1393726-17-4

Basic information

• Product Name: 7-(3-chlorophenylamino)-2-(4-bromophenyl)-1-(4-chlorophenyl)-6,7-dihydro-1H-indol-4(5H)-one
• CAS NO: 1393726-17-4
• Molecular Weight: 526.26
• Mol File: 1393726-17-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-(3-chlorophenylamino)-2-(4-bromophenyl)-1-(4-chlorophenyl)-6,7-dihydro-1H-indol-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(3-chlorophenylamino)-2-(4-bromophenyl)-1-(4-chlorophenyl)-6,7-dihydro-1H-indol-4(5H)-one(1393726-17-4)
• EPA Substance Registry System: 7-(3-chlorophenylamino)-2-(4-bromophenyl)-1-(4-chlorophenyl)-6,7-dihydro-1H-indol-4(5H)-one(1393726-17-4)

Safety Data

• Hazardous Substances Data: 1393726-17-4(Hazardous Substances Data)

Upstream product

• 36646-75-0 3-(4-choloroaniline)-2-cyclohexen-1-one 
• 80352-42-7 1-(4-bromophenyl)-2,2-dihydroxyethanone 
• 108-42-9 3-chloro-aniline 

Relevant articles and documents

Allylic amination and N-arylation-based domino reactions providing rapid three-component strategies to fused pyrroles with different substituted patterns

New three-component domino reaction providing divergent approaches to multifunctionalized fused pyrroles with different substituted patterns have been established (40 examples). The direct C(sp3)-N bond formation was achieved through intermolecular allylic amination in a one-pot operation, and N-arylation of amines was realized by varying N-amino acid enaminones. The reaction is easy to perform simply by mixing three common reactants in acetic acid under microwave heating. The reaction proceeds at fast rates and can be finished within 30 min, which makes workup convenient to give good chemical yields.