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3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is a chemical compound characterized by the molecular formula C18H19BN2O3. It is distinguished by the presence of a boronic acid group, which endows it with unique reactivity in organic synthesis. 3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is particularly notable for its role in the Suzuki-Miyaura cross-coupling reaction, a widely used method for the formation of carbon-carbon bonds. Its versatility in chemical reactions and potential biological activities make it a significant entity in the fields of pharmaceuticals, agrochemicals, and materials science, as well as in the development of new drug candidates.

957060-98-9

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957060-98-9 Usage

Uses

Used in Organic Synthesis:
3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is used as a reagent in organic synthesis for its ability to form carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction. This reaction is crucial for the creation of complex organic molecules, which are essential in the synthesis of pharmaceuticals, agrochemicals, and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is utilized as a key intermediate in the synthesis of various drug molecules. Its participation in cross-coupling reactions allows for the construction of diverse molecular frameworks that can exhibit a range of therapeutic effects.
Used in Agrochemical Industry:
3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is also used in the agrochemical industry as a component in the synthesis of pesticides and other agrochemical products. Its ability to form stable carbon-carbon bonds contributes to the development of effective and durable agrochemicals.
Used in Materials Science:
In materials science, 3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is employed in the development of new materials with specific properties. Its role in cross-coupling reactions can lead to the creation of materials with tailored characteristics for various applications, such as in electronics or advanced materials research.
Used in Drug Development:
3-(2,4-Dimethylphenylcarbamoyl)phenylboronic acid is studied for its potential biological activities and is considered in the development of new drug candidates. Its unique structure and reactivity may contribute to the discovery of novel therapeutic agents with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 957060-98-9 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 957060-98:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*0)+(2*9)+(1*8)=199
199 % 10 = 9
So 957060-98-9 is a valid CAS Registry Number.

957060-98-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H53293)  3-(2,4-Dimethylphenylcarbamoyl)benzeneboronic acid, 98%   

  • 957060-98-9

  • 250mg

  • 552.0CNY

  • Detail
  • Alfa Aesar

  • (H53293)  3-(2,4-Dimethylphenylcarbamoyl)benzeneboronic acid, 98%   

  • 957060-98-9

  • 1g

  • 1764.0CNY

  • Detail

957060-98-9SDS

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-[(2,4-dimethylphenyl)carbamoyl]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names OR2097

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:957060-98-9 SDS

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