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29627-62-1

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29627-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29627-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,2 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29627-62:
(7*2)+(6*9)+(5*6)+(4*2)+(3*7)+(2*6)+(1*2)=141
141 % 10 = 1
So 29627-62-1 is a valid CAS Registry Number.

29627-62-1SDS

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 N,4-dimethyl-N-[2-[methyl-(4-methylphenyl)sulfonylamino]phenyl]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 1,2-bis(N-p-toluenesulfonyl-N-methylamino)benzene

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:29627-62-1 SDS

29627-62-1Relevant articles and documents

Absolute Helical Arrangement of Sulfonamide in the Crystal

Azumaya, Isao,Kato, Takako,Okamoto, Iwao,Yamasaki, Ryu,Tanatani, Aya,Yamaguchi, Kentaro,Kagechika, Hiroyuki,Takayanagi, Hiroaki

, p. 3939 - 3942 (2003)

(Matrix presented) 1,2-Bis(N-benzenesulfonyl-N-methylamino)benzene (2), which has no fixed asymmetric element, was crystallized from ethyl acetate as chiral crystals belonging to space group P41212 (No. 92) or P4321/

BORYLIMIDE CATALYSTS

-

Paragraph 0081, (2020/06/10)

The present invention provides a borylimide catalyst and further relates to compositions comprising the borylimide catalysts and processes for the polymerisation of olefins (e.g. ethylene) using the borylimide catalysts or the compositions comprising the

Carbon–carbon bond formation via benzoyl umpolung attained by photoinduced electron-transfer with benzimidazolines

Igarashi, Tomohito,Tayama, Eiji,Iwamoto, Hajime,Hasegawa, Eietsu

supporting information, p. 6874 - 6877 (2019/04/10)

A photoreaction between benzoyl compounds, such as benzoylformate derivatives, and 2-(p-anisyl)-1,3-dimethylbenzimidazoline in the presence of allyl bromide was found to give various allylated alcohols. In the reaction of benzoylformates, α-hydroxy ester enolates, for which the negative charge occurs on the carbonyl carbon of benzoyl (umpolung reactivity), are proposed to be generated as intermediates by electron-transfer from benzimidazolines to the photoexcited benzoylformates; these species react with allyl bromide to produce α-allyl-α-hydroxy esters.

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