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75822-51-4

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75822-51-4 Usage

General Description

2-(4-Bromo-benzoyl)-1H-indole-3-carboxylic acid is a chemical compound with the molecular formula C16H10BrNO3. It is a derivative of indole-3-carboxylic acid and contains a bromo-benzoyl group. 2-(4-BROMO-BENZOYL)-1H-INDOLE-3-CARBOXYLIC ACID has been used in research as a building block for the synthesis of various organic molecules and pharmaceuticals. Its chemical properties make it a valuable compound for the development of new drugs and materials. It is important to handle this compound with care and follow proper safety protocols when working with it in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 75822-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,2 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75822-51:
(7*7)+(6*5)+(5*8)+(4*2)+(3*2)+(2*5)+(1*1)=144
144 % 10 = 4
So 75822-51-4 is a valid CAS Registry Number.

75822-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromobenzoyl)-1H-indole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-(2-CHLOROPHENYL)-1,2-DIHYDRO-5-PHENYL-3H-1,2,4-TRIAZOL-3-ONE

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:75822-51-4 SDS

75822-51-4Relevant articles and documents

Syntheses of 1-alkyl-2-acylindoles, 1-alkyl-2-acylindole-3-carboxylic acids, and their esters, in superbasic media

Rekhter

, p. 408 - 417 (2007/10/03)

2-Acylindoles and 2-acylindole-3-carboxylic acids are readily alkylated at the nitrogen atom by haloalkanes in a superbasic medium (DMSO + NaOH). For the carboxylic acids, this reaction may proceed either entirely at the nitrogen atom, or at both the the

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