161957-60-4 Usage
Description
1-(2-bromo-3-chlorophenyl)ethanone is a chemical compound characterized by the molecular formula C8H6BrClO. It is a ketone derivative featuring a bromo-chloro-phenyl group attached to the ethanone molecule, which endows it with unique chemical properties and reactivity.
Uses
Used in Pharmaceutical Synthesis:
1-(2-bromo-3-chlorophenyl)ethanone serves as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its specific structural features make it a valuable component in the creation of complex organic molecules with potential medicinal applications.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-bromo-3-chlorophenyl)ethanone is utilized as an intermediate for the synthesis of various agrochemicals, including pesticides and herbicides. Its role in these processes is crucial for enhancing crop protection and agricultural productivity.
Used in Organic Chemistry Research:
1-(2-bromo-3-chlorophenyl)ethanone holds potential as a building block in organic chemistry, facilitating the preparation of a wide array of complex molecules. Its unique properties and reactivity are of significant interest to researchers and chemists engaged in organic synthesis and the innovation of novel chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 161957-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 161957-60:
(8*1)+(7*6)+(6*1)+(5*9)+(4*5)+(3*7)+(2*6)+(1*0)=154
154 % 10 = 4
So 161957-60-4 is a valid CAS Registry Number.
161957-60-4Relevant articles and documents
Lithiations directed by carboxylic acid, fluorine and chlorine: The regioselective synthesis of polysubstituted benzoic acids and acetophenones
Moyroud, Joel,Guesnet, Jean-Luc,Bennetau, Bernard,Mortier, Jacques
, p. 133 - 141 (2007/10/03)
Lithiation/electrophilic quenching of ortho-lithiated benzoates allows the totally regiocontrolled synthesis of a wide range of 2,3-, 2,3,4-, and 2,3,4,5-polysubstituted benzoic acids and related acetophenones. Elsevier,.
