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3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid is a chemical compound with the molecular formula C13H12BClNO3. It is a boronic acid derivative used in organic synthesis and medicinal chemistry. 3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid contains a boronic acid group, which has been widely utilized in the development of biologically active compounds and pharmaceutical agents. The presence of the chloro and methyl groups in the phenyl ring make 3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid important for structure-activity relationship studies in drug design and discovery. Additionally, the carbamoyl group in the molecule may contribute to its potential biological activity, such as enzyme inhibition or receptor binding. Overall, 3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid is a valuable chemical building block for the development of new pharmaceuticals and biologically active compounds.

957060-97-8

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957060-97-8 Usage

Uses

Used in Organic Synthesis:
3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid is used as a chemical building block for the synthesis of complex organic molecules. Its boronic acid group allows for versatile reactions, such as Suzuki-Miyaura cross-coupling, which is a powerful method for the formation of carbon-carbon bonds.
Used in Medicinal Chemistry:
3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid is used as a starting material or intermediate in the development of new pharmaceuticals. Its structural features, including the chloro and methyl groups, make it a valuable compound for structure-activity relationship studies, which are essential for optimizing the potency and selectivity of drug candidates.
Used in Drug Design and Discovery:
3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid is used as a key component in the design and discovery of new drugs. The carbamoyl group in the molecule may contribute to its potential biological activity, such as enzyme inhibition or receptor binding, making it a promising candidate for the development of novel therapeutic agents.
Used in Biologically Active Compounds:
3-(2-Chloro-4-methylphenylcarbamoyl)phenylboronic acid is used as a precursor in the synthesis of biologically active compounds. Its unique structural features and potential for chemical modification make it an attractive building block for the creation of new molecules with potential applications in various fields, such as agriculture, materials science, and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 957060-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 957060-97:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*0)+(2*9)+(1*7)=198
198 % 10 = 8
So 957060-97-8 is a valid CAS Registry Number.

957060-97-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H52706)  3-(2-Chloro-4-methylphenylcarbamoyl)benzeneboronic acid, 98%   

  • 957060-97-8

  • 250mg

  • 552.0CNY

  • Detail
  • Alfa Aesar

  • (H52706)  3-(2-Chloro-4-methylphenylcarbamoyl)benzeneboronic acid, 98%   

  • 957060-97-8

  • 1g

  • 1764.0CNY

  • Detail

957060-97-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[(2-chloro-4-methylphenyl)carbamoyl]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names OR7420

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:957060-97-8 SDS

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