73611-42-4

Basic information

• Product Name: 10-oxa-4-aza-tricyclo[5.2.1.0(2,6)]decane
• Synonyms: 10-oxa-4-aza-tricyclo[5.2.1.0(2,6)]decane
• CAS NO: 73611-42-4
• Molecular Weight: 139.197
• Mol File: 73611-42-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 10-oxa-4-aza-tricyclo[5.2.1.0(2,6)]decane(CAS DataBase Reference)
• NIST Chemistry Reference: 10-oxa-4-aza-tricyclo[5.2.1.0(2,6)]decane(73611-42-4)
• EPA Substance Registry System: 10-oxa-4-aza-tricyclo[5.2.1.0(2,6)]decane(73611-42-4)

Safety Data

• Hazardous Substances Data: 73611-42-4(Hazardous Substances Data)

Upstream product

• 28871-92-3 7-oxabicyclo[2.2.1]heptane-2,3-dicarboximide 
• 19878-26-3 (3aR,4R,7S,7aS)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione 
• 272449-67-9 (+/-)-(3aR,4S,7R,7aS)-2-benzyl-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione 
• 29745-04-8 norcantharidin 
• 4938-65-2 C₁₅H₁₉NO 
• 6118-51-0 exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride 

Relevant articles and documents

IBX-mediated oxidation of unactivated cyclic amines: application in highly diastereoselective oxidative Ugi-type and aza-Friedel-Crafts reactions

The first o-iodoxybenzoic acid (IBX) mediated oxidation of unactivated amines to imines is described. A range of meso-pyrrolidines were shown to be suitable substrates. The chemical space was further explored with one-pot oxidative Ugi-type and aza-Friedel-Crafts reactions, which proved to be highly diastereoselective.