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4-(4-BROMOPHENYLCARBAMOYL)PHENYLBORONIC ACID is a boronic acid derivative that features a boronic acid functional group and a carbamoylphenyl group. It is widely recognized for its role as a building block in the synthesis of pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity.
Used in Pharmaceutical Industry:
4-(4-BROMOPHENYLCARBAMOYL)PHENYLBORONIC ACID is used as a key intermediate for the synthesis of complex organic molecules, particularly in the development of new drugs. Its specific structure allows for the introduction of the boronic acid moiety into organic molecules, which is crucial for the creation of pharmaceutical compounds with desired therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(4-BROMOPHENYLCARBAMOYL)PHENYLBORONIC ACID is utilized as a precursor in the synthesis of various agrochemicals. Its ability to be incorporated into organic molecules makes it a valuable component in the development of pesticides, herbicides, and other agricultural chemicals that are designed to protect crops and enhance agricultural productivity.
Used in Materials Science:
4-(4-BROMOPHENYLCARBAMOYL)PHENYLBORONIC ACID is employed as a building block in the synthesis of advanced materials with specific properties. Its reactivity and the presence of the bromine substituent on the phenyl group enable the creation of materials with tailored characteristics for applications in various industries, such as electronics, coatings, and polymers.
Used in Organic Chemistry Research:
As a versatile boronic acid derivative, 4-(4-BROMOPHENYLCARBAMOYL)PHENYLBORONIC ACID is used in Suzuki-Miyaura coupling reactions and other organic transformations. Researchers leverage its reactivity to construct complex organic molecules and explore new synthetic pathways, contributing to the advancement of organic chemistry and the discovery of novel compounds with potential applications in various fields.

874287-99-7

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874287-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874287-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 874287-99:
(8*8)+(7*7)+(6*4)+(5*2)+(4*8)+(3*7)+(2*9)+(1*9)=227
227 % 10 = 7
So 874287-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H11BBrNO3/c15-11-5-7-12(8-6-11)16-13(17)9-1-3-10(4-2-9)14(18)19/h1-8,18-19H,(H,16,17)

874287-99-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H53174)  4-(4-Bromophenylcarbamoyl)benzeneboronic acid, 98%   

  • 874287-99-7

  • 250mg

  • 552.0CNY

  • Detail

  • Alfa Aesar

  • (H53174)  4-(4-Bromophenylcarbamoyl)benzeneboronic acid, 98%   

  • 874287-99-7

  • 1g

  • 1764.0CNY

  • Detail

874287-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[(4-bromophenyl)carbamoyl]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names OR3787

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:874287-99-7 SDS

874287-99-7Downstream Products

874287-99-7Relevant academic research and scientific papers

From arylureas to biarylamides to aminoquinazolines: Discovery of a novel, potent TRPV1 antagonist

Zheng, Xiaozhang,Hodgetts, Kevin J.,Brielmann, Harry,Hutchison, Alan,Burkamp, Frank,Brian Jones,Blurton, Peter,Clarkson, Robert,Chandrasekhar, Jayaraman,Bakthavatchalam, Rajagopal,De Lombaert, Stephane,Crandall, Marci,Cortright, Daniel,Blum, Charles A.

, p. 5217 - 5221 (2007/10/03)

Bioisosteric replacement of piperazine with an aryl ring in lead VR1 antagonist 1 led to the biarylamide series. The development of B-ring SAR led to the conformationally constrained analog 70. The resulting aminoquinazoline 70 represents a novel VR1 anta

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