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2-氟苯甲腈

2-氟苯甲腈用途

【用途一】
用作医药、农药中间体

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2-氟苯甲腈名称

[ CAS 号 ]:
394-47-8

[ 中文名 ]:
2-氟苯腈

[ 英文名 ]:
2-Fluorobenzonitrile

[中文别名 ]:

[英文别名 ]:

Benzonitrile, 2-fluoro-
NCR BF
Benzonitrile,o-fluoro
o-Fluorobenzonitrile
EINECS 206-897-7
2-Fluorobenzenenitrile
1-CYANO-2-FLUOROBENZENE
o-Cyanofluorobenzene
Benzonitrile,2-fluoro
2-Fluorobenzonitrile

2-氟苯甲腈物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
193.6±0.0 °C at 760 mmHg

[ 熔点 ]:
35 - 37ºC

[ 分子式 ]:
C₇H₄FN

[ 分子量 ]:
121.112

[ 闪点 ]:
73.9±0.0 °C

[ 精确质量 ]:
121.032776

[ PSA ]:
23.79000

[ LogP ]:
1.51

[ 外观性状 ]:
透明至白色半固体

[ 蒸汽压 ]:
0.5±0.3 mmHg at 25°C

[ 折射率 ]:
1.511

[ 储存条件 ]:
Refrigerator

[ 水溶解性 ]:
不溶

2-氟苯甲腈MSDS

2-氟苯甲腈安全信息

[ 符号 ]:

GHS05, GHS07

[ 信号词 ]:
Danger

[ 危害声明 ]:
H302-H315-H318-H335

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

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 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) ]:
S26-S39-S36/37/39

[ 危险品运输编码 ]:
3276

[ WGK德国 ]:
3

[ 包装等级 ]:
III

[ 海关编码 ]:
29269095

2-氟苯甲腈合成路线

2-氟苯甲腈上下游产品

2-氟苯甲腈上游产品

2-氟苯甲腈下游产品

2-氟苯甲腈海关

[ 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%

2-氟苯甲腈文献

High-sensitivity elemental ionization for quantitative detection of halogenated compounds.

Analyst 140 , 8177-85, (2015)

The rising importance of organohalogens in environmental, pharmaceutical, and biological applications has drawn attention to analysis of these compounds in recent years. Elemental mass spectrometry (M...

Studies on the synthetic compatibility of aryloxime linkers in the solid-phase synthesis of 3-aminobenzisoxazoles.

J. Org. Chem. 65(10) , 2924-32, (2000)

Further exploration of the scope of our solid-phase method for the synthesis of 3-aminobenzisoxazoles (using the Kaiser oxime resin 1) is described. The effects of base, leaving group, and solvent on ...

Aminoborohydrides. 12. Novel tandem S(N)Ar amination-reduction reactions of 2-halobenzonitriles with lithium N,N-dialkylaminoborohydrides.

J. Org. Chem. 66(6) , 1999-2004, (2001)

A novel tandem amination-reduction reaction has been developed in which 2-(N,N-dialkylamino)benzylamines are generated from 2-halobenzonitriles and lithium N,N-dialkylaminoborohydride (LAB) reagents. ...

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