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7697-25-8 Usage

General Description

2-Chloro-4-methylbenzoic acid is a chemical compound with the molecular formula C8H7ClO2. It is a derivative of benzoic acid with a chlorine atom and a methyl group attached to the benzene ring. 2-CHLORO-4-METHYLBENZOIC ACID is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of dyes and pigments. 2-Chloro-4-methylbenzoic acid is a white crystalline solid with a slightly aromatic odor. It is soluble in organic solvents such as ethanol and acetone, but only slightly soluble in water. 2-CHLORO-4-METHYLBENZOIC ACID should be handled and stored with appropriate safety precautions due to its potential to cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 7697-25-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7697-25:
138 % 10 = 8
So 7697-25-8 is a valid CAS Registry Number.



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017


1.1 GHS Product identifier

Product name 2-Chloro-4-Methylbenzoic Acid

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-methylbenzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7697-25-8 SDS

7697-25-8Relevant articles and documents

Benzohydroxamic acids as potent and selective anti-HCV agents

Kozlov, Maxim V.,Kleymenova, Alla A.,Romanova, Lyudmila I.,Konduktorov, Konstantin A.,Smirnova, Olga A.,Prasolov, Vladimir S.,Kochetkov, Sergey N.

supporting information, p. 5936 - 5940 (2013/10/22)

A diverse collection of 40 derivatives of benzohydroxamic acid (BHAs) of various structural groups were synthesized and tested against hepatitis C virus (HCV) in full-genome replicon assay. Some of these compounds demonstrated an exceptional activity, suppressing viral replication at sub-micromolar concentrations. The compounds were inactive against key viral enzymes NS3, and NS5B in vitro assays, suggesting host cell inhibition target(s). The testing results were consistent with metal coordination by the BHAs hydroxamic group in complex with a target(s). Remarkably, this class of compounds did not suppress poliomyelitis virus (PV) propagation in RD cells indicating a specific antiviral activity of BHAs against HCV.

Regiospecific chlorination of xylenes using K-10 montmorrillonite clay

Thirumamagal,Narayanasamy, Sureshbabu,Venkatesan

experimental part, p. 2820 - 2825 (2009/05/07)

Regiospecific chlorination of xylenes has been developed by employing NCS as a reagent and K-10 montmorrillonite clay as a solid support. Copyright Taylor & Francis Group, LLC.

Substituted alkylidene imidazoles


, (2008/06/13)

This disclosure relates to a class of novel substituted alkylidene imidazole derivatives and pharmaceutically acceptable salts thereof. The disclosure further describes pharmaceutical compositions containing such compounds and to the use of such compounds

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