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

63740-28-3

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63740-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63740-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,4 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63740-28:
(7*6)+(6*3)+(5*7)+(4*4)+(3*0)+(2*2)+(1*8)=123
123 % 10 = 3
So 63740-28-3 is a valid CAS Registry Number.

63740-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-ethenylphenyl)benzenesulfonamide

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:63740-28-3 SDS

63740-28-3Downstream Products

63740-28-3Relevant academic research and scientific papers

Visible-Light-Driven Neutral Nitrogen Radical Mediated Intermolecular Styrene Difunctionalization

Zhao, Quan-Qing,Li, Man,Xue, Xiao-Song,Chen, Jia-Rong,Xiao, Wen-Jing

, p. 3861 - 3865 (2019/05/24)

A neutral nitrogen radical-mediation strategy, wherein the existing N-H moiety of substrates serves as a neutral nitrogen radical precursor to enable room-temperature intermolecular radical difunctionalization of styrenes under photoredox catalysis, is reported. The reaction shows high functional group tolerance and substrate scope with respect to both components, giving the corresponding products with generally good yields. Preliminary control experiments and DFT calculations are performed to explain the reaction mechanism.

N-(Vinylphenyl) sulfonamides

-

, (2008/06/13)

Novel N-(vinylphenyl)sulfonamides and polymers thereof including copolymers of N-(vinylphenyl)sulfonamides and styrene are prepared by reacting 4-vinylaniline with an amine and a sulfonyl chloride in the presence of an acid acceptor to produce the monomer

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