370861-83-9

Basic information

• Product Name: tert-butyl 7-[(diphenoxyphosphoryl)oxo]-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate
• Synonyms: tert-butyl 7-[(diphenoxyphosphoryl)oxo]-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate
• CAS NO: 370861-83-9
• Molecular Weight: 445.452
• Mol File: 370861-83-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: tert-butyl 7-[(diphenoxyphosphoryl)oxo]-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 7-[(diphenoxyphosphoryl)oxo]-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate(370861-83-9)
• EPA Substance Registry System: tert-butyl 7-[(diphenoxyphosphoryl)oxo]-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate(370861-83-9)

Safety Data

• Hazardous Substances Data: 370861-83-9(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 105-60-2 caprolactam 
• 106412-36-6 tert-butyl 2-oxoazepane-1-carboxylate 
• 2524-64-3 chlorophosphoric acid diphenyl ester 

Downstream Products

• 1372716-11-4 tert-butyl 7-((2-methoxyphenyl)(phenyl)phosphino)-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate-borane complex 
• 1372716-18-1 7-((2S,5S)-1-oxo-2,5-diphenyl-λ5-phospholan-1-yl)-2,3,4,5-tetrahydro-azepine-1-carboxylic acid tert-butyl ester 
• 1372716-08-9 tert-butyl 7-(diphenylphosphino)-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate-borane complex 
• 1097200-67-3 tert-butyl 7-(phenylethynyl)-2,3,4,5-tetrahydroazepine-1-carboxylate 
• 64944-51-0 (α-hexahydroazepinylidene)-acetophenone 
• 370861-90-8 tert-butyl 7-phenyl-2,3,4,5-tetrahydro-1H-azepine-1-carboxylate 

Relevant articles and documents

Gold-catalysed synthesis of exocyclic vinylogous amides and β-amino ketones: A detailed study on the 5-exo/6-endo-dig selectivity, methodology and scope

The gold(I)-catalysed reaction of N-Boc-protected 6-alkynyl-3,4-dihydro-2H-pyridines, which gives synthetically useful vinylogous amides (β-enaminones), has been studied in detail, in order to optimize the reaction conditions, enlarge the scope and gain i

Palladium-catalyzed coupling of vinyl phosphates with aryl or heteroaryl boronic acids. Application to the synthesis of substituted nitrogen containing heterocycles

Substituted nitrogen-containing heterocycles were prepared in three steps from commercially available derivatives via an extension of the Suzuki reaction involving the palladium-catalyzed coupling of vinyl phosphates with aryl or heteroaryl boronic acids.