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1026-19-3

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1026-19-3 Usage

Also Known As

2-Methyl-1H-indole-2-carbonyl chloride

Type of Compound

Chemical compound used in synthesis

Base Structure

Indole (heterocyclic aromatic compound)

Modification

Benzoyl group attached to the 2 position of the indole ring

Uses

Key intermediate for the synthesis of pharmaceuticals, agrochemicals, and dyes; manufacturing of organic compounds; building block in organic chemistry; development of new drugs and chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1026-19-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1026-19:
(6*1)+(5*0)+(4*2)+(3*6)+(2*1)+(1*9)=43
43 % 10 = 3
So 1026-19-3 is a valid CAS Registry Number.

1026-19-3SDS

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 1H-indol-2-yl-(2-methylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2-o-Methylbenzoylindol

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:1026-19-3 SDS

1026-19-3Downstream Products

1026-19-3Relevant articles and documents

A Novel Pd-Catalysed Annulation Reaction for the Syntheses of Pyrroloindoles and Pyrroloquinolines

Dethe, Dattatraya H.,Boda, Raghavender

, p. 106 - 110 (2016)

Pd-catalysed annulation reactions between indole derivatives and internal alkyne esters leading to various pyrrolo[1,2-a]indoles and pyrroloquinolines have been developed. The strategy involves an intermolecular addition of the indole nitrogen on to the internal alkyne ester followed by an intramolecular insertion of a vinyl-palladium complex into the carbonyl group. This method offers a facile and practical approach to pyrrolo[1,2-a]indoles and pyrroloquinolines.

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