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5621-13-6

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5621-13-6 Usage

General Description

2,7-Dimethyl-1H-indole is a chemical compound with the molecular formula C10H11N. It is a derivative of indole, a heterocyclic aromatic organic compound. 2,7-Dimethyl-1H-indole is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its diverse biological activities, including anti-inflammatory, antimicrobial, and anti-tumor properties. 2,7-Dimethyl-1H-indole is also used as a key intermediate in the production of dyes and perfumes, as well as in the preparation of other organic compounds. It is a light brown solid with a distinct odor and is considered to be a relatively stable compound under normal conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 5621-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5621-13:
(6*5)+(5*6)+(4*2)+(3*1)+(2*1)+(1*3)=76
76 % 10 = 6
So 5621-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N/c1-7-4-3-5-9-6-8(2)11-10(7)9/h3-6,11H,1-2H3

5621-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dimethyl-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-Indole, 2,7-dimethyl-

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:5621-13-6 SDS

5621-13-6Relevant articles and documents

The Thermolysis of Polyazapentadienes. Part 4. Formation of Indoles and Quinoxalines from 5-(2,6-Disubstituted phenyl)-1,2,5-triazapentadienes and Related Compounds

McNab, Hamish

, p. 377 - 380 (2007/10/02)

7-Methylindole and 5-substituted quinoxalines are the principal cyclised products from the qas-phase thermolyses of the hydrazones (2) and (5) and the oxime ester (7).Both heterocyclic systems arise by competitive decomposition of the spirodienyl radical, e.g. (18), the indole by loss of MeCN and a hydrogen atom, and the quinoxalines by loss of a methyl radical.

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