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28819-38-7

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28819-38-7 Usage

General Description

5-Pyridin-3-yl-1,3,4-thiadiazole-2-thiol is a chemical compound with the molecular formula C8H6N4S2. It is a heterocyclic organic compound with a thiadiazole ring and a pyridine ring. 5-PYRIDIN-3-YL-1,3,4-THIADIAZOLE-2-THIOL is commonly used as a building block in the synthesis of various organic compounds. It has potential applications in the pharmaceutical industry for the development of new drugs due to its pharmacological properties. Additionally, 5-Pyridin-3-yl-1,3,4-thiadiazole-2-thiol has been researched as a potential corrosion inhibitor for metal surfaces. Its unique structure and properties make it a versatile and valuable compound in organic chemistry and various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 28819-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,1 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28819-38:
(7*2)+(6*8)+(5*8)+(4*1)+(3*9)+(2*3)+(1*8)=147
147 % 10 = 7
So 28819-38-7 is a valid CAS Registry Number.

28819-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-pyridin-3-yl-3H-1,3,4-thiadiazole-2-thione

1.2 Other means of identification

Product number -
Other names 2-(3-pyridine)-1H-1,3,4-thiadiazole-5-thioketone

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:28819-38-7 SDS

28819-38-7Downstream Products

28819-38-7Relevant articles and documents

Efficient formation of C–S bond using heterocyclic thiones and arynes

An, Yu,Xu, Gang,Cai, Menglu,Wang, Shihui,Wang, Xiao zhong,Chen, Yingqi,Dai, Liyan

, (2020/12/23)

Phenylthio heterocyclic compounds are widely used because of their diverse biological activities and medicinal prospects. Here, a facile method was reported. An arylation of 1,3,4-oxa(thia)diazol-2-thiones reacting with arynes to build C(aryl)-S bonds in the presence of CsF had good yields and excellent selectivity. The reaction was completed in short time without using expensive reagents and catalysts. Present reaction system is an efficient procedure to process phenylthio heterocyclic compounds and reveals a sustainable method and better application prospects in future organic synthesis.

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