1429308-40-6

Basic information

• Product Name: N-isopropyl-2-(prop-1-en-2-yl)benzenamine
• Synonyms: N-isopropyl-2-(prop-1-en-2-yl)benzenamine
• CAS NO: 1429308-40-6
• Molecular Weight: 175.274
• Mol File: 1429308-40-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-isopropyl-2-(prop-1-en-2-yl)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-isopropyl-2-(prop-1-en-2-yl)benzenamine(1429308-40-6)
• EPA Substance Registry System: N-isopropyl-2-(prop-1-en-2-yl)benzenamine(1429308-40-6)

Safety Data

• Hazardous Substances Data: 1429308-40-6(Hazardous Substances Data)

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 78350-37-5 1-(2-(isopropylamino)phenyl)ethan-1-one 
• 52562-19-3 2-isopropenylaniline 
• 67-64-1 acetone 

Downstream Products

• 2540-20-7 1-isopropyl-4-methylquinolin-2(1H)-one 

Relevant articles and documents

Borane-Catalyzed Synthesis of Quinolines Bearing Tetrasubstituted Stereocenters by Hydride Abstraction-Induced Electrocyclization

The borane-catalyzed synthesis of quinoline derivatives bearing tetrasubstituted stereocenters from vinyl anilines has been developed. Mechanistic studies and quantum-mechanical investigations support the hydride abstraction/electrocyclization/hydride add

Synthesis of 2(1 H)-quinolinones via Pd-catalyzed oxidative cyclocarbonylation of 2-vinylanilines

Palladium-catalyzed oxidative cyclocarbonylation of N-monosubstituted-2- vinylanilines constitutes a simple, direct, and selective method for the synthesis of 2(1H)-quinolinones. The reaction conditions are attractive in terms of environmental considerations and operational simplicity. 2(1H)-Quinolinones with a variety of functional groups were prepared in up to 97% yield.