1416767-53-7

Basic information

• Product Name: 5,5-dibenzyl-2,3,4,5-tetrahydropyridine
• Synonyms: 5,5-dibenzyl-2,3,4,5-tetrahydropyridine
• CAS NO: 1416767-53-7
• Molecular Weight: 263.382
• Mol File: 1416767-53-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5,5-dibenzyl-2,3,4,5-tetrahydropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-dibenzyl-2,3,4,5-tetrahydropyridine(1416767-53-7)
• EPA Substance Registry System: 5,5-dibenzyl-2,3,4,5-tetrahydropyridine(1416767-53-7)

Safety Data

• Hazardous Substances Data: 1416767-53-7(Hazardous Substances Data)

Upstream product

• 85908-96-9 2-oxopiperidine-1-carboxylic acid tert-butyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 1416767-41-3 6,6-dibenzyl-6,7,8,9-tetrahydrobenzo[e]pyrido[2,1-b][1,3]oxazin-11(5aH)-one 
• 1416767-40-2 dimethyl 1,1-dibenzyl-6-oxo-1,3,4,11a-tetrahydro-2H-pyrido[1,2-b]isoquinoline-11,11(6H)-dicarboxylate 
• 1416767-42-4 6,6-dibenzyl-2-nitro-6,7,8,9-tetrahydrobenzo[e]pyrido[2,1-b][1,3]oxazin-11(5aH)-one 
• 1416767-43-5 4,4-dibenzyl-2,3,4,4a-tetrahydronaphtho[2,3-e]pyrido[2,1-b][1,3]oxazin-12(1H)-one 
• 1416767-44-6 12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one 
• 1416767-45-7 10,10-dibenzyl-8,9,10,10a-tetrahydrodipyrido[2,1-b:3',2'-e][1,3]oxazin-5(7H)-one 
• 1416767-46-8 6,6-dibenzyl-6,7,8,9-tetrahydrobenzo[e]pyrido[2,1-b][1,3]thiazin-11(5aH)-one 
• 1416767-47-9 6,6-dibenzyl-5-methyl-6,7,8,9-tetrahydro-5H-pyrido[2,1-b]quinazolin-11(5aH)-one 
• 1416767-48-0 1,3-dichloro-10,10-dibenzyl-8,9,10,10a-tetrahydro-7H-pyrido[1,2-b][4,1,2]benzoxathiazine 5,5-dioxide 
• 1547397-17-0 9,9-dibenzylhexahydropyrido[2,1-b][1,3]oxazin-4(6H)-one 
• 1547397-58-9 8,8-dibenzylhexahydroimidazo[1,2-a]pyridin-3(5H)-one 
• 1547397-61-4 9,9-dibenzylhexahydro-1H-pyrido[1,2-a]pyrimidin-4(6H)-one 
• 1547397-75-0 9,9-dibenzylhexahydropyrido[2,1-b][1,3]thiazin-4(6H)-one 

Relevant articles and documents

Direct imine acylation: Rapid access to diverse heterocyclic scaffolds

A simple and efficient procedure to prepare a range of diverse heterocycles by the direct acylation of imines using a variety of functionalized benzoic acids is described. The methodology features a novel method for N-acyliminium ion generation followed by in situ intramolecular trapping by oxygen-, nitrogen-, sulfur-and carbon-based nucleophiles. Preliminary mechanistic studies, using ReactIR, are also reported.