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61922-00-7

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61922-00-7 Usage

Functional groups

Formyl, acetamide

Structure

Indole ring with a methyl substituent

Potential applications

Pharmaceutical research and development, medicinal chemistry, drug discovery

Relevance

Indole-based scaffolds for pharmacological properties and biological activities

Need for further studies

To fully understand its potential in various applications

Check Digit Verification of cas no

The CAS Registry Mumber 61922-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,2 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61922-00:
(7*6)+(6*1)+(5*9)+(4*2)+(3*2)+(2*0)+(1*0)=107
107 % 10 = 7
So 61922-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c1-8-10(7-15)9-4-2-3-5-11(9)14(8)6-12(13)16/h2-5,7H,6H2,1H3,(H2,13,16)

61922-00-7 Well-known Company Product Price

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  • Aldrich

  • (CBR01113)  2-(3-Formyl-2-methyl-1H-indol-1-yl)acetamide  AldrichCPR

  • 61922-00-7

  • CBR01113-1G

  • 644.67CNY

  • Detail

61922-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Formyl-2-methyl-1H-indol-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names 2-(3-formyl-2-methylindol-1-yl)acetamide

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:61922-00-7 SDS

61922-00-7Downstream Products

61922-00-7Relevant articles and documents

2-Substituted-indole-1-lower-alkanecarboxamides

-

, (2008/06/13)

2-Substituted-indole-1-lower-alkanecarboxamides, prepared by amidation of the corresponding acid or ester; by hydrolysis or thiohydrolysis of the corresponding carbonitrile; by alkylation of a suitable indole with a halo-lower-alkanecarboxamide; or by hydrolysis of a 1-indolechlorosulfonylcarbamyl derivative, have anti-secretory and anti-ulcer activities.

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