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Methanesulfonamide, N-(3,4-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71270-52-5

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71270-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71270-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,7 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71270-52:
(7*7)+(6*1)+(5*2)+(4*7)+(3*0)+(2*5)+(1*2)=105
105 % 10 = 5
So 71270-52-5 is a valid CAS Registry Number.

71270-52-5SDS

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 (3,4-dimethylphenyl)methanesulfonamide

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:71270-52-5 SDS

71270-52-5Relevant academic research and scientific papers

Palladium-Catalyzed cascade sp2 c?H bond functionalizations allowing one-Pot access to 4?Aryl-1,2,3,4-tetrahydroquinolines from n?Allyl?N?arylsulfonamides

Yuan, Kedong,Soule, Jean-Francois,Dorcet, Vincent,Doucet, Henri

, p. 8121 - 8126 (2016)

We have developed a palladium-catalyzed cascade reaction allowing an efficient synthesis of 4-aryl-1,2,3,4-tetrahydroquinolines from N-allyl-N-arylsulfonamides and benzenesulfonyl chlorides. In this transformation, two C(sp2)?C(sp3) bonds were formed via activation of C(sp2)?H bonds. The reaction proceeds using the easily accessible catalyst PdCl2, with Li2CO3 as inexpensive base and CuBr as additive, and tolerates a wide variety of substituents on both reaction partners.

Nitration and Bromination of N-(dimethylphenyl)methanesulfonamides

Al-Khafaji, Sarah,Cardinale, Nina,Hanson, James R.

, p. 701 - 714 (2007/10/03)

The orientation of the products of nitrosation: nitration and bromination of the methanesulfonamides of the six isomeric dimethylanilines have been established by 1H NMR nuclear Overhauser experiments.

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