(2-chlorophenyl)hydrazine hydrochloride
Names
[ CAS No. ]:
41052-75-9
[ Name ]:
(2-chlorophenyl)hydrazine hydrochloride
[Synonym ]:
O-CHLOROPHENYLHYDRAZINE HYDROCHLORIDE
O-ChlOrOphenyl HydrOazine HydrOchlOride
2-Chlorophenyl)hydrazine hydrochloride
Hydrazine, (2-chlorophenyl)-, hydrochloride (1:1)
N-CHLOROSUCCINIMIDE
1-(2-chlorophenyl)hydrazine hydrochloride
Hydrazine, (2-chlorophenyl)-, monohydrochloride
2-CHLOROPHENYLHYDRAZINE HCL
(2-Chlorophenyl)hydrazine hydrochloride (1:1)
EINECS 255-194-1
(2-chlorophenyl)hydrazine hydrochloride
o-chlorophenylhydrazine*HCl
MFCD00012928
2-CHLORO PHENYL HYDRAZXINE HYDROCHLORIDE
1-(2-chlorophenyl)hydrazine
2-Chloro Phenyl Hydrazine Hydrochloride
Chemical & Physical Properties
[ Density]:
1.32g/cm3
[ Boiling Point ]:
252.1ºC at 760 mmHg
[ Melting Point ]:
200-203 °C (dec.)(lit.)
[ Molecular Formula ]:
C6H8Cl2N2
[ Molecular Weight ]:
179.047
[ Flash Point ]:
106.2ºC
[ Exact Mass ]:
178.006454
[ PSA ]:
38.05000
[ LogP ]:
3.20090
[ Water Solubility ]:
SOLUBLE
MSDS
Safety Information
[ Symbol ]:
GHS07, GHS09
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302 + H312 + H332-H400
[ Precautionary Statements ]:
P273-P280
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xn:Harmful;N:Dangerousfortheenvironment;
[ Risk Phrases ]:
R20/21/22;R50/53
[ Safety Phrases ]:
S36/37-S61-S36/37/39-S29-S26-S22
[ RIDADR ]:
UN 3077 9/PG 3
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
6.1(b)
[ HS Code ]:
29280090
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
Antimicrob. Agents Chemother. 45(12) , 3387-92, (2001)
The fluoroquinolones (FQ) are used in the treatment of Mycobacterium tuberculosis, but the development of resistance could limit their effectiveness. FQ resistance (FQ(R)) is a multistep process invol...
Trisubstituted and tetrasubstituted pyrazolines as a novel class of cell-growth inhibitors in tumor cells with wild type p53Bioorg. Med. Chem. 21(23) , 7343-56, (2013)
Designing the new pyrazoline derivatives based on the structure of the reference compounds I–V.