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2-溴-4-氟苯胺

2-溴-4-氟苯胺名称

[ CAS 号 ]:
1003-98-1

[ 中文名 ]:
2-溴-4-氟苯胺

[ 英文名 ]:
2-Bromo-4-fluoroaniline

[英文别名 ]:

2-brom-4-fluoranilin
MFCD00042462
Benzenamine, 2-bromo-4-fluoro-
2-Bromo-4-fluoroaniline
2-bromo-4-fluorophenylamine
ZR DF BE
4-fluoro-2-bromo-aniline
2-bromo-4-fluoro-aniline
4-Bromo-4-fluoroaniline
2-Bromo-4-fluorobenzenamine

2-溴-4-氟苯胺物理化学性质

[ 密度 ]:
1.7±0.1 g/cm3

[ 沸点 ]:
221.0±0.0 °C at 760 mmHg

[ 熔点 ]:
41

[ 分子式 ]:
C₆H₅BrFN

[ 分子量 ]:
190.013

[ 闪点 ]:
104.4±0.0 °C

[ 精确质量 ]:
188.958939

[ PSA ]:
26.02000

[ LogP ]:
2.40

[ 外观性状 ]:
透明黄色-棕色液体

[ 蒸汽压 ]:
0.1±0.4 mmHg at 25°C

[ 折射率 ]:
1.597

[ 储存条件 ]:
室温

2-溴-4-氟苯胺MSDS

2-溴-4-氟苯胺安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

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

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S37/39

[ 危险品运输编码 ]:
UN2810

[ WGK德国 ]:
3

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1

[ 海关编码 ]:
2921420090

2-溴-4-氟苯胺合成路线

2-溴-4-氟苯胺上下游产品

2-溴-4-氟苯胺上游产品

2-溴-4-氟苯胺下游产品

2-溴-4-氟苯胺海关

[ 海关编码 ]: 2921420090

[ 中文概述 ]:
2921420090 其他苯胺衍生物及其盐. 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:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

2-溴-4-氟苯胺文献

Synthesis, reactions, and biological activities of some new thieno[3,2-c]quinoline and pyrrolo[3,2-c]quinoline derivatives.

Arch. Pharm. (Weinheim) 347(2) , 142-52, (2014)

2-Bromo-4-fluoroaniline (1) was condensed with ethyl 2-cyano-3-ethoxyacrylate (2) in ethanol to afford 3, which upon refluxing in paraffin oil at 250°C gave 8-bromo-3-cyano-6-fluoroquinoline-4(1H)-one...

Synthesis of fluorescent tetracyclic lactams by a “one pot” three steps palladium-catalyzed borylation, Suzuki coupling (BSC) and lactamization: DNA and polynucleotides binding studies. Queiroz M-JRP, et al.

J. Photochem. Photobiol. A: Chem. 190(1) , 45-52, (2007)

An efficient synthesis of enantiomerically pure aromatic-fused N-containing heterocycles from common chiral aziridines. Chan Kim J, et al.

Tetrahedron 66(40) , 8108-14, (2010)

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