 p. 449 Full Text View citing articles Show Details
Spectrum
Gonikberg et al.
Doklady Chemistry, 1969 , vol. 185, p. 276 Dokl. Akad. Nauk SSSR Ser. Khim., 1969 , vol. 185, p. 828 Full Text Show Details
Bands
Hecker,E.; Meyer,E.
Chemische Berichte, 1964 , vol. 97, p. 1926 - 1939
Journal of the American Chemical Society, 1992 , vol. 114, # 1 p. 173 - 186 Title/Abstract Full Text View citing articles Show Details
Full Text View citing articles Show Details
Hide facts Description (IR Spectroscopy)
Comment (IR Spectroscopy)
Reference
Bands
1667 - 667 cm**(-1)
Yates et al.
Journal of the American Chemical Society, 1956 , vol. 78, p. 650 Full Text View citing articles Show Details
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1959 , vol. 626, p. 215,217 Full Text Show Details
Mass Spectrometry (8) Description (Mass Spectrometry)
Location
Reference
spectrum
Seuwen, P.; Warneck, P.
International Journal of Chemical Kinetics, 1996 , vol. 28, # 5 p. 315 - 332 Title/Abstract Full Text Show Details
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Hailu, Solomon Legese; Nair, Balachandran Unni; Redi-Abshiro, Mesfin; Diaz, Isabel; Aravindhan, Rathinam; Tessema, Merid
Chinese Journal of Catalysis, 2016 , vol. 37, # 1 p. 135 - 145 Title/Abstract Full Text Show Details
high resolution mass spectrometry (HRMS) electron impact (EI) spectrum
supporting information
Yoshida, Ryota; Isozaki, Katsuhiro; Yokoi, Tomoya; Yasuda, Nobuhiro; Sadakane, Koichiro; Iwamoto, Takahiro; Takaya, Hikaru; Nakamura, Masaharu
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 31 p. 7468 - 7479 Title/Abstract Full Text View citing articles Show Details
liquid chromatography mass spectrometry (LCMS) electrospray ionisation (ESI) spectrum
Wang, Shaomang; Li, Dinglong; Sun, Cheng; Yang, Shaogui; Guan, Yuan; He, Huan
Journal of Molecular Catalysis A: Chemical, 2014 , vol. 383-384, p. 128 - 136 Title/Abstract Full Text View citing articles Show Details
high resolution mass spectrometry (HRMS) time-of-flight mass spectra (TOFMS) gas chromatography mass spectrometry (GCMS) electron impact (EI) spectrum
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
EI (Electron impact) GCMS (Gas chromatography mass spectrometry) Spectrum
supporting information
Kamata, Keigo; Yamaura, Taiyo; Mizuno, Noritaka
Angewandte Chemie - International Edition, 2012 , vol. 51, # 29 p. 7275 - 7278 Title/Abstract Full Text View citing articles Show Details
HRMS (High resolution mass spectrometry) EI (Electron impact) Spectrum
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Shannon et al.
Chemical Communications (London), 1966 , p. 478 Full Text View citing articles Show Details
Aplin; Pike
Chemistry and Industry (London, United Kingdom), 1966 , p. 2009 Full Text Show Details
Wheeler et al.
Tetrahedron Letters, 1972 , p. 4635 Full Text View citing articles Show Details
Bowie; Blumenthal
Australian Journal of Chemistry, 1976 , vol. 29, p. 115 Full Text Show Details
Maquestian et al.
Organic Mass Spectrometry, 1977 , vol. 12, p. 631,633 Full Text Show Details
Kato; Mizushima; Kurata; Fujimaki
Agricultural and Biological Chemistry, 1973 , vol. 37, # 11 p. 2677 - 2678 Title/Abstract Full Text View citing articles Show Details
Suhr et al.
Organic Mass Spectrometry, 1979 , vol. 14, p. 399,400 Full Text Show Details
Chen; Kwan
Tetrahedron Letters, 1973 , p. 2651 Full Text Show Details
Bowie et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1966 , p. 335,336 Full Text Show Details
ion-cyclotron resonance
Suhr et al.
Organic Mass Spectrometry, 1979 , vol. 14, p. 399,400 Full Text Show Details
UV/VIS Spectroscopy (27) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Absorption Maxima (UV/VIS)
Ext./Abs. Coefficient
Log epsilon
Comment (UV/VIS Spectroscopy)
Spectrum
259 nm 325 nm
Bell, Jeffrey G.; Green, James R.; Wang, Jichang
Journal of Physical Chemistry A, 2014 , vol. 118, # 42 p. 9795 - 9800 Title/Abstract Full Text View citing articles Show Details
1,4-dioxane water
278.2 nm 312.3 nm 422.6 nm
4.15 2.75 1.31
Hadjila, Dokari; Mohamed, Hammadi
Asian Journal of Chemistry, 2013 , vol. 25, # 11 p. 6112 - 6116 Title/Abstract Full Text View citing articles Show Details
Spectrum
methanol
Kostikov, Alexey P.; Popik, Vladimir V.
Journal of Organic Chemistry, 2007 , vol. 72, # 24 p. 9190 - 9194 Title/Abstract Full Text View citing articles Show Details
methanol
246 nm
Kostikov, Alexey P.; Popik, Vladimir V.
Journal of Organic Chemistry, 2007 , vol. 72, # 24 p. 9190 - 9194 Title/Abstract Full Text View citing articles Show Details
Triplet-triplet band
Goerner, Helmut
Photochemistry and Photobiology, 2003 , vol. 78, # 5 p. 440 - 448 Title/Abstract Full Text View citing articles Show Details
dioxane H2O
278.2 nm 312.3 nm 422.6 nm
14125 l·mol-1cm-1
Ratio of solvents: dioxane/H2O = 70:30
Villemin, Didier; Hammadi, Mohamed; Hachemi, Messaoud
Synthetic Communications, 2002 , vol. 32, # 10 p. 1501 - 1515 Title/Abstract Full Text View citing articles Show Details
aq. H2SO4 various solvent(s)
324 nm
570 l·mol-1cm-1
Remark: air-saturated solution; pH 3.7 ambient temperature
Anastasio; Faust; Rao
Environmental Science and Technology, 1997 , vol. 31, # 1 p. 218 - 232 Title/Abstract Full Text View citing articles Show Details
Absorption maxima
CCl4
425.53 nm 313.48 nm 250 nm
Kalnin'sh; Bursian
Russian Journal of Physical Chemistry A, 1996 , vol. 70, # 12 p. 2048 2053 Title/Abstract Full Text View citing articles Show Details
Absorption maxima
ethanol
299 nm
3100 l·mol-1cm-1
Keum; Gregory; Bruice
Journal of the American Chemical Society, 1990 , vol. 112, # 7 p. 2711 2715 Title/Abstract Full Text View citing articles Show Details
Spectrum
Baly; Stewart
Journal of the Chemical Society, 1906 , vol. 89, p. 508,620 Full Text Show Details
Herre; Weis
Chemical Physics Letters, 1970 , vol. 7, p. 276 Full Text View citing articles Show Details
Trommsdorf et al.
Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1970 , vol. 271, p. 45 Full Text Show Details
Arai; Onozuka
Nippon Kagaku Kaishi, 1978 , p. 997,998 Full Text Show Details
Trommsdorff
Chemical Physics Letters, 1971 , vol. 10, p. 176 Full Text View citing articles Show Details
Merienne-Lafore
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1977 , vol. 33, p. 453 Full Text View citing articles Show Details
Trommsdorff
Journal of Chemical Physics, 1972 , vol. 56, p. 5358,5364 Full Text Show Details
Kuboyama
Bulletin of the Chemical Society of Japan, 1962 , vol. 35, p. 295 Full Text Show Details
UV/VIS
Abd El-Halim et al.
Egyptian Journal of Chemistry, 1976 , vol. 19, p. 203 Full Text Show Details
562 l·mol-1cm-1
20 l·mol-1cm-1
Reference
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
Band anisotropy
Trommsdorff
Molecular Physics, 1972 , vol. 24, p. 519 Full Text Show Details
Singlet-triplet band
Trommsdorff
Molecular Physics, 1972 , vol. 24, p. 519 Full Text Show Details
Absorption maxima
Hecker,E.; Meyer,E.
Chemische Berichte, 1964 , vol. 97, p. 1926 - 1939 Full Text View citing articles Show Details
Hunt et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1967 , p. 791,795 Full Text Show Details
Spectrum
hexane
220 - 500 nm
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 117,137 Full Text Show Details
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Absorption maxima
ethanol
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 117,137 Full Text Show Details
Absorption maxima
acetonitrile
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 117,137 Full Text Show Details
Absorption maxima
CHCl3
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 117,137 Full Text Show Details
Absorption maxima
CCl4
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 117,137 Full Text Show Details
Spectrum
CCl4
220 - 500 nm
Flaig et al.
Zeitschrift fuer Naturforschung, 1955 , vol. 10b, p. 668,669 Full Text Show Details
Hide facts Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Comment (UV/VIS Spectroscopy)
Spectrum
cyclohexane
200 - 500 nm
Martynoff
Bulletin de la Societe Chimique de France, 1949 , p. 258 Full Text Show Details
Spectrum
ethanol
200 - 500 nm
Martynoff
Bulletin de la Societe Chimique de France, 1949 , p. 258 Full Text Show Details
Spectrum
CHCl3
220 - 500 nm
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Spectrum
340 - 500 nm der Schmelze.
Hunter; Northey
Journal of Physical Chemistry, 1933 , vol. 37, p. 875,877, 878 Full Text View citing articles Show Details
Spectrum
ethanol
Lifschitz et al.
Recueil des Travaux Chimiques des Pays-Bas, 1924 , vol. 43, p. 274,413 Full Text Show Details
Light
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1926 , vol. 122, p. 418 Full Text Show Details
Reference
Spectrum
hexane
Light
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1926 , vol. 122, p. 418 Full Text Show Details
Spectrum
von dampffoermigem Toluchinon.
Purvis
Journal of the Chemical Society, 1923 , vol. 123, p. 1847 Full Text Show Details
ESR Spectroscopy (4) Description (ESR Spectroscopy)
Reference
ENDOR (electron-nuclear double resonance)
Lichtenbelt; Wiersma
Chemical Physics, 1978 , vol. 34, p. 47 Full Text View citing articles Show Details
ESR-hyperfine coupling constants
Yoshida et al.
Bulletin of the Chemical Society of Japan, 1972 , vol. 45, p. 3515,3516, 3518, 3519 Full Text Show Details
Warashina et al.
Bulletin of the Chemical Society of Japan, 1975 , vol. 48, p. 636,637 Full Text Show Details
ESR
Yoshida et al.
Bulletin of the Chemical Society of Japan, 1972 , vol. 45, p. 3515,3516, 3518, 3519 Full Text Show Details
Warashina et al.
Bulletin of the Chemical Society of Japan, 1975 , vol. 48, p. 636,637 Full Text Show Details
Spectrum
Yoshida et al.
Bulletin of the Chemical Society of Japan, 1972 , vol. 45, p. 3515,3516, 3518, 3519 Full Text Show Details
Raman Spectroscopy (2) Description (Raman Spectroscopy)
Comment (Raman Spectroscopy)
Reference
Bands
neat (no solvent, solid phase)
Clough, S.; Heidemann, A.; Lichtenbelt, J. H.; Paley, M. N. J.; Silbey, R.; et al.
Journal of Chemical Physics, 1984 , vol. 81, # 7 p. 2879 - 2883 Title/Abstract Full Text View citing articles Show Details
Bands
Rossetti, R.; Beck, S. M.; Brus, L. E.
Journal of Physical Chemistry, 1983 , vol. 87, # 16 p. 3058 - 3061 Title/Abstract Full Text View citing articles Show Details
Luminescence Spectroscopy (3) Description (Luminescence Spectroscopy)
Reference
Luminescence quenching
Al-Saigh, Hisham Y.; Kemp, Terence J.
Journal of Chemical Research, Miniprint, 1984 , # 7 p. 2001 - 2046 Title/Abstract Full Text Show Details
Luminescence lifetime
Ronfard-Haret, Jean-Claude; Bensasson, Rene V.; Amouyal, Edmond
Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1980 , vol. 76, p. 2432 - 2436 Title/Abstract Full Text View citing articles Show Details
Luminescence
Herre; Weis
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1973 , vol. 29, p. 203 Full Text View citing articles Show Details
Jayswal; Singh
Journal of Molecular Spectroscopy, 1965 , vol. 17, p. 6 Full Text View citing articles Show Details
Phosphorescence Spectroscopy (3) Description (Phosphorescence Spectroscopy)
Comment (Phosphorescence Spectroscopy)
Reference
Triplet state quenching
Goerner, Helmut
Journal of Physical Chemistry A, 2003 , vol. 107, # 51 p. 11587 - 11595 Title/Abstract Full Text View citing articles Show Details
Triplet state lifetime
solvent dependence. Object(s) of Study: dependence on excitation wavelength
Goerner, Helmut
Journal of Physical Chemistry A, 2003 , vol. 107, # 51 p. 11587 - 11595 Title/Abstract Full Text View citing articles Show Details
Phosphorescence
Herre; Weis
Chemical Physics Letters, 1970 , vol. 7, p. 276 Full Text View citing articles Show Details
Veenvliet; Wiersma
Chemical Physics, 1975 , vol. 8, p. 432 Full Text View citing articles Show Details
Other Spectroscopic Methods (1) Description (Other Spectroscopic Methods)
Reference
Photoelectron spectrum
Dougherty,D. et al.
Journal of the American Chemical Society, 1978 , vol. 100, p. 5597 - 5603 Full Text View citing articles Show Details
Bioactivity Pharmacological Data (73) 1 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Garnett, Inc.
Patent: US6340468 B1, 2002 ; Title/Abstract Full Text Show Details
Bosshard,H.
Helvetica Chimica Acta, 1972 , vol. 55, p. 32 - 37 Full Text View citing articles Show Details
Weichert,J. et al.
Collection of Czechoslovak Chemical Communications, 1964 , vol. 29, p. 197 - 205 Full Text View citing articles Show Details
Seiko Kagaku Kabushiki Kaisha
Patent: EP812816 A1, 1997 ; Title/Abstract Full Text Show Details
Inouye,H.; Arai,T.
Chemical and Pharmaceutical Bulletin, 1964 , vol. 12, p. 533 - 539 Full Text View citing articles Show Details
Yoshihira,K. et al.
Chemical and Pharmaceutical Bulletin, 1968 , vol. 16, p. 2383 - 2389 Full Text View citing articles Show Details
Spinner,I.H. et al.
Canadian Journal of Chemistry, 1963 , vol. 41, p. 483 - 494 Full Text View citing articles Show Details
Wilgus,H.S.; Gates,J.W.
Canadian Journal of Chemistry, 1967 , vol. 45, p. 1975 - 1980 Full Text View citing articles Show Details
Canadian Patents and Development Limited
Patent: US4158822 A1, 1979 ; Title/Abstract Full Text Show Details
Hecker,E.; Meyer,E.
Chemische Berichte, 1964 , vol. 97, p. 1926 - 1939 Full Text View citing articles Show Details
Sun Tech, Inc.
Patent: US4482756 A1, 1984 ; Title/Abstract Full Text Show Details
Allen Jr.; Pidacks; Weiss
Journal of the American Chemical Society, 1966 , vol. 88, # 11 p. 2536 - 2544 Title/Abstract Full Text View citing articles Show Details
Bayer Aktiengesellschaft
Patent: US4621138 A1, 1986 ; Title/Abstract Full Text Show Details
Evans,D.A. et al.
Journal of the American Chemical Society, 1973 , vol. 95/17, p. 5822 - 5823 Full Text View citing articles Show Details
Dougherty,D. et al.
Journal of the American Chemical Society, 1978 , vol. 100, p. 5597 - 5603 Full Text View citing articles Show Details
Flaig,W. et al.
Justus Liebigs Annalen der Chemie, 1968 , vol. 719, p. 96 - 111 Full Text View citing articles Show Details
Terdic,M.
Justus Liebigs Annalen der Chemie, 1971 , vol. 746, p. 200 - 206 Full Text View citing articles Show Details
Baiocchi,F. et al.
J. Med. Chem., 1963 , vol. 6, p. 431 - 435 Title/Abstract Full Text View citing articles Show Details
Mathur,R.K.; Rao,A.S.
Tetrahedron, 1967 , vol. 23, p. 1259 - 1265 Full Text View citing articles Show Details
McKillop,A. et al.
Tetrahedron, 1970 , vol. 26, p. 4031 - 4039 Full Text View citing articles Show Details
2 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Cranwell,P.A.; Haworth,R.D.
Tetrahedron, 1971 , vol. 27, p. 1831 - 1837 Full Text View citing articles Show Details
Holmberg,K. et al.
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1974 , vol. 28, p. 913 - 921 Full Text View citing articles Show Details
Sharma,S.C.; Torssell,K.
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1978 , vol. 32, p. 347 - 353 Full Text View citing articles Show Details
Hoegberg,H.-E.; Komlos,P.
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1979 , vol. 33, p. 271 - 276 Full Text View citing articles Show Details
Gripenberg,J.; Hase,T.
Acta Chemica Scandinavica (1947-1973), 1963 , vol. 17, p. 2250 - 2252 Full Text View citing articles Show Details
Schildknecht,H. et al.
Angewandte Chemie, 1963 , vol. 75, p. 762 - 771 Full Text View citing articles Show Details
Ichihara,A. et al.
Bulletin of the Chemical Society of Japan, 1978 , vol. 51, p. 826 - 829 Full Text View citing articles Show Details
Merck and Co., Inc.
Patent: US4978679 A1, 1990 ; Title/Abstract Full Text Show Details
L'Oreal
Patent: US5053053 A1, 1991 ; Title/Abstract Full Text Show Details
Takeshita,H. et al.
Chemistry Letters, 1976 , p. 445 - 448 Full Text View citing articles Show Details
Buchan,R.; Musgrave,O.C.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1975 , p. 2185 - 2189 Full Text View citing articles Show Details
Ansell,M.F.; Knights,B.A.
Journal of the Chemical Society, 1961 , p. 2903 - 2907 Full Text View citing articles Show Details
Cookson,R.C. et al.
Journal of the Chemical Society, 1961 , p. 4499 - 4506 Full Text View citing articles Show Details
Alberola,A. et al.
Journal of the Chemical Society, 1962 , p. 3941 - 3945 Full Text View citing articles Show Details
Lindsey,A.S. et al.
Journal of the Chemical Society, 1962 , p. 4558 - 4569 Full Text View citing articles Show Details
Birch,A.J. et al.
Journal of the Chemical Society, 1964 , p. 2932 - 2941 Full Text View citing articles Show Details
Eastman Kodak Company
Patent: US5107003 A1, 1992 ; Title/Abstract Full Text Show Details
Bayer Aktiengesellschaft
Patent: US5138054 A1, 1992 ; Title/Abstract Full Text Show Details
Mandelbaum,A.; Cais,M.
Journal of Organic Chemistry, 1961 , vol. 26, p. 2633 - 2640 Full Text View citing articles Show Details
Georgian,V.; Lepe M.,J.
Journal of Organic Chemistry, 1964 , vol. 29, p. 45 - 50 Full Text View citing articles Show Details
3 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Lau,P.T.S.; Gompf,T.E.
Journal of Organic Chemistry, 1970 , vol. 35, p. 4103 - 4108 Full Text View citing articles Show Details
Balogh,V. et al.
Journal of Organic Chemistry, 1971 , vol. 36, # 10 p. 1339 - 1341 Full Text View citing articles Show Details
Brown,E.R. et al.
Journal of Organic Chemistry, 1971 , vol. 36, # 19 p. 2849 - 2853 Full Text View citing articles Show Details
L'Oreal
Patent: US5180400 A1, 1993 ; Title/Abstract Full Text Show Details
Horak,V.; Manning,W.B.
Journal of Organic Chemistry, 1979 , vol. 44, # 1 p. 120 - 123 Full Text View citing articles Show Details
Betkerur,S.N.; Siddappa,S.
Journal of the Chemical Society [Section] C: Organic, 1967 , p. 296 - 298 Full Text View citing articles Show Details
da Silva Correa,C.M.M.; Waters,W.A.
Journal of the Chemical Society [Section] C: Organic, 1968 , p. 1874 - 1879 Full Text View citing articles Show Details
Yamada,Y.; Hosaka,K.
Synthesis, 1977 , p. 53 - 54 Full Text View citing articles Show Details
Board of Supervisors of Louisiana State University; Agricultural and Mechanical College
Patent: US6653311 B1, 2003 ; Title/Abstract Full Text Show Details
General Electric Company
Patent: US6693221 B1, 2004 ; Title/Abstract Full Text Show Details
Council of Scientific and Industrial Research
Patent: US6872857 B1, 2005 ; Title/Abstract Full Text Show Details
Mahalingam, Rathinam Jothi; Ashtekar, Sunil; Thampi, Jegadeesh; Kumbhar, Pramod Shankar
Patent: US2005/137380 A1, 2005 ; Title/Abstract Full Text Show Details
COUNCIL OF SCIENTIFIC and INDUSTRIAL RESEARCH
Patent: WO2005/63664 A1, 2005 ; Title/Abstract Full Text Show Details
Thampi, Jegadeesh; Ashtekar, Sunil; Kumbhar, Pramod; Mahalingam, Rathinam Jothi
Patent: US2006/25634 A1, 2006 ; Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2008/35078 A1, 2008 ; Title/Abstract Full Text Show Details
Graebe; Levy
Justus Liebigs Annalen der Chemie, 1894 , vol. 283, p. 265 Full Text View citing articles Show Details
Fieser; Hartwell
Journal of the American Chemical Society, 1935 , vol. 57, p. 1479,1481 Full Text View citing articles Show Details
Lora-Tamayo et al.
Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica, 1957 , vol. 53, p. 63,66 Full Text View citing articles Show Details
Fieser; Ardao
Journal of the American Chemical Society, 1956 , vol. 78, p. 774,779 Full Text View citing articles Show Details
4 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Ladenburg
Chemische Berichte, 1877 , vol. 10, p. 1125 Full Text View citing articles Show Details
Staudinger; Bereza
Justus Liebigs Annalen der Chemie, 1911 , vol. 380, p. 260 Full Text View citing articles Show Details
Garner; Sugden
Journal of the Chemical Society, 1927 , p. 2881 Full Text View citing articles Show Details
Smith et al.
Journal of the American Chemical Society, 1941 , vol. 63, p. 1018,1019 Journal of the American Chemical Society, 1942 , vol. 64, p. 447,448 Full Text View citing articles Show Details
Stern et al.
Journal of the American Chemical Society, 1947 , vol. 69, p. 869,874 Full Text View citing articles Show Details
Karrer; Dutta
Helvetica Chimica Acta, 1948 , vol. 31, p. 2080,2086 Full Text View citing articles Show Details
Erdtman
Svensk Kemisk Tidskrift, 1932 , vol. 44, p. 135,143, 147 Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences, 1934 , vol. 143, p. 191,213 Full Text View citing articles Show Details
Posternak et al.
Helvetica Chimica Acta, 1956 , vol. 39, p. 1556,1562 Full Text View citing articles Show Details
Henry; Smith
Journal of the American Chemical Society, 1952 , vol. 74, p. 278 Full Text View citing articles Show Details
Koptzik
Izvestiya Akademii Nauk SSSR, Seriya Fizicheskaya, 1956 , vol. 20, p. 219,222; engl. Ausg. S. 201 Chem.Abstr., 1956 , p. 11742 Full Text View citing articles Show Details
Schmid; Czerny
Monatshefte fuer Chemie, 1952 , vol. 83, p. 31,34 Full Text Show Details
Spruit
Recueil des Travaux Chimiques des Pays-Bas, 1955 , vol. 74, p. 737,743 Full Text Show Details
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 117,137 Full Text Show Details
Pratesi
Gazzetta Chimica Italiana, 1936 , vol. 66, p. 215,220 Full Text Show Details
Guendel; Pummerer
Justus Liebigs Annalen der Chemie, 1937 , vol. 529, p. 11,27 Full Text Show Details
Fischer,O.; Hepp
Justus Liebigs Annalen der Chemie, 1890 , vol. 256, p. 252 Justus Liebigs Annalen der Chemie, 1891 , vol. 262, p. 246 Full Text Show Details
Leicester
Chemische Berichte, 1890 , vol. 23, p. 2796 Full Text Show Details
Cooper; Haines
Biochemical Journal, 1928 , vol. 22, p. 320 Full Text Show Details
Cooper; Nicholas
Journal of the Society of Chemical Industry, London, 1927 , vol. 46, p. 60 T Chem. Zentralbl., 1927 , vol. 98, # I p. 2203 Full Text Show Details
Bullock
Canadian Journal of Chemistry, 1958 , vol. 36, p. 1744 Full Text Show Details
5 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Goldschmidt; Schmid
Chemische Berichte, 1884 , vol. 17, p. 2067 Full Text Show Details
Fichter
Justus Liebigs Annalen der Chemie, 1908 , vol. 361, p. 391 Full Text Show Details
Anslow; Raistrick
Biochemical Journal, 1940 , vol. 34, p. 1124,1130 Full Text Show Details
Grinew et al.
Vestnik Moskovskogo Universiteta, 1956 , vol. 11, # 2 p. 91,93 Chem.Abstr., 1956 , p. 16737 Full Text Show Details
Grinew et al.
Vestnik Moskovskogo Universiteta, 1956 , vol. 11, # 2 p. S 91, 93 Chem.Abstr., 1956 , p. 16737 Full Text Show Details
Page; Robinson
Journal of the Chemical Society, 1943 , p. 133 Full Text Show Details
Moehlau; Redlich
Chemische Berichte, 1911 , vol. 44, p. 3615 Full Text Show Details
Wallenfels; Gellrich
Justus Liebigs Annalen der Chemie, 1959 , vol. 621, p. 149,158 Full Text Show Details
Beer et al.
Journal of the Chemical Society, 1951 , p. 2029,2031 Full Text Show Details
Bayer and Co.
Patent: DE101607 ; Full Text Show Details
v.Auwers
Chemische Berichte, 1927 , vol. 60, p. 2138 Full Text Show Details
Borsche; Mueller; Bodenstein
Justus Liebigs Annalen der Chemie, 1929 , vol. 475, p. 122 Full Text Show Details
Mustafa
Nature (London, United Kingdom), 1948 , vol. 162, p. 856 Chem.Abstr., 1949 , p. 6515 Full Text View citing articles Show Details
Fischer,E.; Schrader
Chemische Berichte, 1910 , vol. 43, p. 527 Full Text Show Details
Johnson; Jobling; Bodamer
Journal of the American Chemical Society, 1941 , vol. 63, p. 134 Full Text Show Details
Rembaum.Szwarc
Journal of the American Chemical Society, 1955 , vol. 77, p. 4468 Full Text View citing articles Show Details
Sarett et al.
Journal of the American Chemical Society, 1952 , vol. 74, p. 1393,1395 Full Text Show Details
Murakami; Senoh
Kagaku Kenkyusho Hokoku, 1953 , vol. 29, p. 533,538 Chem.Abstr., 1955 , p. 10249 Full Text Show Details
Graebe; Levy
Justus Liebigs Annalen der Chemie, 1894 , vol. 283, p. 246 Full Text Show Details
Noelting; Kohn
Chemische Berichte, 1884 , vol. 17, p. 363 Full Text Show Details
6 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Bridge; Morgan
American Chemical Journal, 1898 , vol. 20, p. 766 Full Text Show Details
Claus; Jackson
Journal fuer Praktische Chemie (Leipzig), 1888 , vol. <2> 38, p. 328 Full Text Show Details
Claus; Krauss
Chemische Berichte, 1887 , vol. 20, p. 3089 Full Text Show Details
Kumagai; Wolffenstein
Chemische Berichte, 1908 , vol. 41, p. 298 Full Text Show Details
Nietzki
Chemische Berichte, 1877 , vol. 10, p. 1934,2005 Chemische Berichte, 1878 , vol. 11, p. 1103 Full Text Show Details
Clark
American Chemical Journal, 1892 , vol. 14, p. 571 Full Text Show Details
Valeur
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1897 , vol. 125, p. 872 Annales de Chimie (Cachan, France), 1900 , vol. <7> 21, p. 478 Full Text Show Details
Sabatier; Mailhe
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1908 , vol. 146, p. 458 Annales de Chimie (Cachan, France), 1909 , vol. <8> 16, p. 88 Full Text Show Details
Canzoneri; Spica
Gazzetta Chimica Italiana, 1882 , vol. 12, p. 471 Full Text Show Details
Noelting; Baumann
Chemische Berichte, 1885 , vol. 18, p. 1152 Full Text Show Details
Nietzki
Justus Liebigs Annalen der Chemie, 1882 , vol. 215, p. 155 Chemische Berichte, 1892 , vol. 25, p. 282,284 Full Text Show Details
Posner; Lipsky
Justus Liebigs Annalen der Chemie, 1904 , vol. 336, p. 163 Full Text Show Details
Fichter; Stocker
Chemische Berichte, 1914 , vol. 47, p. 2016 Full Text Show Details
Bach
Chem. Zentralbl., 1916 , vol. 87, # II p. 743 Full Text Show Details
Schmidlin; Wohl; Thommen
Chemische Berichte, 1910 , vol. 43, p. 1300 Full Text Show Details
Fichter; Ris
Helvetica Chimica Acta, 1924 , vol. 7, p. 810
Full Text Show Details
Fichter; Rinderspacher
Helvetica Chimica Acta, 1927 , vol. 10, p. 40 Full Text Show Details
Fichter; Meyer
Helvetica Chimica Acta, 1925 , vol. 8, p. 79 Full Text Show Details
Swietoslawski; Starczewska
Journal de Chimie Physique et de Physico-Chimie Biologique, 1926 , vol. 23, p. 822 Full Text Show Details
Biilmann; Jensen; Pedersen
Journal of the Chemical Society, 1925 , vol. 127, p. 207 Full Text Show Details
7 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Goldschmidt; Strohmenger
Chemische Berichte, 1922 , vol. 55, p. 2465 Full Text Show Details
Erdtman
Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences, 1934 , vol. 143, p. 196,197 Chem. Zentralbl., 1934 , vol. 105, # I p. 3054 Full Text Show Details
Ramart-Lucas; Martynoff
Bulletin de la Societe Chimique de France, 1949 , p. 53,64 Full Text Show Details
Cason; Allen; Goodwin
Journal of Organic Chemistry, 1948 , vol. 13, p. 403,406 Full Text Show Details
Sumerford; Dalton
Journal of the American Chemical Society, 1944 , vol. 66, p. 1330 Full Text View citing articles Show Details
Hunter; Kvalnes
Journal of the American Chemical Society, 1932 , vol. 54, p. 2869,2874 Full Text Show Details
Posternak et al.
Helvetica Chimica Acta, 1948 , vol. 31, p. 525,535 Full Text Show Details
Luettringhaus; Gralheer
Justus Liebigs Annalen der Chemie, 1942 , vol. 550, p. 67,83 Full Text Show Details
Cohen
Journal of the American Chemical Society, 1947 , vol. 69, p. 1057,1063 Full Text Show Details
Neunhoeffer; Pelz
Chemische Berichte, 1939 , vol. 72, p. 433,439 Full Text Show Details
Dodgson
Journal of the Chemical Society, 1930 , p. 2498,2500 Full Text Show Details
Fieser; Tishler; Wendler
Journal of the American Chemical Society, 1940 , vol. 62, p. 2861,2865 Full Text Show Details
Cardani
Gazzetta Chimica Italiana, 1952 , vol. 82, p. 155,162 Full Text Show Details
Gaertner
Journal of the American Chemical Society, 1954 , vol. 76, p. 6150,6155 Full Text Show Details
Chuang; Han
Chemische Berichte, 1935 , vol. 68, p. 876,881 Full Text Show Details
Tishler; Fieser; Wendler
Journal of the American Chemical Society, 1940 , vol. 62, p. 2866,2868 Full Text Show Details
I. G. Farbenind.
Patent: DE521621 , 1927 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 17, p. 692 Full Text Show Details
Gen. Aniline Works
Patent: US1891168 , 1929 ; Full Text Show Details
I. G. Farbenind.
Patent: GB324661 , 1928 ; Full Text Show Details
Fieser; Chang
Journal of the American Chemical Society, 1942 , vol. 64, p. 2043,2047 Full Text Show Details
8 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Osstroshinsskaja
Zhurnal Obshchei Khimii, 1946 , vol. 16, p. 1053,1055 Chem.Abstr., 1947 , p. 2720 Full Text Show Details
Okahara; Murata
Nippon Kagaku Kaishi, 1942 , vol. 63, p. 1354,1360 Chem.Abstr., 1947 , p. 3088 Full Text Show Details
Bergmann; Bergmann
Journal of Organic Chemistry, 1938 , vol. 3, p. 125,131 Full Text Show Details
Velsicol Corp.
Patent: US2584139 , 1947 ; Full Text Show Details
Hill; Adams
Journal of the American Chemical Society, 1931 , vol. 53, p. 3453,3456 Full Text Show Details
Grinew; Terentjew
Zhurnal Obshchei Khimii, 1958 , vol. 28, p. 75,77 J. Gen. Chem. USSR (Engl. Transl.), 1958 , vol. 28, p. 77,78 Full Text Show Details
Ried; Schmidt
Chemische Berichte, 1957 , vol. 90, p. 2553,2556 Full Text Show Details
Jacini
Gazzetta Chimica Italiana, 1947 , vol. 77, p. 252,254 Full Text Show Details
Alcalay
Helvetica Chimica Acta, 1947 , vol. 30, p. 578,584 Full Text Show Details
Kvalnes
Journal of the American Chemical Society, 1934 , vol. 56, p. 670 Full Text View citing articles Show Details
Burton; Praill
Journal of the Chemical Society, 1952 , p. 755,759 Full Text Show Details
Mackenzie; Winter
Transactions of the Faraday Society, 1948 , vol. 44, p. 171,179 Full Text Show Details
Underwood; Walsh
Journal of the American Chemical Society, 1936 , vol. 58, p. 646 Organic Syntheses, 1943 , vol. Coll. Vol. II, p. 553 Full Text View citing articles Show Details
Teuber; Rau
Chemische Berichte, 1953 , vol. 86, p. 1036,1044 Full Text Show Details
Baxendale; Hardy
Transactions of the Faraday Society, 1954 , vol. 50, p. 808,811 Full Text Show Details
Anliker et al.
Journal of the American Chemical Society, 1957 , vol. 79, p. 220,226 Full Text Show Details
Grinew; Terent'ew
Vestnik Moskovskogo Universiteta, 1957 , vol. 12, # 6 p. 147,155 Chem.Abstr., 1959 , p. 3187 Full Text Show Details
Burton; Praill
Journal of the Chemical Society, 1952 , p. 2546 Full Text Show Details
Wessely; Sinwel
Monatshefte fuer Chemie, 1950 , vol. 81, p. 1055,1069 Full Text Show Details
Andrews et al.
Journal of the Chemical Society, 1956 , p. 1844,1850 Full Text Show Details
9 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Lopez Aparicio; Waters
Journal of the Chemical Society, 1952 , p. 4666,4672 Full Text Show Details
Grdinic; Jugovic
Arhiv za Kemiju, 1951 , vol. 23, p. 73,75 Full Text Show Details
Robins; Walker
Journal of the Chemical Society, 1952 , p. 642,647 Full Text Show Details
Lora-Tamayo
Tetrahedron, 1958 , vol. 4, p. 17,22, 24 Full Text View citing articles Show Details
Lora-Tamayo et al.
Anales de la Real Sociedad Espanola de Fisica y Quimica, 1957 , vol. <B> 53, p. 63,68 Full Text Show Details
Hoffmann-La Roche
Patent: US2626960 , 1950 ; Full Text Show Details
Lora-Tamayo; Corral
Anales de la Real Sociedad Espanola de Fisica y Quimica, 1957 , vol. <B> 53, p. 45,50 Full Text Show Details
Metlesics
Monatshefte fuer Chemie, 1957 , vol. 88, p. 804,808 Full Text Show Details
Siegel; Antony
Monatshefte fuer Chemie, 1955 , vol. 86, p. 292,298 Full Text Show Details
Teuber; Jellinek
Chemische Berichte, 1952 , vol. 85, p. 95,100 Full Text Show Details
Koenig; Letsch
Chemische Berichte, 1959 , vol. 92, p. 1789,1797 Full Text Show Details
Metlesics et al.
Monatshefte fuer Chemie, 1957 , vol. 88, p. 1069,1075 Full Text Show Details
Bamberger
Chemische Berichte, 1895 , vol. 28, p. 248 Chemische Berichte, 1894 , vol. 27, p. 1348 Full Text Show Details
Henderson; Boyd
Journal of the Chemical Society, 1910 , vol. 97, p. 1661 Full Text Show Details
Chattaway; Parkes
Journal of the Chemical Society, 1925 , vol. 127, p. 1309 Full Text Show Details
Bogdanow
Zhurnal Obshchei Khimii, 1943 , vol. 13, p. 797 Chem. Zentralbl., 1945 918 Full Text Show Details
Fichter; Mueller
Helvetica Chimica Acta, 1935 , vol. 18, p. 831,833, 838 Full Text Show Details
Hunter; Northey
Journal of Physical Chemistry, 1933 , vol. 37, p. 875,877, 878 Full Text View citing articles Show Details
Thiele; Winter
Justus Liebigs Annalen der Chemie, 1900 , vol. 311, p. 355 Chem. Zentralbl., 1901 , vol. 72, # II p. 70 Full Text Show Details
Borsche
Justus Liebigs Annalen der Chemie, 1904 , vol. 334, p. 186 Full Text Show Details
10 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Nietzki
Chemische Berichte, 1877 , vol. 10, p. 835 Justus Liebigs Annalen der Chemie, 1882 , vol. 215, p. 160 Full Text Show Details
Posner; Lipsky
Justus Liebigs Annalen der Chemie, 1904 , vol. 336, p. 159 Full Text Show Details
Biltris
Chem. Zentralbl., 1898 , vol. 69, # I p. 887 Full Text Show Details
Zincke; v. Hagen
Chemische Berichte, 1883 , vol. 16, p. 1559 Full Text Show Details
Baly; Stewart
Journal of the Chemical Society, 1906 , vol. 89, p. 508,620 Full Text Show Details
Carstanjen
Journal fuer Praktische Chemie (Leipzig), 1881 , vol. <2> 23, p. 423,425 Full Text Show Details
Schniter
Chemische Berichte, 1887 , vol. 20, p. 2283 Full Text Show Details
Bayrac
Bulletin de la Societe Chimique de France, 1894 , vol. <3> 11, p. 1130,1133 Annales de Chimie (Cachan, France), 1897 , vol. <7> 10, p. 55,56, 68 Full Text Show Details
Borsche
Justus Liebigs Annalen der Chemie, 1907 , vol. 357, p. 187 Full Text Show Details
Heller
Justus Liebigs Annalen der Chemie, 1919 , vol. 418, p. 263 Full Text Show Details
Fichter
Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie, 1913 , vol. 19, p. 782
Full Text Show Details
Heilbron; Henderson
Journal of the Chemical Society, 1913 , vol. 103, p. 1407 Full Text Show Details
Suida,H.; Suida,W.
Justus Liebigs Annalen der Chemie, 1918 , vol. 416, p. 160 Full Text Show Details
Lifschitz et al.
Recueil des Travaux Chimiques des Pays-Bas, 1924 , vol. 43, p. 274,413 Full Text Show Details
Light
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1926 , vol. 122, p. 418 Full Text Show Details
Linke
Journal fuer Praktische Chemie (Leipzig), 1921 , vol. <2> 101, p. 271 Full Text Show Details
Brass; Papp
Chemische Berichte, 1920 , vol. 53, p. 452 Full Text Show Details
Purvis
Journal of the Chemical Society, 1923 , vol. 123, p. 1847 Full Text Show Details
Angeletti
Atti della Accademia delle Scienze di Torino, Classe di Scienze Fisiche, Matematiche e Naturali, 1934 , vol. # 70, p. 326,328 Full Text Show Details
Leighton; Dresia
Journal of the American Chemical Society, 1930 , vol. 52, p. 3556,3560 Full Text Show Details
11 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Rosenblatt
Journal of the American Chemical Society, 1940 , vol. 62, p. 1092 Full Text View citing articles Show Details
Martynoff
Bulletin de la Societe Chimique de France, 1949 , p. 258 Full Text Show Details
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Velasco
Anales de la Real Sociedad Espanola de Fisica y Quimica, 1934 , vol. 32, p. 345,365, 369 Full Text Show Details
Ashley
Journal of the Chemical Society, 1937 , p. 1471 Full Text Show Details
Angeletti
Atti della Accademia delle Scienze di Torino, Classe di Scienze Fisiche, Matematiche e Naturali, 1935 , vol. # 70, p. 326,328 Full Text Show Details
Angeletti
Gazzetta Chimica Italiana, 1934 , vol. 64, p. 346,347 Full Text Show Details
Yokoyama; Ishikawa
Bulletin of the Chemical Society of Japan, 1931 , vol. 6, p. 275,281 Full Text Show Details
Harman
Organic Syntheses, 1963 , vol. Coll. Vol. IV, p. 148,152 Note 13 Full Text Show Details
Smith; Irwin
Journal of the American Chemical Society, 1941 , vol. 63, p. 1036,1040 Full Text Show Details
Neumann; Gould
Analytical Chemistry, 1953 , vol. 25, p. 751,755 Full Text Show Details
Bridges; Porter
Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences, 1958 , vol. 244, p. 259,271 Full Text Show Details
Yates et al.
Journal of the American Chemical Society, 1956 , vol. 78, p. 650 Full Text View citing articles Show Details
Bobrowa
Zhurnal Fizicheskoi Khimii, 1952 , vol. 26, p. 822,832 Chem.Abstr., 1952 , p. 10961 Full Text Show Details
Flaig et al.
Zeitschrift fuer Naturforschung, 1955 , vol. 10b, p. 668,669 Full Text Show Details
Barlin; Riggs
Journal of the Chemical Society, 1954 , p. 3125,3127 Full Text Show Details
Flaig; Salfeld
Justus Liebigs Annalen der Chemie, 1959 , vol. 626, p. 215,217 Full Text Show Details
Brassard; L'Ecuyer
Canadian Journal of Chemistry, 1959 , vol. 37, p. 1505
Full Text Show Details
Pickholz
Journal of the Chemical Society, 1946 , p. 685 Full Text Show Details
Terent'ew; Grinew
Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 1049,1054;engl.Ausg.S.1049,1052 Full Text Show Details
12 of 73
13 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Bielecki; Koleniew
Chem. Zentralbl., 1908 , vol. 79, # II p. 877 Full Text Show Details
Teutscher
Justus Liebigs Annalen der Chemie, 1918 , vol. 416, p. 210 Full Text Show Details
Teutscher
Justus Liebigs Annalen der Chemie, 1918 , vol. 416, p. 201 Full Text Show Details
Bamberger; Blangey
Justus Liebigs Annalen der Chemie, 1911 , vol. 384, p. 318 Anm. 2 Full Text Show Details
Fichter; Mueller
Helvetica Chimica Acta, 1925 , vol. 8, p. 297 Full Text Show Details
Mc Pherson
American Chemical Journal, 1899 , vol. 22, p. 366 Full Text Show Details
Posner
Justus Liebigs Annalen der Chemie, 1904 , vol. 336, p. 160 Full Text Show Details
Bamberger; Blangey
Chemische Berichte, 1903 , vol. 36, p. 1626 Justus Liebigs Annalen der Chemie, 1911 , vol. 384, p. 317 Full Text Show Details
Bamberger; Blangey
Justus Liebigs Annalen der Chemie, 1911 , vol. 384, p. 291 Chemische Berichte, 1903 , vol. 36, p. 1627 Full Text Show Details
Stromberg; Reinus
Zhurnal Obshchei Khimii, 1946 , vol. 16, p. 1431,1437 Chem.Abstr., 1947 , p. 5479 Full Text Show Details
Blackhall; Thomson
Journal of the Chemical Society, 1953 , p. 1138,1141 Full Text Show Details
Agnello; Laubach
Journal of the American Chemical Society, 1960 , vol. 82, p. 4293,4297 Full Text Show Details
McPherson; Gore
American Chemical Journal, 1901 , vol. 25, p. 492 Full Text Show Details
Borsche; Ockinga
Justus Liebigs Annalen der Chemie, 1905 , vol. 340, p. 105 Full Text Show Details
McPherson; Stratton
Journal of the American Chemical Society, 1915 , vol. 37, p. 911 Full Text Show Details
Woroshzow; Mamaew
Sb. Statei Obshch. Khim., 1953 , p. 533,536 Chem.Abstr., 1959 , p. 925 Full Text Show Details
Petersen et al.
Angewandte Chemie, 1955 , vol. 67, p. 217,219 Full Text Show Details
Moerner
Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1921 , vol. 117, p. 69,73 Full Text Show Details
Riedel
Chemische Berichte, 1880 , vol. 13, p. 126 Full Text Show Details
Ettel; Semonsky
Collection of Czechoslovak Chemical Communications, 1948 , vol. 13, p. 601,607 Full Text Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
Borsche
Chemische Berichte, 1921 , vol. 54, p. 1288 Full Text Show Details
v. Hagen; Zincke
Chemische Berichte, 1883 , vol. 16, p. 1558,1559 Full Text Show Details
v. Hagen; Zincke
Chemische Berichte, 1883 , vol. 16, p. 1560 Full Text Show Details
Suchanek
Journal fuer Praktische Chemie (Leipzig), 1914 , vol. <2> 90, p. 479 Full Text Show Details
Becke; Suida; Suida
Patent: DE300706 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 13, p. 353 Full Text Show Details
Barton; Linnell; Senior
Quar. J. Pharm. Pharmacol., 1944 , vol. 17, p. 325,329 Full Text Show Details
Bentley; Dominguez
Journal of Organic Chemistry, 1956 , vol. 21, p. 1348,1349, 1351 Full Text View citing articles Show Details
Berger,S.; Rieker,A.
Tetrahedron, 1972 , vol. 28, p. 3123 Full Text View citing articles Show Details
Chen; Wentworth
Journal of Chemical Physics, 1975 , vol. 63, p. 3183,3189 Full Text Show Details
Dalton; Teitei
Australian Journal of Chemistry, 1969 , vol. 22, p. 1525,1529 Full Text Show Details
Allen et al.
Journal of the American Chemical Society, 1964 , vol. 86, p. 3877 Full Text View citing articles Show Details
Betkerur; Siddappa
Journal of the Chemical Society [Section] C: Organic, 1968 , p. 1795 Full Text View citing articles Show Details
Wilgus et al.
Journal of Organic Chemistry, 1964 , vol. 29, p. 594,597 Full Text Show Details
Beitz; Miller
Journal de Chimie Physique et de Physico-Chimie Biologique, 1979 , vol. 71, p. 4579 Full Text View citing articles Show Details
Pettersson
Acta Chemica Scandinavica (1947-1973), 1966 , vol. 20, p. 657 Full Text View citing articles Show Details
Birch et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1976 , p. 898,903 Full Text Show Details
O'Neill; Jenkins
Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1979 , vol. 75, p. 1912,1914 Full Text Show Details
Shannon et al.
Chemical Communications (London), 1966 , p. 478 Full Text View citing articles Show Details
Foster; Hanson
Biochimica et Biophysica Acta, 1966 , vol. 112, p. 482,484 Full Text Show Details
Aplin; Pike
Chemistry and Industry (London, United Kingdom), 1966 , p. 2009 Full Text Show Details
14 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Srivastava; Shukla
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical, 1977 , vol. 15, p. 603 Full Text Show Details
Wheeler et al.
Tetrahedron Letters, 1972 , p. 4635 Full Text View citing articles Show Details
Bowie; Blumenthal
Australian Journal of Chemistry, 1976 , vol. 29, p. 115 Full Text Show Details
Johnson et al.
Journal of the American Chemical Society, 1962 , vol. 84, p. 2181,2191 Full Text Show Details
Hansson; Stjernstroem
Arkiv foer Kemi, 1963 , vol. 21, p. 81,84 Full Text Show Details
Bowie et al.
Tetrahedron, 1966 , vol. 22, p. 1771,1772 Full Text Show Details
Peover
Transactions of the Faraday Society, 1964 , vol. 60, p. 479 Full Text View citing articles Show Details
Alder et al.
Chemische Berichte, 1960 , vol. 93, p. 1896,1898 Full Text Show Details
Foster; Hanson
Transactions of the Faraday Society, 1964 , vol. 60, p. 2189,2193 Full Text Show Details
Govil
Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical, 1967 , p. 1420 Full Text Show Details
Maquestian et al.
Organic Mass Spectrometry, 1977 , vol. 12, p. 631,633 Full Text Show Details
Bryce-Smith; Gilbert
Proceedings of the Chemical Society, London, 1964 , p. 87 Full Text Show Details
Rao; Hayon
Analytical Chemistry, 1976 , vol. 48, p. 564,565 Full Text Show Details
Klemm; Geiger
Justus Liebigs Annalen der Chemie, 1969 , vol. 726, p. 103 Full Text Show Details
Nilsson et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1973 , p. 2337,2338 Full Text Show Details
Schildknecht et al.
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1968 , vol. 23, p. 637 Full Text Show Details
Foster; Thomson
Transactions of the Faraday Society, 1963 , vol. 59, p. 296,298 Full Text Show Details
Herre; Weis
Chemical Physics Letters, 1970 , vol. 7, p. 276 Full Text View citing articles Show Details
Norris; Sternhell
Australian Journal of Chemistry, 1966 , vol. 19, p. 617,625 Full Text Show Details
Amonkar; Ghosh
Current Science, 1973 , vol. 42, p. 718 Full Text Show Details
15 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Kato; Mizushima; Kurata; Fujimaki
Agricultural and Biological Chemistry, 1973 , vol. 37, # 11 p. 2677 - 2678 Title/Abstract Full Text View citing articles Show Details
Hegedus et al.
Journal of the American Chemical Society, 1972 , vol. 94, p. 7155 Full Text View citing articles Show Details
Laskowski
Analytical Chemistry, 1960 , vol. 32, p. 1171,1173 Full Text Show Details
Jacobsen
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1979 , p. 569 Full Text Show Details
Hunt et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1967 , p. 791,795 Full Text Show Details
McKillop; Young
Synthetic Communications, 1977 , vol. 7, p. 467,470 Full Text Show Details
Sharma; Torssell
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1978 , vol. 32, p. 347,350 Full Text Show Details
Rao et al.
Journal of Organic Chemistry, 1975 , vol. 40, p. 2548 Full Text View citing articles Show Details
Wagner et al.
Tetrahedron Letters, 1965 , p. 4233,4236 Full Text Show Details
Suhr et al.
Organic Mass Spectrometry, 1979 , vol. 14, p. 399,400 Full Text Show Details
Abd El-Halim et al.
Egyptian Journal of Chemistry, 1976 , vol. 19, p. 203 Full Text Show Details
Meinwald et al.
Journal of the American Chemical Society, 1966 , vol. 88, p. 1590 Full Text View citing articles Show Details
Herre; Weis
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1973 , vol. 29, p. 203 Full Text View citing articles Show Details
Trommsdorf et al.
Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1970 , vol. 271, p. 45 Full Text Show Details
Markow et al.
Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk, 1968 , vol. 3, p. 36,37 Chem.Abstr., 1969 , vol. 70, # 6864 Full Text Show Details
Veenvliet; Wiersma
Chemical Physics, 1975 , vol. 8, p. 432 Full Text View citing articles Show Details
Elliot; Wan
Journal of Physical Chemistry, 1978 , vol. 82, p. 444,447 Full Text Show Details
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
Hutchinson et al.
Molecular Physics, 1975 , vol. 29, p. 1767 Full Text Show Details
Jacob 3rd.; Callery; Shulgin; Castagnoli Jr.
The Journal of organic chemistry, 1976 , vol. 41, # 22 p. 3627 - 3629 Title/Abstract Full Text View citing articles Show Details
16 of 73
17 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Stadnik et al.
J. Anal. Chem. USSR (Engl. Transl.), 1977 , vol. 32, p. 1801,1426,1427, 1428 Full Text Show Details
Takamura; Hayakawa
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1971 , vol. 31, p. 225 Full Text View citing articles Show Details
Takamura; Takamura
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1968 , vol. 18, p. 159 Full Text View citing articles Show Details
Koyanagi et al.
Journal of Molecular Spectroscopy, 1970 , vol. 34, p. 450,453 Full Text Show Details
Steenken; Raghavan
Journal of Physical Chemistry, 1979 , vol. 83, p. 3101 Full Text View citing articles Show Details
DuPont de Nemours Co.
Patent: US3987068 , 1976 ; Chem.Abstr., vol. 85, # 192379 Full Text Show Details
Trommsdorff
Molecular Physics, 1972 , vol. 24, p. 519 Full Text Show Details
Arai; Onozuka
Nippon Kagaku Kaishi, 1978 , p. 997,998 Full Text Show Details
McKillop et al.
Angewandte Chemie, 1970 , vol. 82, p. 84 Full Text Show Details
Sasaki; Osugi
Nippon Kagaku Zasshi, 1969 , vol. 90, p. 1231,1233,1238 Chem.Abstr., vol. 72, # 78113 Full Text Show Details
White; Tolln
Photochemistry and Photobiology, 1971 , vol. 14, p. 43,56 Full Text Show Details
Ali
Pakistan Journal of Scientific and Industrial Research, 1968 , vol. 11, p. 9,10 Full Text Show Details
Arshad et al.
Revue Roumaine de Chimie, 1970 , vol. 15, p. 1653,1656,1658,1660 Full Text Show Details
Maruyama et al.
Bulletin of the Chemical Society of Japan, 1973 , vol. 46, p. 2470,2474 Full Text Show Details
Lichtenbelt; Wiersma
Chemical Physics, 1978 , vol. 34, p. 47 Full Text View citing articles Show Details
Gonikberg et al.
Doklady Chemistry, 1969 , vol. 185, p. 276 Dokl. Akad. Nauk SSSR Ser. Khim., 1969 , vol. 185, p. 828 Full Text Show Details
Zaitsev; Trankvillitskaya
Russian Journal of Physical Chemistry, 1974 , vol. 48, p. 963 p. 1621 Full Text Show Details
Jacobs et al.
Biochemistry, 1974 , vol. 13, p. 60,61,62,63 Full Text View citing articles Show Details
Dezina et al.
Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk, 1979 , vol. 2, p. 84,88 Chem.Abstr., 1979 , vol. 91, # 56554 Full Text Show Details
Merienne-Lafore
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1976 , vol. 32, p. 1235,1237,1238 Full Text View citing articles Show Details
Comment (Pharmacological Data)
Bioactivities present
18 of 73
Reference
Patel; Willson
Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1973 , vol. 69, p. 814 Full Text View citing articles Show Details
Trommsdorff
Chemical Physics Letters, 1971 , vol. 10, p. 176 Full Text View citing articles Show Details
Potapov; Sorokin
High Energy Chemistry, 1971 , vol. 5, p. 435 p. 487 Full Text Show Details
van't Hof; Schmidt
Chemical Physics Letters, 1975 , vol. 36, p. 457 Full Text View citing articles Show Details
Merienne-Lafore
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1977 , vol. 33, p. 453 Full Text View citing articles Show Details
Trommsdorff
Journal of Chemical Physics, 1972 , vol. 56, p. 5358,5364 Full Text Show Details
Yoshida et al.
Bulletin of the Chemical Society of Japan, 1972 , vol. 45, p. 3515,3516, 3518, 3519 Full Text Show Details
Minematsu et al.
Journal of Organometallic Chemistry, 1975 , vol. 91, p. 389,390 Full Text Show Details
McKillop; Ray
Synthesis, 1977 , p. 847 Full Text Show Details
Imp. Chem. Ind.
Patent: DE2119726 , 1971 ; Chem.Abstr., 1972 , vol. 76, # 33964 Full Text Show Details
Jayswal; Singh
Journal of Molecular Spectroscopy, 1965 , vol. 17, p. 6 Full Text View citing articles Show Details
Chen; Kwan
Tetrahedron Letters, 1973 , p. 2651 Full Text Show Details
Warashina et al.
Bulletin of the Chemical Society of Japan, 1975 , vol. 48, p. 636,637 Full Text Show Details
Bratchikov et al.
Russian Journal of Physical Chemistry, 1976 , vol. 50, p. 333 p. 563 Full Text Show Details
Vyas et al.
Spectroscopy Letters, 1976 , vol. 9, p. 663,666,668 Full Text Show Details
Davis et al.
Transactions of the Faraday Society, 1965 , vol. 61, p. 1516,1517 Full Text Show Details
Takamura; Takamura
Transactions of the Faraday Society, 1965 , vol. 61, p. 1270 Full Text View citing articles Show Details
Peover
Transactions of the Faraday Society, 1962 , vol. 58, p. 1656,1657 Full Text Show Details
Fritzsche
Zeitschrift fuer Physikalische Chemie (Muenchen, Germany), 1964 , vol. 43, p. 154 Full Text Show Details
Schildknecht; Holoubek
Angewandte Chemie, 1961 , vol. 73, p. 1,5 Full Text Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
Peover
Journal of the Chemical Society, 1962 , p. 4540,4543 Full Text Show Details
Zuman
Collection of Czechoslovak Chemical Communications, 1962 , vol. 27, p. 2035,2048 Full Text Show Details
Laskowski
Analytical Chemistry, 1966 , vol. 38, p. 1188,1193 Chem.Abstr., 1961 , # 607 Full Text Show Details
Moriconi et al.
Journal of Organic Chemistry, 1962 , vol. 27, p. 2772,2774, 2775 Full Text View citing articles Show Details
Berg; Kramarczyk
Berichte der Bunsen-Gesellschaft, 1964 , vol. 68, p. 296 Full Text Show Details
Musso et al.
Chemische Berichte, 1961 , vol. 94, p. 1107,1115 Full Text Show Details
Pettersson
Acta Chemica Scandinavica (1947-1973), 1964 , vol. 18, p. 1428,1429 Full Text Show Details
Fasman et al..
Doklady Physical Chemistry, 1964 , vol. 154-156, p. 298 Doklady Akademii Nauk SSSR, 1964 , vol. 155, p. 434 Full Text Show Details
Monti
Journal of Organic Chemistry, 1966 , vol. 31, p. 2669,2671 Full Text Show Details
Zaitsev; Trankvillitskaya
Journal of Applied Spectroscopy, 1973 , vol. 18, p. 332 p. 449 Full Text View citing articles Show Details
Heitz
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1965 , vol. 261, p. 3158,3160 Full Text Show Details
Kuboyama
Bulletin of the Chemical Society of Japan, 1962 , vol. 35, p. 295 Full Text Show Details
Takamura
Bulletin of the Chemical Society of Japan, 1963 , vol. 36, p. 1053 Full Text Show Details
Hammond
Journal of the Chemical Society, 1964 , p. 471,473, 475 Full Text Show Details
Berg; Gollmick
Collection of Czechoslovak Chemical Communications, 1965 , vol. 30, p. 4192,4196 Full Text Show Details
Beg; Siddiqui
Tetrahedron, 1966 , vol. 22, p. 2203,2211 Full Text Show Details
Bowie et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1966 , p. 335,336 Full Text Show Details
Turcsanyi; Tudos
Acta Chimica Academiae Scientiarum Hungaricae, 1965 , vol. 43, p. 63,65 Full Text Show Details
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 757 Full Text Show Details
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1961 , vol. 16, p. 810 Full Text Show Details
19 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 200 Full Text Show Details
Barbier
Journal of Chromatography, 1959 , vol. 2, p. 649 Full Text View citing articles Show Details
Jones; Murrell
Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical, 1966 , p. 1421 Full Text View citing articles Show Details
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
Georgian; Skaletzky
Journal of Organic Chemistry, 1964 , vol. 29, p. 51,56 Full Text Show Details
Kumanotani et al.
Bulletin of the Chemical Society of Japan, 1968 , vol. 41, p. 2118,2120 Full Text Show Details
Charton
Journal of Organic Chemistry, 1968 , vol. 33, # 10 p. 3878 Full Text View citing articles Show Details
Lau; Kestner
Journal of Organic Chemistry, 1968 , vol. 33, # 12 p. 4426 Full Text View citing articles Show Details
Lounasmaa
Acta Chemica Scandinavica (1947-1973), 1967 , vol. 21, p. 2807,2814 Full Text Show Details
Bothner-By; Moser
Journal of the American Chemical Society, 1968 , vol. 90, p. 2347,2350 Full Text Show Details
Bruce et al.
Journal of the Chemical Society [Section] C: Organic, 1967 , p. 1486 Full Text Show Details
Jalyowiczor
Roczniki Chemii, 1968 , vol. 42, p. 355 Full Text Show Details
Ryba et al.
Collection of Czechoslovak Chemical Communications, 1968 , vol. 33, p. 26
Full Text Show Details
Tolstikov, G. A.; Shul'ts, E. E.; Vafina, G. F.; Spirikhin, L. V.; Panasenko, A. A.
Journal of Organic Chemistry USSR (English Translation), 1989 , vol. 25, # 6.2 p. 1109 - 1121 Zhurnal Organicheskoi Khimii, 1989 , vol. 25, # 6 p. 1231 - 1246 Title/Abstract Full Text Show Details
Aoyama, Toyohiko; Nakano, Takao; Nishigaki, Satoshi; Shioiri, Takayuki
Heterocycles, 1990 , vol. 30, # 1 p. 375 - 379 Title/Abstract Full Text View citing articles Show Details
Keum; Gregory; Bruice
Journal of the American Chemical Society, 1990 , vol. 112, # 7 p. 2711 - 2715 Title/Abstract Full Text View citing articles Show Details
Gready, Jill E.; Hata, Kazumi; Sternhell, Sever; Tansey, Charles W.
Australian Journal of Chemistry, 1990 , vol. 43, # 3 p. 593 - 600 Title/Abstract Full Text Show Details
Okunowski, J. K.; Dam, H. E. van; Bekkum, H. van
Recueil des Travaux Chimiques des Pays-Bas, 1990 , vol. 109, # 2 p. 103 - 106 Title/Abstract Full Text Show Details
Grieco, Paul A.; Nunes, Joseph J.; Gaul, Micheal D.
Journal of the American Chemical Society, 1990 , vol. 112, # 11 p. 4595 - 4596 Title/Abstract Full Text View citing articles Show Details
Gu, Lianquan; Liu, Cuihua; Xu, Jingxing; King, Tsoo E.
Tetrahedron, 1990 , vol. 46, # 9 p. 3199 - 3210 Title/Abstract Full Text View citing articles Show Details
20 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Boykin, D. W.; Baumstark, A. L.; Mehdizadeh, A.; Venkatramanan, M. K.
Magnetic Resonance in Chemistry, 1990 , vol. 28, p. 305 - 310 Title/Abstract Full Text Show Details
Barton, Derek H. R.; Sas, Woijciech
Tetrahedron, 1990 , vol. 46, # 10 p. 3419 - 3430 Title/Abstract Full Text View citing articles Show Details
Khanna, R.N.; Singh, Prem Kumar
Synthetic Communications, 1990 , vol. 20, # 12 p. 1743 - 1749 Title/Abstract Full Text Show Details
O'Shea, Kevin E.; Fox, Marye Anne
Journal of the American Chemical Society, 1991 , vol. 113, # 2 p. 611 - 615 Title/Abstract Full Text View citing articles Show Details
Fukuhara, Tsuyoshi; Yoneda, Norihiko; Takamura, Kouki; Suzuki, Akira
Journal of Fluorine Chemistry, 1991 , vol. 51, # 2 p. 299 - 304 Title/Abstract Full Text View citing articles Show Details
Kajigaeshi, Shoji; Morikawa, Yukihiro; Fujisaki, Shizuo; Kakinami, Takaaki; Nishihira, Keigo
Bulletin of the Chemical Society of Japan, 1991 , vol. 64, # 1 p. 336 - 338 Title/Abstract Full Text Show Details
Giannotti, C.; Mousset, G.
Tetrahedron Letters, 1980 , vol. 21, p. 2155 - 2158 Title/Abstract Full Text View citing articles Show Details
Fischer, Alfred; Mathivanan, N.
Tetrahedron Letters, 1988 , vol. 29, # 16 p. 1869 - 1872 Title/Abstract Full Text View citing articles Show Details
Thompson, Malcolm J.; Zeegers, Petrus J.
Tetrahedron Letters, 1988 , vol. 29, # 20 p. 2471 - 2474 Title/Abstract Full Text View citing articles Show Details
Errazuriz, B.; Tapia, R.; Valderrama, J. A.
Tetrahedron Letters, 1985 , vol. 26, # 7 p. 819 - 822 Title/Abstract Full Text View citing articles Show Details
Fischer, A.; Henderson, N.
Tetrahedron Letters, 1980 , vol. 21, p. 701 - 704 Title/Abstract Full Text View citing articles Show Details
Malesani, Giorgio; Galiano, Fabio; Ferlin, Maria Grazia; Masiero, Sergio
Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 563 - 569 Title/Abstract Full Text Show Details
Myers, John A.; Moore, Lloyd D.; Whitter, Willie L.; Council, Samuel L.; Waldo, Rosalyn M.; et al.
Journal of Organic Chemistry, 1980 , vol. 45, # 7 p. 1202 - 1206 Title/Abstract Full Text View citing articles Show Details
Nan'ya, Seiko; Tange, Toshiaki; Maekawa, Eturo; Ueno, Yoshio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 1267 - 1271 Title/Abstract Full Text Show Details
Conway, Gregory A.; Loeffler, Larry J.
Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 1315 - 1320 Title/Abstract Full Text Show Details
Hiranuma Hidetoshi; Miller, Sidney I.
Journal of Organic Chemistry, 1982 , vol. 47, # 26 p. 5083 - 5088 Title/Abstract Full Text View citing articles Show Details
Minisci, Francesco; Citterio, Attilio; Vismara, Elena; Fontana, Francesca; Bernardinis, Silvia De; Correale, Mariano
Journal of Organic Chemistry, 1989 , vol. 54, # 3 p. 728 - 731 Title/Abstract Full Text View citing articles Show Details
Fischer, Alfred; Henderson, George N.
Synthesis, 1985 , # 6/7 p. 641 - 643 Title/Abstract Full Text Show Details
Ishii, Fumio; Kishi, Ken-ichi
Synthesis, 1980 , # 9 p. 706 - 708 Title/Abstract Full Text Show Details
Liotta, Dennis; Saindane, Manohar; Barnum, Christopher
Journal of Organic Chemistry, 1981 , vol. 46, # 16 p. 3369 - 3370
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Fukuzumi, Shunichi; Nishizawa, Nobuaki; Tanaka, Toshio
Journal of Organic Chemistry, 1984 , vol. 49, # 19 p. 3571 - 3578 Title/Abstract Full Text View citing articles Show Details
Hiranuma, Hidetoshi; Miller, Sidney I.
Journal of Organic Chemistry, 1983 , vol. 48, # 18 p. 3096 - 3102 Title/Abstract Full Text View citing articles Show Details
Takata, Toshikazu; Tajima, Rieko; Ando, Wataru
Journal of Organic Chemistry, 1983 , vol. 48, # 24 p. 4764 - 4766 Title/Abstract Full Text View citing articles Show Details
Aoyama, Yasuhiro; Asakawa, Masumi; Matsui, Yuichi; Ogoshi, Hisanobu
Journal of the American Chemical Society, 1991 , vol. 113, # 16 p. 6233 - 6240 Title/Abstract Full Text View citing articles Show Details
Hung, Shang-Cheng; Liao, Chun-Chen
Tetrahedron Letters, 1991 , vol. 32, # 32 p. 4011 - 4014 Title/Abstract Full Text View citing articles Show Details
Schubert-Zsilavecz, Manfred; Likussar, Werner; Gusterhuber, Dagmar; Michelitsch, Astrid
Monatshefte fuer Chemie, 1991 , vol. 122, # 5 p. 383 - 387 Title/Abstract Full Text View citing articles Show Details
Uno, Hidemitsu; Shiraishi, Yasukazu; Matsushima, Yuji; Yayama, Ayumi; Suzuki, Hitomi
Bulletin of the Chemical Society of Japan, 1991 , vol. 64, # 3 p. 842 - 850 Title/Abstract Full Text Show Details
Yogo; Ito; Furukawa
Chemical and Pharmaceutical Bulletin, 1991 , vol. 39, # 2 p. 328 - 334 Title/Abstract Full Text View citing articles Show Details
Hanaya, Minoru; Iwaizumi, Masamoto
Journal of Organometallic Chemistry, 1991 , vol. 417, # 3 p. 407 - 420 Title/Abstract Full Text View citing articles Show Details
Muathen, H A
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1991 , vol. 30, # 5 p. 522 - 524 Title/Abstract Full Text Show Details
Binstead, Robert A.; McGuire, Mark E.; Dovletoglou, Angelos; Seok, Won K.; Roecker, Lee E.; Meyer, Thomas J.
Journal of the American Chemical Society, 1992 , vol. 114, # 1 p. 173 - 186 Title/Abstract Full Text View citing articles Show Details
Komaguchi, Kenji; Hatsusegawa, Yasuhiro; Kitani, Akira; Sasaki, Kazuo
Bulletin of the Chemical Society of Japan, 1991 , vol. 64, # 9 p. 2686 - 2690 Title/Abstract Full Text Show Details
Kasa, S.; Maekelae, R.; Salo, E.; Hannonen, K.; Joela, H.
Journal of the Chemical Society, Faraday Transactions, 1991 , vol. 87, # 19 p. 3163 - 3170 Title/Abstract Full Text View citing articles Show Details
Nishina, Atsuyoshi; Uchibori, Tsuyoshi
Agricultural and Biological Chemistry, 1991 , vol. 55, # 9 p. 2395 - 2398 Title/Abstract Full Text Show Details
McKillop, Alexander; Tarbin, Jonathan A.
Tetrahedron, 1987 , vol. 43, # 8 p. 1753 - 1758 Title/Abstract Full Text View citing articles Show Details
Nickel, Ulrich; Jaenicke, Walther
Journal of the Chemical Society, Perkin Transactions 2, 1980 , # 11 p. 1601 - 1605 Title/Abstract Full Text View citing articles Show Details
Mehta; Murthy; Reddy
Tetrahedron Letters, 1987 , vol. 28, # 13 p. 1467 - 1468 Title/Abstract Full Text View citing articles Show Details
Barton, Derek H. R.; Bridon, Dominique; Zard, Samir Z.
Tetrahedron, 1987 , vol. 43, # 22 p. 5307 - 5314 Title/Abstract Full Text View citing articles Show Details
Ashnagar, Alamdar; Bruce, J. Malcolm; Lloyd-Williams, Paul
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988 , p. 559 - 562 Title/Abstract Full Text Show Details
Fukuzumi, Shunichi; Ishikawa, Masashi; Tanaka, Toshio
Tetrahedron, 1986 , vol. 42, # 4 p. 1021 - 1034 Title/Abstract Full Text View citing articles Show Details
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Bioactivities present
Reference
Nallaiah, C.; Strickson, J. A.
Tetrahedron, 1986 , vol. 42, # 14 p. 4083 - 4088 Title/Abstract Full Text View citing articles Show Details
Baldwin, Jack E.; Norris, Robert K.
Journal of Organic Chemistry, 1981 , vol. 46, # 4 p. 697 - 703 Title/Abstract Full Text View citing articles Show Details
Cossio, Fernando P.; Lopez, Concepcion M.; Palomo, Claudio
Tetrahedron, 1987 , vol. 43, # 17 p. 3963 - 3974 Title/Abstract Full Text View citing articles Show Details
Bruce, Malcolm; Heatley, Frank; Ryles, Roderick G.; Scrivens, James H.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1980 , p. 860 - 866 Title/Abstract Full Text View citing articles Show Details
Chudek, John A.; Foster, Roy; Reid, Francis J.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984 , # 2 p. 287 - 292 Title/Abstract Full Text View citing articles Show Details
Thompson, Malcolm J.; Zeegers, Petrus J.
Tetrahedron, 1989 , vol. 45, # 1 p. 191 - 202 Title/Abstract Full Text View citing articles Show Details
Chetcuti, Michael J.; Howard, Judith A. K.; Pfeffer, Michael; Spencer, John L.; Stone, F. Gordon A.
Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1981 , p. 276 - 283 Title/Abstract Full Text View citing articles Show Details
Chetcuti, Michael J.; Herbert, Judith A.; Howard, Judith A. K.; Pfeffer, Michel; Spencer, John L.; et al.
Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1981 , p. 284 - 291 Title/Abstract Full Text View citing articles Show Details
Lecea, B.; Aizpurua, J. M.; Palomo, C.
Tetrahedron, 1985 , vol. 41, # 20 p. 4657 - 4666 Title/Abstract Full Text View citing articles Show Details
Ronfard-Haret, Jean-Claude; Bensasson, Rene V.; Amouyal, Edmond
Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1980 , vol. 76, p. 2432 - 2436 Title/Abstract Full Text View citing articles Show Details
Veltwisch, Dieter; Asmus, Klaus-Dieter
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 1147 - 1152 Title/Abstract Full Text View citing articles Show Details
Shimizu, Masao; Orita, Hideo; Hayakawa, Takashi; Takehira, Katsuomi
Tetrahedron Letters, 1989 , vol. 30, # 4 p. 471 - 474 Title/Abstract Full Text View citing articles Show Details
Kucklaender, Uwe; Toeberich, Hildegard
Chemische Berichte, 1981 , vol. 114, # 6 p. 2238 - 2244 Title/Abstract Full Text Show Details
Aumueller, Alexander; Huenig, Siegfried
Liebigs Annalen der Chemie, 1986 , # 1 p. 165 - 176 Title/Abstract Full Text Show Details
Aumueller, Alexander; Huenig, Siegfried
Liebigs Annalen der Chemie, 1986 , # 1 p. 142 - 164 Title/Abstract Full Text Show Details
Kharchuk, V. G.; Kolenko, I. P.; Petrov, L. A.; Gus'kova, L. M.
Journal of Organic Chemistry USSR (English Translation), 1986 , vol. 22, # 11 p. 2071 - 2078 Zhurnal Organicheskoi Khimii, 1986 , vol. 22, # 11 p. 2306 - 2315 Title/Abstract Full Text Show Details
Turchaninov, V. K.; Gorshkov, A. G.; Petrushenko, K. B.; Vokin, A. I.; Skvortsova, G. G.
Journal of Organic Chemistry USSR (English Translation), 1984 , vol. 20, # 5 p. 986 - 990 Zhurnal Organicheskoi Khimii, 1984 , vol. 20, # 5 p. 1084 - 1089 Title/Abstract Full Text Show Details
Nan'ya, Seiko; Katsuraya, Kaname; Maekawa, Eturo; Kondo, Kazumoto; Eguchi, Shoji
Journal of Heterocyclic Chemistry, 1987 , vol. 24, p. 971 - 975 Title/Abstract Full Text Show Details
Pratt, Daniel V.; Ruan, Fuqiang; Hopkins, Paul B.
Journal of Organic Chemistry, 1987 , vol. 52, # 22 p. 5053 - 5055 Title/Abstract Full Text View citing articles Show Details
Johnson; Soria; O'Connor; Dobson
Journal of Medicinal Chemistry, 1981 , vol. 24, # 11 p. 1314 - 1319 Title/Abstract Full Text View citing articles Show Details
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Reference
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Journal of Organic Chemistry, 1988 , vol. 53, # 11 p. 2647 - 2650 Title/Abstract Full Text View citing articles Show Details
Youngblood, Michael P.
Journal of the American Chemical Society, 1989 , vol. 111, # 5 p. 1843 - 1849 Title/Abstract Full Text View citing articles Show Details
Willis, John P.; Gogins, Kitty A.; Miller, Larry L.
Journal of Organic Chemistry, 1981 , vol. 46, # 16 p. 3215 - 3218 Title/Abstract Full Text View citing articles Show Details
Ipaktschi, Junes; Heydari, Akbar
Angewandte Chemie, 1992 , vol. 104, # 3 p. 335 - 336 Title/Abstract Full Text Show Details
Barnish, Ian T.; Gibson, Martin S.
Journal of Chemical Research, Miniprint, 1992 , # 7 p. 1740 - 1757 Title/Abstract Full Text Show Details
Mukhopadhyay; Suryawanshi; Bhakuni
Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry, 1990 , vol. 29, # 11 p. 1060 - 1061 Title/Abstract Full Text View citing articles Show Details
Hanaya, Minoru; Iwaizumi, Masamoto
Journal of Organometallic Chemistry, 1992 , vol. 435, # 3 p. 337 - 345 Title/Abstract Full Text View citing articles Show Details
Ipaktschi, Junes; Heydari, Akbar
Chemische Berichte, 1992 , vol. 125, # 6 p. 1513 - 1516 Title/Abstract Full Text Show Details
Inoue, Masami; Uragaki, Toshitaka; Enomoto, Saburo
Chemistry Letters, 1986 , p. 2075 - 2078 Title/Abstract Full Text Show Details
Maruyama, Kazuhiro; Tai, Seiji
Chemistry Letters, 1985 , p. 681 - 684 Title/Abstract Full Text Show Details
Cossio, Fernando P.; Aizpurua, Jesus M.; Palomo, Claudio
Canadian Journal of Chemistry, 1986 , vol. 64, p. 225 - 231 Title/Abstract Full Text Show Details
Aizpurua, Jesus M.; Lecea, Begona; Palomo, Claudio
Canadian Journal of Chemistry, 1986 , vol. 64, p. 2342 - 2347
Title/Abstract Full Text Show Details
Matsumoto, Hideyuki; Koike, Shunji; Matsubara, Ikuya; Nakano, Taichi; Nagai, Yoichiro
Chemistry Letters, 1982 , p. 533 - 534 Title/Abstract Full Text Show Details
Furukawa, Hiroshi; Yogo, Motoi; Ito, Chihiro; Wu, Tian-Shung; Kuoh, Chang-Shung
Chemical and Pharmaceutical Bulletin, 1985 , vol. 33, # 3 p. 1320 - 1322 Title/Abstract Full Text Show Details
Juaristi, M.; Aizpurua, J. M.; Lecea, B.; Palomo, C.
Canadian Journal of Chemistry, 1984 , vol. 62, p. 2941 - 2944 Title/Abstract Full Text Show Details
Colter, Allan K.; Lai, Charles C.; Parsons, A. Gregg; Ramsay, N. Bruce; Saito, Gunzi
Canadian Journal of Chemistry, 1985 , vol. 63, p. 445 - 451 Title/Abstract Full Text Show Details
Askari, Syed; Lee, Susan; Perkins, Robert R.; Scheffer, John R.
Canadian Journal of Chemistry, 1985 , vol. 63, p. 3526 - 3529 Title/Abstract Full Text Show Details
Kallmayer; Tappe
Pharmazie, 1986 , vol. 41, # 1 p. 29 - 33 Title/Abstract Full Text View citing articles Show Details
Schulze; Gutsche; Wohlrabe; Tresselt; Horn; Fleck
Pharmazie, 1986 , vol. 41, # 2 p. 99 - 101 Title/Abstract Full Text View citing articles Show Details
Bindl, Johann; Burgemeister, Thomas; Daub, Joerg
Liebigs Annalen der Chemie, 1985 , # 7 p. 1346 - 1359 Title/Abstract Full Text Show Details
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Reference
Jurczak, Janusz; Kawczynski, Andrzej L.; Kozluk, Tomasz
Journal of Organic Chemistry, 1985 , vol. 50, # 7 p. 1106 - 1107 Title/Abstract Full Text View citing articles Show Details
Coppa, Fausta; Fontana, Francesca; Lazzarini, Edoardo; Minisci, Francesco
Chemistry Letters, 1992 , # 7 p. 1299 - 1302 Title/Abstract Full Text Show Details
Sartori, Giovanni; Maggi, Raimondo; Bigi, Franca; Arienti, Attilio; Casnati, Giuseppe
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1993 , # 1 p. 39 - 42 Title/Abstract Full Text View citing articles Show Details
Morey; Saa
Tetrahedron, 1993 , vol. 49, # 1 p. 105 - 112 Title/Abstract Full Text View citing articles Show Details
Meng, Qing-Xiang; Suzuki, Kouei; Maeda, Kiminori; Terazima, Masahide; Azumi, Tohru
Journal of Physical Chemistry, 1993 , vol. 97, # 7 p. 1265 - 1269 Title/Abstract Full Text View citing articles Show Details
Carlson, Brian W.; Miller, Larry L.
Journal of the American Chemical Society, 1985 , vol. 107, # 2 p. 479 - 485 Title/Abstract Full Text View citing articles Show Details
Bushnell, Gordon W.; Fischer, Alfred; Ibrahim, Prabha N.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1988 , p. 1281 - 1286 Title/Abstract Full Text Show Details
Miller; Beitz; Huddleston
Journal of the American Chemical Society, 1984 , vol. 106, # 18 p. 5057 - 5068 Title/Abstract Full Text View citing articles Show Details
Fukuzumi, Shunichi; Koumitsu, Shintaro; Hironaka, Katsuhiko; Tanaka, Toshio
Journal of the American Chemical Society, 1987 , vol. 109, # 2 p. 305 - 316 Title/Abstract Full Text View citing articles Show Details
Tanner, Dennis D.; Deonarian, Natasha; Kharrat, Abdelmajid
Canadian Journal of Chemistry, 1989 , vol. 67, p. 171 - 175 Title/Abstract Full Text Show Details
Fukuzumi, Shunichi; Nishizawa, Nobuaki; Tanaka, Toshio
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1985 , p. 371 - 378 Title/Abstract Full Text View citing articles Show Details
Fukuzumi, Shunichi; Ishikawa, Masashi; Tanaka, Toshio
Chemistry Letters, 1989 , p. 1227 - 1230 Title/Abstract Full Text Show Details
Ott, Robert; Pinter, Erfried; Kajtna, Peter
Monatshefte fuer Chemie, 1980 , vol. 111, p. 813 - 820 Title/Abstract Full Text View citing articles Show Details
Kurov, G. N.; Svyatkina, L. I.; Skvortsova, G. G.; Naumova, I. P.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 10 p. 1969 - 1972 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 10 p. 2235 - 2238 Title/Abstract Full Text View citing articles Show Details
Cassis, R.; Valderrama, J. A.
Synthetic Communications, 1983 , vol. 13, # 5 p. 347 - 356 Title/Abstract Full Text Show Details
Hayakawa, T.; Araki, K.; Shiraishi, S.
Bulletin of the Chemical Society of Japan, 1984 , vol. 57, # 6 p. 1643 - 1649 Title/Abstract Full Text Show Details
Mori, Akira; Mametsuka, Hiroaki; Takeshita, Hitoshi
Bulletin of the Chemical Society of Japan, 1985 , vol. 58, # 7 p. 2072 - 2077 Title/Abstract Full Text Show Details
Kucklaender; Toeberich; Toberich
Archiv der Pharmazie, 1981 , vol. 314, # 4 p. 379 - 380 Title/Abstract Full Text View citing articles Show Details
Rao, A. V. Rama; Deshpande, V. H.; Ravichandran, K.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1985 , vol. 24, p. 233 - 235
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Barranco, Elena; Martin, Nazario; Segura, Jose L.; Seoane, Carlos; De La Cruz, Pilar; Langa, Fernando; Gonzalez, Araceli; Pingarron, Jose M.
Tetrahedron, 1993 , vol. 49, # 22 p. 4881 - 4892 Title/Abstract Full Text View citing articles Show Details
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Bioactivities present
Reference
Jones; Storey
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Bruce, J. Malcolm; Lloyd-Williams, Paul
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1992 , # 21 p. 2877 - 2884 Title/Abstract Full Text View citing articles Show Details
Grimsrud, Eric P.; Caldwell, Gary; Chowdhury, Swapan; Kebarle, Paul
Journal of the American Chemical Society, 1985 , vol. 107, # 16 p. 4627 - 4634 Title/Abstract Full Text View citing articles Show Details
Heinis, Thomas; Chowdhury, Swapan; Scott, Susannah L.; Kebarle, Paul
Journal of the American Chemical Society, 1988 , vol. 110, # 2 p. 400 - 407 Title/Abstract Full Text View citing articles Show Details
Patil; Curtin; I. C. Paul
Journal of the American Chemical Society, 1984 , vol. 106, # 2 p. 348 - 353 Title/Abstract Full Text View citing articles Show Details
Seok, Won K.; Meyer, Thomas J.
Journal of the American Chemical Society, 1988 , vol. 110, # 22 p. 7358 - 7367 Title/Abstract Full Text View citing articles Show Details
Lopez, C.; Gonzalez, A.; Cossio, F. P.; Palomo, C.
Synthetic Communications, 1985 , vol. 15, # 13 p. 1197 - 1212 Title/Abstract Full Text Show Details
Shiraishi, Shinsaku; Holla, B. Shivarama; Imamura, Kiyoshi
Bulletin of the Chemical Society of Japan, 1983 , vol. 56, # 11 p. 3457 - 3463 Title/Abstract Full Text Show Details
Kajiwara, M.; Sakamoto, O.; Ohta, S.
Heterocycles, 1980 , vol. 14, # 12 p. 1995 - 1998 Title/Abstract Full Text Show Details
Kucklander; Toberich; Kuna
Archiv der Pharmazie, 1987 , vol. 320, # 4 p. 308 - 312 Title/Abstract Full Text View citing articles Show Details
Jempty, Thomas C.; Gogins, Kitty A. Z.; Mazur, Yehuda; Miller, Larry L.
Journal of Organic Chemistry, 1981 , vol. 46, # 22 p. 4545 - 4551 Title/Abstract Full Text View citing articles Show Details
Chowdhury, Swapan; Heinis, Thomas; Grimsrud, Eric P.; Kebarle, Paul
Journal of Physical Chemistry, 1986 , vol. 90, # 12 p. 2747 - 2752 Title/Abstract Full Text View citing articles Show Details
Mataga, Noboru; Karen, Akiya; Okada, Tadashi; Nishitani, Shinji; Sakata, Yoshiteru; Misumi, Soichi
Journal of Physical Chemistry, 1984 , vol. 88, # 20 p. 4650 - 4655 Title/Abstract Full Text View citing articles Show Details
Kenley, Richard A.; Davenport, John E.; Hendry, Dale G.
Journal of Physical Chemistry, 1981 , vol. 85, # 19 p. 2740 - 2746 Title/Abstract Full Text View citing articles Show Details
Jurczak, Janusz; Kozluk, Tomasz; Tkacz, Marek; Eugster, Conrad Hans
Helvetica Chimica Acta, 1983 , vol. 66, # 1 p. 218 - 221 Title/Abstract Full Text Show Details
Jurczak, Janusz; Kozluk, Tomasz; Filipek, Stanislaw; Eugster, Conrad Hans
Helvetica Chimica Acta, 1983 , vol. 66, # 1 p. 222 - 225 Title/Abstract Full Text Show Details
Wilford, J. H.; Archer, M. D.; Bolton, J. R.; Ho, T.-F.; Schmidt, J. A.; Weedon, A. C.
Journal of Physical Chemistry, 1985 , vol. 89, # 25 p. 5395 - 5398 Title/Abstract Full Text View citing articles Show Details
Mataga, Noboru; Karen, Akiya; Okada, Tadashi
Journal of the American Chemical Society, 1984 , vol. 106, # 8 p. 2442 - 2443 Title/Abstract Full Text View citing articles Show Details
Rossetti, R.; Beck, S. M.; Brus, L. E.
Journal of Physical Chemistry, 1983 , vol. 87, # 16 p. 3058 - 3061 Title/Abstract Full Text View citing articles Show Details
Beltrame, Paolo; Beltrame, Pier Luigi; Bussola, Marzio; Carniti, Paolo
Gazzetta Chimica Italiana, 1980 , vol. 110, # 2/3 p. 141 - 146 Title/Abstract Full Text Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
Kucklaender, Uwe; Bastian, Udo
Zeitschrift fuer Naturforschung, B: Chemical Sciences, 1987 , vol. 42, # 12 p. 1567 - 1577 Title/Abstract Full Text Show Details
Kucklaender, Uwe; Schneider, Bettina
Chemische Berichte, 1988 , vol. 121, p. 577 - 580 Title/Abstract Full Text Show Details
Gleiter, Rolf; Schaefer, Wolfgang; Staab, Heinz A.
Chemische Berichte, 1988 , vol. 121, p. 1257 - 1264 Title/Abstract Full Text Show Details
Rodriguez, Jose Gonzalo; Pablo, Alfonso de; Lerma, Julian Lopez de; Perales, Aurea
Journal of Crystallographic and Spectroscopic Research, 1989 , vol. 19, # 2 p. 307 - 316 Title/Abstract Full Text View citing articles Show Details
Dockal, Edward R.; Cass, Quezia B.; Brocksom, Timothy J.; Brocksom, Ursula; Correa, Arlene G.
Synthetic Communications, 1985 , vol. 15, # 11 p. 1033 - 1036 Title/Abstract Full Text Show Details
Kucklander; Kuna; Schneider
Archiv der Pharmazie, 1993 , vol. 326, # 7 p. 415 - 419 Title/Abstract Full Text View citing articles Show Details
Aversa, M. C.; Giannetto, P.; Saija, A.
Magnetic Resonance in Chemistry, 1985 , vol. 23, # 5 p. 322 - 326 Title/Abstract Full Text Show Details
Meyerson, Matthew L.
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy, 1985 , vol. 41, # 11 p. 1263 - 1268 Title/Abstract Full Text View citing articles Show Details
Stegmann, Werner; Uebelhart, Peter; Heimgartner, Heinz
Helvetica Chimica Acta, 1983 , vol. 66, # 7 p. 2252 - 2268 Title/Abstract Full Text Show Details
Duthaler, Rudolf O.; Lyle, Paulette A.; Heuberger, Christoph
Helvetica Chimica Acta, 1984 , vol. 67, p. 1406 - 1426 Title/Abstract Full Text Show Details
Al-Saigh, Hisham Y.; Kemp, Terence J.
Journal of Chemical Research, Miniprint, 1984 , # 7 p. 2001 - 2046 Title/Abstract Full Text Show Details
Coxon, James M.; O'Connell, Michael J.; Steel, Peter J.
Australian Journal of Chemistry, 1986 , vol. 39, # 10 p. 1537 - 1557 Title/Abstract Full Text Show Details
Pandey, Bipin; Dalvi, Pramod V.
Angewandte Chemie, 1993 , vol. 105, # 11 p. 1724 - 1726 Title/Abstract Full Text Show Details
Singh; Khanna
Synthetic Communications, 1993 , vol. 23, # 15 p. 2083 - 2089 Title/Abstract Full Text View citing articles Show Details
Meng, Q.; Yamakage, Y.; Maeda, K.; Azumi, T.
Zeitschrift fuer Physikalische Chemie (Muenchen, Germany), 1993 , vol. 180, # 1/2 p. 95 - 110 Title/Abstract Full Text Show Details
Singh, J. P.; Sirohi, S. J. S.; Aishwati
Journal of the Indian Chemical Society, 1987 , vol. 64, # 7 p. 440 - 442 Title/Abstract Full Text Show Details
Sviridov, B. D.; Nikolaeva, T. D.; Venderina, V. F.; Zhdanov, S. I.
J. Gen. Chem. USSR (Engl. Transl.), 1985 , vol. 55, # 4 p. 821 - 824,732 - 734 Title/Abstract Full Text Show Details
Gur'yanova, E. N.; Muravlyanskii, D. V.; Romm, I. P.; Sviridov, B. D.; Shifrina, R. R.
J. Gen. Chem. USSR (Engl. Transl.), 1984 , vol. 54, # 4 p. 817 - 824,725 - 731 Title/Abstract Full Text Show Details
Kutyrev, A. A.; Ovrutskii, D. G.; Moskva, V. V.
J. Gen. Chem. USSR (Engl. Transl.), 1988 , vol. 58, # 4 p. 790 - 796,699 - 705 Title/Abstract Full Text Show Details
Varma, R. G.; Yadav, R. L.
Journal of the Indian Chemical Society, 1983 , vol. 60, p. 554 - 556 Title/Abstract Full Text Show Details
27 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Gonzalez, Monica C.; McIntosh, Alan R.; Bolton, James R.; Weedon, Alan C.
Journal of the Chemical Society, Chemical Communications, 1984 , # 17 p. 1138 - 1140 Title/Abstract Full Text View citing articles Show Details
Deacon, Glen B.; O'Donoghue, Michael F.; McKillop, Alexander; Young, Derek W.
Synthetic Communications, 1980 , vol. 10, # 8 p. 615 - 622 Title/Abstract Full Text Show Details
Hegedus, Louis S.; Perry, Robert J.
Journal of Organic Chemistry, 1985 , vol. 50, # 24 p. 4955 - 4960 Title/Abstract Full Text View citing articles Show Details
Ikeda, Tokuji; Katasho, Isao; Kamei, Masugu; Senda, Mitsugi
Agricultural and Biological Chemistry, 1984 , vol. 48, p. 1969 - 1976 Title/Abstract Full Text Show Details
Thapliyal; Singh; Khanna
Synthetic Communications, 1994 , vol. 24, # 8 p. 1079 - 1083 Title/Abstract Full Text View citing articles Show Details
Raju, K. Vijaya; Raju, G. Bangar; Yadav, M. Rajasekhar
Indian Journal of Chemistry, Section A: Inorganic, Bio-inorganic, Physical, Theoretical & Analytical Chemistry, 1993 , vol. 32, # 11 p. 1012 - 1014 Title/Abstract Full Text Show Details
Sain, Bir; Murthy, Pappu S.; Venkateshwar Rao; Prasada Rao; Joshi, Girish C.
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Costantini; D'Ischia; Prota
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Chemistry Letters, 1994 , # 7 p. 1345 - 1348
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28 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
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D'Souza, Francis
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30 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
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Tetrahedron Letters, 1996 , vol. 37, # 29 p. 5221 - 5224 Title/Abstract Full Text View citing articles Show Details
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Kalnin'sh; Bursian
Russian Journal of Physical Chemistry A, 1996 , vol. 70, # 12 p. 2048 - 2053 Title/Abstract Full Text View citing articles Show Details
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Journal of Chemical Research - Part S, 1996 , # 10 p. 474 - 475 Title/Abstract Full Text View citing articles Show Details
Liu, Chunjian; Burnell, D. Jean
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Kazak; Chudaeva; Rodionova; Trofimov
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Journal of Agricultural and Food Chemistry, 1996 , vol. 44, # 8 p. 2167 - 2175 Title/Abstract Full Text View citing articles Show Details
Haraguchi, Hiroyuki; Yamano, Kaori; Kusunoki, Naoko; Fukuda, Ayumi
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Journal of the Chemical Society. Perkin Transactions 2, 1998 , # 5 p. 1123 - 1128 Title/Abstract Full Text View citing articles Show Details
Borovikov; Sivachek; Makovetskii; Novikov
Russian Journal of General Chemistry, 1997 , vol. 67, # 6 p. 936 - 941 Title/Abstract Full Text View citing articles Show Details
Hashemi, Mohammed M.; Beni, Yousef Ahmadi
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Kalnin'sh; Pavlova
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Comment (Pharmacological Data)
Bioactivities present
Reference
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Shumakovich; Yaropolov; Dubova; Antonova; Bachurin
Doklady Chemistry, 1996 , vol. 348, # 4-6 p. 149 - 152 Title/Abstract Full Text View citing articles Show Details
Roginsky, Vitaly A.; Pisarenko, Leonid M.; Bors, Wolf; Michel, Christa
Journal of the Chemical Society. Perkin Transactions 2, 1999 , # 4 p. 871 - 876 Title/Abstract Full Text View citing articles Show Details
Mahalingam, Rathinam J.; Selvam, Parsuraman
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Schmid, Ralf; Goebel, Friederike; Warnecke, Andre; Labahn, Andreas
Journal of the Chemical Society. Perkin Transactions 2, 1999 , # 6 p. 1199 - 1202 Title/Abstract Full Text View citing articles Show Details
Ahvazi, Behzad C.; Crestini, Claudia; Argyropoulos, Dimitris S.
Journal of Agricultural and Food Chemistry, 1999 , vol. 47, # 1 p. 190 - 201 Title/Abstract Full Text View citing articles Show Details
Baldwin; Staszak-Kozinski; Davidson
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Anastasio; Faust; Rao
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Journal of Chemical Research - Part S, 1999 , # 11 p. 672 - 673 Title/Abstract Full Text View citing articles Show Details
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31 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
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Advanced Synthesis and Catalysis, 2000 , vol. 342, # 8 p. 825 - 827 Title/Abstract Full Text View citing articles Show Details
Barun; Chakrabarti; Ila; Junjappa
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Tetrahedron, 2001 , vol. 57, # 23 p. 4863 - 4866 Title/Abstract Full Text View citing articles Show Details
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Journal of the Chemical Society, Perkin Transactions 2, 2001 , # 5 p. 843 - 860 Title/Abstract Full Text View citing articles Show Details
Tohma, Hirofumi; Morioka, Hironori; Harayama, Yu; Hashizume, Miki; Kita, Yasuyuki
Tetrahedron Letters, 2001 , vol. 42, # 39 p. 6899 - 6902 Title/Abstract Full Text View citing articles Show Details
D'Souza; Deviprasad
Journal of Organic Chemistry, 2001 , vol. 66, # 13 p. 4601 - 4609 Title/Abstract Full Text View citing articles Show Details
Eguchi, Tadashi; Kanai, Shinobu; Kakinuma, Katsumi; Okazaki, Tadayasu; Mizoue, Kazutoshi
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Del Corral; Gordaliza; Castro; Mahiques; Chamorro; Molinari; Garcia-Gravalo; Broughton; San Feliciano
Journal of Medicinal Chemistry, 2001 , vol. 44, # 8 p. 1257 - 1267 Title/Abstract Full Text View citing articles Show Details
Swann; Barraja; Oberlander; Gardipee; Hudnott; Beall; Moody
Journal of Medicinal Chemistry, 2001 , vol. 44, # 20 p. 3311 - 3319 Title/Abstract Full Text View citing articles Show Details
Villemin, Didier; Hammadi, Mohamed; Hachemi, Messaoud
Synthetic Communications, 2002 , vol. 32, # 10 p. 1501 - 1515 Title/Abstract Full Text View citing articles Show Details
Ling, Taotao; Poupon, Erwan; Rueden, Erik J.; Kim, Sun H.; Theodorakis, Emmanuel A.
Journal of the American Chemical Society, 2002 , vol. 124, # 41 p. 12261 - 12267 Title/Abstract Full Text View citing articles Show Details
Eipert, Martin; Maichle-Moessmer, Caecilia; Maier, Martin E.
Journal of Organic Chemistry, 2002 , vol. 67, # 24 p. 8692 - 8695 Title/Abstract Full Text View citing articles Show Details
Singh, Vasundhara; Sapehiyia, Varinder; Kad, Goverdhan L.
Synthesis, 2003 , # 2 p. 198 - 200 Title/Abstract Full Text View citing articles Show Details
Hashemi, Mohammed M.; Ahmadibeni, Yusef
Monatshefte fur Chemie, 2003 , vol. 134, # 3 p. 411 - 418 Title/Abstract Full Text View citing articles Show Details
Obushak; Martyak; Matiychuk
Polish Journal of Chemistry, 2002 , vol. 76, # 10 p. 1419 - 1424 Title/Abstract Full Text View citing articles Show Details
Saladino, Raffaele; Neri, Veronica; Mincione, Enrico; Filippone, Paolino
Tetrahedron, 2002 , vol. 58, # 42 p. 8493 - 8500 Title/Abstract Full Text View citing articles Show Details
Yadav; Reddy; Kondaji
Synthesis, 2003 , # 7 p. 1100 - 1104 Title/Abstract Full Text View citing articles Show Details
Knoelker, Hans-Joachim; Reddy, Kethiri R.
Heterocycles, 2003 , vol. 60, # 5 p. 1049 - 1052 Title/Abstract Full Text View citing articles Show Details
32 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
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Journal of Physical Organic Chemistry, 2003 , vol. 16, # 5 p. 265 - 270 Title/Abstract Full Text View citing articles Show Details
Yadav; Reddy; Swamy
Tetrahedron Letters, 2003 , vol. 44, # 26 p. 4861 - 4864 Title/Abstract Full Text View citing articles Show Details
Evans, David A.; Wu, Jimmy
Journal of the American Chemical Society, 2003 , vol. 125, # 34 p. 10162 - 10163 Title/Abstract Full Text View citing articles Show Details
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Journal of Organic Chemistry, 2003 , vol. 68, # 12 p. 4988 - 4990 Title/Abstract Full Text View citing articles Show Details
Fukuzumi, Shunichi; Nishimine, Mari; Ohkubo, Kei; Tkachenko, Nikolai V.; Lemmetyinen, Helge
Journal of Physical Chemistry B, 2003 , vol. 107, # 45 p. 12511 - 12518 Title/Abstract Full Text View citing articles Show Details
Yadav, J. S.; Reddy, B. V. S.; Swamy, T.
Tetrahedron Letters, 2003 , vol. 44, # 51 p. 9121 - 9124 Title/Abstract Full Text Show Details
Gacem, Badra; Jenner, Gerard
Journal of Physical Organic Chemistry, 2004 , vol. 17, # 3 p. 221 - 225 Title/Abstract Full Text View citing articles Show Details
Yadav; Reddy; Swamy
Synthesis, 2004 , # 1 p. 106 - 110 Title/Abstract Full Text View citing articles Show Details
Goerner, Helmut
Journal of Physical Chemistry A, 2003 , vol. 107, # 51 p. 11587 - 11595 Title/Abstract Full Text View citing articles Show Details
Kudryasheva; Vetrova; Kuznetsov; Kratasyuk; Stom
Ecotoxicology and Environmental Safety, 2002 , vol. 53, # 2 p. 221 - 225 Title/Abstract Full Text View citing articles Show Details
Nair, Vijay; Vinod, A. Unni; Abhilash; Menon, Rajeev S.; Santhi; Varma, R. Luxmi; Viji; Mathew, Saumini; Srinivas
Tetrahedron, 2003 , vol. 59, # 51 p. 10279 - 10286 Title/Abstract Full Text View citing articles Show Details
Goerner, Helmut
Photochemistry and Photobiology, 2003 , vol. 78, # 5 p. 440 - 448 Title/Abstract Full Text View citing articles Show Details
Yadav; Reddy, B. V. Subba; Swamy; Rao, K. Raghavender
Tetrahedron Letters, 2004 , vol. 45, # 31 p. 6037 - 6039 Title/Abstract Full Text View citing articles Show Details
Yadav; Reddy; Swamy; Ramireddy
Synthesis, 2004 , # 11 p. 1849 - 1853 Title/Abstract Full Text View citing articles Show Details
Niedermeyer, Timo H. J.; Mikolasch, Annett; Lalk, Michael
Journal of Organic Chemistry, 2005 , vol. 70, # 6 p. 2002 - 2008 Title/Abstract Full Text View citing articles Show Details
Jenner, Gerard; Salem, Ridha Ben
New Journal of Chemistry, 2000 , vol. 24, # 4 p. 203 - 207 Title/Abstract Full Text View citing articles Show Details
Hashemi, Mohammed M.; Karimi-Jaberi, Zahed; Eftekhari-Sis, Bagher
Journal of Chemical Research, 2005 , # 3 p. 160 - 161 Title/Abstract Full Text View citing articles Show Details
Silvero, Guadalupe; Arevalo, Maria Jose; Bravo, Jose Luis; Avalos, Martin; Jimenez, Jose Luis; Lopez, Ignacio
Tetrahedron, 2005 , vol. 61, # 30 p. 7105 - 7111 Title/Abstract Full Text View citing articles Show Details
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Kim, MeeKyoung; Wiemer, David F.
Tetrahedron Letters, 2005 , vol. 46, # 44 p. 7583 - 7587 Title/Abstract Full Text View citing articles Show Details
33 of 73
34 of 73
Comment (Pharmacological Data)
Bioactivities present
Reference
Maloney, David J.; Hecht, Sidney M.
Organic Letters, 2005 , vol. 7, # 19 p. 4297 - 4300 Title/Abstract Full Text View citing articles Show Details
Ganiev; Ganieva; Kabal'nova
Russian Chemical Bulletin, 2004 , vol. 53, # 10 p. 2281 - 2284 Title/Abstract Full Text View citing articles Show Details
Hashemi; Akhbari
Russian Journal of Organic Chemistry, 2005 , vol. 41, # 6 p. 935 - 936 Title/Abstract Full Text View citing articles Show Details
Hong, Bor-Cherng; Chen, Zhong-Yi; Chen, Wei-Hung; Sun, Hsu-I.; Lee, Gene-Hsiang
Journal of the Chinese Chemical Society, 2005 , vol. 52, # 1 p. 181 - 200 Title/Abstract Full Text View citing articles Show Details
Khazaei, Ardeshir; Zolfigol, Mohammad Ali; Manesh, Abbas Amini
Journal of the Chinese Chemical Society, 2005 , vol. 52, # 3 p. 515 - 518 Title/Abstract Full Text View citing articles Show Details
Zhang, Hai-Bo; Liu, Li; Chen, Yong-Jun; Wang, Dong; Li, Chao-Jun
Advanced Synthesis and Catalysis, 2006 , vol. 348, # 1-2 p. 229 - 235 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Chen, Chao; Xi, Chanjuan; Ai, Zhezhe; Hong, Xiaoyin
Organic Letters, 2006 , vol. 8, # 18 p. 4055 - 4058 Title/Abstract Full Text View citing articles Show Details
Algi, Fatih; Balci, Metin
Synthetic Communications, 2006 , vol. 36, # 16 p. 2293 - 2297 Title/Abstract Full Text View citing articles Show Details
Watanabe, Hiroto; Hiraoka, Ryota; Senna, Mamoru
Tetrahedron Letters, 2006 , vol. 47, # 26 p. 4481 - 4484 Title/Abstract Full Text View citing articles Show Details
Scheepers, Brent A.; Klein, Rosalyn; Davies-Coleman, Michael T.
Tetrahedron Letters, 2006 , vol. 47, # 47 p. 8243 - 8246 Title/Abstract Full Text View citing articles Show Details
Zhou, Guanglian; Zheng, Deping; Da, Shijun; Xie, Zhixiang; Li, Ying
Tetrahedron Letters, 2006 , vol. 47, # 20 p. 3349 - 3352 Title/Abstract Full Text View citing articles Show Details
Bernardo, Paul H.; Chai, Christina L.L.; Guen, Maurice Le; Smith, Geoffrey D.; Waring, Paul
Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 1 p. 82 - 85 Title/Abstract Full Text View citing articles Show Details
Zhizhina; Simonova; Russkikh; Matveev
Russian Journal of Applied Chemistry, 2005 , vol. 78, # 5 p. 758 - 764 Title/Abstract Full Text View citing articles Show Details
Komiyama, Takuzo; Takaguchi, Yutaka; Tsuboi, Sadao
Synthesis, 2006 , # 9 p. 1405 - 1407 Title/Abstract Full Text View citing articles Show Details
Shimada, Hideaki; Hirashima, Takaomi; Imamura, Yorishige
European Journal of Pharmacology, 2006 , vol. 540, # 1-3 p. 46 - 52 Title/Abstract Full Text View citing articles Show Details
Mal, Dipakranjan; Ray, Sutapa; Sharma, Indrajeet
Journal of Organic Chemistry, 2007 , vol. 72, # 13 p. 4981 - 4984 Title/Abstract Full Text View citing articles Show Details
Jakober, Chris A.; Riddle, Sarah G.; Robert, Michael A.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.
Environmental Science and Technology, 2007 , vol. 41, # 13 p. 4548 - 4554 Title/Abstract Full Text View citing articles Show Details
Coeur-Tourneur, Cecile; Henry, Francoise; Janquin, Marie-Andree; Brutier, Laurent
International Journal of Chemical Kinetics, 2006 , vol. 38, # 9 p. 553 - 562 Title/Abstract Full Text View citing articles Show Details
Cape, Jonathan L.; Bowman, Michael K.; Kramer, David M.
Phytochemistry, 2006 , vol. 67, # 16 p. 1781 - 1788 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
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BASF Aktiengesellschaft
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Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
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Comment (Pharmacological Data)
physiological behaviour discussed
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physiological behaviour discussed
Reference
Bremer, Paul T.; Hixon, Mark S.; Janda, Kim D.
Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 15 p. 3971 - 3981 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
physiological behaviour discussed
Reference
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
enzyme activity; inhibition of
Species or Test-System (Pharmacological Data)
thioredoxin reductase of Entamoeba histolytica
Kind of Dosing (Pharmacological Data)
DTNB; 0.3 mmol/l NADPH
Method (Pharmacological Data)
name of assay/method: spectrophotometric assay
Further Details (Pharmacological Data)
DTNB: 5-5'-dithio-nitrobenzoic acid; Kic related to: disulfide reductase activity
Type (Pharmacological Data)
Kic
Value of Type (Pharmacological Data)
2.5 μmol/l
Reference
Arias, Diego G.; Regner, Erika L.; Iglesias, Alberto A.; Guerrero, Sergio A.
Biochimica et Biophysica Acta - General Subjects, 2012 , vol. 1820, # 12 p. 1859 - 1866 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
enzyme activity; inhibition of
Species or Test-System (Pharmacological Data)
thioredoxin reductase of Entamoeba histolytica
Kind of Dosing (Pharmacological Data)
DTNB; 0.3 mmol/l NADPH
Method (Pharmacological Data)
name of assay/method: spectrophotometric assay
Further Details (Pharmacological Data)
DTNB: 5-5'-dithio-nitrobenzoic acid; Kiu related to: disulfide reductase activity
Type (Pharmacological Data)
Kiu
Value of Type (Pharmacological Data)
3.7 μmol/l
Reference
Arias, Diego G.; Regner, Erika L.; Iglesias, Alberto A.; Guerrero, Sergio A.
Biochimica et Biophysica Acta - General Subjects, 2012 , vol. 1820, # 12 p. 1859 - 1866 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
pharmacokinetics
Species or Test-System (Pharmacological Data)
recombinant apoptosis-inducing factor of mouse
Further Details (Pharmacological Data)
catalytic constant (Kcat)
Type (Pharmacological Data)
Kcat
Value of Type (Pharmacological Data)
0.041 1/s
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Reference
Misevicien, Lina; Anusevicius, Zilvinas; Sarlauskas, Jonas; Sevrioukova, Irina F.; Cnas, Narimantas
Archives of Biochemistry and Biophysics, 2011 , vol. 512, # 2 p. 183 - 189 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Example 3 - activity asainst P. acnes (other quinones)A series of quinones was tested with zinc pyrithione (ZP) in a similar manner to that described in Example 1. The MIC and MBC results are shown in Table 4 below and the (S)DDA results in Tables 5 (unsupplemented assays) and 6 (assays supplemented with salt and lipid). All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc with the exception of 2-t-butyl-p-benzoquinone which was used at 50 μg per disc in unsupplemented and 100 μg per disc in supplemented assays. The test compounds were dissolved in DMSO, with the exception of /?-benzoquinone and thymoquinone which were dissolved in ethanol.Table 4 Table 5 (unsupplemented (S)DDAs)Table 6 (supplemented (S)DDAs) (SL-(S)DDA = (S)DDA carried out in the presence of salt and lipid)Again these data demonstrate a synergistic antimicrobial interaction when a quinone is combined with zinc pyrithione, there being a significant increase in zone diameter over that exhibited by either compound alone. This synergistic interaction is maintained in nearly all cases in the presence of salt and lipid; furthermore the activity of the quinones alone appears in all cases to be enhanced by the presence of the supplements. Indeed, in some cases, for example the combination of 2-methyl-/?hydroquinone or 2- ethyl-p-hydroquinone with zinc pyrithione, antimicrobial synergy appears to be far more marked under the supplemented conditions than the unsupplemented ones, indicating the potential value of such a combination in topical skin treatment formulations, in particular to treat acne.Example 5 - activity against Propionibacterium spp (copper pyrithione)Copper (II) pyrithione (CuP) was tested against P. acnes NCTC 737 with a number of quinones, using the same procedure as in Example 3. The MIC and MBC results are shown in Table 9 below and the (S)DDA results in Table 10. All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc, with the exception of 2-t-butyl-p-benzoquinone which was used at 100 μg per disc. The TBHQ was dissolved in ethanol and the copper pyrithione, 2-methyl-p- benzoquinone and 2-chloro-p-benzoquinone in DMSO.Table 9 Table 10* Denotes data obtained in a separate series of experiments to those involving TBHQ and CuP.These data demonstrate a synergistic antimicrobial interaction when a quinone is combined with copper pyrithione, there being in nearly all cases a significant increase in zone diameter over that exhibited by either compound alone.
Type (Pharmacological Data)
MIC
Value of Type (Pharmacological Data)
15.6 μg/ml
Results
MBC is 31.25 μg/ml, MIC/MBC is 0.5
Location
Page/Page column 22-24; 28; 33-34
Reference
SYNTOPIX LIMITED
Patent: WO2008/35078 A1, 2008 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Example 3 - activity asainst P. acnes (other quinones)A series of quinones was tested with zinc pyrithione (ZP) in a similar manner to that described in Example 1. The MIC and MBC results are shown in Table 4 below and the (S)DDA results in Tables 5 (unsupplemented assays) and 6 (assays supplemented with salt and lipid). All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc with the exception of 2-t-butyl-p-benzoquinone which was used at 50 μg per disc in unsupplemented and 100 μg per disc in supplemented assays. The test compounds were dissolved in DMSO, with the exception of /?-benzoquinone and thymoquinone which were dissolved in ethanol.Table 4 Table 5 (unsupplemented (S)DDAs)Table 6 (supplemented (S)DDAs) (SL-(S)DDA = (S)DDA carried out in the presence of salt and lipid)Again these data demonstrate a synergistic antimicrobial interaction when a quinone is combined with zinc pyrithione, there being a significant increase in zone diameter over that exhibited by either compound alone. This synergistic interaction is maintained in nearly all cases in the presence of salt and lipid; furthermore the activity of the quinones alone appears in all cases to be enhanced by the presence of the supplements. Indeed, in some cases, for example the combination of 2-methyl-/?hydroquinone or 2- ethyl-p-hydroquinone with zinc pyrithione, antimicrobial synergy appears to be far more marked under the supplemented conditions than the unsupplemented ones, indicating the potential value of such a combination in topical skin treatment formulations, in particular to treat acne.Example 5 - activity against Propionibacterium spp (copper pyrithione)Copper (II) pyrithione (CuP) was tested against P. acnes NCTC 737 with a number of quinones, using the same procedure as in Example 3. The MIC and MBC results are shown in Table 9 below and the (S)DDA results in Table 10. All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc, with the exception of 2-t-butyl-p-benzoquinone which was used at 100 μg per disc. The TBHQ was dissolved in ethanol and the copper pyrithione, 2-methyl-p- benzoquinone and 2-chloro-p-benzoquinone in DMSO.Table 9 Table 10* Denotes data obtained in a separate series of experiments to those involving TBHQ and CuP.These data demonstrate a synergistic antimicrobial interaction when a quinone is combined with copper pyrithione, there being in nearly all cases a significant increase in zone diameter over that exhibited by either compound alone.
Results
unsupplemented disc diffusion assay value is 34.50 mm, 39.90 mm, supplemented (Triolein at 1percent v/v, sodium chloride, 100 mM) disc diffusion assay value is 44.99 mm
Location
Page/Page column 22-25; 28-30; 33-34
Reference
SYNTOPIX LIMITED
Patent: WO2008/35078 A1, 2008 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
cytotoxicity
Species or Test-System (Pharmacological Data)
hepatocytes of Sprague-Dawley rat
Sex
male
Method (Pharmacological Data)
cells incubated with title comp. for up to 3 h at 37 deg C under atmosphere of 95percent O2 and 5percent CO2; cell viability detd. trypan blue exclusion test
Further Details (Pharmacological Data)
control: untreated cells; LC50: conc. of title comp. required to cause 50percent decrease in cell viability in 2 h
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Type (Pharmacological Data)
LC50
Value of Type (Pharmacological Data)
46 μmol/l
Reference
Chan, Katie; Jensen, Neil; O'Brien, Peter J.
Journal of Applied Toxicology, 2008 , vol. 28, # 5 p. 608 - 620 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cytotoxicity
Species or Test-System (Pharmacological Data)
hepatocytes of human
Sex
male
Method (Pharmacological Data)
cells incubated with title comp. for up to 3 h at 37 deg C; MTT added; incubated for another 3 h; absorbance of MTT formazan was measured at 572 nm and 690 nm; cytotoxicity determined
Further Details (Pharmacological Data)
control: untreated cells; LC50: conc. of title comp. required to cause 50percent decrease in cell viability in 2 h
Type (Pharmacological Data)
LC50
Value of Type (Pharmacological Data)
117 μmol/l
Reference
Chan, Katie; Jensen, Neil; O'Brien, Peter J.
Journal of Applied Toxicology, 2008 , vol. 28, # 5 p. 608 - 620 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Test micro-organismsThe principal test micro-organism used was Propionibacterium acnes NCTC 737. Other propionibacterial strains, including some P. granulosum strains and including some having antibiotic resistance, were also used as test organisms in Example 4.Propionibacteria are known to be involved in acne, which is a complex, multi-factorial skin disease in which P. acnes and other Propionibacterium spp. play key roles. Activity observed against the chosen test organisms is therefore expected to be a reasonable qualitative predictor of activity against micro-organisms responsible for skin and skin structure infections, in particular acne.All the propionibacteria were cultured and maintained on Wilkins-Chalgren Anaerobe Medium (agar and broth) at pH 6.0; all cultures were incubated anaerobically at 37 °C for 72 hours. Also tested was Porphyromonas gingivalis NCTC 11834 - this is a black pigmented gram-negative anaerobic bacterium belonging to the genus Porphyromonas. Porphyromonas are a human commensal bacterium, predominantly associated with the oral cavity. Clinically, Por. gingivalis is associated with periodontal lesions, infections and adult periodontal disease. Gingivitis (inflammation of the gums that causes bleeding and exposes the base of the teeth) can be a precursor to periodontal disease by allowing Por. gingivalis to infect the areas near the roots of the teeth and thus cause tooth decay and infection.Activity observed against this micro-organism is expected to be a reasonable qualitative predictor of antimicrobial activity, in particular against micro-organisms responsible for periodontal lesions, infections, and periodontal disease.Por. gingivalis was cultured and maintained on Wilkins-Chalgren Anaerobe Medium (agar and broth) at pH 7.0; all cultures were incubated anaerobically at 37 0C for 5-7 days.The following tests were carried out to assess antimicrobial activity against the test organisms. (d) Disc diffusion assay (DDA)This is an internationally recognised standard method for qualitatively assessing the antimicrobial activity of a compound.A sterile paper disc was impregnated with a sample of the test compound in a suitable solvent and 30 minutes allowed for the solvents to evaporate (where possible). The disc was then placed on an agar plate onto which the test micro-organism had been inoculated. The plate was then incubated under the conditions described above, following which it was examined visually for signs of microbial growth. If the test compound had antimicrobial activity, a circular zone of no growth would be obtained around the disc. The diameter of this zone of "inhibition" was measured using a ProtoCOL.(TM). automated zone sizer (Synbiosis, Cambridge, UK). In general, a greater diameter and/or area of the zone of inhibition indicates a greater antimicrobial activity in the relevant test compound, although other factors such as test compound mobility through the agar gel may also influence the result.
Results
The diameter of zone of inhibition = 39.90 mm
Location
Page/Page column 27-28; 30; 34-35
Reference
SYNTOPIX LIMITED
Patent: WO2008/35085 A1, 2008 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
insecticidal
Species or Test-System (Pharmacological Data)
Coptotermes formosanus Shiraki, Formosan subterranean termite
Kind of Dosing (Pharmacological Data)
administered via filter paper disk treated with solution of title comp. in acetone (1percent wt/wt) after evaporation of solvent
Further Details (Pharmacological Data)
filter paper disk assay; results obtained at days 3-21 of treatment
Type (Pharmacological Data)
percent mortality
Value of Type (Pharmacological Data)
1.7 - 20 percent
Reference
Mozaina, Kobaisy; Cantrell, Charles L.; Mims, Amelia B.; Lax, Alan R.; Tellez, Maria R.; Osbrink, Weste L. A.
Journal of Agricultural and Food Chemistry, 2008 , vol. 56, # 11 p. 4021 - 4026
Title/Abstract Full Text View citing articles Show Details
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Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Example 8 - activity against P. acnes (other quinones)A number of different quinones was tested with both copper (II) sulphate pentahydrate (CSPH) and copper (II) silicate (CSL) against P. acnes NCTC 737 using (S)DDA tests as described in Example 1.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc, with the exception of copper (II) silicate (62 μg/disc) and 2-t-butyl-l,4- benzoquinone (100 μg/disc). The quinones were dissolved in DMSO and the copper (II) sulphate pentahydrate in deionised water, whilst the copper (II) silicate was used as a 0.62 percent (w/w) solution in water.All the quinones were sourced from Thermo Fisher Scientific, UK with the exception of 2-t-butyl-l,4-benzoquinone (Sigma- Aldrich) and 2-ethyl-p-hydroquinone (Apin Chemicals Ltd, UK).The DDA results are shown in Table 13 below and the SDDA results in Tables 14 and 15 (unsupplemented assays) and 16 and 17 (supplemented assays).Table 13 f-lpercent(v/v) trioleinTable 14Table 15Table 16 (SL SDDA = SDDA with salt and lipid (1percent (v/v) triolein) supplements)Table 17(SL SDDA = SDDA with salt and lipid (1percent (v/v) triolein) supplements)These data demonstrate synergistic antimicrobial activity against P. acnes NCTC 737 for a range of different benzo- and hydroquinones with copper salts. On the whole these synergies are retained under the supplemented conditions.
Results
title compound demonstrated an antimicrobial activity with zone of diameter of 33.74 mm (DDA) and 35.18 mm (DDA + salt and lipid)
Location
Page/Page column 47-49
Reference
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
metabolism; inhibition of
Species or Test-System (Pharmacological Data)
pig heart cytosol
Concentration (Pharmacological Data)
10 μmol/l
Kind of Dosing (Pharmacological Data)
title comp. was dissolved in dimethyl sulfoxide
Method (Pharmacological Data)
test system incubated with 0.5 mmol/l all-trans retinal, NADPH-generating system, sodium potassium phosphate buffer and title comp. at 37 deg C for 10 min; centrifuged; concentration of all-trans retinol determined by HPLC
Results
title comp. inhibited reduction of all-trans retinal to all-trans retinol; fig.
Reference
Shimada, Hideaki; Hirashima, Takaomi; Imamura, Yorishige
European Journal of Pharmacology, 2006 , vol. 540, # 1-3 p. 46 - 52 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
toxic to aquatic plants
Species or Test-System (Pharmacological Data)
T. isochrysis galbana
Method (Pharmacological Data)
Culture was allowed to grow under continuous fluorescent light following the exposure treatments; chlorophyll fluorescence determination. In-vivo fluorimetry with the Hitachi F4500 recording the emission spectra from 600-720 nm. End-points for compound toxicity include cell motility, inhibition of cell division, inhibition of chlorophyll synthesis and chloroplate bleaching
Value of Type (Pharmacological Data)
500 ppb
Results
toxic
Location
Page column 10-12
Comment (Pharmacological Data)
potential area of application: agro
Reference
Garnett, Inc.
Patent: US6340468 B1, 2002 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
mutagenic (microorganism)
Species or Test-System (Pharmacological Data)
Escherichia coli IC206
Concentration (Pharmacological Data)
40 μg/plate
Kind of Dosing (Pharmacological Data)
title comp. dissolved in DMSO; diluted with water
Method (Pharmacological Data)
in vitro; plate incorporation assay; Difco agar; minimal ET4 plates; 37 deg C; 2 d; number of revertants per plates counted
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Further Details (Pharmacological Data)
mutY WP2 uvrA/pKM101 bacterial strain
Comment (Pharmacological Data)
No effect
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
mutagenic (microorganism)
Species or Test-System (Pharmacological Data)
Escherichia coli IC208
Concentration (Pharmacological Data)
40 μg/plate
Kind of Dosing (Pharmacological Data)
title comp. dissolved in DMSO; diluted with water
Method (Pharmacological Data)
in vitro; plate incorporation assay; Difco agar; minimal ET4 plates; 37 deg C; 2 d; number of revertants per plates counted
Further Details (Pharmacological Data)
mutY oxyR WP2 uvrA/pKM101 bacterial strain
Comment (Pharmacological Data)
No effect
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
mutagenic (microorganism)
Species or Test-System (Pharmacological Data)
Escherichia coli IC204
Concentration (Pharmacological Data)
40 μg/plate
Kind of Dosing (Pharmacological Data)
title comp. dissolved in DMSO; diluted with water
Method (Pharmacological Data)
in vitro; plate incorporation assay; Difco agar; minimal ET4 plates; 37 deg C; 2 d; number of revertants per plates counted
Further Details (Pharmacological Data)
mut+ WP2 uvrA/pKM101 bacterial strain
Comment (Pharmacological Data)
No effect
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cytotoxicity
Endpoint of Effect (Pharmacological Data)
growth
Species or Test-System (Pharmacological Data)
Escherichia coli IC203
Concentration (Pharmacological Data)
50 μg/disc
Kind of Dosing (Pharmacological Data)
paper discs (6 mm in diameter) impregnated with title comp. dissolved in DMSO and diluted with water
Method (Pharmacological Data)
in vitro; LA plates; paper discs impregnated with title comp. placed on solidified top agar; in the pres. and abs. of S9 mix; inhibition zone determined
Further Details (Pharmacological Data)
WP2 uvrA/pKM101 bacterial strain deficient in OxyR
Results
diameter of inhibition zone 12-16 mm; cytotoxicity of title comp. weakly inhibited by S9
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
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Effect (Pharmacological Data)
cytotoxicity
Endpoint of Effect (Pharmacological Data)
growth
Species or Test-System (Pharmacological Data)
Escherichia coli IC188
Concentration (Pharmacological Data)
50 μg/disc
Kind of Dosing (Pharmacological Data)
paper discs (6 mm in diameter) impregnated with title comp. dissolved in DMSO and diluted with water
Method (Pharmacological Data)
in vitro; LA plates; paper discs impregnated with title comp. placed on solidified top agar; incubated overnight; diameter of inhibition zone determined
Further Details (Pharmacological Data)
parent WP2 uvrA/pKM101 bacterial strain
Results
diameter of inhibition zone 8 mm
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
mutagenic (microorganism)
Species or Test-System (Pharmacological Data)
Escherichia coli IC203
Concentration (Pharmacological Data)
20 - 40 μg/plate
Kind of Dosing (Pharmacological Data)
title comp. dissolved in DMSO; diluted with water
Method (Pharmacological Data)
in vitro; plate incorporation assay; Difco agar; minimal ET4 plates; 37 deg C; 2 d; with and without metabolic activation with rat S9 mix; number of revertants per plates counted
Further Details (Pharmacological Data)
WP2 uvrA/pKM101 bacterial strain deficient in OxyR
Results
oxidative mutagenesis both in the pres. and abs. of S9 mix
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
mutagenic (microorganism)
Species or Test-System (Pharmacological Data)
Escherichia coli IC188
Concentration (Pharmacological Data)
20 - 40 μg/plate
Kind of Dosing (Pharmacological Data)
title comp. dissolved in DMSO; diluted with water
Method (Pharmacological Data)
in vitro; plate incorporation assay; Difco agar; minimal ET4 plates; 37 deg C; 2 d; number of revertants per plates counted
Further Details (Pharmacological Data)
parent WP2 uvrA/pKM101 bacterial strain
Comment (Pharmacological Data)
No effect
Reference
Martinez, Alicia; Urios, Amparo; Blanco, Manuel
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2000 , vol. 467, # 1 p. 41 - 53 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
enzyme; examination of
Species or Test-System (Pharmacological Data)
NADPH-cytochrome P450 reductase
Sex
male
Concentration (Pharmacological Data)
10 - 100 μmol/l
Method
Incubation mixture contained: purified reductase (from liver microsomes of phenobarbital-treated rats), the title comp., complete medium, and Hepes (pH 7.4); quinone
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(Pharmacological Data)
reductase activity estimated as quinone-dependent NADPH oxidation (340 nm); 25 deg C
Further Details (Pharmacological Data)
complete medium: L-<2,3-3H>arginine, L-arginine, NADPH, (6R)-5,6,7,8-tetrahydro-L-biopterin, CaCl2, calmodulin; Hepes=4-(2-hydroxyethyl)-1-piperazineethane-sulfonic acid; specific activity of P450 reductase was 34.53 U/mg
Type (Pharmacological Data)
reductase activity
Value of Type (Pharmacological Data)
4.35 μmol/mg/min
Reference
Kumagai, Yoshito; Nakajima, Hiromi; Midorikawa, Kazumi; Homma-Takeda, Shino; Shimojo, Nobuhiro
Chemical Research in Toxicology, 1998 , vol. 11, # 6 p. 608 - 613 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
enzyme; examination of
Species or Test-System (Pharmacological Data)
neuronal nitric oxide synthase nNOS from Wistar rat
Sex
male
Concentration (Pharmacological Data)
10 - 100 μmol/l
Method (Pharmacological Data)
Incubation mixture contained: purified nNOS (from cerebellum), the title comp., complete medium, and Hepes (pH 7.4); quinone reductase activity was estimated as quinonedependent NADPH oxidation (measurements at 340 nm); 25 deg C
Further Details (Pharmacological Data)
complete medium: L-<2,3-3H>arginine, L-arginine, NADPH, (6R)-5,6,7,8-tetrahydro-L-biopterin, CaCl2, calmodulin; Hepes=4-(2-hydroxyethyl)-1-piperazineethane-sulfonic acid; specific activity of nNOS was 364 nmol of L-citrulline formed/mg/min
Type (Pharmacological Data)
reductase activity
Value of Type (Pharmacological Data)
0 μmol/mg/min
Reference
Kumagai, Yoshito; Nakajima, Hiromi; Midorikawa, Kazumi; Homma-Takeda, Shino; Shimojo, Nobuhiro
Chemical Research in Toxicology, 1998 , vol. 11, # 6 p. 608 - 613 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
enzyme; inhib. of
Species or Test-System (Pharmacological Data)
Wistar rat
Sex
male
Method (Pharmacological Data)
Rat (5 weeks) cerebellum homogenized and centrifuged at 20000g for 1 h; supernatants containing nNOS incubated with the title comp. in DMSO and complete medium at 37 deg C for 10 min in Hepes; pH 7.4; formation of <3H>citrulline was determined
Further Details (Pharmacological Data)
nNOS=neuronal nitric oxide synthase; complete medium: L-<2,3-3H>arginine, L-arginine, NADPH, (6R)-5,6,7,8-tetrahydro-L-biopterin, CaCl2, calmodulin; Hepes=4-(2hydroxyethyl)-1-piperazineethane-sulfonic acid; citrulline: the coproduct of NO biosynthesis
Type (Pharmacological Data)
IC50
Value of Type (Pharmacological Data)
63.8 μmol/l
Reference
Kumagai, Yoshito; Nakajima, Hiromi; Midorikawa, Kazumi; Homma-Takeda, Shino; Shimojo, Nobuhiro
Chemical Research in Toxicology, 1998 , vol. 11, # 6 p. 608 - 613 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
inhibition of yeast acetolactate synthase, IC50: 12.8 μM
Reference
Haraguchi, Hiroyuki; Yamano, Kaori; Kusunoki, Naoko; Fukuda, Ayumi
Journal of Agricultural and Food Chemistry, 1997 , vol. 45, # 7 p. 2784 - 2787 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
cytotoxicity against human chronic leukemia K562 cells, IC50=2.75 μM (in vitro); DNA interstrand cross-linking in plasmid DNA.
Reference
Mayalarp, Stephen P.; Hargreaves, Rob H. J.; Butler, John; Caroline O'Hare; Hartley, John A.
Journal of Medicinal Chemistry, 1996 , vol. 39, # 2 p. 531 - 537 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
slight inhibitory activity against porcine lens aldose reductase and no activity against porcine kidney aldehyde reductase; effect on bovine liver mitochondrial NADH oxidase
Reference
Haraguchi, Hiroyuki; Ohmi, Isao; Kubo, Isao
Bioorganic and Medicinal Chemistry, 1996 , vol. 4, # 1 p. 49 - 53 Title/Abstract Full Text View citing articles Show Details
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Effect (Pharmacological Data)
toxicity, acute
Species or Test-System (Pharmacological Data)
mitochondria from liver of Sprague-Dawley rats
Sex
male
Method (Pharmacological Data)
liver mitochondria fractions were isolated from 225- to 250-g rats from Dominion Laboratories; the average protein concentration of the isolated mitochondria fractions was 25 mg/ml
Further Details (Pharmacological Data)
all assays using an individual mitochondrial fraction were completed on the day of isolation; rates of states 3 and 4 respiration were determined
Type (Pharmacological Data)
IC50
Value of Type (Pharmacological Data)
23 μM
Results
simultaneous decline of state 3 and 4 respiration upon exposure to increasing concentration of quinone indicates electron-transport inhibition as the mechanism of mitochondria toxicity
Reference
Bramble; Boardman; Bevan; Dietrich
Environmental Toxicology and Chemistry, 1994 , vol. 13, # 2 p. 307 - 316 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
microsomal oxygen consumption rates
Species or Test-System (Pharmacological Data)
microsomal fractions from liver of Sprague-Dawley rats
Sex
male
Method (Pharmacological Data)
liver microsomal fractions were isolated from 225- to 250-g rats from Dominion Laboratories; the average protein concentration of the isolated microsomal fractions was 27 mg/ml
Further Details (Pharmacological Data)
immediately before use, frozen microsomez were thawed in iced water and quickly placed on ice; one batch was used within 2 h of thawing
Results
the ability to stimulate microsomal oxygen uptake reflects their capability to redox cycle and form reactive oxygen species
Reference
Bramble; Boardman; Bevan; Dietrich
Environmental Toxicology and Chemistry, 1994 , vol. 13, # 2 p. 307 - 316 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
antibacterial activity against S. aureus (MIC=200 ppm), B. subtilis (MIC=200 ppm), S. lutea (MIC=200 ppm), E. coli (MIC=200 ppm), S. typhi (MIC=400 ppm), P. aeruginosa (MIC=800 ppm)
Reference
Nishina, Atsuyoshi; Uchibori, Tsuyoshi
Agricultural and Biological Chemistry, 1991 , vol. 55, # 9 p. 2395 - 2398 Title/Abstract Full Text Show Details
Comment (Pharmacological Data)
antifungal activity against Candida albicans (MIC=400 ppm), Saccharomyces cerevisiae (MIC=50 ppm), Trichophyton interdigitale (MIC=25 ppm), Microsporium gypseum (MIC=10 ppm), Penicillum chrysogenum (MIC=800 ppm), Aspergillus niger (MIC > 800 ppm)
Reference
Nishina, Atsuyoshi; Uchibori, Tsuyoshi
Agricultural and Biological Chemistry, 1991 , vol. 55, # 9 p. 2395 - 2398 Title/Abstract Full Text Show Details
Ecotoxicology (7) 1 of 7
Effect (Ecotoxicology)
pheromone activity
Species or Test-System (Ecotoxicology)
Tribolium confusum (du Val), flour beetle
Sex
male and female
Concentration (Ecotoxicology)
1 - 1E4 ng
Kind of Dosing (Ecotoxicology)
title comp. dissolved in methanol
Method (Ecotoxicology)
species transferred in vials and placed in the center of olfactometer; then allowed to respond to title comp. released from glass capillary for 5 min; 22.5 deg C, 60percent relative humidity; species collec. upwind from release point counted as responding
Further Details (Ecotoxicology)
control: methanol; active control: 1 μg of title comp.
Results
title comp. attracted both sexes compared to methanol; no difference in behavior between male and female in response to title comp.; fig.
Reference
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
2 of 7
3 of 7
4 of 7
5 of 7
Effect (Ecotoxicology)
electrophysiology; effect on
Species or Test-System (Ecotoxicology)
antenna of Tribolium confusum (du Val), flour beetle
Sex
male and female
Concentration (Ecotoxicology)
1 - 1E6 ng
Kind of Dosing (Ecotoxicology)
title comp. impregnated in a piece of 0.5-cm2 filter paper
Method (Ecotoxicology)
insect antenna mounted between 2 glass electrodes; exposed to title comp. puff by means of a stimulus controller; EAG responses recorded
Further Details (Ecotoxicology)
control: n-hexane; active control: 10 μg of title comp.; EAG: electroantennography
Results
title comp. elicited higher EAG response than the control; males were more sensitive than females; fig.
Reference
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
bioluminescence; inhibition of
Species or Test-System (Ecotoxicology)
Photobacterium phosphoreum
Concentration (Ecotoxicology)
<= 0.0001 mol/l
Method (Ecotoxicology)
assays were performed in 3 percent NaCl; measurements were performed using bioluminometer; inhibition constants calc.
Type (Ecotoxicology)
inhibition constant
Value of Type (Ecotoxicology)
280E4 l/mol
Reference
Kudryasheva; Vetrova; Kuznetsov; Kratasyuk; Stom
Ecotoxicology and Environmental Safety, 2002 , vol. 53, # 2 p. 221 - 225 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
bioluminescence; inhibition of
Species or Test-System (Ecotoxicology)
Photobacterium leiognathi NADH:FMN-oxidoreductase/luciferase
Concentration (Ecotoxicology)
<= 0.0001 mol/l
Method (Ecotoxicology)
assays were performed in 0.1 M phosphate buffer (pH 6.8); measurements were performed using bioluminometer; room temp.
Further Details (Ecotoxicology)
enzyme system immobilized in starch gel; 0.1 mg/ml enzymes, 5E-4 mol/l FMN, 5E-4 mol/l NADH, 0.002 percent tetradecanal; inhib. const. K from I/I(max)=e-KC (I=luminesc. intensity, I(max): uninhibited; C: conc. title comp.)
Type (Ecotoxicology)
inhibition constant
Value of Type (Ecotoxicology)
150E4 l/mol
Reference
Kudryasheva; Vetrova; Kuznetsov; Kratasyuk; Stom
Ecotoxicology and Environmental Safety, 2002 , vol. 53, # 2 p. 221 - 225 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
bioluminescence; inhibition of
Species or Test-System (Ecotoxicology)
Photobacterium leiognathi NADH:FMN-oxidoreductase/luciferase
Concentration (Ecotoxicology)
<= 0.0001 mol/l
Method (Ecotoxicology)
assays were performed in 0.1 M phosphate buffer (pH 6.8); measurements were performed using bioluminometer; room temp.
Further Details (Ecotoxicology)
water-soluble coupled enzyme system; 0.1 mg/ml enzymes, 5E-4 mol/l FMN, 5E-4 mol/l NADH, 0.002 percent tetradecanal; inhib. const. K from I/I(max)=e-KC (I=luminesc. intensity, I(max): uninhibited; C: conc. title comp.)
Type (Ecotoxicology)
inhibition constant
Value of Type (Ecotoxicology)
340E4 l/mol
Reference
Kudryasheva; Vetrova; Kuznetsov; Kratasyuk; Stom
Ecotoxicology and Environmental Safety, 2002 , vol. 53, # 2 p. 221 - 225 Title/Abstract Full Text View citing articles Show Details
6 of 7
7 of 7
Effect (Ecotoxicology)
toxicity to aquatic invertebrates
Endpoint of Effect (Ecotoxicology)
population density
Species or Test-System (Ecotoxicology)
Tetrahymena pyriformis
Exposure Period (Ecotoxicology)
40 h
Method (Ecotoxicology)
static population growth assay; six to eight different concentrations; two controls: no test material but had been inoculated with T. pyriformis strain GL-C; blank (neither test material nor Tetrahymena); measured spectrophotometrically at 540 nm
Results
50 percent growth inhibitory concentration, IGC50; log (1/IGC50) = 2.41
Reference
Schultz; Sinks; Cronin
Aquatic Toxicology, 1997 , vol. 39, # 3-4 p. 267 - 278 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
reproductive effects
Endpoint of Effect (Ecotoxicology)
germination
Species or Test-System (Ecotoxicology)
Nicotiana attenuata Torr. ex. Watson, Solanaceae
Concentration (Ecotoxicology)
0.0005 - 0.5 mg/ml
Exposure Period (Ecotoxicology)
7 d
Method (Ecotoxicology)
seeds
Further Details (Ecotoxicology)
14 light : 10 dark photoperiod with 200 μM/m2/sec PAR; 30 deg C day - 22 deg C night temp. cycle; 9.8 mM aq. KNO3
Results
no stimulation of germination in compared with extract of wood smoke
Reference
Baldwin; Staszak-Kozinski; Davidson
Journal of Chemical Ecology, 1994 , vol. 20, # 9 p. 2345 - 2371 Title/Abstract Full Text View citing articles Show Details
Other Data Concentration in the Environment (2) 1 of 2
2 of 2
Media (Concentration in the Environment)
air
Location
California, USA
Contamination Concentration
35 - 480 μg/l
Method, Remarks (Concentration in the Environment)
gas-phase emissions sampled from light-duty gasoline and heavy-duty diesel vehicles operating on chassis dynamometers using annular denuders, quartz filters and PUF substrates; Aug.-Sept. 2002, June 2003; GC-ITMS and HPLC-APCI-ITMS analyzed
Reference
Jakober, Chris A.; Riddle, Sarah G.; Robert, Michael A.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.
Environmental Science and Technology, 2007 , vol. 41, # 13 p. 4548 - 4554 Title/Abstract Full Text View citing articles Show Details
Media (Concentration in the Environment)
air
Location
California, USA
Contamination Concentration
79 μg/l
Method, Remarks (Concentration in the Environment)
particle-phase emissions sampled from light-duty gasoline vehicles operating on chassis dynamometers using annular denuders, quartz filters and PUF substrates; Aug.-Sept. 2002; GC-ITMS and HPLC-APCI-ITMS analyzed
Reference
Jakober, Chris A.; Riddle, Sarah G.; Robert, Michael A.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.
Environmental Science and Technology, 2007 , vol. 41, # 13 p. 4548 - 4554 Title/Abstract Full Text View citing articles Show Details
Use (62) Use Pattern
Reference
depletes glutathione (GSH) by forming an adduct or conjugate with GSH
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ;
Title/Abstract Full Text Show Details
Cancer
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
malignant cells
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Cancerous cells
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Malignant tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Leukemias
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Lymphomas
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Solid tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
bladder tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
bone tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
brain tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
breast tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
cervical tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
colon tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
esophageal tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ;
kidney tumors
Title/Abstract Full Text Show Details
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ;
laryngeal tumors
Title/Abstract Full Text Show Details
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ;
liver tumors
Title/Abstract Full Text Show Details
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ;
lung tumors
Title/Abstract Full Text Show Details
Show next 20
Hide facts
Use Pattern
Reference
melanoma
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
ovary tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
pancreas tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
prostate tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
rectal tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
skin tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
testicular tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
uterine tumors
Redoxia Israel Ltd.
Patent: US2008/287541 A1, 2008 ; Title/Abstract Full Text Show Details
Antimicrobial
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Skin structure conditions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Acne
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Eczema
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Superficial infected traumatic lesions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
wounds
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Burns
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
ulcers
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Folliculitis
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Mycoses
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Acne lesions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Bacteria associated with acne
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Skin conditions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Staphylococcal infection
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Atopic dermatitis
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Primary skin infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Secondary skin infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Primary skin structure infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Secondary skin structure infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Acne-related scarring
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
methicillin resistant S. aureus (MRSA)-associated infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Skin care
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Hair care
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Cosmeceutical preparation
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Toiletry product
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Laundry product
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Fabric treatment product
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Bath additive
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Shower additive
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Cleansing preparation
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Agricultural product
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Horticultural product
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
veterinary preparation
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Monomers for preparation of polymers
General Electric Company
Patent: US6693221 B1, 2004 ;
Title/Abstract Full Text Show Details
Isolation from Natural Product (8) Isolation from Natural Product
Reference
Chavesincola inexpectabilis; Magnispina neptunus
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Bledius mandibularis, B. spectabilis
Wheeler et al.
Tetrahedron Letters, 1972 , p. 4635 Full Text View citing articles Show Details
Extrahiert aus Pyridial glands of Blendins mandibukris and B. spectabilis
Wheeler et al.
Tetrahedron Letters, 1972 , p. 4635 Full Text View citing articles Show Details
Pygidialeoehrblasen von Laufkaefern
Schildknecht et al.
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1968 , vol. 23, p. 637 Full Text Show Details
im 'Pulverdampf' von Bombardierkaefern u. anderen Kaefern
Schildknecht,H. et al.
Angewandte Chemie, 1963 , vol. 75, p. 762 - 771 Full Text View citing articles Show Details
V.: in den Abwehrblasen von Diplopoden, neben 2-Methyl-3-methoxy-p-benzochinon
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1961 , vol. 16, p. 810 Full Text Show Details
V. im Sekret des Totenkaefers, neben Ethylchinon
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 200 Full Text Show Details
V. in Blaps mortisaga, Blaps mucronata, Blaps requienii, Blaps lethifera, Gnaptor spinimanus Pall., Pimelia confusa u. Morisia plan. tingitan.
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 757 Full Text Show Details
Quantum Chemical Calculations (1) Calculated Properties
Method (Quantum Chemical Calculations)
Reference
Molecular orbitals
Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)
Nafikova; Asfandiarov; Kalimullina; El'Kin, Yu. N.
Russian Chemical Bulletin, 2014 , vol. 63, # 3 p. 572 - 576 Izvestiya Akademii Nauk. Seriya Khimicheskaya, 2014 , # 3 p. 572 - 576,5 Title/Abstract Full Text View citing articles Show Details
Chemical Name: 2-ethyl-1,4-benzoquinone
2
Reaxys Registry Number: 1931753
CAS Registry Number: 4754-26-1 Type of Substance: isocyclic Molecular Formula: C8H8O2
Linear Structure Formula: C6H4O2CH2CH2
Molecular Weight: 136.15
InChI Key: IGRSQEOIAAGSGS-UHFFFAOYSA-N
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-ethyl-1,4-benzoquinone, 2-ethylcyclohexa-2,5-diene-1,4-dione, 2-ethyl-p-benzoquinone, ethyl-1,4-benzoquinone, 2-ethylbenzoquinone, ethyl[1,4]benzoquinone, Aethyl-[1,4]benzochinon Identification
20 prep out of 41 reactions.
Identification Physical Data (15) Spectra (17) Bioactivity (5) Other Data (5)
47
Substance Label (5) Label
Reference
2b
Eipert, Martin; Maichle-Moessmer, Caecilia; Maier, Martin E.
Journal of Organic Chemistry, 2002 , vol. 67, # 24 p. 8692 - 8695 Title/Abstract Full Text View citing articles Show Details
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
7
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
EBQ
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
Q3
Roginsky, Vitaly; Barsukova, Tatyana
Journal of the Chemical Society. Perkin Transactions 2, 2000 , # 7 p. 1575 - 1582 Title/Abstract Full Text View citing articles Show Details
Q3
Roginsky, Vitaly A.; Pisarenko, Leonid M.; Bors, Wolf; Michel, Christa
Journal of the Chemical Society. Perkin Transactions 2, 1999 , # 4 p. 871 - 876 Title/Abstract Full Text View citing articles Show Details
Patent-Specific Data (1)
Prophetic Compound
Reference
prophetic product
Bayer Aktiengesellschaft
Patent: US4621138 A1, 1986 ; Title/Abstract Full Text Show Details
Bayer Aktiengesellschaft
Patent: US5138054 A1, 1992 ; Title/Abstract Full Text Show Details
Derivative (3) Comment (Derivative)
Reference
Ethylchinhydron: Abs.-Sp. in wss. THF
Moser; Cassidy
Journal of Organic Chemistry, 1965 , vol. 30, p. 3336,3337 Full Text Show Details
compound with phenylmethanethiol (mp: 76-78 degree , Blue Black) Further Data see Handbook
Loconti; Roth
Ann. entomol. Soc. Am., 1953 , vol. 46, p. 281,283 Full Text Show Details
compound with 2-ethyl-hydroquinone (mp: 81-82 degree , Blue Black) Further Data see Handbook
Loconti; Roth
Ann. entomol. Soc. Am., 1953 , vol. 46, p. 281,283 Full Text Show Details
Physical Data Melting Point (6) Melting Point
Solvent (Melting Point)
Reference
34 °C
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
37 - 38 °C
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
34 - 37 °C
Orlando jun. et al.
Journal of Organic Chemistry, 1968 , vol. 33, p. 2512 Full Text View citing articles Show Details
37 - 39 °C
diethyl ether
Allen Jr.; Pidacks; Weiss
Journal of the American Chemical Society, 1966 , vol. 88, # 11 p. 2536 - 2544
Title/Abstract Full Text View citing articles Show Details
37 °C
Clemmensen
Chemische Berichte, 1914 , vol. 47, p. 62 Full Text Show Details
38.2 °C
diethyl ether
Bayrac
Bulletin de la Societe Chimique de France, 1894 , vol. <3> 11, p. 1130,1133 Annales de Chimie (Cachan, France), 1897 , vol. <7> 10, p. 55,56, 68 Full Text Show Details
Crystal Property Description (3) Colour & Other Properties
Reference
yellow
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
gelbe Nadeln
Bayrac
Bulletin de la Societe Chimique de France, 1894 , vol. <3> 11, p. 1130,1133 Annales de Chimie (Cachan, France), 1897 , vol. <7> 10, p. 55,56, 68 Full Text Show Details
Electrochemical Behaviour (1) Description (Electrochemical Behaviour)
Reference
Polarography
Zuman
Collection of Czechoslovak Chemical Communications, 1962 , vol. 27, p. 2035,2048 Full Text Show Details
Electrochemical Characteristics (2) Description (Electrochemical Characteristics)
Solvent (Electrochemical Characteristics)
pH-Value (Electrochemical Characteristics)
Product XRN (Electrochemical Characteristics)
Product
redox potential
H2O
4.5
1936246
2ethylhydroquinone
redox potential
Comment (Electrochemical Characteristics) 0.44 V Product: /BRN= 1936246/. No. of transm. electrons: 2 Method: potentiometry. Description: vs. NHE
Raju, K. Vijaya; Raju, G. Bangar; Yadav, M. Rajasekhar
Indian Journal of Chemistry, Section A: Inorganic, Bioinorganic, Physical, Theoretical & Analytical Chemistry, 1993 , vol. 32, # 11 p. 1012 - 1014 Title/Abstract Full Text Show Details
des Systems Aethyl-benzochinon(1.4)/2-Aethyl-hydrochinon.
Kvalnes
Journal of the American Chemical Society, 1934 , vol. 56, p. 670 Full Text View citing articles Show Details
Further Information (3) Description (Further Information)
Reference
Further information
Meinwald et al.
Journal of the American Chemical Society, 1966 , vol. 88, p. 1590 Full Text View citing articles Show Details
Further information
Moser; Cassidy
Journal of Organic Chemistry, 1965 , vol. 30, p. 3336,3337 Full Text Show Details
Further information
Barbier
Journal of Chromatography, 1959 , vol. 2, p. 649 Full Text View citing articles Show Details
Spectra NMR Spectroscopy (6)
Reference
Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts
1H
chloroform-d1
COSY (Correlation Spectroscopy)
1H 1H
HSQC (Heteronuclear Single Quantum Coherence)
Location
Reference
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
chloroform-d1
400.1 MHz
supporting information
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
1H 13C
supporting information
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
1H
chloroform-d1
400.1 MHz
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
13C
chloroform-d1
100.6 MHz
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
NMR
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
IR Spectroscopy (2) Description (IR Spectroscopy)
Comment (IR Spectroscopy)
Reference
IR
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Bands
1667 - 833 cm**(-1)
Yates et al.
Journal of the American Chemical Society, 1956 , vol. 78, p. 650 Full Text View citing articles Show Details
Mass Spectrometry (3) Description (Mass Spectrometry)
Location
Reference
high resolution mass spectrometry (HRMS) time-of-flight mass spectra (TOFMS) gas chromatography mass spectrometry (GCMS) electron impact (EI) spectrum
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
EI (Electron impact) GCMS (Gas chromatography mass spectrometry) Spectrum
supporting information
Kamata, Keigo; Yamaura, Taiyo; Mizuno, Noritaka
Angewandte Chemie - International Edition, 2012 , vol. 51, # 29 p. 7275 - 7278 Title/Abstract Full Text View citing articles Show Details
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
UV/VIS Spectroscopy (6) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Comment (UV/VIS Spectroscopy)
UV/VIS
Reference Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Orlando jun. et al.
Journal of Organic Chemistry, 1968 , vol. 33, p. 2512
Full Text View citing articles Show Details
Spectrum
Moser; Cassidy
Journal of Organic Chemistry, 1965 , vol. 30, p. 3336,3337 Full Text Show Details
Moser; Cassidy
Journal of Organic Chemistry, 1965 , vol. 30, p. 2602,2603 Full Text Show Details
Spectrum
ethanol
220 - 320 nm
Loconti; Roth
Ann. entomol. Soc. Am., 1953 , vol. 46, p. 281,285 Full Text Show Details
Spectrum
CHCl3
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Spectrum
hexane
Alexander; Barton
Biochemical Journal, 1943 , vol. 37, p. 463 Full Text Show Details
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Spectrum
ethanol
Alexander; Barton
Biochemical Journal, 1943 , vol. 37, p. 463 Full Text Show Details
Bioactivity Pharmacological Data (3) 1 of 3
Comment (Pharmacological Data)
Bioactivities present
Reference
Allen Jr.; Pidacks; Weiss
Journal of the American Chemical Society, 1966 , vol. 88, # 11 p. 2536 - 2544 Title/Abstract Full Text View citing articles Show Details
Bayer Aktiengesellschaft
Patent: US4621138 A1, 1986 ; Title/Abstract Full Text Show Details
Schildknecht,H. et al.
Angewandte Chemie, 1963 , vol. 75, p. 762 - 771 Full Text View citing articles Show Details
Bayer Aktiengesellschaft
Patent: US5138054 A1, 1992 ; Title/Abstract Full Text Show Details
Erdtman; Stjernstroem
Acta Chemica Scandinavica (1947-1973), 1959 , vol. 13, p. 653,656 Full Text View citing articles Show Details
Clemmensen
Chemische Berichte, 1914 , vol. 47, p. 62 Full Text Show Details
Hackman; Pryor; Todd
Biochemical Journal, 1948 , vol. 43, p. 474,477 Full Text Show Details
Alexander; Barton
Biochemical Journal, 1943 , vol. 37, p. 463 Full Text Show Details
Loconti; Roth
Ann. Entomol. Soc. Am., 1953 , vol. 46, p. 281,283 Full Text Show Details
Kvalnes
Journal of the American Chemical Society, 1934 , vol. 56, p. 670 Full Text View citing articles Show Details
Trave et al.
Chimica e l'Industria (Milan, Italy), 1959 , vol. 41, p. 19,25 Full Text Show Details
Bayrac
Bulletin de la Societe Chimique de France, 1894 , vol. <3> 11, p. 1130,1133 Annales de Chimie (Cachan, France), 1897 , vol. <7> 10, p. 55,56, 68 Full Text Show Details
Ono
Helvetica Chimica Acta, 1927 , vol. 10, p. 46,47, 51 Full Text Show Details
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Loconti; Roth
Ann. entomol. Soc. Am., 1953 , vol. 46, p. 281,283 Full Text Show Details
Yates et al.
Journal of the American Chemical Society, 1956 , vol. 78, p. 650 Full Text View citing articles Show Details
Harman; Cason
Journal of Organic Chemistry, 1952 , vol. 17, p. 1058,1060 Full Text Show Details
Loconti; Roth
Ann. entomol. Soc. Am., 1953 , vol. 46, p. 281,285 Full Text Show Details
Ladisch
Patent: US2840571 , 1956 ; Full Text Show Details
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
2 of 3
3 of 3
Comment (Pharmacological Data)
Bioactivities present
Reference
Meinwald et al.
Journal of the American Chemical Society, 1966 , vol. 88, p. 1590 Full Text View citing articles Show Details
Moser; Cassidy
Journal of Organic Chemistry, 1965 , vol. 30, p. 3336,3337 Full Text Show Details
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
Moser; Cassidy
Journal of Organic Chemistry, 1965 , vol. 30, p. 2602,2603 Full Text Show Details
Zuman
Collection of Czechoslovak Chemical Communications, 1962 , vol. 27, p. 2035,2048 Full Text Show Details
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 757 Full Text Show Details
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 200 Full Text Show Details
Barbier
Journal of Chromatography, 1959 , vol. 2, p. 649 Full Text View citing articles Show Details
Orlando jun. et al.
Journal of Organic Chemistry, 1968 , vol. 33, p. 2512 Full Text View citing articles Show Details
Thompson, Malcolm J.; Zeegers, Petrus J.
Tetrahedron Letters, 1988 , vol. 29, # 20 p. 2471 - 2474 Title/Abstract Full Text View citing articles Show Details
Errazuriz, B.; Tapia, R.; Valderrama, J. A.
Tetrahedron Letters, 1985 , vol. 26, # 7 p. 819 - 822 Title/Abstract Full Text View citing articles Show Details
Raju, K. Vijaya; Raju, G. Bangar; Yadav, M. Rajasekhar
Indian Journal of Chemistry, Section A: Inorganic, Bio-inorganic, Physical, Theoretical & Analytical Chemistry, 1993 , vol. 32, # 11 p. 1012 - 1014 Title/Abstract Full Text Show Details
Lau, Tai-Chu; Mak, Chi-Keung
Journal of the Chemical Society, Chemical Communications, 1995 , # 9 p. 943 - 944 Title/Abstract Full Text View citing articles Show Details
Farina, F.; Fernandez, E.; Gimeno, V.; Valderrama, J. A.
Anales de Quimica, 1995 , vol. 91, # 3-4 p. 220 - 229 Title/Abstract Full Text Show Details
Mayalarp, Stephen P.; Hargreaves, Rob H. J.; Butler, John; Caroline O'Hare; Hartley, John A.
Journal of Medicinal Chemistry, 1996 , vol. 39, # 2 p. 531 - 537 Title/Abstract Full Text View citing articles Show Details
Roginsky, Vitaly A.; Pisarenko, Leonid M.; Bors, Wolf; Michel, Christa; Saran, Manfred
Journal of the Chemical Society - Faraday Transactions, 1998 , vol. 94, # 13 p. 1835 - 1840 Title/Abstract Full Text View citing articles Show Details
Roginsky, Vitaly A.; Pisarenko, Leonid M.; Bors, Wolf; Michel, Christa
Journal of the Chemical Society. Perkin Transactions 2, 1999 , # 4 p. 871 - 876 Title/Abstract Full Text View citing articles Show Details
Roginsky, Vitaly; Barsukova, Tatyana
Journal of the Chemical Society. Perkin Transactions 2, 2000 , # 7 p. 1575 - 1582 Title/Abstract Full Text View citing articles Show Details
Eipert, Martin; Maichle-Moessmer, Caecilia; Maier, Martin E.
Journal of Organic Chemistry, 2002 , vol. 67, # 24 p. 8692 - 8695 Title/Abstract Full Text View citing articles Show Details
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
Murahashi, Shun-Ichi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
Tetrahedron Letters, 2010 , vol. 51, # 17 p. 2339 - 2341 Title/Abstract Full Text View citing articles Show Details
Liu, Qiuyuan; Zhu, Liangfang; Li, Li; Guo, Bin; Hu, Xiaoke; Hu, Changwei
Journal of Molecular Catalysis A: Chemical, 2010 , vol. 331, # 1-2 p. 71 - 77 Title/Abstract Full Text View citing articles Show Details
Neu, Heather M.; Zhdankin, Viktor V.; Nemykin, Victor N.
Tetrahedron Letters, 2010 , vol. 51, # 50 p. 6545 - 6548 Title/Abstract Full Text View citing articles Show Details
Kamata, Keigo; Yamaura, Taiyo; Mizuno, Noritaka
Angewandte Chemie - International Edition, 2012 , vol. 51, # 29 p. 7275 - 7278 Title/Abstract Full Text View citing articles Show Details
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Nazareth, Taís M.; Sudatti, Daniela B.; Machado, Glauco
Journal of Chemical Ecology, 2016 , vol. 42, # 10 p. 1047 - 1051 Title/Abstract Full Text Show Details
Ecotoxicology (2) 1 of 2
2 of 2
Effect (Ecotoxicology)
pheromone activity
Species or Test-System (Ecotoxicology)
Tribolium confusum (du Val), flour beetle
Sex
male and female
Concentration (Ecotoxicology)
1E-1 - 1E4 ng
Kind of Dosing (Ecotoxicology)
title comp. dissolved in methanol
Method (Ecotoxicology)
species transferred in vials and placed in the center of olfactometer; then allowed to respond to title comp. released from glass capillary for 5 min; 22.5 deg C, 60percent relative humidity; species collec. upwind from release point counted as responding
Further Details (Ecotoxicology)
control: methanol; active control: 1 μg of title comp.
Results
there was an interaction between dose and sex with title comp.; female and male attraction were found to be dose-depend.; fig.
Reference
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
electrophysiology; effect on
Species or Test-System (Ecotoxicology)
antenna of Tribolium confusum (du Val), flour beetle
Sex
male and female
Concentration (Ecotoxicology)
1 - 1E5 ng
Kind of Dosing (Ecotoxicology)
title comp. impregnated in a piece of 0.5-cm2 filter paper
Method (Ecotoxicology)
insect antenna mounted between 2 glass electrodes; exposed to title comp. puff by means of a stimulus controller; EAG responses recorded
Further Details (Ecotoxicology)
control: n-hexane; active control: 10 μg of title comp.; EAG: electroantennography
Results
title comp. elicited higher EAG response than the control; males were more sensitive than females; fig.
Reference
Verheggen; Ryne; Olsson; Arnaud; Lognay; Hoegberg; Persson; Haubruge; Loefstedt
Journal of Chemical Ecology, 2007 , vol. 33, # 3 p. 525 - 539 Title/Abstract Full Text View citing articles Show Details
Other Data Isolation from Natural Product (5) Isolation from Natural Product
Reference
Chavesincola inexpectabilis; Magnispina neptunus
Rocha, Daniele F.O.; Wouters, Felipe C.; Zampieri, Davila S.; Brocksom, Timothy J.; Machado, Glauco; Marsaioli, Anita J.
Molecules, 2013 , vol. 18, # 9 p. 11429 - 11451 Title/Abstract Full Text View citing articles Show Details
Tenebrioniden
Schildknecht,H. et al.
Angewandte Chemie, 1963 , vol. 75, p. 762 - 771
Full Text View citing articles Show Details
V. im Sekret des Totenkaefers, neben Toluchinon
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 200 Full Text Show Details
V. in Blaps mortisaga, Blaps mucronata, Blaps requienii, Blaps lethifera u. Gnaptor spinimanus Pall.
Schildknecht; Weis
Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,, 1960 , vol. 15, p. 757 Full Text Show Details
Vorkommen in Tribolium castaneum und Tribolium confusum
Hackman; Pryor; Todd
Biochemical Journal, 1948 , vol. 43, p. 474,477 Full Text Show Details
Alexander; Barton
Biochemical Journal, 1943 , vol. 37, p. 463 Full Text Show Details
Loconti; Roth
Ann. entomol. Soc. Am., 1953 , vol. 46, p. 281,283 Full Text Show Details
Chemical Name: 2-isopropyl-1,4-benzoquinone
3
Reaxys Registry Number: 1934578
CAS Registry Number: 15232-10-7 Type of Substance: isocyclic Molecular Formula: C9H10O2
Linear Structure Formula: C9H10O2
Molecular Weight: 150.177
InChI Key: XLTSBDOZTUSCMX-UHFFFAOYSA-N
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-isopropyl-1,4-benzoquinone, 2-Isopropyl-1,4-benzoquinone, 2-i-propyl-1,4-benzoquinone, 2-isopropyl-p-benzoquinone, 2-isopropyl-1,4-quinone, isopropyl-[1,4]benzoquinone, Isopropyl-[1,4]benzochinon Identification Substance Label (10) Label
Reference
5
Miller, Natalie A.; Willis, Anthony C.; Sherburn, Michael S.
Chemical Communications, 2008 , # 10 p. 1226 - 1228 Title/Abstract Full Text View citing articles Show Details
e
Maurya, Mannar R.; Kumar, Umesh; Manikandan
European Journal of Inorganic Chemistry, 2007 , # 16 p. 2303 - 2314 Title/Abstract Full Text View citing articles Show Details
16
Jankowski; Savoie; Lesage; Boivin; Leclair; Diaz T; Reyes-Chilpa; Jimenez-Estrada; Barrios
Polish Journal of Chemistry, 2005 , vol. 79, # 2 p. 429 - 440 Title/Abstract Full Text View citing articles Show Details
7cA
Yamago, Shigeru; Hashidume, Masahiro; Yoshida, Jun-Ichi
Tetrahedron, 2002 , vol. 58, # 34 p. 6805 - 6813 Title/Abstract Full Text View citing articles Show Details
2
Parsons; Gold; Semple; Montagnon
Synlett, 2000 , # 8 p. 1184 - 1186 Title/Abstract Full Text View citing articles Show Details
3cA
Yamago, Shigeru; Hashidume, Masahiro; Yoshida, Jun-Ichi
Chemistry Letters, 2000 , # 11 p. 1234 - 1235 Title/Abstract Full Text View citing articles Show Details
7
Jacobsen
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1979 , p. 569 Full Text Show Details
27 prep out of 33 reactions.
Identification Physical Data (7) Spectra (15)
25
Mayelvaganan; Hadimani, Shreeshailkumar B.; Bhat, Sujata V.
Tetrahedron, 1997 , vol. 53, # 6 p. 2185 - 2188 Title/Abstract Full Text View citing articles Show Details
3b
Murahashi, Shun-Ichi; Naota, Takeshi; Miyaguchi, Noriko; Noda, Shinji
Journal of the American Chemical Society, 1996 , vol. 118, # 10 p. 2509 - 2510 Title/Abstract Full Text View citing articles Show Details
III
Citterio, Attilio; Vismara, Elena; Bernardi, Rosanna
Journal of Chemical Research, Miniprint, 1983 , # 4 p. 876 - 890 Title/Abstract Full Text Show Details
20
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
Patent-Specific Data (1)
Prophetic Compound
Reference
prophetic product
Bayer Aktiengesellschaft
Patent: US4621138 A1, 1986 ; Title/Abstract Full Text Show Details
Bayer Aktiengesellschaft
Patent: US5138054 A1, 1992 ; Title/Abstract Full Text Show Details
Physical Data Melting Point (6) Melting Point
Solvent (Melting Point)
Reference
35 - 36 °C
Citterio, Attilio; Vismara, Elena; Bernardi, Rosanna
Journal of Chemical Research, Miniprint, 1983 , # 4 p. 876 - 890 Title/Abstract Full Text Show Details
35.5 - 36.5 °C
Jacobsen
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1979 , p. 569 Full Text Show Details
33 - 36 °C
methanol H2O
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
34 - 36 °C
ethanol
Bogoljubskii
J. Gen. Chem. USSR (Engl. Transl.), 1962 , vol. 32, p. 869,862 Chem.Abstr., 1963 , vol. 58, # 2391 Full Text Show Details
34 - 36 °C
Zenker; Jorgensen
Journal of Organic Chemistry, 1959 , vol. 24, p. 1351 Full Text View citing articles Show Details
28.4 °C
Bayrac
Bulletin de la Societe Chimique de France, 1895 , vol. <3> 13, p. 979 Annales de Chimie (Cachan, France), 1897 , vol. <7> 10, p. 66,73 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelbe Prismen
Bayrac
Bulletin de la Societe Chimique de France, 1895 , vol. <3> 13, p. 979 Annales de Chimie (Cachan, France), 1897 , vol. <7> 10, p. 66,73 Full Text Show Details
Spectra NMR Spectroscopy (10)
Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Coupling Nuclei
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts
1H
chloroform-d1
270 MHz
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
chloroform-d1
68 MHz
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
200 MHz
Jankowski; Savoie; Lesage; Boivin; Leclair; Diaz T; Reyes-Chilpa; Jimenez-Estrada; Barrios
Polish Journal of Chemistry, 2005 , vol. 79, # 2 p. 429 - 440 Title/Abstract Full Text View citing articles Show Details
1H
1H
CDCl3
200 MHz
Jankowski; Savoie; Lesage; Boivin; Leclair; Diaz T; Reyes-Chilpa; Jimenez-Estrada; Barrios
Polish Journal of Chemistry, 2005 , vol. 79, # 2 p. 429 - 440 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
50 MHz
Jankowski; Savoie; Lesage; Boivin; Leclair; Diaz T; Reyes-Chilpa; Jimenez-Estrada; Barrios
Polish Journal of Chemistry, 2005 , vol. 79, # 2 p. 429 - 440 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
300 MHz
Yamago, Shigeru; Hashidume, Masahiro; Yoshida, Jun-Ichi
Tetrahedron, 2002 , vol. 58, # 34 p. 6805 - 6813 Title/Abstract Full Text View citing articles Show Details
1H
1H
CDCl3
300 MHz
Yamago, Shigeru; Hashidume, Masahiro; Yoshida, Jun-Ichi
Tetrahedron, 2002 , vol. 58, # 34 p. 6805 - 6813 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
Spectrum
Johnson; Tully
Journal of Chemical Physics, 1964 , vol. 40, p. 1744 Full Text Show Details
NMR
Johnson; Tully
Journal of Chemical Physics, 1964 , vol. 40, p. 1744 Full Text Show Details
Reference
IR Spectroscopy (2) Description (IR Spectroscopy)
Comment (IR Spectroscopy)
Reference
Bands
neat (no solvent)
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
Bands
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
Mass Spectrometry (2) Description (Mass Spectrometry)
Location
Reference
EI (Electron impact) GCMS (Gas chromatography mass spectrometry) Spectrum
supporting information
Kamata, Keigo; Yamaura, Taiyo; Mizuno, Noritaka
Angewandte Chemie - International Edition, 2012 , vol. 51, # 29 p. 7275 - 7278 Title/Abstract Full Text View citing articles Show Details
HRMS (High resolution mass spectrometry) EI (Electron impact) Spectrum
Murahashi, Shun-Ichi; Miyaguchi, Noriko; Noda, Shinji; Naota, Takeshi; Fujii, Akiko; Inubushi, Yasutaka; Komiya, Naruyoshi
European Journal of Organic Chemistry, 2011 , # 27 p. 5355 - 5365 Title/Abstract Full Text View citing articles Show Details
ESR Spectroscopy (1) Description (ESR Spectroscopy)
Reference
Pedersen
Molecular Physics, 1974 , vol. 28, p. 1031,1033 Full Text Show Details
ESR
Chemical Name: 2-n-propyl-1,4-benzoquinone
4
8 prep out of 17 reactions.
Reaxys Registry Number: 3237805
CAS Registry Number: 55811-48-8 Type of Substance: isocyclic Molecular Formula: C9H10O2
Linear Structure Formula: C9H10O2
Molecular Weight: 150.177
InChI Key: NBHAZVWKRHTWRW-UHFFFAOYSA-N
Identification Physical Data (1) Spectra (2)
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-n-propyl-1,4-benzoquinone, propyl-p-benzoquinone, 2-propylcyclohexa-2,5-diene-1,4-dione, 2-propyl-p-benzoquinone, propyl-1,4-benzoquinone, propyl-[1,4]benzoquinone, Propyl-[1,4]benzochinon Identification Substance Label (2) Label
Reference
28
Wang, Dawei; Ge, Bingyang; Ju, Anqi; Zhou, Yucheng; Xu, Chongying; Ding, Yuqiang
Journal of Organometallic Chemistry, 2015 , vol. 780, p. 30 - 33 Title/Abstract Full Text View citing articles Show Details
2c
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Patent-Specific Data (1)
Prophetic Compound
Reference
prophetic product
Bayer Aktiengesellschaft
Patent: US4621138 A1, 1986 ; Title/Abstract Full Text Show Details
Bayer Aktiengesellschaft
Patent: US5138054 A1, 1992 ; Title/Abstract Full Text Show Details
Physical Data Boiling Point (1) Boiling Point
Pressure (Boiling Point)
Comment (Boiling Point)
Reference
98 °C
19 Torr
gelbes Oel.
Hiraiwa
Yakugaku Zasshi, 1940 , vol. 60, p. 569,574 Full Text Show Details
Spectra NMR Spectroscopy (2) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts Spectrum
1H
chloroform-d1
400 MHz
Location
Reference
supporting information
Wang, Dawei; Ge, Bingyang; Ju, Anqi; Zhou, Yucheng; Xu, Chongying; Ding, Yuqiang
Journal of Organometallic Chemistry, 2015 , vol. 780, p. 30 - 33
9
Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
supporting information
Chemical Name: 2-tert-butyl-1,4-benzoquinone
5
Reaxys Registry Number: 1860944
CAS Registry Number: 3602-55-9 Type of Substance: isocyclic Molecular Formula: C10H12O2
Linear Structure Formula: (CH3)3CC6H3O2
Molecular Weight: 164.204
InChI Key: NCCTVAJNFXYWTM-UHFFFAOYSA-N
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
26 prep out of 119 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-tert-butyl-1,4-benzoquinone, 2-tert-Butyl-1,4-benzoquinone, tert-butyl-1,4-benzoquinone Identification Substance Label (27) Label
Reference
2c
Yang, Wei; Wang, Jingyi; Wei, Zhonglin; Zhang, Qian; Xu, Xianxiu
Journal of Organic Chemistry, 2016 , vol. 81, # 4 p. 1675 - 1680 Title/Abstract Full Text View citing articles Show Details
Gelis, Coralie; Bekkaye, Mathieu; Lebée, Clément; Blanchard, Florent; Masson, Géraldine
Organic Letters, 2016 , vol. 18, # 14 p. 3422 - 3425 Title/Abstract Full Text View citing articles Show Details
1e
Jardim, Guilherme A. M.; Bower, John F.; Da Silva Júnior, Eufrânio N.
Organic Letters, 2016 , vol. 18, # 18 p. 4454 - 4457 Title/Abstract Full Text Show Details
2F
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
2
Vilipi, Jovana; Novakovi, Irena; Stanojkovi, Tatjana; Mati, Ivana; egan, Dejan; Kljaji, Zoran; Sladi, Duan
Bioorganic and Medicinal Chemistry, 2015 , vol. 23, # 21 p. 6930 - 6942 Title/Abstract Full Text View citing articles Show Details
TQ
Li, Jun; Bi, Yanlan; Liu, Wei; Sun, Shangde
Journal of Agricultural and Food Chemistry, 2015 , vol. 63, # 38 p. 8584 - 8591 Title/Abstract Full Text View citing articles Show Details
9
Michman, Michael; Oron, Miriam; Schaefer, Hans J.
Collection of Czechoslovak Chemical Communications, 2000 , vol. 65, # 6 p. 924 - 940 Title/Abstract Full Text View citing articles Show Details
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valrie; Li, Haiyan; Shah, Nimesh; Kumar, Rahul; John, Jubi; Namboothiri, Irishi N.N.; Doris, Eric
Tetrahedron, 2014 , vol. 70, # 36 p. 6140 - 6145 Title/Abstract Full Text View citing articles Show Details
2f
Zhang, Hai-Bo; Liu, Li; Chen, Yong-Jun; Wang, Dong; Li, Chao-Jun
Advanced Synthesis and Catalysis, 2006 , vol. 348, # 1-2 p. 229 - 235 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
2b
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valerie; Li, Haiyan; Shah, Nimesh; Namboothiri, Irishi N. N.; Doris, Eric
ChemCatChem, 2014 , vol. 6, # 3 p. 719 - 723
Identification Physical Data (30) Spectra (48) Bioactivity (40) Other Data (34)
172
Title/Abstract Full Text View citing articles Show Details
2-tBuBQ
Tomita, Ren; Mantani, Kohei; Hamasaki, Akiyuki; Ishida, Tamao; Tokunaga, Makoto
Chemistry - A European Journal, 2014 , vol. 20, # 32 p. 9914 - 9917 Title/Abstract Full Text View citing articles Show Details
1c
Nunes, Ruth Leandro; Bieber, Lothar Wilhelm
Tetrahedron Letters, 2001 , vol. 42, # 2 p. 219 - 221 Title/Abstract Full Text View citing articles Show Details
Zhang, Shuai; Song, Feijie; Zhao, Dongbing; You, Jingsong
Chemical Communications, 2013 , vol. 49, # 40 p. 4558 - 4560 Title/Abstract Full Text View citing articles Show Details
3c
Meazza, Giovanni; Dayan, Franck E.; Wedge, David E.
Journal of Agricultural and Food Chemistry, 2003 , vol. 51, # 13 p. 3824 - 3828 Title/Abstract Full Text View citing articles Show Details
Reddy, B.V.Subba; Reddy, P. Sivaramakrishna; Reddy, Y. Jayasudhan; Bhaskar; Reddy, B. Chandra Obula
Bulletin of the Korean Chemical Society, 2013 , vol. 34, # 10 p. 2968 - 2972 Title/Abstract Full Text View citing articles Show Details
TBQ
Peters, Melanie M. C. G.; Lau, Serrine S.; Dulik, Deanne; Murphy, Darlene; Van Ommen, Ben; Van Bladeren, Peter J.; Monks, Terrence J.
Chemical Research in Toxicology, 1996 , vol. 9, # 1 p. 133 - 139 Title/Abstract Full Text View citing articles Show Details
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Li, Yunbo; Seacat, Andrew; Kuppusamy, Periannan; Zweier, Jay L; Yager, James D; Trush, Michael A
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2002 , vol. 518, # 2 p. 123 - 133 Title/Abstract Full Text View citing articles Show Details
Endo, Satoshi; Arai, Yuki; Hara, Akira; Kitade, Yukio; Bunai, Yasuo; El-Kabbani, Ossama; Matsunaga, Toshiyuki
Biological and Pharmaceutical Bulletin, 2013 , vol. 36, # 9 p. 1514 - 1518 Title/Abstract Full Text View citing articles Show Details
q2d
Hall, Gabriel B.; Chen, Jinzhu; Mebi, Charles A.; Okumura, Noriko; Swenson, Matthew T.; Ossowski, Stephanie E.; Zakai, Uzma I.; Nichol, Gary S.; Lichtenberger, Dennis L.; Evans, Dennis H.; Glass, Richard S.
Organometallics, 2013 , vol. 32, # 21 p. 6605 - 6612 Title/Abstract Full Text View citing articles Show Details
TBBQ
SYNTOPIX LIMITED
Patent: WO2008/35078 A1, 2008 ; Title/Abstract Full Text Show Details
Watanabe, Hiroto; Hiraoka, Ryota; Senna, Mamoru
Tetrahedron Letters, 2006 , vol. 47, # 26 p. 4481 - 4484 Title/Abstract Full Text View citing articles Show Details
4d
Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
Chemistry Letters, 2008 , vol. 37, # 3 p. 360 - 361 Title/Abstract Full Text View citing articles Show Details
Table 1, entry 3, prod.
Bar-Nahum, Itsik; York, John T.; Young Jr., Victor G.; Tolman, William B.
Angewandte Chemie - International Edition, 2008 , vol. 47, # 3 p. 533 - 536 Title/Abstract Full Text View citing articles Show Details
3e
Yakura, Takayuki; Konishi, Tatsuya
Synlett, 2007 , # 5 p. 765 - 768 Title/Abstract Full Text View citing articles Show Details
prod., Tab. 1, entry 10
Shang, Yongjia; But, Tracy Yuen Sze; Togo, Hideo; Toy, Patrick H.
Synlett, 2007 , # 1 p. 67 - 70 Title/Abstract Full Text View citing articles Show Details
4c
Maeda, Chihiro; Shinokubo, Hiroshi; Osuka, Atsuhiro
Organic and Biomolecular Chemistry, 2006 , vol. 4, # 2 p. 200 - 202 Title/Abstract Full Text View citing articles Show Details
Tab. 2, entry 19, prod.
Tajbakhsh, Mahmood; Lakouraj, Moslem Mansour; Ramzanian-Lehmali, Farhad
Synlett, 2006 , # 11 p. 1724 - 1728 Title/Abstract Full Text View citing articles Show Details
Hide facts Label
Reference
2d
Iwasa, Seiji; Fakhruddin, Ahmad; Widagdo, Herman Setyo; Nishiyama, Hisao
Advanced Synthesis and Catalysis, 2005 , vol. 347, # 4 p. 517 - 520 Title/Abstract Full Text View citing articles Show Details
6E
Yamago, Shigeru; Hashidume, Masahiro; Yoshida, Jun-Ichi
Tetrahedron, 2002 , vol. 58, # 34 p. 6805 - 6813 Title/Abstract Full Text View citing articles Show Details
3
Dayan, Franck E.
Journal of Chemical Research - Part S, 2002 , # 10 p. 518 - 519 Title/Abstract Full Text View citing articles Show Details
2E
Yamago, Shigeru; Hashidume, Masahiro; Yoshida, Jun-Ichi
Chemistry Letters, 2000 , # 11 p. 1234 - 1235 Title/Abstract Full Text View citing articles Show Details
2,R1=t-Bu,R2=R3=R4=H
Eguchi, Tadashi; Kanai, Shinobu; Kakinuma, Katsumi; Okazaki, Tadayasu; Mizoue, Kazutoshi
Chemical and Pharmaceutical Bulletin, 2000 , vol. 48, # 10 p. 1470 - 1473 Title/Abstract Full Text View citing articles Show Details
Q4
Roginsky, Vitaly; Barsukova, Tatyana
Journal of the Chemical Society. Perkin Transactions 2, 2000 , # 7 p. 1575 - 1582 Title/Abstract Full Text View citing articles Show Details
Q4
Roginsky, Vitaly A.; Pisarenko, Leonid M.; Bors, Wolf; Michel, Christa
Journal of the Chemical Society. Perkin Transactions 2, 1999 , # 4 p. 871 - 876 Title/Abstract Full Text View citing articles Show Details
Patent-Specific Data (3)
Prophetic Compound
Location in Patent
Reference
prophetic product
Pasquier, Cecile; Duc-Reichlin, Nadia; Braun, Hans-Jurgen
Patent: US2007/73 A1, 2007 ; Title/Abstract Full Text Show Details
Rockhurst University
Patent: US5780515 A1, 1998 ;
Claim
Title/Abstract Full Text Show Details
BetzDearborn Inc.
Patent: US5648573 A1, 1997 ; Title/Abstract Full Text Show Details
prophetic product
Canadian Patents and Development Limited
Patent: US4158822 A1, 1979 ;
Claim
Title/Abstract Full Text Show Details
Purification (1) Reference McKillop; Young
Synthetic Communications, 1977 , vol. 7, p. 467,470 Full Text Show Details
Physical Data Melting Point (15) Melting Point
Solvent (Melting Point)
Comment (Melting Point)
56 - 58 °C
Dohi, Toshifumi; Nakae, Tomofumi; Takenaga, Naoko; Uchiyama, Teruyoshi; Fukushima, Kei-Ichiro; Fujioka, Hiromichi; Kita, Yasuyuki
Synthesis, 2012 , vol. 44, # 8 p. 1183 - 1189 Title/Abstract Full Text View citing articles Show Details
59 °C
Bruce; Chaudhry
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 372,379 Full Text Show Details
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Blatchly et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 2286,2290 Full Text Show Details
Reference
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
48 - 51 °C
Costantini; D'Ischia; Prota
Synthesis, 1994 , # 12 p. 1399 - 1400 Title/Abstract Full Text View citing articles Show Details
56 - 57 °C
McKillop; Ray
Synthesis, 1977 , p. 847 Full Text Show Details
56 - 58 °C
Cuntze,U.; Musso,H.
Chemische Berichte, 1970 , vol. 103, p. 62 - 70 Full Text View citing articles Show Details
Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
57 - 58 °C
methanol H2O
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
53 °C
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
57 - 58 °C
McKillop,A. et al.
Tetrahedron, 1970 , vol. 26, p. 4031 - 4039 Full Text View citing articles Show Details
59 °C
with Sublimation
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
55 - 57 °C
Orlando et al.
Journal of the American Chemical Society, 1967 , vol. 89, p. 6527,6531 Full Text Show Details
49 - 50 °C
Petranek et al.
Collection of Czechoslovak Chemical Communications, 1967 , vol. 32, p. 2140 Full Text Show Details
59 - 60 °C
ethanol
Karpov; Chidekel'
Zhurnal Organicheskoi Khimii, 1967 , vol. 3, p. 1669,1625 Full Text Show Details
49 - 50 °C
petroleum ether
Norris; Sternhell
Australian Journal of Chemistry, 1966 , vol. 19, p. 617,625 Full Text Show Details
58.5 - 59 °C
hexane
Horswill,E.C.; Ingold,K.U.
Canadian Journal of Chemistry, 1966 , vol. 44, p. 269 - 277 Full Text View citing articles Show Details
58 - 59 °C
Hewgill et al.
Journal of the Chemical Society, 1965 , p. 2904,2910 Full Text Show Details
Association (MCS) (1) Description (Association (MCS))
Partner (Association (MCS))
Solvent (Association (MCS))
Reference
UV/VIS spectrum of the complex
cresol
neat (no solvent)
Watanabe, Hiroto; Hiraoka, Ryota; Senna, Mamoru
Tetrahedron Letters, 2006 , vol. 47, # 26 p. 4481 - 4484 Title/Abstract Full Text View citing articles Show Details
Chromatographic Data (1) Chromatographic data
Original string
Reference
TLC (Thin layer chromatography)
Rf=0.47 (n-hexane/EtOAc=10:1)
Abu-Elfotoh, Abdel-Moneim; Tsuzuki, Kazuyuki; Nguyen, Tram Bao; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Tetrahedron, 2013 , vol. 69, # 40 p. 8612 - 8617 Title/Abstract Full Text View citing articles Show Details
Crystal Property Description (7) Colour & Other Properties
Location
Reference
yellow-orange
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
green
Abu-Elfotoh, Abdel-Moneim; Tsuzuki, Kazuyuki; Nguyen, Tram Bao; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Tetrahedron, 2013 , vol. 69, # 40 p. 8612 - 8617 Title/Abstract Full Text View citing articles Show Details
yellow
Albrecht, Marcel; Schneider, Oliver; Schmidt, Andreas
Organic and Biomolecular Chemistry, 2009 , vol. 7, # 7 p. 1445 - 1453 Title/Abstract Full Text View citing articles Show Details
Dohi, Toshifumi; Nakae, Tomofumi; Takenaga, Naoko; Uchiyama, Teruyoshi; Fukushima, Kei-Ichiro; Fujioka, Hiromichi; Kita, Yasuyuki
Synthesis, 2012 , vol. 44, # 8 p. 1183 - 1189 Title/Abstract Full Text View citing articles Show Details
brown
Uyanik, Muhammet; Mutsuga, Tatsuya; Ishihara, Kazuaki
Molecules, 2012 , vol. 17, # 7 p. 8604 - 8616 Title/Abstract Full Text View citing articles Show Details
orange
Yakura, Takayuki; Tian, Yuan; Yamauchi, Yu; Omoto, Masanori; Konishi, Tatsuya
Chemical and Pharmaceutical Bulletin, 2009 , vol. 57, # 3 p. 252 - 256 Title/Abstract Full Text View citing articles Show Details
Yakura, Takayuki; Omoto, Masanori; Yamauchi; Tian, Yuan; Ozono, Ayaka
Tetrahedron, 2010 , vol. 66, # 31 p. 5833 - 5840 Title/Abstract Full Text View citing articles Show Details
Yakura, Takayuki; Ozono, Ayaka; Morimoto, Kohei
Chemical and Pharmaceutical Bulletin, 2011 , vol. 59, # 1 p. 132 - 134 Title/Abstract Full Text View citing articles Show Details
yellow
supporting information
Hu, Peng; Huang, Shijun; Xu, Jing; Shi, Zhang-Jie; Su, Weiping
Angewandte Chemie - International Edition, 2011 , vol. 50, # 42 p. 9926 - 9930 Title/Abstract Full Text View citing articles Show Details
gelb
Universal Oil Prod. Co.
Patent: US2573136 , 1949 ; Full Text Show Details
Electrochemical Behaviour (1) Description (Electrochemical Behaviour)
Reference
Polarography
Ryba et al.
Collection of Czechoslovak Chemical Communications, 1968 , vol. 33, p. 26 Full Text Show Details
Electrochemical Characteristics (3) Description (Electrochemical Characteristics)
Solvent (Electrochemical Characteristics)
Temperature (Electrochemical Characteristics)
Product XRN (Electrochemical Characteristics)
Product
cyclovoltammetry
dimethyl sulfoxide
25 °C
transmitted electrons -1; Standard potential; -0.933 V; Other electrode; potential diagram; 0.1 M tetraethylammonium perchlorate
Vilipi, Jovana; Novakovi, Irena; Stanojkovi, Tatjana; Mati, Ivana; egan, Dejan; Kljaji, Zoran; Sladi, Duan
Bioorganic and Medicinal Chemistry, 2015 , vol. 23, # 21 p. 6930 6942 Title/Abstract Full Text View citing articles Show Details
cyclovoltammetry
dichloromethane
1878687
2-tertbutylsemiquinone radical anion
transmitted electrons -1; Standard potential; -1.083 V; Ferrocene/ferrocenium; 0.10 M tetrabutylammonium hexafluorophosphate
Hall, Gabriel B.; Chen, Jinzhu; Mebi, Charles A.; Okumura, Noriko; Swenson, Matthew T.; Ossowski, Stephanie E.; Zakai, Uzma I.; Nichol, Gary S.; Lichtenberger, Dennis L.; Evans, Dennis H.; Glass, Richard S.
Organometallics, 2013 , vol. 32, # 21 p. 6605 - 6612 Title/Abstract Full Text View citing articles Show Details
polarographic halfwave potential
Ryba et al.
Collection of Czechoslovak Chemical Communications, 1968 , vol. 33, p. 26 Full Text Show Details
Further Information (1)
Comment (Electrochemical Characteristics)
Reference
Description (Further Information)
Reference
Further information
McKillop et al.
Angewandte Chemie, 1970 , vol. 82, p. 84 Full Text Show Details
Partition octan-1-ol/water (MCS) (1) log POW
Temperature (Partition octan-1-ol/water (MCS))
Reference
1.65
25 °C
Dayan, Franck E.
Journal of Chemical Research - Part S, 2002 , # 10 p. 518 - 519 Title/Abstract Full Text View citing articles Show Details
Spectra NMR Spectroscopy (27) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Temperature (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts Spectrum
1H
chloroform-d1
Chemical shifts Spectrum
13C
chloroform-d1
Chemical shifts
1H
Chemical shifts
Original Text (NMR Spectroscopy)
Signals
Kind of signal
400 MHz
100 MHz
chloroform-d1
300 MHz
13C
chloroform-d1
Chemical shifts
1H
chloroform-d1
Chemical shifts
13C
Chemical shifts
Location
Reference
supporting information
Yasukawa, Tomohiro; Miyamura, Hiroyuki; Kobayashi, Shu
Chemistry Letters, 2015 , vol. 44, # 1 p. 50 - 52 Title/Abstract Full Text View citing articles Show Details
supporting information
Yasukawa, Tomohiro; Miyamura, Hiroyuki; Kobayashi, Shu
Chemistry Letters, 2015 , vol. 44, # 1 p. 50 - 52 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
75 MHz
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valerie; Li, Haiyan; Shah, Nimesh; Namboothiri, Irishi N. N.; Doris, Eric
ChemCatChem, 2014 , vol. 6, # 3 p. 719 - 723 Title/Abstract Full Text View citing articles Show Details
chloroform-d1
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valerie; Li, Haiyan; Shah, Nimesh; Namboothiri, Irishi N. N.; Doris, Eric
ChemCatChem, 2014 , vol. 6, # 3 p. 719 - 723 Title/Abstract Full Text View citing articles Show Details
1H
chloroform-d1
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
1H
NMR (400 MHz, CDCl3): δ
1.28 ppm 6.59 ppm 6.67 ppm
s, 9H s, 1H m, 2H
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valrie; Li, Haiyan; Shah, Nimesh; Kumar, Rahul; John, Jubi; Namboothiri, Irishi N.N.; Doris, Eric
Tetrahedron, 2014 , vol. 70, # 36 p. 6140 - 6145 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
chloroform-d1
NMR (300 MHz, CDCl3) δ
1.29 ppm
s, 9H
supporting
Abu-Elfotoh, Abdel-Moneim; Tsuzuki,
1.28 (s, 9H), 6.59 (s, 1H), 6.67 (m, 2H) ppm
300 MHz
1H
6.59 ppm 6.68 ppm
s, 1H d, J=1.0 Hz, 2H
information
Kazuyuki; Nguyen, Tram Bao; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Tetrahedron, 2013 , vol. 69, # 40 p. 8612 - 8617 Title/Abstract Full Text View citing articles Show Details
29.3 ppm 35.5 ppm 131.7 ppm 135.1 ppm 138.9 ppm 156.3 ppm 187.7 ppm 188.6 ppm
supporting information
Abu-Elfotoh, Abdel-Moneim; Tsuzuki, Kazuyuki; Nguyen, Tram Bao; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Tetrahedron, 2013 , vol. 69, # 40 p. 8612 - 8617 Title/Abstract Full Text View citing articles Show Details
Dohi, Toshifumi; Nakae, Tomofumi; Takenaga, Naoko; Uchiyama, Teruyoshi; Fukushima, Kei-Ichiro; Fujioka, Hiromichi; Kita, Yasuyuki
Synthesis, 2012 , vol. 44, # 8 p. 1183 - 1189 Title/Abstract Full Text View citing articles Show Details
100 MHz
Dohi, Toshifumi; Nakae, Tomofumi; Takenaga, Naoko; Uchiyama, Teruyoshi; Fukushima, Kei-Ichiro; Fujioka, Hiromichi; Kita, Yasuyuki
Synthesis, 2012 , vol. 44, # 8 p. 1183 - 1189 Title/Abstract Full Text View citing articles Show Details
400 MHz
Uyanik, Muhammet; Mutsuga, Tatsuya; Ishihara, Kazuaki
Molecules, 2012 , vol. 17, # 7 p. 8604 - 8616 Title/Abstract Full Text View citing articles Show Details
chloroform-d1
100 MHz
Uyanik, Muhammet; Mutsuga, Tatsuya; Ishihara, Kazuaki
Molecules, 2012 , vol. 17, # 7 p. 8604 - 8616 Title/Abstract Full Text View citing articles Show Details
1H
chloroform-d1
600 MHz
supporting information
Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
Angewandte Chemie - International Edition, 2008 , vol. 47, # 42 p. 8093 - 8095 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
chloroform-d1
150 MHz
supporting information
Miyamura, Hiroyuki; Shiramizu, Mika; Matsubara, Ryosuke; Kobayashi, Shu
Angewandte Chemie - International Edition, 2008 , vol. 47, # 42 p. 8093 - 8095 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
75 MHz
Iwasa, Seiji; Fakhruddin, Ahmad; Widagdo, Herman Setyo; Nishiyama, Hisao
Advanced Synthesis and Catalysis, 2005 , vol. 347, # 4 p. 517 - 520 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
300 MHz
Iwasa, Seiji; Fakhruddin, Ahmad; Widagdo, Herman Setyo; Nishiyama, Hisao
Advanced Synthesis and Catalysis, 2005 , vol. 347, # 4 p. 517 - 520 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles
Spectrum
Chemical shifts Spectrum
13C
chloroform-d1
Chemical shifts
1H
chloroform-d1
25 °C
400 MHz
Chemical shifts
13C
chloroform-d1
25 °C
Chemical shifts
1H
chloroform-d1
Chemical shifts
13C
Chemical shifts
100 MHz
1.29 (s, 9H), 6.59 (s, 1H), 6.68 (d, J=1.0 Hz, 2H)
13C
NMR (100 MHz, CDCl3) δ
29.3, 35.5, 131.7, 135.1, 138.9, 156.3, 187.7, 188.6
Show Details
Chemical shifts
1H
CDCl3
200 MHz
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
50 MHz
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Hide facts Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Temperature (NMR Spectroscopy)
Comment (NMR Spectroscopy)
Chemical shifts
1H
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
Michman, Michael; Oron, Miriam; Schaefer, Hans J.
Collection of Czechoslovak Chemical Communications, 2000 , vol. 65, # 6 p. 924 940 Title/Abstract Full Text View citing articles Show Details
Spectrum
17O
acetonitrile
75 °C
Boykin, D. W.; Baumstark, A. L.; Mehdizadeh, A.; Venkatramanan, M. K.
Magnetic Resonance in Chemistry, 1990 , vol. 28, p. 305 - 310 Title/Abstract Full Text Show Details
Chemical shifts
1H
CDCl3
Barton, Derek H. R.; Sas, Woijciech
Tetrahedron, 1990 , vol. 46, # 10 p. 3419 - 3430 Title/Abstract Full Text View citing articles Show Details
Natake, Masato; Kawamura, Kazuhiko; Danno, Gen-ichi; Kanazawa, Kazuki
Agricultural and Biological Chemistry, 1982 , vol. 46, # 4 p. 1083 - 1084 Title/Abstract Full Text Show Details
Chemical shifts
17O
acetonitrile
75 °C
Boykin, D. W.; Baumstark, A. L.; Mehdizadeh, A.; Venkatramanan, M. K.
Magnetic Resonance in Chemistry, 1990 , vol. 28, p. 305 - 310 Title/Abstract Full Text Show Details
Chemical shifts
1H
CD3CN
Fischer, Alfred; Henderson, George N.
Synthesis, 1985 , # 6/7 p. 641 - 643 Title/Abstract Full Text Show Details
Spin-spin coupling constants
CD3CN
1H-1H.
Fischer, Alfred; Henderson, George N.
Synthesis, 1985 , # 6/7 p. 641 - 643 Title/Abstract Full Text Show Details
NMR
Norris; Sternhell
Australian Journal of Chemistry, 1966 , vol. 19, p. 617,625 Full Text Show Details
Blatchly et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 2286,2290 Full Text Show Details
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Original Text (IR Spectroscopy)
Comment (IR Spectroscopy)
Bands
film
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
Bands
neat (no solvent, solid phase)
IR (neat) ν 1654.6 cm-1
Abu-Elfotoh, Abdel-Moneim; Tsuzuki, Kazuyuki; Nguyen, Tram Bao; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Tetrahedron, 2013 , vol. 69, # 40 p. 8612 - 8617
Reference
IR Spectroscopy (9) Reference
Title/Abstract Full Text View citing articles Show Details
Intensity of IR bands Bands
potassium bromide
Dohi, Toshifumi; Nakae, Tomofumi; Takenaga, Naoko; Uchiyama, Teruyoshi; Fukushima, Kei-Ichiro; Fujioka, Hiromichi; Kita, Yasuyuki
Synthesis, 2012 , vol. 44, # 8 p. 1183 - 1189 Title/Abstract Full Text View citing articles Show Details
Bands
film
Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel
Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759 Title/Abstract Full Text View citing articles Show Details
Bands
KBr
Iwasa, Seiji; Fakhruddin, Ahmad; Widagdo, Herman Setyo; Nishiyama, Hisao
Advanced Synthesis and Catalysis, 2005 , vol. 347, # 4 p. 517 - 520 Title/Abstract Full Text View citing articles Show Details
Bands
CHCl3
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 7 p. 1530 - 1532 Title/Abstract Full Text View citing articles Show Details
Bands
CCl4
2963 - 1588 cm**(-1)
Barton, Derek H. R.; Sas, Woijciech
Tetrahedron, 1990 , vol. 46, # 10 p. 3419 - 3430 Title/Abstract Full Text View citing articles Show Details
Bands
KBr
1650 - 840 cm**(-1)
Natake, Masato; Kawamura, Kazuhiko; Danno, Gen-ichi; Kanazawa, Kazuki
Agricultural and Biological Chemistry, 1982 , vol. 46, # 4 p. 1083 - 1084 Title/Abstract Full Text Show Details
Bands
Jacobsen,N.; Torrsell,K.
Justus Liebigs Annalen der Chemie, 1972 , vol. 763, p. 135 - 147 Full Text View citing articles Show Details
Mass Spectrometry (2) Description (Mass Spectrometry)
Reference
spectrum
Michman, Michael; Oron, Miriam; Schaefer, Hans J.
Collection of Czechoslovak Chemical Communications, 2000 , vol. 65, # 6 p. 924 - 940 Title/Abstract Full Text View citing articles Show Details
Dewkar, Gajanan K.; Shaikh, Tanveer M.; Pardhy; Kulkarni, Swati S.; Sudalai, Arumugam
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Kwong Chip; Grossert
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 1629 Full Text Show Details
UV/VIS Spectroscopy (9)
Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Absorption Maxima (UV/VIS)
Spectrum
248 nm 310 nm
Spectrum
ethyl acetate
in the presence of additive(s) Spectrum
various solvent(s)
252 nm
Spectrum
acetonitrile
Ext./Abs. Coefficient
Location
Comment (UV/VIS Spectroscopy)
Reference
supporting information
Li, Jun; Bi, Yanlan; Liu, Wei; Sun, Shangde
Journal of Agricultural and Food Chemistry, 2015 , vol. 63, # 38 p. 8584 - 8591 Title/Abstract Full Text View citing articles Show Details
252 nm
Bekdeser, Burcu; Oezyuerek, Mustafa; Gueclue, Kubilay; Apak, Resat
Analytical Chemistry, 2011 , vol. 83, # 14 p. 5652 - 5660 Title/Abstract Full Text View citing articles Show Details
252 nm
20000 l·mol-1cm-1
Wang, Xiu Jun; Hayes, John D.; Higgins, Larry G.; Wolf, C. Roland; Dinkova-Kostova, Albena T.
Chemistry and Biology, 2010 , vol. 17, # 1 p. 75 - 85 Title/Abstract Full Text View citing articles Show Details
in the presence of inorganic compounds. Object(s) of Study: in the presence of organic compounds
Li, Yunbo; Seacat, Andrew; Kuppusamy, Periannan; Zweier, Jay L; Yager, James D; Trush, Michael A
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2002 , vol. 518, # 2 p. 123 - 133 Title/Abstract Full Text View citing articles Show Details
200 - 800 nm
Mure, Minae; Klinman, Judith P.
Journal of the American Chemical Society, 1995 , vol. 117, # 34 p. 8698 - 8706
Title/Abstract Full Text View citing articles Show Details
Absorption maxima
Absorption maxima
acetonitrile
ethanol
250 nm 312 nm
17300 l·mol-1cm-1
Mure, Minae; Klinman, Judith P.
Journal of the American Chemical Society, 1995 , vol. 117, # 34 p. 8698 - 8706 Title/Abstract Full Text View citing articles Show Details
Natake, Masato; Kawamura, Kazuhiko; Danno, Gen-ichi; Kanazawa, Kazuki
Agricultural and Biological Chemistry, 1982 , vol. 46, # 4 p. 1083 - 1084 Title/Abstract Full Text Show Details
700 l·mol-1cm-1
248 nm 269 nm 420 nm
15600 l·mol-1cm-1 1360 l·mol-1cm-1
46 l·mol-1cm-1
UV/VIS
Bruce; Chaudhry
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 372,379 Full Text Show Details
Maruyama; Otsuki
Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 2873 Full Text Show Details
Absorption maxima
Orlando et al.
Journal of the American Chemical Society, 1967 , vol. 89, p. 6527,6531 Full Text Show Details
ESR Spectroscopy (1) Description (ESR Spectroscopy)
Reference
ESR
Pedersen
Molecular Physics, 1974 , vol. 28, p. 1031,1033 Full Text Show Details
Barbarin et al.
Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques, 1973 , vol. 276, p. 339 Full Text Show Details
Bioactivity Pharmacological Data (37) 1 of 37
Comment (Pharmacological Data)
Bioactivities present
Reference
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Seiko Kagaku Kabushiki Kaisha
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Horswill,E.C.; Ingold,K.U.
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Canadian Patents and Development Limited
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Cuntze,U.; Musso,H.
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Universal Oil Prod. Co.
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Orlando et al.
Journal of the American Chemical Society, 1967 , vol. 89, p. 6527,6531 Full Text Show Details
Bruce; Chaudhry
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1972 , p. 372,379 Full Text Show Details
2 of 37
Comment (Pharmacological Data)
Bioactivities present
Reference
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Karpov; Chidekel'
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Pedersen
Molecular Physics, 1974 , vol. 28, p. 1031,1033 Full Text Show Details
Barbarin et al.
Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques, 1973 , vol. 276, p. 339 Full Text Show Details
McKillop et al.
Angewandte Chemie, 1970 , vol. 82, p. 84 Full Text Show Details
Pilar et al.
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Ho et al.
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3 of 37
4 of 37
Comment (Pharmacological Data)
Bioactivities present
Reference
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Comment (Pharmacological Data)
Bioactivities present
Reference
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Comment (Pharmacological Data)
Bioactivities present
Reference
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6 of 37
Comment (Pharmacological Data)
Bioactivities present
Reference
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SYNTOPIX LIMITED
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SYNTOPIX LIMITED
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7 of 37
Comment (Pharmacological Data)
Bioactivities present
Reference
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Uyanik, Muhammet; Mutsuga, Tatsuya; Ishihara, Kazuaki
Molecules, 2012 , vol. 17, # 7 p. 8604 - 8616 Title/Abstract Full Text View citing articles Show Details
Hernandez-Juarez, Martin; Garcia-Baez, Efren V.; Padilla-Martinez, Itzia I.; Salazar, Veronica; Hoepfl, Herbert; Rosales-Hoz, Maria De Jesus
Organometallics, 2012 , vol. 31, # 15 p. 5438 - 5451,14 Title/Abstract Full Text Show Details
Endo, Satoshi; Matsunaga, Toshiyuki; Kumada, Sho; Fujimoto, Airi; Hara, Akira; Ohno, Satoshi; El-Kabbani, Ossama; Hu, Dawei; Toyooka, Naoki; Mano, Jun'Ichi; Tajima, Kazuo
Archives of Biochemistry and Biophysics, 2012 , vol. 527, # 1 p. 23 - 30,8 Title/Abstract Full Text Show Details
Endo, Satoshi; Matsunaga, Toshiyuki; Kumada, Sho; Fujimoto, Airi; Ohno, Satoshi; El-Kabbani, Ossama; Hu, Dawei; Toyooka, Naoki; Mano, Jun'Ichi; Tajima, Kazuo; Hara, Akira
Archives of Biochemistry and Biophysics, 2012 , vol. 527, # 1 p. 23 - 30 Title/Abstract Full Text View citing articles Show Details
Nielsen, Christian B.; Brock-Nannestad, Theis; Hammershoj, Peter; Reenberg, Theis K.; Schau-Magnussen, Magnus; Trpcevski, Denis; Hensel, Thomas; Salcedo, Roberto; Baryshnikov, Gleb V.; Minaev, Boris F.; Pittelkow, Michael
Chemistry - A European Journal, 2013 , vol. 19, # 12 p. 3898 - 3904 Title/Abstract Full Text View citing articles Show Details
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Comment (Pharmacological Data)
Bioactivities present
Reference
Zhang, Shuai; Song, Feijie; Zhao, Dongbing; You, Jingsong
Chemical Communications, 2013 , vol. 49, # 40 p. 4558 - 4560 Title/Abstract Full Text View citing articles Show Details
Grafton, Mark W.; Farrugia, Louis J.; Sutherland, Andrew
Journal of Organic Chemistry, 2013 , vol. 78, # 14 p. 7199 - 7207 Title/Abstract Full Text View citing articles Show Details
Siraki, Arno G.; Chan, Tom S.; O'Brien, Peter J.
Toxicological Sciences, 2004 , vol. 81, # 1 p. 148 - 159 Title/Abstract Full Text View citing articles Show Details
Abu-Elfotoh, Abdel-Moneim; Tsuzuki, Kazuyuki; Nguyen, Tram Bao; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Tetrahedron, 2013 , vol. 69, # 40 p. 8612 - 8617 Title/Abstract Full Text View citing articles Show Details
Ikeda, Atsushi; Hoshino, Kazuya; Komatsuzaki, Hidehito; Satoh, Minoru; Nakazawa, Jun; Hikichi, Shiro
New Journal of Chemistry, 2013 , vol. 37, # 8 p. 2377 - 2383 Title/Abstract Full Text View citing articles Show Details
Endo, Satoshi; Arai, Yuki; Hara, Akira; Kitade, Yukio; Bunai, Yasuo; El-Kabbani, Ossama; Matsunaga, Toshiyuki
Biological and Pharmaceutical Bulletin, 2013 , vol. 36, # 9 p. 1514 - 1518 Title/Abstract Full Text View citing articles Show Details
Hall, Gabriel B.; Chen, Jinzhu; Mebi, Charles A.; Okumura, Noriko; Swenson, Matthew T.; Ossowski, Stephanie E.; Zakai, Uzma I.; Nichol, Gary S.; Lichtenberger, Dennis L.; Evans, Dennis H.; Glass, Richard S.
Organometallics, 2013 , vol. 32, # 21 p. 6605 - 6612 Title/Abstract Full Text View citing articles Show Details
EADY, Elizabeth, Anne; QURESHI, Andleeb
Patent: WO2008/35078 A1, 2008 ; Title/Abstract Full Text Show Details
FITZGERALD, Daniel, James; GOTTARDELLO, Priscila
Patent: WO2008/35085 A1, 2008 ; Title/Abstract Full Text Show Details
FITZGERALD, Daniel, James; GOTTARDELLO, Priscila
Patent: WO2008/35085 A1, 2008 ; Title/Abstract Full Text Show Details
Reddy, B.V.Subba; Reddy, P. Sivaramakrishna; Reddy, Y. Jayasudhan; Bhaskar; Reddy, B. Chandra Obula
Bulletin of the Korean Chemical Society, 2013 , vol. 34, # 10 p. 2968 - 2972 Title/Abstract Full Text View citing articles Show Details
Liu, Xiao; Pan, Ling; Dong, Jinhuan; Xu, Xianxiu; Zhang, Qian; Liu, Qun
Organic Letters, 2013 , vol. 15, # 24 p. 6242 - 6245 Title/Abstract Full Text View citing articles Show Details
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valerie; Li, Haiyan; Shah, Nimesh; Namboothiri, Irishi N. N.; Doris, Eric
ChemCatChem, 2014 , vol. 6, # 3 p. 719 - 723 Title/Abstract Full Text View citing articles Show Details
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Tomita, Ren; Mantani, Kohei; Hamasaki, Akiyuki; Ishida, Tamao; Tokunaga, Makoto
Chemistry - A European Journal, 2014 , vol. 20, # 32 p. 9914 - 9917 Title/Abstract Full Text View citing articles Show Details
Nafikova; Asfandiarov; Kalimullina; El'Kin, Yu. N.
Russian Chemical Bulletin, 2014 , vol. 63, # 3 p. 572 - 576 Izvestiya Akademii Nauk. Seriya Khimicheskaya, 2014 , # 3 p. 572 - 576,5 Title/Abstract Full Text View citing articles Show Details
Moon, Youngtaek; Jeong, Yujeong; Kook, Daehyuk; Hong, Sungwoo
Organic and Biomolecular Chemistry, 2015 , vol. 13, # 13 p. 3918 - 3923 Title/Abstract Full Text View citing articles Show Details
Jawale, Dhanaji V.; Gravel, Edmond; Geertsen, Valrie; Li, Haiyan; Shah, Nimesh; Kumar, Rahul; John, Jubi; Namboothiri, Irishi N.N.; Doris, Eric
Tetrahedron, 2014 , vol. 70, # 36 p. 6140 - 6145 Title/Abstract Full Text View citing articles Show Details
Plesner, Malene; Hensel, Thomas; Nielsen, Bjarne E.; Kamounah, Fadhil S.; Brock-Nannestad, Theis; Nielsen, Christian B.; Tortzen, Christian G.; Hammerich, Ole; Pittelkow, Michael
Organic and Biomolecular Chemistry, 2015 , vol. 13, # 21 p. 5937 - 5943 Title/Abstract Full Text View citing articles Show Details
Yasukawa, Tomohiro; Miyamura, Hiroyuki; Kobayashi, Shu
Chemistry Letters, 2015 , vol. 44, # 1 p. 50 - 52 Title/Abstract Full Text View citing articles Show Details
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Comment (Pharmacological Data)
Bioactivities present
Reference
Li, Jun; Bi, Yanlan; Liu, Wei; Sun, Shangde
Journal of Agricultural and Food Chemistry, 2015 , vol. 63, # 38 p. 8584 - 8591 Title/Abstract Full Text View citing articles Show Details
Ali, Mohammed Hashmat; Welker, Andrea; York, Crystal
Synthesis (Germany), 2015 , vol. 47, # 20 art. no. SS-2015-M0265-OP, p. 3207 - 3211 Title/Abstract Full Text View citing articles Show Details
Vilipi, Jovana; Novakovi, Irena; Stanojkovi, Tatjana; Mati, Ivana; egan, Dejan; Kljaji, Zoran; Sladi, Duan
Bioorganic and Medicinal Chemistry, 2015 , vol. 23, # 21 p. 6930 - 6942 Title/Abstract Full Text View citing articles Show Details
Chen
Asian Journal of Chemistry, 2016 , vol. 28, # 2 p. 450 - 454
Title/Abstract Full Text View citing articles Show Details
Yang, Wei; Wang, Jingyi; Wei, Zhonglin; Zhang, Qian; Xu, Xianxiu
Journal of Organic Chemistry, 2016 , vol. 81, # 4 p. 1675 - 1680 Title/Abstract Full Text View citing articles Show Details
Kiranmayee; Sirisha; Vijaya Rachel; Jha, Anjali
International Journal of Pharmaceutical Sciences Review and Research, 2016 , vol. 38, # 2 art. no. 15, p. 75 - 82 Title/Abstract Full Text View citing articles Show Details
Gelis, Coralie; Bekkaye, Mathieu; Lebée, Clément; Blanchard, Florent; Masson, Géraldine
Organic Letters, 2016 , vol. 18, # 14 p. 3422 - 3425 Title/Abstract Full Text View citing articles Show Details
Wieczorek, Dorota; Marchut-Mikolajczyk, Olga; Strzelecki, Bartosz; Gajewska, Malgorzata; Polewczyk, Arkadiusz; Antczak, Tadeusz
International Biodeterioration and Biodegradation, 2016 , vol. 115, p. 205 - 211 Title/Abstract Full Text Show Details
Jardim, Guilherme A. M.; Bower, John F.; Da Silva Júnior, Eufrânio N.
Organic Letters, 2016 , vol. 18, # 18 p. 4454 - 4457 Title/Abstract Full Text Show Details
Widhalm, Joshua R.; Rhodes, David
Horticulture Research, 2016 , vol. 3, art. no. 16046 Title/Abstract Full Text Show Details
Liu, Cuifang; Li, Jun; Bi, Yanlan; Wang, Xuede; Sun, Shangde; Yang, Guolong
Journal of Oleo Science, 2016 , vol. 65, # 9 p. 739 - 748 Title/Abstract Full Text Show Details
Abiko, Yumi; Lin, Fang-Yu; Lee, Hsinyu; Puga, Alvaro; Kumagai, Yoshito
Journal of Toxicological Sciences, 2016 , vol. 41, # 6 p. 775 - 781 Title/Abstract Full Text Show Details
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Comment (Pharmacological Data)
physiological behaviour discussed
Reference
Vilipi, Jovana; Novakovi, Irena; Stanojkovi, Tatjana; Mati, Ivana; egan, Dejan; Kljaji, Zoran; Sladi, Duan
Bioorganic and Medicinal Chemistry, 2015 , vol. 23, # 21 p. 6930 - 6942 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
pharmacokinetics
Species or Test-System (Pharmacological Data)
recombinant apoptosis-inducing factor of mouse
Further Details (Pharmacological Data)
catalytic constant (Kcat)
Type (Pharmacological Data)
Kcat
Value of Type (Pharmacological Data)
0.04 1/s
Reference
Misevicien, Lina; Anusevicius, Zilvinas; Sarlauskas, Jonas; Sevrioukova, Irina F.; Cnas, Narimantas
Archives of Biochemistry and Biophysics, 2011 , vol. 512, # 2 p. 183 - 189 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
ARE-luciferase reporter activity; induction of
Species or Test-System (Pharmacological Data)
mammary AREc32 reporter cells of human; genetically modified/infected with: ARE-luciferase
Concentration (Pharmacological Data)
2.5 μmol/l
Kind of Dosing (Pharmacological Data)
title comp. dissolved in acetonitrile
Further Details (Pharmacological Data)
ARE: antioxidant response element; test carried out in absence of CuCl2; control luciferase activity was set to 1.0; fold to control related to: luciferase
Type (Pharmacological Data)
fold to control
Value of Type (Pharmacological Data)
4.1
Reference
Wang, Xiu Jun; Hayes, John D.; Higgins, Larry G.; Wolf, C. Roland; Dinkova-Kostova, Albena T.
Chemistry and Biology, 2010 , vol. 17, # 1 p. 75 - 85 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
ARE-luciferase reporter activity; induction of
Species or Test-System (Pharmacological Data)
mammary AREc32 reporter cells of human; genetically modified/infected with: ARE-luciferase
Concentration (Pharmacological Data)
2.5 μmol/l
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Kind of Dosing (Pharmacological Data)
title comp. dissolved in acetonitrile
Further Details (Pharmacological Data)
ARE: antioxidant response element; test carried out in presence of CuCl2; control luciferase activity was set to 1.0; fold to control related to: luciferase
Type (Pharmacological Data)
fold to control
Value of Type (Pharmacological Data)
24.7
Reference
Wang, Xiu Jun; Hayes, John D.; Higgins, Larry G.; Wolf, C. Roland; Dinkova-Kostova, Albena T.
Chemistry and Biology, 2010 , vol. 17, # 1 p. 75 - 85 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
protein binding affinity
Species or Test-System (Pharmacological Data)
N-terminally 6His-tagged macrophage migration inhibitory factor of rat
Further Details (Pharmacological Data)
scintillation proximity assay (SPA); test system protein immobilized on SPA beads; radioligand: [3H]-2-(pyridin-2-yl)-4H-benzo[e][1,3]thiazin-4-one; inhibitory concentration (IC)
Type (Pharmacological Data)
IC50
Value of Type (Pharmacological Data)
1.1 μmol/l
Reference
Kimura, Haruhide; Sato, Yoshimi; Tajima, Yasukazu; Suzuki, Hirobumi; Yukitake, Hiroshi; Imaeda, Toshihiro; Kajino, Masahiro; Oki, Hideyuki; Takizawa, Masayuki; Tanida, Seiichi
Chemistry and Biology, 2010 , vol. 17, # 12 p. 1282 - 1294 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
protein binding affinity
Species or Test-System (Pharmacological Data)
N-terminally 6His-tagged macrophage migration inhibitory factor of rat
Further Details (Pharmacological Data)
scintillation proximity assay (SPA); test system protein immobilized on SPA beads; radioligand: [3H]-2-(pyridin-2-yl)-4H-benzo[e][1,3]thiazin-4-one
Results
molecular target: rat macrophage migration inhibitory factor
Reference
Kimura, Haruhide; Sato, Yoshimi; Tajima, Yasukazu; Suzuki, Hirobumi; Yukitake, Hiroshi; Imaeda, Toshihiro; Kajino, Masahiro; Oki, Hideyuki; Takizawa, Masayuki; Tanida, Seiichi
Chemistry and Biology, 2010 , vol. 17, # 12 p. 1282 - 1294 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Example 3 - activity asainst P. acnes (other quinones)A series of quinones was tested with zinc pyrithione (ZP) in a similar manner to that described in Example 1. The MIC and MBC results are shown in Table 4 below and the (S)DDA results in Tables 5 (unsupplemented assays) and 6 (assays supplemented with salt and lipid). All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc with the exception of 2-t-butyl-p-benzoquinone which was used at 50 μg per disc in unsupplemented and 100 μg per disc in supplemented assays. The test compounds were dissolved in DMSO, with the exception of /?-benzoquinone and thymoquinone which were dissolved in ethanol.Table 4 Table 5 (unsupplemented (S)DDAs)Table 6 (supplemented (S)DDAs) (SL-(S)DDA = (S)DDA carried out in the presence of salt and lipid)Again these data demonstrate a synergistic antimicrobial interaction when a quinone is combined with zinc pyrithione, there being a significant increase in zone diameter over that exhibited by either compound alone. This synergistic interaction is maintained in nearly all cases in the presence of salt and lipid; furthermore the activity of the quinones alone appears in all cases to be enhanced by the presence of the supplements. Indeed, in some cases, for example the combination of 2-methyl-/?hydroquinone or 2- ethyl-p-hydroquinone with zinc pyrithione, antimicrobial synergy appears to be far more marked under the supplemented conditions than the unsupplemented ones, indicating the potential value of such a combination in topical skin treatment formulations, in particular to treat acne. Example 5 - activity against Propionibacterium spp (copper pyrithione)Copper (II) pyrithione (CuP) was tested against P. acnes NCTC 737 with a number of quinones, using the same procedure as in Example 3. The MIC and MBC results are shown in Table 9 below and the (S)DDA results in Table 10. All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc, with the exception of 2-t-butyl-p-benzoquinone which was used at 100 μg per disc. The TBHQ was dissolved in ethanol and the copper pyrithione, 2-methyl-p- benzoquinone and 2-chloro-p-benzoquinone in DMSO.Table 9 Table 10* Denotes data obtained in a separate series of experiments to those involving TBHQ and CuP.These data demonstrate a synergistic antimicrobial interaction when a quinone is combined with copper pyrithione, there being in nearly all cases a significant increase in zone diameter over that exhibited by either compound alone.
Type (Pharmacological Data)
MIC
Value of Type (Pharmacological Data)
7.8 μg/ml
Results
MBC is 15.6 μg/ml, MIC/MBC is 0.5
Location
Page/Page column 22-24; 28; 33-34
Reference
SYNTOPIX LIMITED
Patent: WO2008/35078 A1, 2008 ;
Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Example 3 - activity asainst P. acnes (other quinones)A series of quinones was tested with zinc pyrithione (ZP) in a similar manner to that described in Example 1. The MIC and MBC results are shown in Table 4 below and the (S)DDA results in Tables 5 (unsupplemented assays) and 6 (assays supplemented with salt and lipid). All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc with the exception of 2-t-butyl-p-benzoquinone which was used at 50 μg per disc in unsupplemented and 100 μg per disc in supplemented assays. The test compounds were dissolved in DMSO, with the exception of /?-benzoquinone and thymoquinone which were dissolved in ethanol.Table 4 Table 5 (unsupplemented (S)DDAs)Table 6 (supplemented (S)DDAs) (SL-(S)DDA = (S)DDA carried out in the presence of salt and lipid)Again these data demonstrate a synergistic antimicrobial interaction when a quinone is combined with zinc pyrithione, there being a significant increase in zone diameter over that exhibited by either compound alone. This synergistic interaction is maintained in nearly all cases in the presence of salt and lipid; furthermore the activity of the quinones alone appears in all cases to be enhanced by the presence of the supplements. Indeed, in some cases, for example the combination of 2-methyl-/?hydroquinone or 2- ethyl-p-hydroquinone with zinc pyrithione, antimicrobial synergy appears to be far more marked under the supplemented conditions than the unsupplemented ones, indicating the potential value of such a combination in topical skin treatment formulations, in particular to treat acne.Example 5 - activity against Propionibacterium spp (copper pyrithione)Copper (II) pyrithione (CuP) was tested against P. acnes NCTC 737 with a number of quinones, using the same procedure as in Example 3. The MIC and MBC results are shown in Table 9 below and the (S)DDA results in Table 10. All results are collated from a number of experiments.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc, with the exception of 2-t-butyl-p-benzoquinone which was used at 100 μg per disc. The TBHQ was dissolved in ethanol and the copper pyrithione, 2-methyl-p- benzoquinone and 2-chloro-p-benzoquinone in DMSO.Table 9 Table 10* Denotes data obtained in a separate series of experiments to those involving TBHQ and CuP.These data demonstrate a synergistic antimicrobial interaction when a quinone is combined with copper pyrithione, there being in nearly all cases a significant increase in zone diameter over that exhibited by either compound alone.
Results
unsupplemented disc diffusion assay value is 27.60 mm, 52.61 mm, supplemented (Triolein at 1percent v/v, sodium chloride, 100 mM) disc diffusion assay value is 61.68 mm
Location
Page/Page column 22-25; 28-30; 33-34
Reference
SYNTOPIX LIMITED
Patent: WO2008/35078 A1, 2008 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
cytotoxicity
Species or Test-System (Pharmacological Data)
hepatocytes of Sprague-Dawley rat
Sex
male
Method (Pharmacological Data)
cells incubated with title comp. for up to 3 h at 37 deg C under atmosphere of 95percent O2 and 5percent CO2; cell viability detd. trypan blue exclusion test
Further Details (Pharmacological Data)
control: untreated cells; LC50: conc. of title comp. required to cause 50percent decrease in cell viability in 2 h
Type (Pharmacological Data)
LC50
Value of Type (Pharmacological Data)
32 μmol/l
Reference
Chan, Katie; Jensen, Neil; O'Brien, Peter J.
Journal of Applied Toxicology, 2008 , vol. 28, # 5 p. 608 - 620 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cytotoxicity
Species or Test-System (Pharmacological Data)
hepatocytes of human
Sex
male
Method (Pharmacological Data)
cells incubated with title comp. for up to 3 h at 37 deg C; MTT added; incubated for another 3 h; absorbance of MTT formazan was measured at 572 nm and 690 nm; cytotoxicity determined
Further Details (Pharmacological Data)
control: untreated cells; LC50: conc. of title comp. required to cause 50percent decrease in cell viability in 2 h
Type (Pharmacological Data)
LC50
Value of Type (Pharmacological Data)
160 μmol/l
Reference
Chan, Katie; Jensen, Neil; O'Brien, Peter J.
Journal of Applied Toxicology, 2008 , vol. 28, # 5 p. 608 - 620 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Test micro-organismsThe principal test micro-organism used was Propionibacterium acnes NCTC 737. Other propionibacterial strains, including some P. granulosum strains and including some having antibiotic resistance, were also used as test organisms in Example 4.Propionibacteria are known to be involved in acne, which is a complex, multi-factorial skin disease in which P. acnes and other Propionibacterium spp. play key roles. Activity observed against the chosen test organisms is therefore expected to be a reasonable qualitative predictor of activity against micro-organisms responsible for skin and skin structure infections, in particular acne.All the propionibacteria were cultured and maintained on Wilkins-Chalgren Anaerobe Medium (agar and broth) at pH 6.0; all cultures were incubated anaerobically at 37 °C for 72 hours. Also tested was Porphyromonas gingivalis NCTC 11834 - this is a black pigmented gram-negative anaerobic bacterium belonging to the genus Porphyromonas. Porphyromonas are a human commensal bacterium, predominantly associated with the oral cavity. Clinically, Por. gingivalis is associated with periodontal lesions, infections and adult periodontal disease. Gingivitis (inflammation of the gums that causes bleeding and exposes the base of the teeth) can be a precursor to periodontal disease by allowing Por. gingivalis to infect the areas near the roots of the teeth and thus cause tooth decay and infection.Activity observed against this micro-organism is expected to be a reasonable qualitative predictor of antimicrobial activity, in particular against micro-organisms responsible for periodontal lesions, infections, and periodontal disease.Por. gingivalis was cultured and maintained on Wilkins-Chalgren Anaerobe Medium (agar and broth) at pH 7.0; all cultures were incubated anaerobically at 37 0C for 5-7 days.The following tests were carried out to assess antimicrobial activity against the test organisms. (d) Disc diffusion assay (DDA)This is an internationally recognised standard method for qualitatively assessing the antimicrobial activity of a compound.A sterile paper disc was impregnated with a sample of the test compound in a suitable solvent and 30 minutes allowed for the solvents to evaporate (where possible). The disc was then placed on an agar plate onto which the test micro-organism had been inoculated. The plate was then incubated under the conditions described above, following which it was examined visually for signs of microbial growth. If the test compound had antimicrobial activity, a circular zone of no growth would be obtained around the disc. The diameter of this zone of "inhibition" was measured using a ProtoCOL.(TM). automated zone sizer (Synbiosis, Cambridge, UK). In general, a greater diameter and/or area of the zone of inhibition indicates a greater antimicrobial activity in the relevant test compound, although other factors such as test compound mobility through the agar gel may also influence the result.
Results
The diameter of zone of inhibition = 52.61 mm
Location
Page/Page column 27-28; 30; 34-35
Reference
SYNTOPIX LIMITED
Patent: WO2008/35085 A1, 2008 ; Title/Abstract Full Text Show Details
Hide facts 21 of 37
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Effect (Pharmacological Data)
insecticidal
Species or Test-System (Pharmacological Data)
Coptotermes formosanus Shiraki, Formosan subterranean termite
Kind of Dosing (Pharmacological Data)
administered via filter paper disk treated with solution of title comp. in acetone (1percent wt/wt) after evaporation of solvent
Further Details (Pharmacological Data)
filter paper disk assay; results obtained at days 3-21 of treatment
Type (Pharmacological Data)
percent mortality
Value of Type (Pharmacological Data)
13.3 - 28.3 percent
Reference
Mozaina, Kobaisy; Cantrell, Charles L.; Mims, Amelia B.; Lax, Alan R.; Tellez, Maria R.; Osbrink, Weste L. A.
Journal of Agricultural and Food Chemistry, 2008 , vol. 56, # 11 p. 4021 - 4026 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
antimicrobial
Species or Test-System (Pharmacological Data)
Propionibacterium acnes NCTC 737
Method (Pharmacological Data)
Example 8 - activity against P. acnes (other quinones)A number of different quinones was tested with both copper (II) sulphate pentahydrate (CSPH) and copper (II) silicate (CSL) against P. acnes NCTC 737 using (S)DDA tests as described in Example 1.For the (S)DDA experiments, 200 μg of each test compound was loaded onto each disc, with the exception of copper (II) silicate (62 μg/disc) and 2-t-butyl-l,4- benzoquinone (100 μg/disc). The quinones were dissolved in DMSO and the copper (II) sulphate pentahydrate in deionised water, whilst the copper (II) silicate was used as a 0.62 percent (w/w) solution in water.All the quinones were sourced from Thermo Fisher Scientific, UK with the exception of 2-t-butyl-l,4-benzoquinone (Sigma- Aldrich) and 2-ethyl-p-hydroquinone (Apin Chemicals Ltd, UK).The DDA results are shown in Table 13 below and the SDDA results in Tables 14 and 15 (unsupplemented assays) and 16 and 17 (supplemented assays).Table 13 f-lpercent(v/v) trioleinTable 14Table 15Table 16 (SL SDDA = SDDA with salt and lipid (1percent (v/v) triolein) supplements)Table 17(SL SDDA = SDDA with salt and lipid (1percent (v/v) triolein) supplements)These data demonstrate synergistic antimicrobial activity against P. acnes NCTC 737 for a range of different benzo- and hydroquinones with copper salts. On the whole these synergies are retained under the supplemented conditions.
Results
title compound demonstrated an antimicrobial activity with zone of diameter of 35.18 mm (DDA) and 45.13 mm (DDA + salt and lipid)
Location
Page/Page column 47-49
Reference
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
intracellular ATP levels; effect on
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
Ca. 0.01 - 0.1 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 1 h in presence or absence of glucose (GLU); lysed; centrifuged; supernatant collected; intracellular ATP concentration was determined using luminometer
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Further Details (Pharmacological Data)
control: DMSO
Results
in the absence of GLU, title comp. caused drastic conc.-dependent decrease in ATP at 15 min; at 0.04 mmol/l, ATP decrease was about 10 and 66percent of control in absence/presence of GLU, resp.; in presence of GLU, ATP decrease was moderate; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
apoptosis induction
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 h; cytosolic extracts prepared; cytosolic protein was separated on 15percent SDS-polyacrylamide gel; release of cytochrome c detected by Western blotting
Further Details (Pharmacological Data)
control: cells treated with DMSO; caspase cascade plays an essential role in internucleosomal DNA laddering that typifies apoptotic cell death
Results
title comp. showed denser bands of cytochrome c than control; title comp. treatment caused release of cytochrome c from mitochondria to cytosol; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
glutathione levels; decrease of
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.01 - 0.05 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 h; washed; glutathione was extracted with perchloric acid; after addition of o-phthalaldehyde, fluorescence with excitation at 350 nm and emission at 420 nm; reduced glutathione level determined
Further Details (Pharmacological Data)
control: DMSO
Results
title comp. decreased glutathione levels dose-dependently and showed maximal effect at 0.04 mmol/l title comp. concentration; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
apoptosis induction
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 to 6 h; lysed; cell lysates separated on 14percent SDS-polyacrylamide gel and active caspase-3 and -7 detected by Western blotting
Further Details (Pharmacological Data)
caspase cascade plays an essential role in internucleosomal DNA laddering that typifies apoptotic cell death
Results
title comp. apparently processed procaspase-3 and -7 to active forms in cells; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
apoptosis induction
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. in presence of poly(ADP-ribose) polymerase (PARP) for 1.5 to 6 h; lysed; cell lysates separated on 7.5percent SDS-polyacrylamide gels and PARP cleavage determined by Western blotting
Further Details (Pharmacological Data)
PARP contains DEVD peptide sequence is target of DEVDase (caspase-3, -7); caspase cascade plays an essential role in internucleosomal DNA laddering that typifies apoptotic cell death
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Results
title comp.-treated cells showed PARP cleavage at 1.5 h and almost all 116-kDa peptide was cleaved at 4.5 h; cells treated with title comp., an 89-kDa peptide was detected in addition to original 116-kDa PARP peptide; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
apoptosis induction
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 h; lysed; centrifuged; supernatant collected; caspase-6, -9, -8, and -1/-4 activity determined using VEID, LHED, IETD and YVAD, respectively as substrate
Further Details (Pharmacological Data)
control: cells treated with DMSO; caspase cascade plays an essential role in internucleosomal DNA laddering that typifies apoptotic cell death
Results
title comp. induced caspase-9 and -6, though increase of activity was not great; induction of caspase-1 and -4 activity was barely detected; table
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
apoptosis induction
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.01 - 0.05 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 h or 2-4 h; lysed; centrifuged; supernatant collected; DEVDase (caspase-3 or -9) activity determined using Ac-DEVD-7-amino-4methylcoumarin as substrate
Further Details (Pharmacological Data)
control: DMSO
Results
title comp. increased DEVDase activity in conc., time-dependently; at 0.04 mmol/l highest enzyme activities were obsd. at 3 h, drastically decreased at 4 h; GSH and Nacetylcysteine caused inhibition of title comp. induced DEVDase activity; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
mitochondrial transmembrane potential; effect on
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 1 h; stained with 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolcarbocyanine at room temperature for 20 min; mitochondrial membrane potential was analyzed by FACScalibur flow cytometer
Further Details (Pharmacological Data)
control: untreated cells
Results
title comp. treatment caused disruption in mitochondrial transmembrane potential; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cell morphology; effect on
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 h and replaced with PBS (pH 7.4); stained with 2percent (w/v) aqueous uranyl acetate for 2 h and examined under electron microscopy
Further Details (Pharmacological Data)
control: untreated cells; VLS: vacuole like structure
Results
title comp. caused disruption in mitochondrial structure as compared with control; degradation of cristae and intramitochondrial structure, defects in mitochondrial bilayer, VLS were frequently observed; ultrastructure of cells was also similar; fig.
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Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cell morphology; effect on
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
0.04 mmol/l
Method (Pharmacological Data)
cells treated with title comp. for 3 or 6 h; stained with 4',6-diamidino-2-phenylindole dihydrochloride and examined under fluorescence microscopy
Further Details (Pharmacological Data)
control: DMSO
Results
title comp.-treated cells showed time-dependent increase in nuclear condensation and fragmentation and these changes with title comp. was marked at 6 h but not before at 3 h; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cytotoxicity
Species or Test-System (Pharmacological Data)
human monocytic leukemia U937 cells
Concentration (Pharmacological Data)
Ca. 1E-07 - 0.005 mol/l
Kind of Dosing (Pharmacological Data)
title comp. dissolved in ethanol:dodecane (98:2, v/v)
Method (Pharmacological Data)
cells treated with title comp. for 24 h; medium replaced with RPMI 1640 medium containing neutral red for 3 h; cytotoxicity determined by uptake of neutral red; absorbance read at 540 nm
Further Details (Pharmacological Data)
control: vehicle
Results
title comp. showed concentration dependent inhibition of neutral red uptake; inhibition of neutral red uptake was detected with 1E-6 mol/l title comp. conc. and almost complete inhibition was observed at 2E-5 mol/l title comp. concentration; fig.
Reference
Okubo; Yokoyama; Kano
Food and Chemical Toxicology, 2003 , vol. 41, # 5 p. 679 - 688 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
mutagenicity effect in Ames test using Salmonella typhimurium TA 100
Reference
Mizuno, Masashi; Toda, Masaya; Danno, Gen-ichi; Kanazawa, Kazuki; Natake, Masato
Agricultural and Biological Chemistry, 1988 , vol. 52, # 11 p. 2843 - 2850 Title/Abstract Full Text Show Details
Comment (Pharmacological Data)
ED50 in KB Cells 1.40 μg/mL
Reference
Lam; Garg; Swanson; Pezzuto
Journal of Pharmaceutical Sciences, 1988 , vol. 77, # 5 p. 393 - 395 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
ED50 in P-388 Cells 0.56 μg/mL
Reference
Lam; Garg; Swanson; Pezzuto
Journal of Pharmaceutical Sciences, 1988 , vol. 77, # 5 p. 393 - 395 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
DNA-damaging activity and no mutagenic avtivity toward Salmonella typhimurium strains TA 1535, TA 1536, TA 1537, TA 1538, and TA 98
Reference
Natake, Masato; Kawamura, Kazuhiko; Danno, Gen-ichi; Kanazawa, Kazuki
Agricultural and Biological Chemistry, 1982 , vol. 46, # 4 p. 1083 - 1084 Title/Abstract Full Text Show Details
Ecotoxicology (3) 1 of 3
Effect (Ecotoxicology)
antifungal
Species or Test-System (Ecotoxicology)
Colletotrichum gloeosporioides CG162
2 of 3
3 of 3
Kind of Dosing (Ecotoxicology)
placed on TLC plate as solution in 95 percent methanol
Method (Ecotoxicology)
TLC bioautographic assay; moisture growth chamber; 24 deg C; 12 h photoperiod under 60 μmol/m2/s light; incubated for 4 d; size of inhibitory zone measured
Further Details (Ecotoxicology)
benomyl, captan, and chlorothalonil used as ref. comp.
Comment (Ecotoxicology)
No effect
Reference
Meazza, Giovanni; Dayan, Franck E.; Wedge, David E.
Journal of Agricultural and Food Chemistry, 2003 , vol. 51, # 13 p. 3824 - 3828 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
antifungal
Species or Test-System (Ecotoxicology)
Colletotrichum acutatum CAGoff
Kind of Dosing (Ecotoxicology)
placed on TLC plate as solution in 95 percent methanol
Method (Ecotoxicology)
TLC bioautographic assay; moisture growth chamber; 24 deg C; 12 h photoperiod under 60 μmol/m2/s light; incubated for 4 d; size of inhibitory zone measured
Further Details (Ecotoxicology)
benomyl, captan, and chlorothalonil used as ref. comp.
Comment (Ecotoxicology)
No effect
Reference
Meazza, Giovanni; Dayan, Franck E.; Wedge, David E.
Journal of Agricultural and Food Chemistry, 2003 , vol. 51, # 13 p. 3824 - 3828 Title/Abstract Full Text View citing articles Show Details
Effect (Ecotoxicology)
antifungal
Species or Test-System (Ecotoxicology)
Colletotrichum fragariae CF63
Kind of Dosing (Ecotoxicology)
placed on TLC plate as solution in 95 percent methanol
Method (Ecotoxicology)
TLC bioautographic assay; moisture growth chamber; 24 deg C; 12 h photoperiod under 60 μmol/m2/s light; incubated for 4 d; size of inhibitory zone measured
Further Details (Ecotoxicology)
benomyl, captan, and chlorothalonil used as ref. comp.
Comment (Ecotoxicology)
No effect
Reference
Meazza, Giovanni; Dayan, Franck E.; Wedge, David E.
Journal of Agricultural and Food Chemistry, 2003 , vol. 51, # 13 p. 3824 - 3828 Title/Abstract Full Text View citing articles Show Details
Other Data Use (33) Use Pattern
Reference
Antimicrobial
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Skin structure conditions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Acne
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Eczema
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Superficial infected traumatic lesions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Title/Abstract Full Text Show Details
wounds
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Burns
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
ulcers
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Folliculitis
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Mycoses
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Acne lesions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Bacteria associated with acne
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Skin conditions
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Staphylococcal infection
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Atopic dermatitis
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Primary skin infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Secondary skin infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Primary skin structure infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Secondary skin structure infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Acne-related scarring
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
Hide facts Use Pattern
Reference
methicillin resistant S. aureus (MRSA)-associated infections
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ; Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Skin care
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Hair care
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Cosmeceutical preparation
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Toiletry product
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Laundry product
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Fabric treatment product
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Bath additive
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Shower additive
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Cleansing preparation
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Agricultural product
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
Horticultural product
Title/Abstract Full Text Show Details
SYNTOPIX LIMITED
Patent: WO2007/96601 A2, 2007 ;
veterinary preparation
Title/Abstract Full Text Show Details
Quantum Chemical Calculations (1) Calculated Properties
Method (Quantum Chemical Calculations)
Reference
Molecular orbitals
Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)
Nafikova; Asfandiarov; Kalimullina; El'Kin, Yu. N.
Russian Chemical Bulletin, 2014 , vol. 63, # 3 p. 572 - 576 Izvestiya Akademii Nauk. Seriya Khimicheskaya, 2014 , # 3 p. 572 - 576,5 Title/Abstract Full Text View citing articles Show Details
Chemical Name: 2-(sec-butyl)-1,4-benzoquinone
6
2 prep out of 3 reactions.
Reaxys Registry Number: 1941566
CAS Registry Number: 4197-82-4 Type of Substance: isocyclic Molecular Formula: C10H12O2
Linear Structure Formula: C10H12O2
Molecular Weight: 164.204
InChI Key: OMDQHODQKBJJBM-UHFFFAOYSA-N
Physical Data (6) Spectra (7)
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-(sec-butyl)-1,4-benzoquinone, 2-<Butyl-(2)>-benzochinon-(1,4), 2-sec-Butyl-1,4-benzochinon, 2-sek-Butyl-p-benzochinon, Butyl-2-chinon Physical Data Melting Point (1) Melting Point
Reference
65 - 66 °C
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Boiling Point (2) Boiling Point
Pressure (Boiling Point)
Reference
94 - 95 °C
4 Torr
Bogoljubskii
Journal of Organic Chemistry USSR (English Translation), 1966 , vol. 2, p. 1420 Zhurnal Organicheskoi Khimii, 1966 , vol. 2, p. 1433 Full Text Show Details
66 °C
1 Torr
Hawthorne; Reintjes
Journal of the American Chemical Society, 1964 , vol. 86, p. 951 Full Text View citing articles Show Details
Refractive Index (1) Refractive Index
Wavelength (Refractive Index)
Temperature (Refractive Index)
Reference
1.5167
589 nm
20 °C
Bogoljubskii
Journal of Organic Chemistry USSR (English Translation), 1966 , vol. 2, p. 1420 Zhurnal Organicheskoi Khimii, 1966 , vol. 2, p. 1433 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Location
Reference
yellow
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
Further Information (1) Description (Further Information)
Reference
Further information
Hawthorne; Reintjes
Journal of the American Chemical Society, 1965 , vol. 87, p. 4585,4586 Full Text Show Details
Spectra
5
NMR Spectroscopy (3) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts Spectrum
1H
chloroform-d1
Chemical shifts Spectrum
13C
NMR
Location
Reference
500 MHz
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
chloroform-d1
125 MHz
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
IR Spectroscopy (2) Description (IR Spectroscopy)
Location
Comment (IR Spectroscopy)
Reference
Bands
supporting information
neat liquid
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
IR
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Mass Spectrometry (1) Description (Mass Spectrometry)
Location
Reference
HRMS (High resolution mass spectrometry) LCMS (Liquid chromatography mass spectrometry) ESI (Electrospray ionisation) TOFMS (Time of flight mass spectrum) Spectrum
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
UV/VIS Spectroscopy (1) Description (UV/VIS Spectroscopy)
Reference
UV/VIS
Singh; Turner
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974 , p. 2556,2558 Full Text Show Details
Chemical Name: 2-isobutyl-p-benzoquinone
7
Reaxys Registry Number: 2613564
CAS Registry Number: 4197-79-9 Type of Substance: isocyclic Molecular Formula: C10H12O2
Linear Structure Formula: C10H12O2
Molecular Weight: 164.204
InChI Key: OHNSLFRMOCCULR-UHFFFAOYSA-N
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-isobutyl-p-benzoquinone, 2-(2-Methyl-propyl)-benzochinon-(1,4), 2-Methyl-propyl-chinon, Isobutyl-p-benzochinon
2 prep out of 3 reactions.
Identification Physical Data (2) Spectra (2)
4
Identification Substance Label (1) Label
Reference
2e
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Physical Data Melting Point (1) Melting Point
Reference
35 - 36 °C
Hawthorne; Reintjes
Journal of the American Chemical Society, 1964 , vol. 86, p. 951 Full Text View citing articles Show Details
Orlando jun. et al.
Journal of Organic Chemistry, 1968 , vol. 33, p. 2512 Full Text View citing articles Show Details
Further Information (1) Description (Further Information)
Reference
Further information
Hawthorne; Reintjes
Journal of the American Chemical Society, 1965 , vol. 87, p. 4585,4586 Full Text Show Details
Spectra NMR Spectroscopy (1) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Location
Reference
Chemical shifts
1H
chloroform-d1
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
UV/VIS Spectroscopy (1) Description (UV/VIS Spectroscopy)
Reference
UV/VIS
Orlando jun. et al.
Journal of Organic Chemistry, 1968 , vol. 33, p. 2512 Full Text View citing articles Show Details
Chemical Name: 2-(n-butyl)-1,4-benzoquinone
8
Reaxys Registry Number: 2613565
CAS Registry Number: 4197-70-0 Type of Substance: isocyclic Molecular Formula: C10H12O2
Linear Structure Formula: C10H12O2
Molecular Weight: 164.204
InChI Key: AMQCWFKKFGSNNA-UHFFFAOYSA-N
4 prep out of 4 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-(n-butyl)-1,4-benzoquinone, 2-butyl[1,4]benzoquinone, 2-butyl-p-benzoquinone, butyl-[1,4]benzoquinone, Butyl-[1,4]benzochinon, butyl quinone, 2-Butyl-benzochinon-(1,4) Identification
Identification Physical Data (7) Spectra (6)
8
Substance Label (2) Label
Reference
2d
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
6b
Wang, Dawei; Ge, Bingyang; Du, Liyong; Miao, Hongyan; Ding, Yuqiang
Synlett, 2014 , vol. 25, # 20 art. no. ST-2014-W0606-L, p. 2895 - 2898 Title/Abstract Full Text View citing articles Show Details
Patent-Specific Data (1)
Location in Patent
Reference
Claim
Industrial Technology Research Institute
Patent: US5650531 A1, 1997 ; Title/Abstract Full Text Show Details
Physical Data Melting Point (3) Melting Point
Comment (Melting Point)
Reference
34 - 35 °C
Hawthorne; Reintjes
Journal of the American Chemical Society, 1964 , vol. 86, p. 951 Full Text View citing articles Show Details
31.5 °C
Eastman Kodak Co.
Patent: US2533203 , 1948 ; Full Text Show Details
32 °C
Gulland
Biochemical Journal, 1932 , vol. 26, p. 32,43 Full Text Show Details
Sublimation.
Crystal Property Description (3) Colour & Other Properties
Location
Reference
yellow
supporting information
Wang, Dawei; Ge, Bingyang; Du, Liyong; Miao, Hongyan; Ding, Yuqiang
Synlett, 2014 , vol. 25, # 20 art. no. ST-2014-W0606-L, p. 2895 - 2898 Title/Abstract Full Text View citing articles Show Details
yellow
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
orangegelbe Nadeln
Gulland
Biochemical Journal, 1932 , vol. 26, p. 32,43 Full Text Show Details
Further Information (1) Description (Further Information)
Reference
Further information
Hawthorne; Reintjes
Journal of the American Chemical Society, 1965 , vol. 87, p. 4585,4586 Full Text Show Details
Spectra NMR Spectroscopy (4) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Chemical shifts
1H
chloroform-d1
Location
Reference
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
1H
chloroform-d1
400 MHz
supporting information
Wang, Dawei; Ge, Bingyang; Du, Liyong; Miao, Hongyan; Ding, Yuqiang
Synlett, 2014 , vol. 25, # 20 art. no. ST-2014-W0606-L, p. 2895 - 2898 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
1H
dichloromethane-d2
500 MHz
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
Chemical shifts Spectrum
13C
dichloromethane-d2
150 MHz
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
IR Spectroscopy (1) Description (IR Spectroscopy)
Location
Comment (IR Spectroscopy)
Reference
Bands
supporting information
neat liquid
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
Mass Spectrometry (1) Description (Mass Spectrometry)
Location
Reference
HRMS (High resolution mass spectrometry) LCMS (Liquid chromatography mass spectrometry) ESI (Electrospray ionisation) TOFMS (Time of flight mass spectrum) Spectrum
supporting information
Fujiwara, Yuta; Domingo, Victoriano; Seiple, Ian B.; Gianatassio, Ryan; Del Bel, Matthew; Baran, Phil S.
Journal of the American Chemical Society, 2011 , vol. 133, # 10 p. 3292 - 3295 Title/Abstract Full Text View citing articles Show Details
Chemical Name: (3-Methyl-butyl-2)-chinon
9
no reactions.
Physical Data (1)
1
Identification Physical Data (1)
2
Reaxys Registry Number: 2575683
Type of Substance: isocyclic Molecular Formula: C11H14O2
Linear Structure Formula: C11H14O2
Molecular Weight: 178.231
InChI Key: IZCFYTBQHBEGIE-UHFFFAOYSA-N
Synthesize | Hide Details Find similar Chemical Names and Synonyms (3-Methyl-butyl-2)-chinon Physical Data Further Information (1) Description (Further Information)
Reference
Further information
Hawthorne; Reintjes
Journal of the American Chemical Society, 1965 , vol. 87, p. 4585,4586 Full Text Show Details
Chemical Name: 2-tert-amyl-1,4-benzoquinone Reaxys Registry Number: 2614034
CAS Registry Number: 23491-01-2 Type of Substance: isocyclic Molecular Formula: C11H14O2
Linear Structure Formula: C11H14O2
1 prep out of 1 reactions.
Molecular Weight: 178.231
InChI Key: GTBVCZDSESPSAA-UHFFFAOYSA-N
10
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-tert-amyl-1,4-benzoquinone, 2-tert-Pentyl-1,4-benzochinon Identification Patent-Specific Data (1) Location in Patent
Reference
Claim
Rockhurst University
Patent: US5780515 A1, 1998 ; Title/Abstract Full Text Show Details
Physical Data Melting Point (1) Melting Point
Solvent (Melting Point)
Reference
37 °C
aq. ethanol
Perrotti; Castelfranchi
Chimica e l'Industria (Milan, Italy), 1960 , vol. 42, p. 1333,1338 Full Text Show Details
Chemical Name: 2-(2,2-Dimethyl-propyl)-benzochinon-(1,4) Reaxys Registry Number: 3088654
CAS Registry Number: 143427-12-7 Type of Substance: isocyclic Molecular Formula: C11H14O2
Linear Structure Formula: C11H14O2
Molecular Weight: 178.231
InChI Key: WVYIRXGNRGZTGX-UHFFFAOYSA-N
11
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-(2,2-Dimethyl-propyl)-benzochinon-(1,4) Identification Substance Label (1) Label
Reference
IVb
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
2 prep out of 5 reactions.
Identification Physical Data (1)
2
Physical Data Melting Point (1) Melting Point
Reference
33 - 36 °C
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
Chemical Name: 2-n-pentyl-1,4-benzoquinone Reaxys Registry Number: 3245074
CAS Registry Number: 161691-33-4 Type of Substance: isocyclic Molecular Formula: C11H14O2
Linear Structure Formula: C11H14O2
Molecular Weight: 178.231
InChI Key: ASHWETAABNNORQ-UHFFFAOYSA-N
12
9 prep out of 23 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-n-pentyl-1,4-benzoquinone, 2-pentyl-p-benzoquinone, n-pentylbenzoquinone, pentyl-[1,4]benzoquinone, Pentyl-[1,4]benzochinon Identification Substance Label (3) Label
Reference
22
The University of Chicago; MRKSICH, Milan; HODNELAND, Christian
Patent: US2015/369816 A1, 2015 ; Title/Abstract Full Text Show Details
2g
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
6
Tandon, V. K.; Vaish, Meenu; Jain, P. K.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1995 , vol. 34, # 2 p. 93 - 96 Title/Abstract Full Text Show Details
Physical Data Melting Point (1)
Melting Point
Reference
22 °C
Asahina; Yasue
Chemische Berichte, 1936 , vol. 69, p. 643,647 Yakugaku Zasshi, 1936 , vol. 56, p. 549,554 Full Text Show Details
Boiling Point (1) Boiling Point
Pressure (Boiling Point)
Reference
101 °C
5 Torr
Hiraiwa
Yakugaku Zasshi, 1940 , vol. 60, p. 569,574 Full Text Show Details
Crystal Property Description (1)
Identification Physical Data (3) Spectra (4)
5
Colour & Other Properties
Location
Reference
brown
Paragraph 0202
The University of Chicago; MRKSICH, Milan; HODNELAND, Christian
Patent: US2015/369816 A1, 2015 ; Title/Abstract Full Text Show Details
Spectra NMR Spectroscopy (3) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Chemical shifts
1H
chloroform-d1
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
Tandon, V. K.; Vaish, Meenu; Jain, P. K.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1995 , vol. 34, # 2 p. 93 - 96 Title/Abstract Full Text Show Details
Spin-spin coupling constants
CDCl3
1H-1H
Tandon, V. K.; Vaish, Meenu; Jain, P. K.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1995 , vol. 34, # 2 p. 93 - 96 Title/Abstract Full Text Show Details
Location
Comment (NMR Spectroscopy)
Reference
IR Spectroscopy (1) Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Comment (IR Spectroscopy)
Bands
neat (no solvent)
1658 cm**(-1)
Reference Tandon, V. K.; Vaish, Meenu; Jain, P. K.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1995 , vol. 34, # 2 p. 93 96 Title/Abstract Full Text Show Details
Chemical Name: 2-Hexyl-benzochinon-(1,4) Reaxys Registry Number: 2614307
CAS Registry Number: 4197-73-3 Type of Substance: isocyclic Molecular Formula: C12H16O2
Linear Structure Formula: C12H16O2
Molecular Weight: 192.258
InChI Key: FPNBTZLQYJXISJ-UHFFFAOYSA-N
13
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-Hexyl-benzochinon-(1,4), Hexyl-chinon Physical Data Melting Point (1) Melting Point
Reference
48 - 49 °C
Hawthorne; Reintjes
Journal of the American Chemical Society, 1964 , vol. 86, p. 951 Full Text View citing articles Show Details
Further Information (1) Description (Further Information)
Reference
1 prep out of 1 reactions.
Physical Data (2)
2
Hawthorne; Reintjes
Journal of the American Chemical Society, 1965 , vol. 87, p. 4585,4586 Full Text Show Details
Further information
Chemical Name: 2-heptyl-p-benzoquinone
1 prep out of 1 reactions.
Reaxys Registry Number: 19196147
CAS Registry Number: 30100-25-5 Molecular Formula: C13H18O2
Linear Structure Formula: C13H18O2
Molecular Weight: 206.285
InChI Key: KTMJTRUJSDGHGL-UHFFFAOYSA-N
14
Identification Spectra (1)
2
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-heptyl-p-benzoquinone Identification Substance Label (1) Label
Reference
2h
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Spectra NMR Spectroscopy (1) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Location
Reference
Chemical shifts
1H
chloroform-d1
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Chemical Name: 2-(1,1,3,3-Tetramethyl-butyl)-benzochinon-(1,4) Reaxys Registry Number: 3091427
CAS Registry Number: 23491-02-3 Type of Substance: isocyclic Molecular Formula: C14H20O2
Linear Structure Formula: C14H20O2
Molecular Weight: 220.312
InChI Key: AUGHUVMXEYHKMG-UHFFFAOYSA-N
15
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1 prep out of 4 reactions.
Identification Physical Data (1)
1
Label
Reference
IVc
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
Physical Data Melting Point (1) Melting Point
Comment (Melting Point)
Reference
78.5 - 81.5 °C
with Sublimation
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
Chemical Name: 2-Octyl-benzochinon-(1,4) Reaxys Registry Number: 3118499
CAS Registry Number: 21182-43-4 Type of Substance: isocyclic Molecular Formula: C14H20O2
Linear Structure Formula: C14H20O2
Molecular Weight: 220.312
InChI Key: YHQZVSVVXAXCMA-UHFFFAOYSA-N
16
5 prep out of 8 reactions.
Identification Physical Data (1) Spectra (1)
2
Identification
1
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-Octyl-benzochinon-(1,4) Identification Substance Label (1) Label
Reference
III
Ozawa; Momose; Machida; Natori; Yoshihira
Chemical and pharmaceutical bulletin, 1968 , vol. 16, # 5 p. 853 - 862 Title/Abstract Full Text View citing articles Show Details
Physical Data Melting Point (1) Melting Point
Solvent (Melting Point)
Reference
59 - 60 °C
ethanol
Ozawa; Momose; Machida; Natori; Yoshihira
Chemical and pharmaceutical bulletin, 1968 , vol. 16, # 5 p. 853 - 862 Title/Abstract Full Text View citing articles Show Details
Spectra IR Spectroscopy (1) Description (IR Spectroscopy)
Reference
Bands
Ozawa; Momose; Machida; Natori; Yoshihira
Chemical and pharmaceutical bulletin, 1968 , vol. 16, # 5 p. 853 - 862 Title/Abstract Full Text View citing articles Show Details
Reaxys Registry Number: 4416636
Type of Substance: isocyclic Molecular Formula: C14H20O2
Linear Structure Formula: C14H20O2
Molecular Weight: 220.312
1 prep out of 1 reactions.
InChI Key: RCAURTUQGOGWHN-UHFFFAOYSA-N
17
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Identification Substance Label (1) Label
Reference
2d
Ishii, Fumio; Kishi, Ken-ichi
Synthesis, 1980 , # 9 p. 706 - 708 Title/Abstract Full Text Show Details
Chemical Name: 2-nonyl-p-benzoquinone
1 prep out of 1 reactions.
Reaxys Registry Number: 26683512
CAS Registry Number: 1585912-89-5 Molecular Formula: C15H22O2
Linear Structure Formula: C15H22O2
Molecular Weight: 234.338
InChI Key: RCMFCEUDXVDZIY-UHFFFAOYSA-N
18
Identification Spectra (1)
1
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-nonyl-p-benzoquinone Identification Substance Label (1) Label
Reference
2i
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Spectra NMR Spectroscopy (1) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Location
Reference
Chemical shifts
1H
chloroform-d1
supporting information
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
Chemical Name: 2-undecyl-1,4-benzoquinone
5 prep out of
Identification Physical Data (3)
4
5 reactions.
Reaxys Registry Number: 2455422
CAS Registry Number: 52431-54-6 Type of Substance: isocyclic Molecular Formula: C17H26O2
Linear Structure Formula: C17H26O2
Molecular Weight: 262.392
InChI Key: CJKAOSXSHTYWOT-UHFFFAOYSA-N
19
Spectra (9)
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-undecyl-1,4-benzoquinone, 2-undecyl-p-benzoquinone, undecyl-[1,4]benzoquinone, Undecyl-[1,4]benzochinon, 2-Undecyl-1,4-benzochinon Identification Substance Label (3) Label
Reference
2j
Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997 Title/Abstract Full Text View citing articles Show Details
18
Asakawa, Yoshinori; Masuya, Toru; Tori, Motoo; Campbell, Ella O.
Phytochemistry (Elsevier), 1987 , vol. 26, # 3 p. 735 - 738 Title/Abstract Full Text View citing articles Show Details
16
Jacobsen,N.; Torssell,K.
Acta Chemica Scandinavica (1947-1973), 1973 , vol. 27, # 9 p. 3211 - 3216 Full Text View citing articles Show Details
Physical Data Melting Point (2) Melting Point
Solvent (Melting Point)
Reference
59 - 60 °C
methanol
Jacobsen,N.; Torssell,K.
Acta Chemica Scandinavica (1947-1973), 1973 , vol. 27, # 9 p. 3211 - 3216 Full Text View citing articles Show Details
57 - 59 °C
ethanol
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelbe Nadeln
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Spectra NMR Spectroscopy (4) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Location
Chemical shifts
1H
chloroform-d1
supporting information
Comment (NMR Spectroscopy)
Reference Love, Brian E.; Duffy, Brian C.; Simmons, Alexander L.
Tetrahedron Letters, 2014 , vol. 55, # 12 p. 1994 - 1997
Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
Asakawa, Yoshinori; Masuya, Toru; Tori, Motoo; Campbell, Ella O.
Phytochemistry (Elsevier), 1987 , vol. 26, # 3 p. 735 - 738 Title/Abstract Full Text View citing articles Show Details
Spin-spin coupling constants
CDCl3
1H-1H
Asakawa, Yoshinori; Masuya, Toru; Tori, Motoo; Campbell, Ella O.
Phytochemistry (Elsevier), 1987 , vol. 26, # 3 p. 735 - 738 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
Jacobsen,N.; Torssell,K.
Acta Chemica Scandinavica (1947-1973), 1973 , vol. 27, # 9 p. 3211 - 3216 Full Text View citing articles Show Details
IR Spectroscopy (2) Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Comment (IR Spectroscopy)
Reference
Bands
CHCl3
1665 - 902 cm**(-1)
Asakawa, Yoshinori; Masuya, Toru; Tori, Motoo; Campbell, Ella O.
Phytochemistry (Elsevier), 1987 , vol. 26, # 3 p. 735 - 738 Title/Abstract Full Text View citing articles Show Details
Bands
Jacobsen,N.; Torssell,K.
Acta Chemica Scandinavica (1947-1973), 1973 , vol. 27, # 9 p. 3211 - 3216 Full Text View citing articles Show Details
Mass Spectrometry (1) Description (Mass Spectrometry)
Reference
spectrum
Asakawa, Yoshinori; Masuya, Toru; Tori, Motoo; Campbell, Ella O.
Phytochemistry (Elsevier), 1987 , vol. 26, # 3 p. 735 - 738 Title/Abstract Full Text View citing articles Show Details
UV/VIS Spectroscopy (2) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Absorption Maxima (UV/VIS)
Ext./Abs. Coefficient
Reference
Absorption maxima
ethanol
204 nm 246 nm
3236 l·mol-1cm-1
8511 l·mol-1cm-1
Asakawa, Yoshinori; Masuya, Toru; Tori, Motoo; Campbell, Ella O.
Phytochemistry (Elsevier), 1987 , vol. 26, # 3 p. 735 - 738 Title/Abstract Full Text View citing articles Show Details
Absorption maxima
Jacobsen,N.; Torssell,K.
Acta Chemica Scandinavica (1947-1973), 1973 , vol. 27, # 9 p. 3211 3216 Full Text View citing articles Show Details
Chemical Name: (1-methyl-decyl)-[1,4]benzoquinone Reaxys Registry Number: 3302729
Type of Substance: isocyclic Molecular Formula: C17H26O2
Linear Structure Formula: C17H26O2
Molecular Weight: 262.392
InChI Key: JTWBFTHCJLBKDI-UHFFFAOYSA-N
20
Synthesize | Hide Details Find similar Chemical Names and Synonyms (1-methyl-decyl)-[1,4]benzoquinone, (1-Methyl-decyl)-[1,4]benzochinon
1 prep out of 1 reactions.
Physical Data (1)
1
Physical Data Boiling Point (1) Boiling Point
Pressure (Boiling Point)
Reference
122 - 125 °C
0.5 Torr
Eastman Kodak Co.
Patent: US2701197 , 1951 ; Full Text Show Details
Chemical Name: 2-(1,1,3,3,5,5-Hexamethyl-hexyl)-benzochinon-(1,4) Reaxys Registry Number: 3095822
CAS Registry Number: 23491-03-4 Type of Substance: isocyclic Molecular Formula: C18H28O2
Linear Structure Formula: C18H28O2
Molecular Weight: 276.419
InChI Key: CMGXUTUQHRXUBR-UHFFFAOYSA-N
21
2 prep out of 2 reactions.
Identification Physical Data (1)
1
Physical Data (7) Spectra (2)
4
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-(1,1,3,3,5,5-Hexamethyl-hexyl)-benzochinon-(1,4) Identification Substance Label (1) Label
Reference
IVd
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
Physical Data Melting Point (1) Melting Point
Comment (Melting Point)
Reference
48 - 49 °C
with Sublimation
Buben,I.; Pospisil,J.
Collection of Czechoslovak Chemical Communications, 1969 , vol. 34, p. 1991 - 2001 Full Text View citing articles Show Details
Chemical Name: dodecyl-[1,4]benzoquinone Reaxys Registry Number: 3295553
CAS Registry Number: 30100-26-6 Type of Substance: isocyclic Molecular Formula: C18H28O2
Linear Structure Formula: C18H28O2
Molecular Weight: 276.419
InChI Key: DZKQVYPBPFZBMD-UHFFFAOYSA-N
22
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6 prep out of 6 reactions.
dodecyl-[1,4]benzoquinone, Dodecyl-[1,4]benzochinon Physical Data Melting Point (6) Melting Point
Solvent (Melting Point)
Reference
70 °C
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
72 °C
Cook; Heilbron; Lewis
Journal of the Chemical Society, 1942 , p. 659 Full Text Show Details
74 °C
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
81 °C
ethanol
Hasan; Stedman
Journal of the Chemical Society, 1931 , p. 2112,2120 Full Text Show Details
81 °C
ethanol diethyl ether
Hasan; Stedman
Journal of the Chemical Society, 1931 , p. 2112,2120 Full Text Show Details
81 °C
petroleum ether
Hasan; Stedman
Journal of the Chemical Society, 1931 , p. 2112,2120 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelblich
Hasan; Stedman
Journal of the Chemical Society, 1931 , p. 2112,2120 Full Text Show Details
Spectra UV/VIS Spectroscopy (2) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Reference
Absorption maxima
hexane
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Absorption maxima
CHCl3
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Chemical Name: tetradecyl-[1,4]benzoquinone Reaxys Registry Number: 3317809
CAS Registry Number: 102310-43-0 Type of Substance: isocyclic Molecular Formula: C20H32O2
Linear Structure Formula: C20H32O2
Molecular Weight: 304.473
InChI Key: RVJDXEPKISKLNE-UHFFFAOYSA-N
23
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4 prep out of 4 reactions.
Physical Data (3) Spectra (2)
3
Chemical Names and Synonyms tetradecyl-[1,4]benzoquinone, Tetradecyl-[1,4]benzochinon Physical Data Melting Point (2) Melting Point
Solvent (Melting Point)
Reference
77.5 °C
Cook; Heilbron; Lewis
Journal of the Chemical Society, 1942 , p. 659 Full Text Show Details
78 - 79 °C
ethanol
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelbe Nadeln
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Spectra UV/VIS Spectroscopy (2) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Reference
Absorption maxima
hexane
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Absorption maxima
CHCl3
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Chemical Name: 2-n-Pentadecyl-1,4-benzoquinone Reaxys Registry Number: 2588447
CAS Registry Number: 41427-22-9 Type of Substance: isocyclic Molecular Formula: C21H34O2
Linear Structure Formula: C21H34O2
Molecular Weight: 318.5
InChI Key: LSWQTJBEJKTFHQ-UHFFFAOYSA-N
24
6 prep out of 8 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms 2-n-Pentadecyl-1,4-benzoquinone, 2-pentadecyl-p-benzoquinone, pentadecyl-[1,4]benzoquinone, Pentadecyl-[1,4]benzochinon, 2-Pentadecylbenzochinon-(1,4) Identification Substance Label (4) Label
Reference
16
Saladino, Raffaele; Neri, Veronica; Mincione, Enrico; Marini, Stefano; Coletta, Massimiliano; Fiorucci, Chiara; Filippone, Paolino
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 4 p. 581 - 586
Identification Physical Data (4) Spectra (4)
6
Title/Abstract Full Text View citing articles Show Details
7a (R=CH3(CH2)14-)
Barton, Derek H. R.; Bridon, Dominique; Zard, Samir Z.
Tetrahedron, 1987 , vol. 43, # 22 p. 5307 - 5314 Title/Abstract Full Text View citing articles Show Details
48
Barton, Derek H.R.; Crich, David; Kretzschmar, Gerhard
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1986 , p. 39 - 54 Title/Abstract Full Text Show Details
36, R1=C15H31
Barton, Derek H. R.; Crich, David; Kretzschmar, Gerhard
Tetrahedron Letters, 1984 , vol. 25, # 10 p. 1055 - 1058 Title/Abstract Full Text View citing articles Show Details
Physical Data Melting Point (3) Melting Point
Solvent (Melting Point)
Reference
70 - 72 °C
methanol
Barton, Derek H. R.; Bridon, Dominique; Zard, Samir Z.
Tetrahedron, 1987 , vol. 43, # 22 p. 5307 - 5314 Title/Abstract Full Text View citing articles Show Details
71 - 72 °C
pentane
Barton, Derek H.R.; Crich, David; Kretzschmar, Gerhard
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1986 , p. 39 - 54 Title/Abstract Full Text Show Details
72 - 74 °C
ethanol
Loev; Dawson
Journal of the American Chemical Society, 1956 , vol. 78, p. 4083,4086 Full Text View citing articles Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelb
Loev; Dawson
Journal of the American Chemical Society, 1956 , vol. 78, p. 4083,4086 Full Text View citing articles Show Details
Spectra NMR Spectroscopy (3) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Coupling Nuclei
Solvents (NMR Spectroscopy)
Comment (NMR Spectroscopy)
1H
1H
CDCl3
Saladino, Raffaele; Neri, Veronica; Mincione, Enrico; Marini, Stefano; Coletta, Massimiliano; Fiorucci, Chiara; Filippone, Paolino
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 4 p. 581 - 586 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
1H
CDCl3
Barton, Derek H.R.; Crich, David; Kretzschmar, Gerhard
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (19721999), 1986 , p. 39 - 54 Title/Abstract Full Text Show Details
Saladino, Raffaele; Neri, Veronica; Mincione, Enrico; Marini, Stefano; Coletta, Massimiliano; Fiorucci, Chiara; Filippone, Paolino
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 4 p. 581 - 586 Title/Abstract Full Text View citing articles Show Details
Spin-spin coupling constants
CDCl3
1H-1H
Barton, Derek H.R.; Crich, David; Kretzschmar, Gerhard
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (19721999), 1986 , p. 39 - 54 Title/Abstract Full Text Show Details
Reference
IR Spectroscopy (1) Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Comment (IR Spectroscopy)
Bands
nujol
1650 cm**(-1)
Reference Barton, Derek H.R.; Crich, David; Kretzschmar, Gerhard
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1986 , p. 39 54 Title/Abstract Full Text Show Details
Chemical Name: hexadecyl-[1,4]benzoquinone
4 prep out of 4 reactions.
Reaxys Registry Number: 1982959
CAS Registry Number: 122142-80-7 Type of Substance: isocyclic Molecular Formula: C22H36O2
Linear Structure Formula: C22H36O2
Molecular Weight: 332.527
InChI Key: KLMXEOXMGYOJEY-UHFFFAOYSA-N
25
Physical Data (5) Spectra (2)
Synthesize | Hide Details Find similar Chemical Names and Synonyms hexadecyl-[1,4]benzoquinone, Hexadecyl-[1,4]benzochinon Physical Data Melting Point (4) Melting Point
Solvent (Melting Point)
Reference
82 - 83 °C
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Neiland; Trybatscha
Patent: SU371196 , 1973 ; Ref. Zh., Khim., 1974 , vol. 8, # N121P Full Text Show Details
ethanol diethyl ether
Cook; Heilbron; Lewis
Journal of the Chemical Society, 1942 , p. 659 Full Text Show Details
83 °C
Cook; Heilbron; Lewis
Journal of the Chemical Society, 1942 , p. 659 Full Text Show Details
ethanol
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelbe Nadeln
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Spectra UV/VIS Spectroscopy (2) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Reference
Absorption maxima
hexane
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Absorption maxima
CHCl3
Braude
4
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Chemical Name: heptadecyl-[1,4]benzoquinone Reaxys Registry Number: 3359072
CAS Registry Number: 102898-50-0 Type of Substance: isocyclic Molecular Formula: C23H38O2
Linear Structure Formula: C23H38O2
Molecular Weight: 346.554
InChI Key: CHBMULNINJJGIE-UHFFFAOYSA-N
26
4 prep out of 4 reactions.
Physical Data (1)
1
Physical Data (4) Spectra (2)
5
Synthesize | Hide Details Find similar Chemical Names and Synonyms heptadecyl-[1,4]benzoquinone, Heptadecyl-[1,4]benzochinon Physical Data Melting Point (1) Melting Point
Solvent (Melting Point)
Reference
72 - 73 °C
ethanol
Lamberton
Australian Journal of Chemistry, 1959 , vol. 12, p. 224,230 Full Text Show Details
Chemical Name: octadecyl-[1,4]benzoquinone Reaxys Registry Number: 1991596
CAS Registry Number: 35175-59-8 Type of Substance: isocyclic Molecular Formula: C24H40O2
Linear Structure Formula: C24H40O2
Molecular Weight: 360.58
InChI Key: UPBVJANJSQRZSO-UHFFFAOYSA-N
27
5 prep out of 7 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms octadecyl-[1,4]benzoquinone, Octadecyl-[1,4]benzochinon, 2-Octadecyl-p-benzochinon Physical Data Melting Point (3) Melting Point
Solvent (Melting Point)
Reference
84 - 85 °C
Neiland; Trybatscha
Patent: SU371196 , 1973 ; Ref. Zh., Khim., 1974 , vol. 8, # N121P Full Text Show Details
76 °C
ethanol diethyl ether
Cook; Heilbron; Lewis
Journal of the Chemical Society, 1942 , p. 659 Full Text Show Details
84 - 85 °C
ethanol
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Crystal Property Description (1) Colour & Other Properties
Reference
gelbe Nadeln
Asano; Hase
Yakugaku Zasshi, 1940 , vol. 60, p. 650,658 Yakugaku Zasshi, 1941 , vol. 61, p. engl. Ref. S. 1, 5 Chem.Abstr., 1942 , p. 83 Full Text Show Details
Spectra UV/VIS Spectroscopy (2) Description (UV/VIS Spectroscopy)
Solvent (UV/VIS Spectroscopy)
Reference
Absorption maxima
hexane
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Absorption maxima
CHCl3
Braude
Journal of the Chemical Society, 1945 , p. 490,492 Full Text Show Details
Chemical Name: nonadecyl-[1,4]benzoquinone Reaxys Registry Number: 3376718
CAS Registry Number: 103044-71-9 Type of Substance: isocyclic Molecular Formula: C25H42O2
Linear Structure Formula: C25H42O2
Molecular Weight: 374.607
InChI Key: IDYNZEXMKYHOLA-UHFFFAOYSA-N
28
4 prep out of 4 reactions.
Synthesize | Hide Details Find similar Chemical Names and Synonyms nonadecyl-[1,4]benzoquinone, Nonadecyl-[1,4]benzochinon Physical Data Melting Point (1) Melting Point
Solvent (Melting Point)
Reference
80 - 81 °C
ethanol
Lamberton
Australian Journal of Chemistry, 1959 , vol. 12, p. 224,230 Full Text Show Details
Physical Data (1)
1