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4113-57-9

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4113-57-9 Usage

General Description

5-Chloro-1,2,3-thiadiazole is a chemical compound with the molecular formula C2HClN2S. It belongs to the class of heterocyclic compounds and contains a five-membered ring consisting of three carbon atoms, one nitrogen atom, and one sulfur atom. 5-Chloro-1,2,3-thiadiazole is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceuticals and agrochemicals. It can also be utilized as a reagent in organic synthesis and as an intermediate in the production of dyes and pigments. 5-Chloro-1,2,3-thiadiazole exhibits moderate toxicity and should be handled and used with appropriate safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 4113-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4113-57:
(6*4)+(5*1)+(4*1)+(3*3)+(2*5)+(1*7)=59
59 % 10 = 9
So 4113-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C2HClN2S/c3-2-1-4-5-6-2/h1H

4113-57-9SDS

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 5-chlorothiadiazole

1.2 Other means of identification

Product number -
Other names 1,2,3-Thiadiazole,5-chloro

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:4113-57-9 SDS

4113-57-9Relevant articles and documents

Substituted 1-propiolylpiperazine compounds, their preparation and use

-

, (2008/06/13)

Substituted 1-propiolylpiperazine compounds corresponding to formula I in which X denotes N or C—R2, and n is an integer from 0 to 8, a method for producing such substituted 1-propiolylpiperazine compounds, pharmaceutical compositions containing such substituted 1-propiolylpiperazine compounds, and the use of such substituted 1-propiolylpiperazine compounds for modulating mGluR5 receptor activity or for treating or inhibiting pain and various other conditions, especially conditions at least partly mediated by the mGluR5 receptor.

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