1416767-44-6

Basic information

• Product Name: 12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one
• Synonyms: 12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one
• CAS NO: 1416767-44-6
• Molecular Weight: 433.55
• Mol File: 1416767-44-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one(1416767-44-6)
• EPA Substance Registry System: 12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one(1416767-44-6)

Safety Data

• Hazardous Substances Data: 1416767-44-6(Hazardous Substances Data)

Upstream product

• 1416767-53-7 5,5-dibenzyl-2,3,4,5-tetrahydropyridine 
• 86-48-6 1-hydroxy-2-naphthoic acid 
• 85908-96-9 2-oxopiperidine-1-carboxylic acid tert-butyl ester 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Substrate scope in the direct imine acylation of ortho-substituted benzoic acid derivatives: The total synthesis (±)-cavidine Dedicated to the memory of Sandy McKillop - Colleague, mentor, collaborator and friend

The direct imine acylation (DIA) and subsequent cyclisation of a range of imines with ortho-substituted benzoic acid derivatives is described. Variation in the coupling reagents, imine and benzoic acid were all examined. The DIA procedure was also applied in the total synthesis of (±)-cavidine.