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70140-60-2

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70140-60-2 Usage

General Description

4-Methylsulfanyl-benzenesulfonic acid, also known as p-tolylsulfonic acid, is a white crystalline solid with the chemical formula C7H8O3S2. It is a sulfonic acid derivative, containing a sulfonic acid group (-SO3H) attached to a benzene ring with a methylthio substituent. 4-Methylsulfanyl-benzenesulfonic acid is used as a catalyst in organic synthesis, particularly in the production of pharmaceuticals and dyes. It is also employed in the synthesis of polymers, plastics, and fragrances. Additionally, 4-Methylsulfanyl-benzenesulfonic acid is used as an intermediate in the manufacture of agricultural chemicals and as a corrosion inhibitor in industrial processes. Due to its acidic nature, it must be handled with care and stored in a cool, dry place.

Check Digit Verification of cas no

The CAS Registry Mumber 70140-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,4 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70140-60:
(7*7)+(6*0)+(5*1)+(4*4)+(3*0)+(2*6)+(1*0)=82
82 % 10 = 2
So 70140-60-2 is a valid CAS Registry Number.

70140-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylsulfanylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 4-(Methylthio)benzenesulfonic acid

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:70140-60-2 SDS

70140-60-2Relevant articles and documents

Sustainable access to sulfonic acids from halides and thiourea dioxide with air

Zhang, Hui,Wang, Ming,Jiang, Xuefeng

supporting information, p. 8238 - 8242 (2020/12/29)

A sustainable and mild one-step strategy is explored for the synthesis of aryl and alkyl sulfonic acids using a facile combination of halides and sulfur dioxide surrogates under air. The cheap industrial material thiourea dioxide was employed as an eco-friendly and easy-handling sulfur dioxide surrogate, while air was used as a green oxidant. Both aryl and alkyl sulfonic acids were obtained under transition metal-catalyzed or transition metal-free conditions. Mechanistic studies demonstrated that sulfinate was involved as an intermediate in this transformation. Notably, this protocol has been applied to the late-stage sulfonation of the drugs naproxen, isoxepac and ibuprofen.

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