60256-44-2

Basic information

• Product Name: Benzenamine, N-(2-bromo-2-propenyl)-N-methyl-
• CAS NO: 60256-44-2
• Molecular Formula: C10H12BrN
• Molecular Weight: 226.116
• Mol File: 60256-44-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-(2-bromo-2-propenyl)-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-(2-bromo-2-propenyl)-N-methyl-(60256-44-2)
• EPA Substance Registry System: Benzenamine, N-(2-bromo-2-propenyl)-N-methyl-(60256-44-2)

Safety Data

• Hazardous Substances Data: 60256-44-2(Hazardous Substances Data)

Upstream product

• 100-61-8 N-methylaniline 
• 513-31-5 2-bromoallyl bromide 

Downstream Products

• 4282-82-0 N-methyl-N-propargylaniline 
• 100-61-8 N-methylaniline 
• 1176684-21-1 N-(2-(indol-1-yl)-allyl)-N-methylaniline 

Relevant articles and documents

Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N?H and Aryl C?H Bond Cleavage

An asymmetric palladium-catalyzed intramolecular oxidative aminoarylation of alkenes has been developed with quinoline–oxazoline chiral ligands and Ag2CO3 as the oxidant. Various indolines containing a quaternary stereogenic center were synthesized in high yield with excellent enantioselectivity. Preliminary mechanistic studies suggest that the addition of a catalytic amount of phenylglyoxylic acid significantly accelerates the reaction and slightly enhances the enantioselectivity.