6206-30-0

Basic information

• Product Name: 4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenyl-
• CAS NO: 6206-30-0
• Molecular Formula: C20H17NO
• Molecular Weight: 287.361
• Mol File: 6206-30-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenyl-(6206-30-0)
• EPA Substance Registry System: 4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenyl-(6206-30-0)

Safety Data

• Hazardous Substances Data: 6206-30-0(Hazardous Substances Data)

Usage

Classification

Indole derivative

Main properties

complex molecular structure, potential biological activities, potential therapeutic effects, important target for drug development

Specific content

4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenylis used in medicinal chemistry and pharmaceutical research, studied for its potential therapeutic effects in treating diseases and disorders, has applications in material science and organic synthesis, versatile and valuable chemical compound.

Upstream product

• 52035-11-7 N-<(3-oxo-2-cyclohexenyl)imino>triphenylphosphorane 
• 1484-50-0 desyl bromide 
• 5220-49-5 3-amino-cyclohex-2-enone 
• 501-65-5 diphenyl acetylene 
• 504-02-9 1,3-cylohexanedione 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 3469-17-8 2-diazo-1,2-diphenylethan-1-one 
• 36625-33-9 3-azido-2-cyclohexen-1-one 
• 113859-86-2 3-(2-Oxo-1,2-diphenyl-ethylamino)-cyclohex-2-enone 

Relevant articles and documents

Coumarin-pyrrolizinone synthetic method of compound

The invention discloses a synthetic method of a coumarin-pyrrole compound. The synthetic method comprises the following step of: in a reactive solvent, with 4-amino coumarin compounds and disubstituted acetylene compounds as raw materials, under the catal

A catalyst- and solvent-free three-component reaction for the regioselective one-pot access to polyfunctionalized pyrroles

A facile method for the regioselective synthesis of tetrasubstituted pyrroles, from readily accessible 1,3-dicarbonyls, benzoin derivatives and ammonium acetate, has been developed. The one-pot three-component reactions were performed to afford tetrasubst

Catalyzed Reaction of Diazodiphenylethanone and Related Diazo Ketones with Enaminones as a Source of Pyrroles

The reaction of copper(II)-stabilized keto carbenes (1, 7, 8), derived from diazo ketones, with enaminones leads to the formation of pyrroles.The cyclic enaminones 3 react with the keto carbenes on nitrogen to form products 5, 9, 11, and/or pyrroles 6, 10