144061
4-(溴甲基)苯甲腈
99%
别名:
α-溴对甲基苯甲腈, 4-氰基苄溴
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关于此项目
线性分子式:
BrCH2C6H4CN
化学文摘社编号:
分子量:
196.04
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-246-0
Beilstein/REAXYS Number:
636717
MDL number:
产品名称
4-(溴甲基)苯甲腈, 99%
InChI key
UMLFTCYAQPPZER-UHFFFAOYSA-N
InChI
1S/C8H6BrN/c9-5-7-1-3-8(6-10)4-2-7/h1-4H,5H2
SMILES string
BrCc1ccc(cc1)C#N
assay
99%
form
solid
mp
115-117 °C (lit.)
functional group
bromo
nitrile
Quality Level
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Application
4-(溴甲基)苄腈可用于合成含有螯合吡唑基-吡啶基团和芳香族腈的配体。
General description
在KOH存在下，4-(溴甲基)苄腈与2H-四唑反应，得到4-[(2H-四唑-2-基)甲基]苄腈。
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
Hazel Fenton et al.
Dalton transactions (Cambridge, England : 2003), 39(16), 3805-3815 (2010-04-08)
Two ligands L(1) and L(2) have been prepared which contain a chelating pyrazolyl-pyridine group with a pendant aromatic nitrile (in L(1), a benzonitrile; in L(2), a naphthonitrile). These ligands react with Ag(I) salts to give a range of infinite coordination
Zheng Xing et al.
Acta crystallographica. Section E, Structure reports online, 64(Pt 2), o445-o445 (2008-01-01)
The title compound, C(9)H(7)N(5), was synthesized by reaction of 4-(bromomethyl)benzonitrile and 2H-tetrazole in the presence of KOH. The relative orientation of the planar tetra-zole ring and the methyl-benzonitrile moiety is (-)-anti-clinal. The crystal packing is dominated by van der Waals
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