1055874-41-3

Basic information

• Product Name: (3S,9S)-3,9-diphenyloctahydro-5H,11H-bis[1,3]oxazolo[3,2-a:3',2'-e][1,5]diazocine
• Synonyms: (3S,9S)-3,9-diphenyloctahydro-5H,11H-bis[1,3]oxazolo[3,2-a:3',2'-e][1,5]diazocine
• CAS NO: 1055874-41-3
• Molecular Weight: 350.461
• Mol File: 1055874-41-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3S,9S)-3,9-diphenyloctahydro-5H,11H-bis[1,3]oxazolo[3,2-a:3',2'-e][1,5]diazocine(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,9S)-3,9-diphenyloctahydro-5H,11H-bis[1,3]oxazolo[3,2-a:3',2'-e][1,5]diazocine(1055874-41-3)
• EPA Substance Registry System: (3S,9S)-3,9-diphenyloctahydro-5H,11H-bis[1,3]oxazolo[3,2-a:3',2'-e][1,5]diazocine(1055874-41-3)

Safety Data

• Hazardous Substances Data: 1055874-41-3(Hazardous Substances Data)

Upstream product

• 20989-17-7 (2S)-2-phenylglycinol 
• 107-02-8 acrolein 

Relevant articles and documents

Facile preparation of 1,5-diazacyclooctanes from unsaturated imines: Effects of the hydroxyl groups on [4+4] dimerization

Hydroxyl groups on an unsaturated imine, which may be readily obtained from the corresponding unsaturated aldehyde and the 1,2-ethanolamine derivative, were found to efficiently activate a [4+4] dimerization reaction to produce the eight-membered 1,5-diazacyclooctane. A novel OH-π interaction between the two imines, in addition to the stabilization of the eight-membered diacetals, was proposed based on density functional theory calculations. Georg Thieme Verlag Stuttgart New York.