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139131-34-3

139131-34-3

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139131-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139131-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,3 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139131-34:
(8*1)+(7*3)+(6*9)+(5*1)+(4*3)+(3*1)+(2*3)+(1*4)=113
113 % 10 = 3
So 139131-34-3 is a valid CAS Registry Number.

139131-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-2-(4-methylphenyl)sulfonylsulfanylethanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names Benzenesulfonothioic acid,4-methyl-,S-(2-(dimethylamino)ethyl) ester,hydrochloride

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:139131-34-3 SDS

139131-34-3Downstream Products

139131-34-3Relevant articles and documents

&β-(N,N-Dialkylamino)ethyl Arylthiosulfonates: New Simulants for O-Ethyl S- Methylphosphonothioate

Davis, Franklin A.,Ray, Jayanta K.,Kasperowicz, Steve,Przeslawski, Robert M.,Durst, H. Dupont

, p. 2594 - 2599 (2007/10/02)

β-(N,N-Dialkylamino)ethyl arylthiosulfonates 2, new simulants for the hydrolysis and oxidation chemistry of VX (1), are prepared in good yield by reaction of a potassium arylthiosulfonate with a 2-chloroethylamine.Alkaline hydrolysis of 2 results in cleavage of the S-S-bond to give sulfinic acids and disulfides.Like VX, oxidation of 2 by N-sulfonyloxaziridine 12 occurs exclusively on nitrogen to give the corresponding amine oxide which subsequently undergoes a Cope elimination reaction affording the vinyl sulfide 14.

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