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42060-28-6

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42060-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42060-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,6 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42060-28:
(7*4)+(6*2)+(5*0)+(4*6)+(3*0)+(2*2)+(1*8)=76
76 % 10 = 6
So 42060-28-6 is a valid CAS Registry Number.

42060-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(p-Tolylmethyl)methansulfonamid

1.2 Other means of identification

Product number -
Other names N-(4-METHYLBENZYL)METHANESULFONAMIDE

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:42060-28-6 SDS

42060-28-6Relevant articles and documents

Electrosynthesis of sulfonamides from DMSO and amines under mild conditions

Lin, Zhiguan,Huang, Liangbin,Yuan, Gaoqing

supporting information, p. 3579 - 3582 (2021/04/14)

With DMSO as the solvent and the precursor of a -SO2Me unit at room temperature, a novel electrochemical oxidization and amination of DMSO with amines was developed for the synthesis of sulfonamides. Our investigations reveal that this transformation may involve a radical process and an electrochemical oxidization of DMSO.

Green and scalable aldehyde-catalyzed transition metal-free dehydrative N-alkylation of amides and amines with alcohols

Xu, Qing,Li, Qiang,Zhu, Xiaogang,Chen, Jianhui

supporting information, p. 73 - 80 (2013/03/13)

In contrast to the borrowing hydrogen-type N-alkylation reactions, in which alcohols were activated by transition metal-catalyzed anaerobic dehydrogenation, the addition of external aldehydes was accidentally found to be a simple and effective protocol for alcohol activation. This interesting finding subsequently led to an efficient and green, practical and scalable aldehyde-catalyzed transition metal-free dehydrative N-alkylation method for a variety of amides, amines, and alcohols. Mechanistic studies revealed that this reaction most possibly proceeds via a simple but interesting transition metal-free relay race mechanism. Copyright

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