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3-chloro-N-methyl-N-phenyl-1-benzothiophene-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105577-05-7

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105577-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105577-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105577-05:
(8*1)+(7*0)+(6*5)+(5*5)+(4*7)+(3*7)+(2*0)+(1*5)=117
117 % 10 = 7
So 105577-05-7 is a valid CAS Registry Number.

105577-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-N-methyl-N-phenyl-1-benzothiophene-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-chloro-N-methyl-1-benzothiophene-2-carboxanilide

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:105577-05-7 SDS

105577-05-7Relevant academic research and scientific papers

Agents and methods for treating ischemic and other diseases

-

Page/Page column 90, (2016/06/01)

This invention relates to compounds that modulate TRPM7 protein activity and use of the same for treatment or prophylaxis of ischemia, cancer, pain or glaucoma.

Photochemical eliminations involving zwitterionic intermediates generated via electrocyclic ring closure of benzothiophene carboxanilides

Sarker, Majher,Shahrin, Tasnuva,Steinmetz, Mark G.

, p. 872 - 875 (2011/05/02)

Leaving groups such as carboxylate, thiolate, and phenolate are expelled via zwitterionic intermediates produced upon photochemical electrocyclic ring closure of benzothiophene carboxanilides in the triplet excited state. Chemical yields generally exceed 90%, while quantum yields vary with basicity of the released leaving group.(Figure Presented)

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