112186
4-溴溴苄
98%
别名:
α,4-二溴甲苯
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关于此项目
线性分子式:
BrC6H4CH2Br
化学文摘社编号:
分子量:
249.93
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-636-5
Beilstein/REAXYS Number:
606498
MDL number:
产品名称
4-溴溴苄, 98%
InChI key
YLRBJYMANQKEAW-UHFFFAOYSA-N
InChI
1S/C7H6Br2/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2
SMILES string
BrCc1ccc(Br)cc1
assay
98%
form
solid
mp
62-64 °C (lit.)
functional group
bromo
Quality Level
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Application
使用4-溴苄基溴通过多种胺的连续N-烷基化制备20元氨基甲基取代的联芳基文库。
signalword
Danger
hcodes
Hazard Classifications
Resp. Sens. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
M G Organ et al.
Journal of combinatorial chemistry, 3(5), 473-476 (2001-09-11)
Described herein is the semiautomated preparation of a 20-member aminomethyl-substituted biaryl library. The two-step solution-phase synthesis was achieved via sequential N-alkylation of various amines with either 3- or 4-bromobenzyl bromide and Suzuki cross-coupling of the resultant aryl bromides with various
E V Sargent et al.
Drug and chemical toxicology, 22(4), 583-593 (1999-10-28)
As part of an occupational hazard evaluation, p-bromobenzyl bromide (p-BBB) was evaluated for genotoxic activity in the Ames microbial mutagenicity assay, the alkaline elution assay for DNA strand breaks in rat hepatocytes and the in vitro chromosome aberration assay in
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