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Benzenesulfonothioic acid, S-(chloromethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113975-44-3

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113975-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113975-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113975-44:
(8*1)+(7*1)+(6*3)+(5*9)+(4*7)+(3*5)+(2*4)+(1*4)=133
133 % 10 = 3
So 113975-44-3 is a valid CAS Registry Number.

113975-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name chloromethylsulfanylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names -

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:113975-44-3 SDS

113975-44-3Downstream Products

113975-44-3Relevant academic research and scientific papers

S-Alkyl Alkanesulfonothioates and S-1-Chloroalkyl Alkanesulfonothioates from Linear Alkanesulfinyl Chlorides

Freeman, Fillmore,Keindl, Monica C.

, p. 2026 - 2031 (1988)

Treatment of linear alkanesulfinyl chlorides 1 with dry N,N-dimethylmethanamide (DMF), N,N-dimethylethanamide (DMA), or 1-methyl-2-pyrrolidone (NMP) in an inert atmosphere, with or without added solvent, gives S-alkyl alkanesulfonothioates 4 (minor products) and S-1-chloroalkyl alkanesulfonothioates 5.The yield of 4 is decreased in the presence of the radical inhibitor 1,4-dihydroxybenzene.Evidence has been obtained for the formation and trapping of sulfines (including methanethial S-oxide) and for formation of sulfinyl radicals, vic-disulfoxides (α-disulfoxides), and O,S-sulfenyl sulfinates as reaction intermediates.S-Phenyl benzenesulfonothioate is a major product from the reaction of alkanesulfinyl chlorides and benzenesulfinyl chloride in the presence of DMF.

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