141584-02-3

Basic information

• Product Name: N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-2,3-dihydro-4-pyridone
• Synonyms: N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-2,3-dihydro-4-pyridone
• CAS NO: 141584-02-3
• Molecular Weight: 371.433
• Mol File: 141584-02-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-2,3-dihydro-4-pyridone(CAS DataBase Reference)
• NIST Chemistry Reference: N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-2,3-dihydro-4-pyridone(141584-02-3)
• EPA Substance Registry System: N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-2,3-dihydro-4-pyridone(141584-02-3)

Safety Data

• Hazardous Substances Data: 141584-02-3(Hazardous Substances Data)

Upstream product

• 140-88-5 ethyl acrylate 
• 501-53-1 benzyl chloroformate 
• 34164-50-6 4-penten-1-ylmagnesium bromide 
• 107971-44-8 N-<(benzyloxy)carbonyl>-2-(4-hydroxybutyl)-2,3-dihydro-4-pyridone 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 141584-01-2 N-<(benzyloxy)carbonyl>-2-(3-formylpropyl)-2,3-dihydro-4-pyridone 
• 620-08-6 4-methoxypyridine 

Downstream Products

• 141584-10-3 N-<(benzyloxy)carbonyl>-2-(trans-5-(ethoxycarbonyl)-4-pentenyl)-4-(triethylsilyloxy)-1,2-dihydropyridine 
• 141584-11-4 N-<(benzyloxy)carbonyl>-11-(ethoxycarbonyl)-2-azatricyclo<5.3.1.0^3,8>undecan-9-one 
• 141584-14-7 5α,6,7,8,9α,10α-hexahydro-1-<(benzyloxy)carbonyl>-5-<1-(ethoxycarbonyl)methyl>-4-quinolone 
• 141660-71-1 N-<(benzyloxy)carbonyl>-11-(ethoxycarbonyl)-2-azatricyclo<5.3.1.0^3,8>undec-9-ene 
• 141584-04-5 N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-4-hydroxy-1,2-dihydropyridine 
• 141584-03-4 N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-4-hydroxy-1,2,3,4-tetrahydropyridine 
• 146253-95-4 N-<(Benzyloxy)carbonyl>-4-chloro-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-1,2-dihydropyridine 

Relevant articles and documents

Studies toward the total synthesis of dihydrolycolucine. Preparation of AB and CEF ring fragments

A strategy for the synthesis of the lycopodium alkaloid dihydrolycolucine (1) has been investigated. Synthetic routes were developed based on N-acylpyridinium salt chemistry to prepare target fragments 3 and 4 that could ultimately converge to the natural