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对氯苯肼盐酸盐

对氯苯肼盐酸盐用途

【用途一】
用作有机合成中间体
【用途二】
1073-70-7（对氯苯肼盐酸盐）是染料及药物的重要中间体，也是一种有机合成的原料。
【用途三】
应用于染料和医药中间体。

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对氯苯肼盐酸盐名称

[ CAS 号 ]:
1073-70-7

[ 中文名 ]:
对氯苯肼盐酸盐

[ 英文名 ]:
4-Chlorophenylhydrazine hydrochloride

[中文别名 ]:

[英文别名 ]:

Hydrazine, (4-chlorophenyl)-, monohydrochloride
p-Chlorophenylhydrazine monohydrochloride
4-CHLORO PHENYL HYDRAZXINE HYDROCHLORIDE
(4-Chlorophenyl)hydrazine hydrochloride (1:1)
4-Chlorophenylhydrazine hydrochloride
1-(4-chlorophenyl)hydrazine hydrochloride
Hydrazine, (p-chlorophenyl)-, monohydrochloride
(4-chlorophenyl)hydrazine hydrochloride
4-CHLOROPHENYLHYDRAZINE HCL
MFCD00012943

对氯苯肼盐酸盐物理化学性质

[ 密度 ]:
1.32g/cm3

[ 沸点 ]:
265.3ºC at 760mmHg

[ 熔点 ]:
216 °C (dec.)(lit.)

[ 分子式 ]:
C₆H₈Cl₂N₂

[ 分子量 ]:
179.047

[ 闪点 ]:
114.2ºC

[ 精确质量 ]:
178.006454

[ PSA ]:
38.05000

[ LogP ]:
3.20090

[ 外观性状 ]:
白色至粉红色粉末

[ 储存条件 ]:
存放于惰性气体之中;避免空气,湿气 (吸湿)

[ 水溶解性 ]:
可溶于：甲醇

对氯苯肼盐酸盐MSDS

对氯苯肼盐酸盐安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H302-H312-H332

[ 警示性声明 ]:
P280

[ 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

[ 安全声明 (欧洲) ]:
S36/37

[ 危险品运输编码 ]:
2811

[ WGK德国 ]:
3

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1(b)

[ 海关编码 ]:
29280090

对氯苯肼盐酸盐合成路线

对氯苯肼盐酸盐上下游产品

对氯苯肼盐酸盐上游产品

对氯苯肼盐酸盐下游产品

对氯苯肼盐酸盐海关

[ 海关编码 ]: 2928000090

[ 中文概述 ]:
2928000090 其他肼（联氨）及胲（羟胺）的有机衍生物。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:6.5%。普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

对氯苯肼盐酸盐文献

Reaction of 3-acetonyl-5-cyano-1,2,4-thiadiazole with phenylhydrazine hydrochlorides: indolization and phenylpyrazolation.

Chem. Pharm. Bull. 48(1) , 160-2, (2000)

Treatment of 3-acetonyl-5-cyano-1,2,4-thiadiazole (1) with 4-methyl or 4-methoxyphenylhydrazine hydrochloride provided 5-cyano-3-(2,5-dimethylindol-3-yl)-1,2,4-thiadiazole (2) or 5-cyano-3-(5-methoxy-...

Reactions of prostaglandin H synthase with monosubstituted hydrazines and diazenes. Formation of iron(II)-diazene and iron(III)-sigma-alkyl or iron(III)-sigma-aryl complexes.

Eur. J. Biochem. 226(2) , 445-57, (1994)

The reaction of p-chlorophenylhydrazine with prostaglandin H synthase (PGHS) Fe(III) under aerobic conditions leads to a partial destruction of the heme and to a new complex absorbing at 436 nm. This ...

Design, synthesis and biological evaluation of indane-2-arylhydrazinylmethylene-1,3-diones and indol-2-aryldiazenylmethylene-3-ones as beta-amyloid aggregation inhibitors.

Eur. J. Med. Chem. 45(4) , 1359-66, (2010)

Biological screening of (hetero)aromatic compounds allowed the identification of some novel inhibitors of Abeta(1-40) aggregation, bearing indane and indole rings as common scaffolds. Molecular decora...

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