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61336-27-4

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61336-27-4 Usage

Potential pharmaceutical applications

+ Inhibitor of the enzyme glyoxalase I (involved in the detoxification of methylglyoxal and other reactive dicarbonyl compounds)
+ Antimicrobial properties
+ Antifungal properties
+ Antioxidant properties
Requires further research to understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 61336-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,3 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61336-27:
(7*6)+(6*1)+(5*3)+(4*3)+(3*6)+(2*2)+(1*7)=104
104 % 10 = 4
So 61336-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H5N3O2S/c8-3(9)1-7-2-5-6-4(7)10/h2H,1H2,(H,6,10)(H,8,9)

61336-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-sulfanylidene-1H-1,2,4-triazol-4-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 4H-1,2,4-Triazole-4-acetic acid,1,5-dihydro-5-thioxo

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:61336-27-4 SDS

61336-27-4Upstream product

61336-27-4Downstream Products

61336-27-4Relevant articles and documents

7-Acyl-3-(substituted triazolyl thiomethyl)cephalosporins

-

, (2008/06/13)

The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a substituted triazolyl thiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.

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