102897-57-4

Basic information

• Product Name: N,N'-(3,4-dimethoxy-β-phenylethyl)succindiamide
• Synonyms: N,N'-(3,4-dimethoxy-β-phenylethyl)succindiamide
• CAS NO: 102897-57-4
• Molecular Weight: 444.528
• Mol File: 102897-57-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N'-(3,4-dimethoxy-β-phenylethyl)succindiamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-(3,4-dimethoxy-β-phenylethyl)succindiamide(102897-57-4)
• EPA Substance Registry System: N,N'-(3,4-dimethoxy-β-phenylethyl)succindiamide(102897-57-4)

Safety Data

• Hazardous Substances Data: 102897-57-4(Hazardous Substances Data)

Upstream product

• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 123-25-1 succinic acid diethyl ester 
• 110-15-6 succinic acid 
• 41828-92-6 N-(3,4-dimethoxy-phenethyl)-succinamic acid methyl ester 

Downstream Products

• 39662-45-8 N-<2-(3,4-dimethoxyphenyl)ethyl>succinimide 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 6275-29-2 N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide 

Relevant articles and documents

Synthesis of bis-Tetrahydroisoquinolines Based on Homoveratrylamine and Several Dibasic Acids. 4. Reaction with Malonic and Succinic Acids

Bischler-Napieralski cyclization of amides synthesized from homoveratrylamine and malonic and succinic acids produced N-(3,4-dimethoxy-β-phenylethyl)-succinimide, 1,1-bis-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)methane, cleavage products, and several intermediates, the structures of which were confirmed using IR and NMR spectral data and x-ray crystal structure analysis.