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Tris(2,3-dibromopropyl) phosphate | CAS:126-72-7

Tris(2,3-dibromopropyl) phosphate

名称：三(2,3-二溴丙基)磷酸酯 | Tris(2,3-dibromopropyl) phosphate
CAS号：126-72-7
别名：3PBR; Anfram 3PB; Apex 462-5; Bromkal P 67-6HP; ES 685; FireMaster LV-T 23P; FireMaster T 23; FireMaster T 23P; Flammex AP; Flammex LV-T 23P; Flammex T 23P; Fyrol HB 32; NSC 3240; Phoscon FR 150; Phoscon PE 60; Phoscon UF-S; T 23P; TDBPP; Tris; Tris (flame retardant); Tris(2,3-dibromopropyl) phosphate; Zetofex ZN
分子式：C₉H₁₅Br₆O₄P
分子量：697.61
EINESC号：204-799-9

产品描述

物理化学性质

熔点	5.5 ºC**
密度	2.27 g/cm3 (25 ºC)*
折射率	1.5772 (589.3 nm 20 ºC)*

安全数据

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SDS

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An enantioselective approach to highly substituted tetrahydrocarbazoles through hydrogen bonding-catalyzed cascade reactions.Xu-Fan Wang et al.Organic letters, 12(5), 1140-1143 (2010-02-12) Synthesis of novel 1-substituted and 1, 9-disubstituted-1, 2, 3, 4-tetrahydro-9H-carbazole derivatives as potential anticancer agentsShmeiss NAMM, et al. Molecules (Basel), 5(10), 1101-1112 (2000) The energetics of tetrahydrocarbazole aromatization over Pd(111): a computational analysis.P Crawford et al.The Journal of chemical physics, 128(10), 105104-105104 (2008-03-19) Binding of methoxy-substituted N1-benzenesulfonylindole analogs at human 5-HT6 serotonin receptors.Uma Siripurapu et al.Bioorganic & medicinal chemistry letters, 16(14), 3793-3796 (2006-05-20) Synthesis and SAR of substituted tetrahydrocarbazole derivatives as new NPY-1 antagonists.Romano Di Fabio et al.Bioorganic & medicinal chemistry letters, 16(6), 1749-1752 (2005-12-21) Solubilization of substituted indole compounds by beta-cyclodextrin in water.J Cao et al.Chemosphere, 40(12), 1411-1416 (2000-05-02) An entry to the azocino[4,3-b]indole framework through a dehydrogenative activation of 1,2,3,4-tetrahydrocarbazoles mediated by DDQ: formal synthesis of (±)-uleine.Süleyman Patir et al.The Journal of organic chemistry, 76(1), 335-338 (2010-12-15) Exploring the Chemistry of Spiroindolenines by Mechanistically-Driven Reaction Development: Asymmetric Pictet-Spengler-type Reactions and Beyond.Chao Zheng et al.Accounts of chemical research, 53(4), 974-987 (2020-04-11) One-pot synthesis of new substituted 1,2,3,4-tetrahydrocarbazoles via Petasis reaction.Subhasish Neogi et al.Journal of combinatorial chemistry, 12(5), 617-629 (2010-07-01) 1,2,3,4-tetrahydrocarbazoles as 5-HT6 serotonin receptor ligands.Jean Chang-Fong et al.Bioorganic & medicinal chemistry letters, 14(8), 1961-1964 (2004-03-31) Pd-catalyzed asymmetric hydrogenation of unprotected indoles activated by bronsted acidsWang D-S, et al. Journal of the American Chemical Society, 132(26), 8909-8911 (2010) Synthesis and in-vitro antitumor activities of some mannich bases of 9-alkyl-1,2,3,4-tetrahydrocarbazole-1-ones.Jing Chen et al.Archiv der Pharmazie, 342(3), 165-172 (2009-02-13) Photooxygenation of 1, 2, 3, 4-Tetrahydrocarbazole: Synthesis of Spiro [cyclopentane-1, 2 `-indolin-3 `-one]Mateo CA, et al. The Journal of Organic Chemistry, 61(2), 810-812 (1996)

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名称	CAS号

产品描述

物理化学性质

安全数据

SDS

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