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106110-61-6

106110-61-6

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106110-61-6 Usage

Chemical class

Indole diones

Physical state

Yellow solid

Usage

Commonly used in organic synthesis and medicinal chemistry

Structural features

a. Diethylaminoethyl group attached to the 1-position of the indole ring
b. Carbonyl group at the 2,3-positions

Biological activities

Potential anti-inflammatory, anti-cancer, and antioxidant properties

Applications

Key intermediate in the synthesis of various pharmaceuticals and agrochemicals

Check Digit Verification of cas no

The CAS Registry Mumber 106110-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,1 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106110-61:
(8*1)+(7*0)+(6*6)+(5*1)+(4*1)+(3*0)+(2*6)+(1*1)=66
66 % 10 = 6
So 106110-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O2/c1-3-15(4-2)9-10-16-12-8-6-5-7-11(12)13(17)14(16)18/h5-8H,3-4,9-10H2,1-2H3/p+1

106110-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(diethylamino)ethyl]indole-2,3-dione

1.2 Other means of identification

Product number -
Other names -

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:106110-61-6 SDS

106110-61-6Relevant articles and documents

Synthesis of an indoloquinoxaline derivative as potential inhibitor of InhA enzyme of mycobacterium tuberculosis

Zanzoul, Asmae,Chollet, Aurélien,Piedra-Arroni, Estefania,Stigliani, Jean-Luc,Bernardes-Génisson, Vania,Essassi, El Mokhtar,Pratviel, Geneviève

, p. 727 - 733 (2016/03/25)

Seven heterocyclic compounds derived from isatin have been synthesized. Isatin was Nsubstituted with four aromatic/aliphatic and benzylic moieties (1a-d). Compounds 1a-c were condensed with o-phenylenediamine to afford indoloquinoxaline derivatives (2a-c). Products were tested as inhibitors of InhA enzyme of M. tuberculosis. Compound 6-(diethylaminoethyl)indoloquinoxaline (2a) inhibited 38% of InhA activity at 50 μM. The possible modes of interaction of 2a with InhA were explored by molecular docking. Docking experiments afford keys to improve compound 2a for the design of new potential active drugs against tuberculosis.

HETEROCYCLIC SEMICARBAZONES AND THIOSEMICARBAZONES. XLIX. ANTIINFLAMMATORY ACTIVITY OF ISATIN THIOSEMICARBAZONES AND THEIR CYCLIZATION PRODUCTS

Tomchin, A. B.,Zhmykhova, I. L.,Ponomareva, M. M.,Pastushenkov, L. G.,Gromova, E. G.

, p. 619 - 624 (2007/10/02)

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