31949-41-4

Basic information

• Product Name: 3-Pyridinecarboxamide, N-[2-(3,4-dimethoxyphenyl)ethyl]-
• CAS NO: 31949-41-4
• Molecular Formula: C16H18N2O3
• Molecular Weight: 286.331
• Mol File: 31949-41-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Pyridinecarboxamide, N-[2-(3,4-dimethoxyphenyl)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinecarboxamide, N-[2-(3,4-dimethoxyphenyl)ethyl]-(31949-41-4)
• EPA Substance Registry System: 3-Pyridinecarboxamide, N-[2-(3,4-dimethoxyphenyl)ethyl]-(31949-41-4)

Safety Data

• Hazardous Substances Data: 31949-41-4(Hazardous Substances Data)

Upstream product

• 59-67-6 nicotinic acid 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 10400-19-8 3-pyridinecarbonyl chloride 
• 123-75-1 pyrrolidine 
• 614-18-6 3-pyridinecarboxylic acid ethyl ester 

Downstream Products

• 3161-08-8 6,7-dimethoxy-1-(pyridin-3-yl)-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Synthesis of anabaseine and anabasine derivatives: Structural modifications of possible nicotinic agonists

Coupling nicotinoyl chloride with 3,4-dimetoxyphenethylamine under Bischler-Napieralski cyclization afforded the isoquinoline (4) in good yield. This latter was used as starting material to obtain with only hydrobromic acid a product with demethylation at

Diazaestrones and analogs. II. Structural modifications of succinimidoethyldihydroisoquinoline, heterosteroid precursor, to establish structure-analgesic activity relationship

β-1-(succinimidoethyl)-6,7-dimethoxydihydroisoquinoline having exihibited a stronger analgesic activity than the methylester of 2-methoxy-8,13-diazaestrone, its structure has been systematically modified in view of establishing a relation between structur