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2-Chloroethanethiol, also known as ethanethiol or 2-chloroethyl mercaptan, is an organic compound with the chemical formula C2H5ClS. It is a colorless, volatile liquid with a strong, pungent odor. 2-chloroethanethiol is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. 2-Chloroethanethiol is also employed as a reagent in organic synthesis and as a building block for the preparation of other sulfur-containing compounds. Due to its reactive nature and potential health hazards, it is essential to handle 2-chloroethanethiol with proper safety measures and precautions.

4325-97-7

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4325-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4325-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4325-97:
(6*4)+(5*3)+(4*2)+(3*5)+(2*9)+(1*7)=87
87 % 10 = 7
So 4325-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C2H5ClS/c3-1-2-4/h4H,1-2H2

4325-97-7SDS

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 2-chloroethanethiol

1.2 Other means of identification

Product number -
Other names Ethanethiol, 2-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:4325-97-7 SDS

4325-97-7Relevant academic research and scientific papers

Selective synthesis of 2-haloalkanethiols and episulfides therefrom

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, (2008/06/13)

Haloalkanethiols are synthesized through the free radical liquid phase reaction of halogenated olefins with an excess of hydrogen sulfide. High product yields to the desired haloalkanethiol products are secured when a 3 to 20 fold molar excess of hydrogen sulfide to halogenated olefin is used. Desirably, the synthesis is carried out to a conversion level not exceeding 90%. The haloalkanethiol products can be subsequently dehydrohalogenated to the corresponding episulfide products by reacting the haloalkanethiol product with a substantially equal molar amount of anhydrous ammonia.

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