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2,3,6-Trichloroquinoxaline | CAS:2958-87-4
2,3,6-Trichloroquinoxaline
  • Name:2,3,6-Trichloroquinoxaline
  • CAS:2958-87-4
  • Synonyms:NSC 203052
  • Molecular Formula:C8H3Cl3N2
  • Molecular Weight:233.48
  • EINESC:220-987-3

Description

Properties

Melting point 143-144 ºC
Density 1.600

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Peer-Reviewed Papers
Ohkuma, T. et al. Journal of the American Chemical Society, 117, 2675-2675 (1995) Genet, J.-P. et al. Tetrahedron Letters, 36, 2063-2063 (1995) Lee, C.W. Alper, H. The Journal of Organic Chemistry, 60, 499-499 (1995) Sci. Synth., 1, 113-264 (2002) Smith, P. et al. Synthetic Communications, 25, 1093-1093 (1995) 2,2'-bis (diphenylphosphino)-1, 1'-binaphthyl (binap): A new atropisomeric bis (triaryl) phosphine. synthesis and its use in the Rh (l)-catalyzed asymmetric hydrogenation of a-(acylamino) acrylic acids.Miyashita A, et al. Tetrahedron, 40(8), 1245-1253 (1984) R. Noyori et al.Accounts of Chemical Research, 23, 345-345 (1990) Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts.Nakcheol Jeong et al.Chemical communications (Cambridge, England), (9), 1134-1135 (2004-04-30) Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound.Masanori Kawasaki et al.Journal of the American Chemical Society, 128(51), 16482-16483 (2006-12-21) Tani, K. et al. Organic Syntheses, 67, 33-33 (1989) Inoue, S.-I. et al. Journal of the American Chemical Society, 112, 4897-4897 (1990) Organic Syntheses, 71, 1-1 (1993) Tetrahedron, 50, 335-335 (1994) Journal of Organometallic Chemistry, 692, 550-550 (2007) The preparation of bi-functional organophosphine oxides as potential antitumor agents.Kim-Hung Lam et al.European journal of medicinal chemistry, 45(11), 5527-5530 (2010-09-14) Kurihara, Y. et al. Chemical & Pharmaceutical Bulletin, 42, 2357-2357 (1994)
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