1402830-73-2

Basic information

• Product Name: C₁₅H₁₉NO₃
• Synonyms: C₁₅H₁₉NO₃
• CAS NO: 1402830-73-2
• Molecular Weight: 261.321
• Mol File: 1402830-73-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₉NO₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₉NO₃(1402830-73-2)
• EPA Substance Registry System: C₁₅H₁₉NO₃(1402830-73-2)

Safety Data

• Hazardous Substances Data: 1402830-73-2(Hazardous Substances Data)

Upstream product

• 6729-50-6 2,3,4,5-tetrahydro-1H-2-benzazepin-1-one 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1402830-69-6 (+)-tert-butyl 1-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carboxylate 

Relevant articles and documents

Copper(I)-catalyzed enantioselective incorporation of ketones to cyclic hemiaminals for the synthesis of versatile alkaloid precursors

A general catalytic enantioselective method that can produce five-, six-, and seven-membered N-heterocycles possessing various ketone moieties starting from stable and easily available cyclic hemiaminals and ketones was developed. The method involves three successive steps in one pot (aldol addition, dehydration, and enantioselective intramolecular aza-Michael reaction), all of which are promoted by a chiral copper(I)-conjugated Bronsted base catalyst. This method is useful for rapid access to versatile chiral building blocks for the synthesis of drug-lead alkaloids.