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120267-05-2

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120267-05-2 Usage

General Description

1,2,4-Triazolo[4,3-a]pyridine-3-sulfonamide(9CI) is a chemical compound with the molecular formula C7H6N4O2S. It is a pyridine derivative with a triazolopyridine and sulfonamide moieties. This chemical has potential applications in pharmaceutical research and drug development due to its structural features and biological activity. It may exhibit pharmacological properties such as antimicrobial, antifungal, or antiproliferative effects. However, further research is required to fully understand and exploit the potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 120267-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,6 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120267-05:
(8*1)+(7*2)+(6*0)+(5*2)+(4*6)+(3*7)+(2*0)+(1*5)=82
82 % 10 = 2
So 120267-05-2 is a valid CAS Registry Number.

120267-05-2SDS

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 [1,2,4]triazolo[4,3-a]pyridine-3-sulfonamide

1.2 Other means of identification

Product number -
Other names -

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:120267-05-2 SDS

120267-05-2Upstream product

120267-05-2Downstream Products

120267-05-2Relevant articles and documents

Treatment of chronic inflammatory joint disease with arylsulfonamides

-

, (2008/06/13)

A method of treating chronic inflammatory joint disease with arylsulfonamides of the formula: wherein R1 and R2 are selected from hydrogen, lower alkyl, lower alkenyl, cycloalkyl, phenyl, loweralkylphenyl, 2 or 3 pyrrolidinyl, 2 or 3-(N-loweralkylpyrrolidinyl, or R1 and R2 taken together may form pyrrolidinyl or piperidinyl heterocyclic amino radicals and Z is an aryl group selected from substituted or unsubstituted tetrazole, 1,3,4-thiadiazole, 1,2,4-triazole, benzothiazole, benzimidazole, imidazole, pyridyl, 4,6-dimethyl pyrimidine, benzene or naphthalene is disclosed.

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