115382-35-9 Usage
Uses
Used in Pharmaceutical Synthesis:
4-carboxy-3-chloroacetophenone is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, contributing to the development of new medications.
Used in Agrochemical Production:
4-carboxy-3-chloroacetophenone is also utilized as an intermediate in the production of agrochemicals, where it can be used to create substances that help protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
Due to its versatile chemical structure, 4-carboxy-3-chloroacetophenone is used as a building block in organic synthesis, allowing for the creation of a wide range of organic compounds for various applications.
Used in Antibacterial and Antifungal Drug Development:
4-carboxy-3-chloroacetophenone is used as a potential candidate for the development of new drugs to combat microbial infections, given its reported antibacterial and antifungal properties. This makes it a valuable component in the search for effective treatments against resistant strains of bacteria and fungi.
Check Digit Verification of cas no
The CAS Registry Mumber 115382-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,8 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115382-35:
(8*1)+(7*1)+(6*5)+(5*3)+(4*8)+(3*2)+(2*3)+(1*5)=109
109 % 10 = 9
So 115382-35-9 is a valid CAS Registry Number.
115382-35-9Relevant articles and documents
Electrosynthesis of aryl-carboxylic acids from chlorobenzene derivatives and carbon dioxide
Heintz, Monique,Sock, Oumar,Saboureau, Christophe,Perichon, Jacques,Troupel, Michel
, p. 1631 - 1636 (2007/10/02)
The electrocarboxylation of a large variety of chlorobenzenic compounds is achieved in N,N-dimethylformamide by constant current electrolysis between a stainless steel cathode and a sacrificial magnesium anode in a diaphragmless cell. Substituted benzoic acids are obtained in high yield in simle conditions thus avoiding the usual preparation of organometallic intermediates.
