1353896-89-5

Basic information

• Product Name: 1-(4-chlorophenyl)-7-(1-(4-chlorophenyl)-4-hydroxy-2-p-tolyl-1H-indol-3-yl)-6,7-dihydro-2-p-tolyl-1H-indol-4(5H)-one
• CAS NO: 1353896-89-5
• Molecular Weight: 667.634
• Mol File: 1353896-89-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-chlorophenyl)-7-(1-(4-chlorophenyl)-4-hydroxy-2-p-tolyl-1H-indol-3-yl)-6,7-dihydro-2-p-tolyl-1H-indol-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)-7-(1-(4-chlorophenyl)-4-hydroxy-2-p-tolyl-1H-indol-3-yl)-6,7-dihydro-2-p-tolyl-1H-indol-4(5H)-one(1353896-89-5)
• EPA Substance Registry System: 1-(4-chlorophenyl)-7-(1-(4-chlorophenyl)-4-hydroxy-2-p-tolyl-1H-indol-3-yl)-6,7-dihydro-2-p-tolyl-1H-indol-4(5H)-one(1353896-89-5)

Safety Data

• Hazardous Substances Data: 1353896-89-5(Hazardous Substances Data)

Upstream product

• 36646-75-0 3-(4-choloroaniline)-2-cyclohexen-1-one 
• 16208-14-3 2,2-dihydroxy-1-(p-tolyl)ethanone 

Relevant articles and documents

A multi-component domino reaction for the direct access to polyfunctionalized indoles via intermolecular allylic esterification and indolation

A novel multi-component reaction for the synthesis of polyfunctionalized indoles and bis-indoles has been established. The reaction pathways were controlled by varying enamines with different substitution patterns to give polyfunctionalized indoles and bis-indoles selectively. The reaction proceeds at a fast speed within 15-30 min with water as the major byproduct, which makes work-up convenient.