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1-{[2-(propylsulfanyl)ethyl]sulfanyl}propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22037-97-4

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22037-97-4 Usage

Physical state

Colorless liquid

Molecular weight

224.45 g/mol

Functional groups

Sulfur-containing compound with two sulfanyl (thiol) groups and an ethyl chain

Central atom

Central carbon atom

Industrial applications

Chemical intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds

Synthesis use

Building block for the synthesis of complex organic molecules

Potential uses

Development of new materials and organic synthesis research

Safety precautions

Proper handling due to potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 22037-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,3 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22037-97:
(7*2)+(6*2)+(5*0)+(4*3)+(3*7)+(2*9)+(1*7)=84
84 % 10 = 4
So 22037-97-4 is a valid CAS Registry Number.

22037-97-4SDS

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-propylsulfanylethylsulfanyl)propane

1.2 Other means of identification

Product number -
Other names 1,2-Dithioaethylenglykoldi-n-propylaether

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:22037-97-4 SDS

22037-97-4Downstream Products

22037-97-4Relevant academic research and scientific papers

Reactions of diorganyl disulfides with dihaloalkanes in basic reductive media. Synthesis of bis(organylthio)alkanes

Alekminskaya,Russavskaya,Korchevin,Deryagina

, p. 75 - 78 (2002)

A convenient preparative synthesis of bis(organylthio)alkanes was developed. It is based on alkylation with dihaloalkanes of solutions of diorganyl disulfides in the basic reductive system hydrazine hydrate-alkali. The generation of organylthiolate anions

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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