205764-47-2

Basic information

• Product Name: (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine
• Synonyms: (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine
• CAS NO: 205764-47-2
• Molecular Weight: 313.44
• Mol File: 205764-47-2.mol

Chemical Properties

• CAS DataBase Reference: (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine(CAS DataBase Reference)
• NIST Chemistry Reference: (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine(205764-47-2)
• EPA Substance Registry System: (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine(205764-47-2)

Safety Data

• Hazardous Substances Data: 205764-47-2(Hazardous Substances Data)

Upstream product

• 2216-51-5 (-)-menthol 
• 165554-70-1 6-ethoxy-3-phenyl-6H-1,2-oxazine 

Downstream Products

• 491838-94-9 (5S,6R)-5-n-butyl-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-5,6-dihydro-4H-1,2-oxazine 
• 491838-93-8 (5R,6S)-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3,5-diphenyl-5,6-dihydro-4H-1,2-oxazine 

Relevant articles and documents

Synthesis of enantioenriched 2-substituted 4-phenylbutylamines by hydrogenolysis of optically pure 6-alkoxy-5,6-dihydro-4H-1,2-oxazines

Lewis acid promoted exchange of the 6-ethoxy group of 6H- 1,2-oxazines 1-3 with (-)-menthol furnished the optically active heterocycles 4-6. Diastereomers 4a and 4b, which could be separated efficiently by chromatography, were excellent substrates for hig