1296208-05-3

Basic information

• Product Name: (3S,3aS,6R,7aR)-6-ethyl-1,3-diphenylhexahydrobenzo[c]isoxazole-5,5(1H)-dicarbonitrile
• Synonyms: (3S,3aS,6R,7aR)-6-ethyl-1,3-diphenylhexahydrobenzo[c]isoxazole-5,5(1H)-dicarbonitrile
• CAS NO: 1296208-05-3
• Molecular Weight: 357.455
• Mol File: 1296208-05-3.mol

Chemical Properties

• CAS DataBase Reference: (3S,3aS,6R,7aR)-6-ethyl-1,3-diphenylhexahydrobenzo[c]isoxazole-5,5(1H)-dicarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,3aS,6R,7aR)-6-ethyl-1,3-diphenylhexahydrobenzo[c]isoxazole-5,5(1H)-dicarbonitrile(1296208-05-3)
• EPA Substance Registry System: (3S,3aS,6R,7aR)-6-ethyl-1,3-diphenylhexahydrobenzo[c]isoxazole-5,5(1H)-dicarbonitrile(1296208-05-3)

Safety Data

• Hazardous Substances Data: 1296208-05-3(Hazardous Substances Data)

Upstream product

• 1576-86-9 2-pentenal 
• 100-65-2 N-Phenylhydroxylamine 

Downstream Products

• 1296208-14-4 (2R,4R,5S)-2-ethyl-5-((S)-hydroxy(phenyl)methyl)-4-(phenylamino)cyclohexane-1,1-dicarbonitrile 
• 1296208-17-7 (1R,2R,4R,5S)-1-cyano-2-ethyl-5-((S)-hydroxy(phenyl)methyl)-4-(phenylamino)cyclohexanecarboxamide 

Relevant articles and documents

Optically active bicyclic N-heterocycles by organocatalytic asymmetric Michael addition/cyclization sequences

Highly stereoselective one-pot syntheses of various optically active N-heterocyclic bicycles have been developed. The protocols are based on an organocatalytic, asymmetric Michael addition followed by a condensation/ cycloaddition sequence to furnish aziridine carbonyls, β-lactams, or octahydrobenzo[c]isoxazoles depending on the reaction conditions and applied nucleophiles. Copyright