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2-amino-4-chloro-5-(methylsulfonyl)Benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51521-76-7

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51521-76-7 Usage

Chemical compound

2-amino-4-chloro-5-(methylsulfonyl)Benzoic acid

Check Digit Verification of cas no

The CAS Registry Mumber 51521-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,2 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51521-76:
(7*5)+(6*1)+(5*5)+(4*2)+(3*1)+(2*7)+(1*6)=97
97 % 10 = 7
So 51521-76-7 is a valid CAS Registry Number.

51521-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4-chloro-5-methylsulphonylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Amino-4-chloro-5-methanesulfonyl-benzoic 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:51521-76-7 SDS

51521-76-7Relevant academic research and scientific papers

Ortho-substituted benzoil acid derivatives

-

, (2008/06/13)

Ortho-substituted benzoic acid derivatives of the formula I STR1 in which R1, R2 and R3 have the given meanings, and Q is guanidyl, and also their physiologically harmless salts, exhibit antiarrhythmic properties and act a

3-Amino-5-sulfonylbenzoic acids

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, (2008/06/13)

Aminobenzoic acids of the structure SPC1 Having saluretic and diuretic properties are described. These compounds are prepared by amidation of a 2-halo analog thereof or by alkylation of the free amino compound.

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