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3-溴氰苄

3-溴氰苄用途

【用途一】
用于有机合成

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3-溴氰苄名称

[ CAS 号 ]:
31938-07-5

[ 中文名 ]:
3-溴氰苄

[ 英文名 ]:
2-(3-Bromophenyl)acetonitrile

[中文别名 ]:

[英文别名 ]:

m-bromophenyl acetonitrile
Benzeneacetonitrile, 3-bromo-
EINECS 250-867-6
3-bromophenylacetonitrile
ACETONITRILE, (m-BROMOPHENYL)-
3-Bromobenzyl cyanide
m-Bromobenzyl cyanide
3-BROMOBENZENEACETONITRILE
Benzeneacetonitrile,3-bromo
(3-Bromophenyl)acetonitrile

3-溴氰苄物理化学性质

[ 密度 ]:
1.5±0.1 g/cm3

[ 沸点 ]:
286.2±15.0 °C at 760 mmHg

[ 熔点 ]:
26-29 °C

[ 分子式 ]:
C₈H₆BrN

[ 分子量 ]:
196.044

[ 闪点 ]:
126.9±20.4 °C

[ 精确质量 ]:
194.968353

[ PSA ]:
23.79000

[ LogP ]:
2.22

[ 外观性状 ]:
白色固体或无色液体

[ 蒸汽压 ]:
0.0±0.6 mmHg at 25°C

[ 折射率 ]:
1.573

[ 储存条件 ]:
Room temperature.

3-溴氰苄MSDS

详细MSDS(安全技术说明书)

3-溴氰苄安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H302 + H312 + H332-H315-H319-H335

[ 警示性声明 ]:
P261-P280-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xn:Harmful;

[ 风险声明 (欧洲) ]:
R20/21/22;R36/37/38

[ 安全声明 (欧洲) ]:
S36/37/39-S26-S26/36/37/39-S36

[ 危险品运输编码 ]:
3449

[ RTECS号 ]:
AL8060000

[ 包装等级 ]:
I

[ 危险类别 ]:
6.1

[ 海关编码 ]:
2926909090

3-溴氰苄上下游产品

3-溴氰苄上游产品

3-溴氰苄下游产品

3-溴氰苄海关

[ 海关编码 ]: 2926909090

[ 中文概述 ]:
2926909090 其他腈基化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

3-溴氰苄文献

Synthesis and structure-activity relationships of 2-alkylidenethiazolidine-4,5-diones as antibiotic agents.

Bioorg. Med. Chem. 13(14) , 4402-7, (2005)

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...

Novel aminoethylbiphenyls as 5-HT7 receptor ligands.

Bioorg. Med. Chem. Lett. 17(11) , 3018-22, (2007)

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) r...

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