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1H-Azepine-2,5-dicarboxylic acid, 1-[(4-methylphenyl)sulfonyl]-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68218-52-0

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68218-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68218-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68218-52:
(7*6)+(6*8)+(5*2)+(4*1)+(3*8)+(2*5)+(1*2)=140
140 % 10 = 0
So 68218-52-0 is a valid CAS Registry Number.

68218-52-0SDS

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-(p-toluenesulphonyl)-2,5-dimethoxycarbonyl-1H-azepine

1.2 Other means of identification

Product number -
Other names 1-(toluene-4-sulfonyl)-1H-azepine-2,5-dicarboxylic acid dimethyl ester

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:68218-52-0 SDS

68218-52-0Downstream Products

68218-52-0Relevant academic research and scientific papers

FACILE SYNTHESIS OF N-SUBSTITUTED 1H-AZEPINE DERIVATIVES

Ayyangar, Nagaraj R.,Bambal, Ramesh B.,Lugade, Ananda G.

, p. 77 - 82 (2007/10/02)

The facile synthesis of N-sulphonyl and N-ethoxycarbonyl substituted 1H-azepines in high yields by the pressure-induced sulphonylnitrene insertion reaction or, in anhydrous solvents, the 1,3-dipolar azide addition reaction with aromatic substrates containing electron-withdrawing substituents (e.g. dimethyl terephthalate) are described.The probable sequences of reactions involved in the two cases have been indicated.

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