Skip to Content
MilliporeSigma
All Photos(2)

Documents

109509

Sigma-Aldrich

2-Chlorophenylhydrazine hydrochloride

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ClC6H4NHNH2·HCl
CAS Number:
Molecular Weight:
179.05
Beilstein/REAXYS Number:
3699381
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

mp

200-203 °C (dec.) (lit.)

SMILES string

Cl.NNc1ccccc1Cl

InChI

1S/C6H7ClN2.ClH/c7-5-3-1-2-4-6(5)9-8;/h1-4,9H,8H2;1H

InChI key

ADODRSVGNHNKAT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

2-Chlorophenylhydrazine hydrochloride was used to study intrinsic resistance of Mycobacterium smegmatis to fluoroquinolones, used for treatment of Mycobacterium tuberculosis. It may be used in pyrazoline synthesis.

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mohammad Abdel-Halim et al.
Bioorganic & medicinal chemistry, 21(23), 7343-7356 (2013-10-22)
Derivatives with scaffolds of 1,3,5-tri-substituted pyrazoline and 1,3,4,5-tetra-substituted pyrazoline were synthesized and tested for their inhibitory effects versus the p53(+/+) HCT116 and p53(-/-) H1299 human tumor cell lines. Several compounds were active against the two cell lines displaying IC50 values
C Montero et al.
Antimicrobial agents and chemotherapy, 45(12), 3387-3392 (2001-11-16)
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 involving alterations in the type II topoisomerases and perhaps in the regulation of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service