83497-60-3

Basic information

• Product Name: 3-Methyl-1,11-diphenyl-2,10-dihydro-1H-indolo[3,2-b]quinoline
• CAS NO: 83497-60-3
• Molecular Weight: 386.496
• Mol File: 83497-60-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Methyl-1,11-diphenyl-2,10-dihydro-1H-indolo[3,2-b]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Methyl-1,11-diphenyl-2,10-dihydro-1H-indolo[3,2-b]quinoline(83497-60-3)
• EPA Substance Registry System: 3-Methyl-1,11-diphenyl-2,10-dihydro-1H-indolo[3,2-b]quinoline(83497-60-3)

Safety Data

• Hazardous Substances Data: 83497-60-3(Hazardous Substances Data)

Upstream product

• 78121-14-9 1-acetyl-2-(1-phenylbutan-3-on-1-yl)indolin-3-one 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 16800-68-3 1-acetyl-2,3-dihydro-1H-indol-3-one 
• 3160-40-5 4-(4-chlorophenyl)-3-buten-2-one 

Relevant articles and documents

NEW METHOD OF SYNTHESIS OF QUINDOLINES FROM 1,5-DIKETONES OF THE INDOLINONE SERIES

By the action of ammonium acetate and α,β-unsaturated carbonyl compounds, 1,5-diketones of the indolinone series undergo not yet known transformations into difficulty accessible 1,2-dihydro-10H-quindolines.Under these conditions, 11-phenyl-1,2,3,4-tetrahydro-10H-quindoline was obtained from 1-acetyl-2-(benzylcyclohexan-1-on-α-yl)indolin-3-one.Dihydroquindolines with identical aryl substituents in the 1- and 11-positions were obtained from 1-acetylindolin-3-one by the action of an excess of certain α,β-unsaturated ketones and ammonium acetate.Dehydrogenation ofdihydroquindolines proceeds smoothly on heating with sulfur.The possible paths of the formation of dihydroquindolines are discussed.