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1,2,4-Thiadiazole-5-carboxylic acid, 3-methyl-, methyl ester (9CI) is a chemical compound with the molecular formula C6H6N2O2S. It is a methyl ester derivative of 1,2,4-thiadiazole-5-carboxylic acid, known for its potential antimicrobial, antifungal, and anticancer properties. 1,2,4-Thiadiazole-5-carboxylicacid,3-methyl-,methylester(9CI) is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and serves as a building block in the creation of heterocyclic compounds and pharmaceuticals. It has also been investigated for its potential use in the development of new materials and chemical processes.

352356-71-9

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352356-71-9 Usage

Uses

Used in Pharmaceutical Industry:
1,2,4-Thiadiazole-5-carboxylic acid, 3-methyl-, methyl ester (9CI) is used as a chemical intermediate for the synthesis of various drugs, contributing to the development of new pharmaceuticals with diverse therapeutic applications.
Used in Antimicrobial Applications:
1,2,4-Thiadiazole-5-carboxylicacid,3-methyl-,methylester(9CI) is studied for its potential antimicrobial properties, making it a candidate for use in the development of new antimicrobial agents to combat resistant bacterial strains.
Used in Antifungal Applications:
1,2,4-Thiadiazole-5-carboxylic acid, 3-methyl-, methyl ester (9CI) is explored for its antifungal capabilities, indicating its potential use in treating fungal infections and developing new antifungal medications.
Used in Anticancer Applications:
1,2,4-Thiadiazole-5-carboxylicacid,3-methyl-,methylester(9CI) has been studied for its potential anticancer properties, suggesting its use in the development of novel anticancer drugs that could target and inhibit the growth of cancer cells.
Used in Heterocyclic Compounds Synthesis:
As a building block, 1,2,4-Thiadiazole-5-carboxylic acid, 3-methyl-, methyl ester (9CI) is utilized in the synthesis of heterocyclic compounds, which are important in various chemical and pharmaceutical applications.
Used in Material Science and Chemical Processes:
This chemical has been investigated for its potential use in the development of new materials and chemical processes, indicating its versatility and applicability in advancing material science and chemical engineering fields.

Check Digit Verification of cas no

The CAS Registry Mumber 352356-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,3,5 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 352356-71:
(8*3)+(7*5)+(6*2)+(5*3)+(4*5)+(3*6)+(2*7)+(1*1)=139
139 % 10 = 9
So 352356-71-9 is a valid CAS Registry Number.

352356-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-methyl-1,2,4-thiadiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names 1,2,4-Thiadiazole-5-carboxylic acid,3-methyl-,methyl ester

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:352356-71-9 SDS

352356-71-9Relevant academic research and scientific papers

NOVEL CHIRAL N-ACYL-5,6,7,(8-SUBSTITUTED)-TETRAHYDRO-[1,2,4]TRIAZOLO[4,3-a]PYRAZINES AS SELECTIVE NK-3 RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITION, METHODS FOR USE IN NK-3 RECEPTOR MEDIATED DISORDERS AND CHIRAL SYNTHESIS THEREOF

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Page/Page column 116-117, (2013/04/24)

The present invention relates to novel compounds of Formula I and their use in therapeutic treatments. The invention further relates to a novel chiral synthesis of 5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines using N-sp3 protective groups. The invention also provides intermediates for use in the synthesis of compounds of Formula I.

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