161687-28-1

Basic information

• Product Name: (5S,9S)-N-((2'S,3'S)-3'-hydroxy-2'-methyl-3'-phenylpropionyl)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one
• Synonyms: (5S,9S)-N-((2'S,3'S)-3'-hydroxy-2'-methyl-3'-phenylpropionyl)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one
• CAS NO: 161687-28-1
• Molecular Weight: 463.485
• Mol File: 161687-28-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5S,9S)-N-((2'S,3'S)-3'-hydroxy-2'-methyl-3'-phenylpropionyl)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5S,9S)-N-((2'S,3'S)-3'-hydroxy-2'-methyl-3'-phenylpropionyl)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one(161687-28-1)
• EPA Substance Registry System: (5S,9S)-N-((2'S,3'S)-3'-hydroxy-2'-methyl-3'-phenylpropionyl)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one(161687-28-1)

Safety Data

• Hazardous Substances Data: 161687-28-1(Hazardous Substances Data)

Upstream product

• 161687-27-0 (5S,9S)-N-(acryloyl)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one 
• 161687-23-6 2,3:4,6-di-O-isopropylidene-2-keto-L-gulofuranose-2-methylazidoformate 
• 161687-24-7 (5S,9S)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one 
• 161687-22-5 2,3:4,6-di-O-isopropylidene-2-keto-L-gulofuranose-2-methylchloroformate 
• 17682-70-1 2,3:4,6-bis-O-isopropylidene-L-sorbose 
• 18467-77-1 dikegulac 
• 100-52-7 benzaldehyde 
• 161687-25-8 (5S,9S)-N-propionyl-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one 

Downstream Products

• 127379-92-4 (1S,2R)-2-methyl-1-phenyl-propane-1,3-diol 
• 161687-24-7 (5S,9S)-4-aza-5,9:6,10-di-O-isopropylidene-2,8-dioxabicyclo<4.3.0>nonan-3-one 

Relevant articles and documents

Highly Regio- and Stereo-specific Preparation of a New Carbohydrate-based 1,3-Oxazin-2-one by the INIR Method and its Applications in Some Asymmetric Transformations

Preliminary experiments show that a new gulonic acid-derived 1,3-oxazin-2-one, prepared by an intramolecular nitrene insertion reaction (INIR) method, serves to control both asymmetric aldol and Diels-Alder reactions with excellent stereo-selection.