4-Chlorophenylhydrazine hydrochloride

Names

[ Name ]:
4-Chlorophenylhydrazine hydrochloride

[Synonym ]:
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
EINECS 214-030-9
4-Chlorophenylhydrazine monohydrochloride
4-Cl-phenylhydrazine hydrochloride
P-CHLOROPHENYLHYDRAZINE HCL
Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1)
P-Chlorophenyluhydrazinehydrochloride

Chemical & Physical Properties

[ Density]:
1.32g/cm3

[ Boiling Point ]:
265.3ºC at 760mmHg

[ Melting Point ]:
216 °C (dec.)(lit.)

[ Molecular Formula ]:
C₆H₈Cl₂N₂

[ Molecular Weight ]:
179.047

[ Flash Point ]:
114.2ºC

[ Exact Mass ]:
178.006454

[ PSA ]:
38.05000

[ LogP ]:
3.20090

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H332

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S36/37

[ RIDADR ]:
2811

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1(b)

[ HS Code ]:
29280090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2928000090

[ 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%

Articles

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...