229342-86-3 Usage
General Description
3-Chloro-4-methyl-2-thiophenecarboxylic acid is a chemical compound with the molecular formula C7H5ClO2S. It is a derivative of thiophene and functions as a carboxylic acid. 3-CHLORO-4-METHYL-2-THIOPHENECARBOXYLIC ACID is commonly used in the synthesis of other pharmaceutical and agricultural chemicals due to its functional group, which allows for further modifications. It is also known for its potential antibacterial and antifungal properties, making it a valuable intermediate in the production of medications and agrochemicals. Additionally, it is used in research and development of new compounds with potential biological activity. Overall, 3-Chloro-4-methyl-2-thiophenecarboxylic acid is an important building block in the production of various useful compounds with applications in medicine and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 229342-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,3,4 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 229342-86:
(8*2)+(7*2)+(6*9)+(5*3)+(4*4)+(3*2)+(2*8)+(1*6)=143
143 % 10 = 3
So 229342-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClO2S/c1-3-2-10-5(4(3)7)6(8)9/h2H,1H3,(H,8,9)
229342-86-3Relevant articles and documents
Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa
Kochanny, Monica J.,Adler, Marc,Ewing, Janice,Griedel, Brian D.,Ho, Elena,Karanjawala, Rushad,Lee, Wheeseong,Lentz, Dao,Liang, Amy M.,Morrissey, Michael M.,Phillips, Gary B.,Post, Joseph,Sacchi, Karna L.,Sakata, Steven T.,Subramanyam, Babu,Vergona, Ron,Walters, Janette,White, Kathy A.,Whitlow, Marc,Ye, Bin,Zhao, Zuchun,Shaw, Kenneth J.
, p. 2127 - 2146 (2008/02/01)
A series of thiophene-containing non-amidine factor Xa inhibitors is described. Simple methyl-substituted thiophene analogs were relatively weak inhibitors. However, introduction of hydrophilic substituents at C-4 or C-5 of the thiophene afforded inhibito
C:Corrosive;
