1159426-14-8

Basic information

• Product Name: 1-[(2-nitrophenyl)sulfonyl]-2-phenyl-1,2-dihydroquinolinemethylsulfonyl-2-phenyl-1,2-dihydroquinoline
• Synonyms: 1-[(2-nitrophenyl)sulfonyl]-2-phenyl-1,2-dihydroquinolinemethylsulfonyl-2-phenyl-1,2-dihydroquinoline
• CAS NO: 1159426-14-8
• Molecular Weight: 392.435
• Mol File: 1159426-14-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-[(2-nitrophenyl)sulfonyl]-2-phenyl-1,2-dihydroquinolinemethylsulfonyl-2-phenyl-1,2-dihydroquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(2-nitrophenyl)sulfonyl]-2-phenyl-1,2-dihydroquinolinemethylsulfonyl-2-phenyl-1,2-dihydroquinoline(1159426-14-8)
• EPA Substance Registry System: 1-[(2-nitrophenyl)sulfonyl]-2-phenyl-1,2-dihydroquinolinemethylsulfonyl-2-phenyl-1,2-dihydroquinoline(1159426-14-8)

Safety Data

• Hazardous Substances Data: 1159426-14-8(Hazardous Substances Data)

Upstream product

• 911312-96-4 N-o-nitrobenzenesulfonyl-2-aminobenzaldehyde 

Relevant articles and documents

Br?nsted Acid-Catalysed Allylic Amination of 1-(2-Aminoaryl)prop-2-en-1-ols to 1,2-Dihydroquinolines

A highly efficient synthetic method to prepare 1,2-dihydroquinolines that relies on trifluoromethanesulfonic acid (TfOH)-catalysed allylic amination of 1-(2-aminoaryl)prop-2-en-1-ols is described. Achieved at a catalyst loading of 0.01 mol-% under mild conditions at room temperature, the reaction was found to be robust, with a wide range of substitution patterns tolerated. The corresponding N-heterocyclic adducts were obtained in good to excellent yields of 45-93 %.