1436868-41-5

Basic information

• Product Name: 2-(4-bromophenyl)-1-(4-chlorophenyl)-3-methoxy-6,7-dihydro-1H-indol-4(5H)-one
• Synonyms: 2-(4-bromophenyl)-1-(4-chlorophenyl)-3-methoxy-6,7-dihydro-1H-indol-4(5H)-one
• CAS NO: 1436868-41-5
• Molecular Weight: 430.728
• Mol File: 1436868-41-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(4-bromophenyl)-1-(4-chlorophenyl)-3-methoxy-6,7-dihydro-1H-indol-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromophenyl)-1-(4-chlorophenyl)-3-methoxy-6,7-dihydro-1H-indol-4(5H)-one(1436868-41-5)
• EPA Substance Registry System: 2-(4-bromophenyl)-1-(4-chlorophenyl)-3-methoxy-6,7-dihydro-1H-indol-4(5H)-one(1436868-41-5)

Safety Data

• Hazardous Substances Data: 1436868-41-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 36646-75-0 3-(4-choloroaniline)-2-cyclohexen-1-one 
• 80352-42-7 1-(4-bromophenyl)-2,2-dihydroxyethanone 

Relevant articles and documents

Three-component synthesis of poly-substituted tetrahydroindoles through p-TsOH promoted alkoxylation

Concise and efficient three-component domino reactions to highly substituted tetrahydroindole derivatives promoted by p-TsOH have been developed under microwave irradiation condition. The direct C3-alkoxylation of indole framework was achieved in a one-pot operation. The reaction proceeds at fast rates and can be finished within 30 min, which makes workup convenient to give good chemical yields.