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S-tert-butyl 4-methylbenzenesulfonothioate, also known as tert-butyl 4-methylbenzenesulfonothioate, is an organic compound with the chemical formula C11H15O2S2. It is a colorless to pale yellow liquid with a molecular weight of 249.36 g/mol. S-tert-butyl 4-methylbenzenesulfonothioate is a derivative of benzene, featuring a tert-butyl group, a methyl group, and a sulfonothioate functional group. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is important to handle S-tert-butyl 4-methylbenzenesulfonothioate with care, following proper safety protocols.

2943-19-3

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2943-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2943-19-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2943-19:
(6*2)+(5*9)+(4*4)+(3*3)+(2*1)+(1*9)=93
93 % 10 = 3
So 2943-19-3 is a valid CAS Registry Number.

2943-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tert-butylsulfanylsulfonyl-4-methylbenzene

1.2 Other means of identification

Product number -
Other names 4-(t-Butylthio)tosylate

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:2943-19-3 SDS

2943-19-3Relevant academic research and scientific papers

Metal-Free Chemoselective Reaction of Sulfoxonium Ylides and Thiosulfonates: Diverse Synthesis of 1,4-Diketones, Aryl Sulfursulfoxonium Ylides, and β-Keto Thiosulfones Derivatives

Wang, Fei,Liu, Bo-Xi,Rao, Weidong,Wang, Shun-Yi

, p. 6600 - 6604 (2020/09/02)

A diverse chemoselective insertion reaction of sulfoxonium ylides and thiosulfonates under transition-metal-free conditions is developed, which successfully affords 1,4-diketone compounds, arylthiosulfoxide-ylides, and β-keto thiosulfones, respectively. The nucleophilic addition of two molecular sulfoxonium ylides to construct sulfone-substituted 1,4-dione compounds is the highlight of this work.

Regioselective cobalt-catalyzed addition of sulfides to unactivated alkenes

Girijavallabhan, Vinay,Alvarez, Carmen,Njoroge, F. George

experimental part, p. 6442 - 6446 (2011/09/16)

A novel method to synthesize tertiary alkyl/aryl sulfides in a mild and regioselective manner from unactivated alkenes using cobalt catalysis is described. The methodology is compatible with sensitive functionalities and is successful with several different types of alkenes and sulfides.

A FACILE SYNTHESIS OF UNSYMMETRICAL THIOSULFONATES VIA SULFONYLATION OF MERCAPTANS

Ranasinghe, M. G.,Fuchs, P. L.

, p. 227 - 232 (2007/10/02)

The reaction of p-toluenesulfonyl bromide with mercaptans provides a convenient procedure for the synthesis of unsymmetrical thiolsulfonates.

Physical Properties and Various Reactions of Thionitrites and Related Substances

Oae, Shigeru,Shinhama, Koichi,Fujimori, Ken,Kim, Yong Hae

, p. 775 - 784 (2007/10/02)

Several new sulfenyl or sulfonyl derivatives, thionitrates (RSNO2), sulfonyl nitrites (RSO2NO), were successfully isolated by treating corresponding thiols and sulfinic acids with dinitrogen tetraoxide (N2O4).Spectroscopic data of both stable and many rather unstable compounds were determined and compared with those of corresponding alkyl nitrites (RONO) or alkyl nitrates (RONO2).Chemical reactivities of these uncommon, novel S-nitroso and S-nitro compounds were investigated.

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