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4303-42-8

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4303-42-8 Usage

General Description

2-Chloroethyl N-propyl sulfide is a chemical compound with the formula C5H11ClS. It is a sulfur mustard and a powerful vesicant that can cause severe skin, eye, and respiratory tract irritation upon contact. 2-CHLOROETHYL N-PROPYL SULFIDE is a liquid at room temperature and has a faint garlic-like odor. It is used as a chemical weapon and is known for its toxic and blistering effects. Exposure to 2-Chloroethyl N-propyl sulfide can result in blistering, tissue damage, and long-term health effects such as respiratory issues and an increased risk of cancer. Therefore, it is considered a highly toxic and harmful chemical and is classified as a chemical weapon.

Check Digit Verification of cas no

The CAS Registry Mumber 4303-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,0 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4303-42:
(6*4)+(5*3)+(4*0)+(3*3)+(2*4)+(1*2)=58
58 % 10 = 8
So 4303-42-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H11ClS/c1-2-4-7-5-3-6/h2-5H2,1H3

4303-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroethylsulfanyl)propane

1.2 Other means of identification

Product number -
Other names 1-chloro-2-propylsulfanyl-ethane

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:4303-42-8 SDS

4303-42-8Relevant articles and documents

New preparative procedure for the synthesis of chloroalkyl sulfides

Russavskaya,Korchevin,Alekminskaya,Sukhomazova,Levanova,Deryagina

, p. 1445 - 1448 (2007/10/03)

Reaction of thiols with dihaloalkanes in the system hydrazine hydrate-base leads to alkyl(chloroalkyl) sulfides with different positions of the chlorine atom with respect to sulfur. The developed one-step procedure for the synthesis of such unsymmetrical sulfides is most suitable for arenethiols and alkanethiols having a long polymethylene chain. The reaction mechanism is discussed.

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