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Merck
CN

260088

3-溴氰苄

98%

别名:

3-溴苯乙腈

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线性分子式:
BrC6H4CH2CN
化学文摘社编号:
分子量:
196.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
250-867-6
MDL number:
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产品名称

3-溴氰苄, 98%

InChI key

UUZYFBXKWIQKTF-UHFFFAOYSA-N

InChI

1S/C8H6BrN/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6H,4H2

SMILES string

Brc1cccc(CC#N)c1

assay

98%

form

solid

bp

145-147 °C/10 mmHg (lit.)

mp

27-28 °C (lit.)

functional group

bromo
nitrile

Quality Level

Application

3-Bromophenylacetonitrile has been used in the synthesis of:
  • a series of aminoethylbiphenyls, novel 5-HT7 receptor ligands
  • 2-(1-cyano-1-(3-bromophenyl))methylidene-3-phenylthiazolidine-4,5-dione

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

>235.4 °F - closed cup

flash_point_c

> 113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

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Magalie Paillet-Loilier et al.
Bioorganic & medicinal chemistry letters, 17(11), 3018-3022 (2007-04-10)
The synthesis of a series of aminoethylbiphenyls as novel 5-HT(7) receptor ligands is described. The novel derivatives exhibit high affinity for the 5-HT(7) receptor with selectivity toward 5-HT(1A) receptor.
Xin-Yang Zhang et al.
Journal of hazardous materials, 403, 124103-124103 (2020-12-04)
Ozonation might increase the risk of wastewater due to byproduct formation, especially in the presence of bromide. In this study, a new analytical method was developed to identify new brominated disinfection byproducts (Br-DBPs) during ozonation, using comprehensive two-dimensional gas chromatography-single
Uwe Albrecht et al.
Bioorganic & medicinal chemistry, 13(14), 4402-4407 (2005-05-21)
2-Alkylidenethiazolidine-4,5-diones were prepared by novel one-pot cyclizations of arylacetonitriles with isothiocyanates and ethyl 2-chloro-2-oxoacetate. The products show antibiotic activity against the Gram-positive bacteria Bacillus subtilis and Staphylococcus aureus.

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