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(4-BROMOPHENYL)SUCCINIC ACID, with the molecular formula C10H9BrO4, is a chemical compound derived from succinic acid, featuring a bromine atom substitution in the phenyl group. This modification endows it with unique properties and potential applications in various fields, particularly in medicine and pharmaceuticals, as well as in organic chemistry.

71471-40-4

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71471-40-4 Usage

Uses

Used in Pharmaceutical Industry:
(4-BROMOPHENYL)SUCCINIC ACID is used as a precursor in the synthesis of bioactive molecules for its ability to be a building block in creating new compounds with potential therapeutic effects.
Used in Organic Chemistry:
(4-BROMOPHENYL)SUCCINIC ACID is used in cross-coupling reactions due to its bromine substituent, which allows for the formation of new carbon-carbon bonds, contributing to the synthesis of complex organic molecules.
Used in Research and Development:
(4-BROMOPHENYL)SUCCINIC ACID is utilized in biological studies and property exploration for its potential biological activities, which may lead to the discovery of new applications in various scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 71471-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,7 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71471-40:
(7*7)+(6*1)+(5*4)+(4*7)+(3*1)+(2*4)+(1*0)=114
114 % 10 = 4
So 71471-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H9BrO4/c11-7-3-1-6(2-4-7)8(10(14)15)5-9(12)13/h1-4,8H,5H2,(H,12,13)(H,14,15)

71471-40-4SDS

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 (4-BROMOPHENYL)SUCCINIC ACID

1.2 Other means of identification

Product number -
Other names 2-(4-Bromophenyl)-butanedioic acid

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:71471-40-4 SDS

71471-40-4Downstream Products

71471-40-4Relevant academic research and scientific papers

Simple synthesis of arylsuccinic acids

Makosza,Marcinowicz

, p. 1311 - 1312 (2007/10/03)

Alkylation of arylacetonitriles with potassium chloroacetate proceeds selectively leading to 3-cyano-3-arylpropionic acids, which are directly hydrolyzed to arylsuccinic acids.

Reductive Arylation of Maleic and Fumaric Acid Derivatives by Arenediazonium and Titanium(III) Salts

Citterio, Attilio,Cominelli, Alberto,Bonavoglia, Francesco

, p. 308 - 309 (2007/10/02)

The titanium(III)-induced decomposition of substituted benzenediazonium salts in the presence of maleic and fumaric acids, alkyl esters, amides, and nitriles gives the corresponding arylsuccinic acid derivatives.

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