136413-53-1

Basic information

• Product Name: 2-(3,4-dimethoxybenzyl)-2-benzamidomalonate de diethyle
• CAS NO: 136413-53-1
• Molecular Weight: 429.47
• Mol File: 136413-53-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(3,4-dimethoxybenzyl)-2-benzamidomalonate de diethyle(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-dimethoxybenzyl)-2-benzamidomalonate de diethyle(136413-53-1)
• EPA Substance Registry System: 2-(3,4-dimethoxybenzyl)-2-benzamidomalonate de diethyle(136413-53-1)

Safety Data

• Hazardous Substances Data: 136413-53-1(Hazardous Substances Data)

Upstream product

• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 21852-32-4 4-bromomethyl-1,2-dimethoxybenzene 
• 96-86-6 diethyl benzamidomalonate 

Downstream Products

• 857805-18-6 6,7-Dimethoxy-1-phenyl-3,4-dihydro-isoquinoline-3-carboxylic acid 
• 57061-11-7 6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinoleine-3-carboxylate de methyle 
• 136413-55-3 6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinoleine-3,3-dicarboxylate de diethyle 

Relevant articles and documents

Cycloaddition d'ylures d'azomethine derives de la 3,4-dihydro-6,7-dimethoxy-3-methoxycarbonyl-isoquinoleine

Three azomethine ylide precursors including the 3,4-dihydro-6,7-dimethoxyisoquinoline-3-carboxylate moiety were synthesized.The 1,3-dipolar species formed from these products react with activated dipolarophilic olefines leading diastereospecifically to derivatives of 4',5'-dimethoxy-1,2-benzo-4,7-imino-4-methoxycarbonyl-1-cycloheptene.Proton magnetic resonance data allowed the determination of the stereochemistry of the cycloadducts. Key words: cyclic azomethine ylide, azabicyclic compounds, stereochemistry.