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1H-Indole-2-carboxamide, N-(1,1-dimethylethyl)-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17537-57-4

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17537-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17537-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,3 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17537-57:
(7*1)+(6*7)+(5*5)+(4*3)+(3*7)+(2*5)+(1*7)=124
124 % 10 = 4
So 17537-57-4 is a valid CAS Registry Number.

17537-57-4SDS

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-tert-butyl-3-methyl-1H-indole-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-methyl-indole-2-carboxylic acid tert-butylamide

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:17537-57-4 SDS

17537-57-4Relevant academic research and scientific papers

Direct carboxamidation of indoles by palladium-catalyzed C-H activation and isocyanide insertion

Peng, Jiangling,Liu, Lanying,Hu, Ziwei,Huang, Jinbo,Zhu, Qiang

supporting information; experimental part, p. 3772 - 3774 (2012/06/15)

A selective C3 carboxamidation of indoles including free (N-H) ones by palladium-catalyzed sequential C-H activation-isocyanide insertion has been developed. The Royal Society of Chemistry 2012.

A convenient synthesis of 2-cyano-3-substituted indoles

Denison, Sophie,Hilton, Stephen T.

, p. 2806 - 2808 (2007/10/03)

A new and mild method for the synthesis of 2-cyano-3-substituted indoles is described which is effective on N-unsubstituted indoles.

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