7697-25-8 Usage
Description
2-Chloro-4-methylbenzoic acid, a derivative of benzoic acid, is a chemical compound characterized by the molecular formula C8H7ClO2. It features a chlorine atom and a methyl group attached to the benzene ring, resulting in a white crystalline solid with a slightly aromatic odor. 2-CHLORO-4-METHYLBENZOIC ACID is soluble in organic solvents such as ethanol and acetone, but only slightly soluble in water. Due to its potential to cause skin and eye irritation, appropriate safety precautions should be taken during handling and storage.
Uses
Used in Pharmaceutical Industry:
2-Chloro-4-methylbenzoic acid serves as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-chloro-4-methylbenzoic acid is utilized as an intermediate in the production of agrochemicals. Its involvement in the synthesis of these chemicals aids in the development of effective solutions for agricultural applications, such as pest control and crop protection.
Used in Dye and Pigment Production:
2-Chloro-4-methylbenzoic acid is also employed in the manufacturing process of dyes and pigments. Its chemical properties make it suitable for creating a wide range of colors and shades, which are used across various industries, including textiles, plastics, and printing inks.
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:
(6*7)+(5*6)+(4*9)+(3*7)+(2*2)+(1*5)=138
138 % 10 = 8
So 7697-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)
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
