1202888-53-6

Basic information

• Product Name: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](phenyl)methyl}acrylate
• Synonyms: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](phenyl)methyl}acrylate
• CAS NO: 1202888-53-6
• Molecular Weight: 371.392
• Mol File: 1202888-53-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](phenyl)methyl}acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](phenyl)methyl}acrylate(1202888-53-6)
• EPA Substance Registry System: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](phenyl)methyl}acrylate(1202888-53-6)

Safety Data

• Hazardous Substances Data: 1202888-53-6(Hazardous Substances Data)

Upstream product

• 956833-12-8 methyl 2-{[(tert-butoxycarbonyl)oxy](phenyl)methyl}acrylate 
• 81-83-4 1,8-Naphthalimide 

Relevant articles and documents

Asymmetric Allylic Amination of Morita-Baylis-Hillman Adducts with Simple Aromatic Amines by Nucleophilic Amine Catalysis

Asymmetric allylic amination of Morita-Baylis-Hillman (MBH) adducts with simple aromatic amines is successfully realized by nucleophilic amine catalysis. A range of substituted α-methylene-β-arylamino esters is accessed in moderate to high yields (up to 8

Enantioselective allylic amination of morita - baylis - hillman carbonates catalysed by modified cinchona alkaloids

An efficient procedure for the asymmetric allylic amination of Morita - Baylis - Hillman carbonates with cyclic imides catalysed by commercially available cinchona alkaloids is reported. It proves to be a facile protocol that affords α-methylene β-amino e