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2-bromo-2-methyl-N-o-tolylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23423-38-3

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23423-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23423-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23423-38:
(7*2)+(6*3)+(5*4)+(4*2)+(3*3)+(2*3)+(1*8)=83
83 % 10 = 3
So 23423-38-3 is a valid CAS Registry Number.

23423-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2-methyl-N-o-tolylpropanamide

1.2 Other means of identification

Product number -
Other names α-Brom-isobuttersaeure-o-toluidid

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:23423-38-3 SDS

23423-38-3Relevant academic research and scientific papers

Friedel-Crafts chemistry. Part 40. An expedient novel synthesis of some dibenz-azepines, -azocines, 11H-benzo[f]pyrido[2,3-b]azepines and 6H-benzo[g]pyrido[2,3-c]azocines

Abd El-Aal, Hassan A.K.,Khalaf, Ali A.

, p. 306 - 322 (2013/10/21)

A new synthetic approach for the synthesis of novel 5H-dibenz[b,f]azepine, 5H-dibenz[b,f]-azocine, 11H-benzo[f]pyrido[2,3-b]azepine and 6H-benzo[g]pyrido[2,3-c]azocine derivatives is reported. The key step of this methodology is based on Friedel-Crafts ring closure of nitrogen containing carboxylic acids and alkanols in the presence of AlCl3, P 2O5 or PPA catalysts in overall high yields. The starting carboxylic acids were prepared via an unequivocal synthetic pathway by the basic hydrolysis of trimethyloxindole followed by N-arylation reactions.

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