21900-24-3 Usage
General Description
4-Chloro-3-methylbenzoyl chloride is a chemical compound with the molecular formula C8H6ClO and a molar mass of 168.58 g/mol. It is a derivative of benzoyl chloride and contains a chlorine atom and a methyl group attached to the benzene ring. 4-Chloro-3-methylbenzoyl chloride is commonly used in organic synthesis as a reagent for the preparation of various derivatives and pharmaceutical intermediates. It is a highly reactive compound that can undergo various chemical reactions, including nucleophilic substitution and addition reactions. Due to its reactivity and versatility, 4-Chloro-3-methylbenzoyl chloride is an important building block in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. However, it should be handled and stored with caution due to its corrosive and toxic nature.
Check Digit Verification of cas no
The CAS Registry Mumber 21900-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,0 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21900-24:
(7*2)+(6*1)+(5*9)+(4*0)+(3*0)+(2*2)+(1*4)=73
73 % 10 = 3
So 21900-24-3 is a valid CAS Registry Number.
21900-24-3Relevant articles and documents
Palladium-Catalyzed C-H Trifluoroethoxylation of N-Sulfonylbenzamides
Yang, Long,Li, Shangda,Cai, Lei,Ding, Yongzheng,Fu, Lei,Cai, Zhihua,Ji, Huafang,Li, Gang
supporting information, p. 2746 - 2749 (2017/05/24)
The trifluoroethyl aryl ethers are important motifs in drug molecules. However, a report devoted specifically to the study of transition-metal-catalyzed C-H trifluoroethoxylation has not been reported to date. A protocol of Pd(II)-catalyzed o-C-H trifluor
Biaryl Benzylamine Derivatives
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Page/Page column 22, (2010/07/08)
The present invention relates to biaryl-benzylamine compounds, to processes for their production, to their use as pharmaceuticals and to pharmaceutical compositions comprising them.
Viral Polymerase Inhibitors
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Page/Page column 50, (2008/06/13)
Compounds of formula I: wherein X, R2, R3, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.