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57688-24-1

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57688-24-1 Usage

General Description

RARECHEM AL BE 0950 is a chemical compound with the molecular formula C7H8BrNO2S. It is a rare and uncommon chemical that is not widely known or used in industrial or commercial applications. RARECHEM AL BE 0950 is classified as a phenol derivative and contains a bromine atom, a nitro group, and a sulfur atom in its structure. It is likely used in specialized research or laboratory settings, but specific information about its properties, uses, and potential hazards is limited. Overall, RARECHEM AL BE 0950 is a relatively obscure chemical compound with limited available information.

Check Digit Verification of cas no

The CAS Registry Mumber 57688-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,8 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57688-24:
(7*5)+(6*7)+(5*6)+(4*8)+(3*8)+(2*2)+(1*4)=171
171 % 10 = 1
So 57688-24-1 is a valid CAS Registry Number.

57688-24-1SDS

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 3-bromo-2-hydroxy-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 3-bromo-2-hydroxy-5-nitrobenzenecarboxylic 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:57688-24-1 SDS

57688-24-1Relevant articles and documents

Rearrangements during nitrosodecarboxylation of isomeric dibromohydroxybenzoic acids

Shishkin,Fadin

experimental part, p. 688 - 692 (2009/04/07)

The reaction of 3,5-dibromo-4-hydroxybenzoic acid, its sodium salt, and also sodium 3,5-dibromo-2-hydroxybenzoate with NaNO2 in a glacial acetic acid at room temperature led to the formation of a mixture of dibromonitrophenol resulting from nitrosodecarboxylation accompanied by a rearrangement processes and followed by oxidation of the arising nitrosophenols.

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