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1H-Indole-4,7-dione,2,3-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62676-76-0

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62676-76-0 Usage

Derivative of indole

The compound is a modified version of the indole chemical structure, which is a common building block in organic synthesis and pharmaceuticals.

Distinct yellow color

The compound has a characteristic yellow color, which may be useful for identification or visual tracking purposes.

Potential applications in organic synthesis and pharmaceuticals

The compound has potential uses in the development of novel drugs and may be a valuable reagent or building block in the creation of more complex organic molecules.

Used as a reagent in chemical reactions

The compound may be useful as a reagent in various chemical reactions, facilitating the formation of new bonds or the modification of existing ones.

Potential biological activities and therapeutic properties

The compound has been studied for its potential biological activities and therapeutic properties, making it a subject of interest for further research and exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 62676-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62676-76:
(7*6)+(6*2)+(5*6)+(4*7)+(3*6)+(2*7)+(1*6)=150
150 % 10 = 0
So 62676-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c1-5-6(2)11-10-8(13)4-3-7(12)9(5)10/h3-4,11H,1-2H3

62676-76-0SDS

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 2,3-dimethyl-1H-indole-4,7-dione

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-indol-4,7-dion

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:62676-76-0 SDS

62676-76-0Downstream Products

62676-76-0Relevant academic research and scientific papers

A procedure for transforming indoles into indolequinones

Eastabrook, Andrew S.,Wang, Christy,Davison, Emma K.,Sperry, Jonathan

, p. 1006 - 1017 (2015/01/30)

A procedure that converts a series of structurally diverse, readily available indole derivatives to their corresponding indolequinones is described. The three-step route commences with an iridium catalyzed C-H borylation to give a 7-borylindole that upon

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