179088-59-6

Basic information

• Product Name: (2S,3S)-4-Benzyl-3-[3-hydroxy-2-methyl-1-oxo-3-[(4-phenylsulfanyl)-3,4,5,6-tetrahydro-(2H)-pyran-4-yl]propionyl]oxazolidin-2-one
• Synonyms: (2S,3S)-4-Benzyl-3-[3-hydroxy-2-methyl-1-oxo-3-[(4-phenylsulfanyl)-3,4,5,6-tetrahydro-(2H)-pyran-4-yl]propionyl]oxazolidin-2-one
• CAS NO: 179088-59-6
• Molecular Weight: 455.575
• Mol File: 179088-59-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,3S)-4-Benzyl-3-[3-hydroxy-2-methyl-1-oxo-3-[(4-phenylsulfanyl)-3,4,5,6-tetrahydro-(2H)-pyran-4-yl]propionyl]oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-4-Benzyl-3-[3-hydroxy-2-methyl-1-oxo-3-[(4-phenylsulfanyl)-3,4,5,6-tetrahydro-(2H)-pyran-4-yl]propionyl]oxazolidin-2-one(179088-59-6)
• EPA Substance Registry System: (2S,3S)-4-Benzyl-3-[3-hydroxy-2-methyl-1-oxo-3-[(4-phenylsulfanyl)-3,4,5,6-tetrahydro-(2H)-pyran-4-yl]propionyl]oxazolidin-2-one(179088-59-6)

Safety Data

• Hazardous Substances Data: 179088-59-6(Hazardous Substances Data)

Upstream product

• 179088-46-1 4-(Methoxy-phenylsulfanyl-methyl)-tetrahydro-pyran 
• 294211-62-4 4-[Methoxy(phenylsulfanyl)methyl]-3,4,5,6-tetrahydro-(2H)-pyran-4-ol 
• 131685-53-5 (S)-4-benzyl-3-propionyl-2-oxazolidinone 
• 13865-50-4 methoxymethyl phenyl sulfide 
• 211504-69-7 di-n-butylboron enolate of (S)-4-benzyl-N-propionyl-2-oxazolidinone 
• 179088-48-3 4-(Phenylsulfanyl)-3,4,5,6-tetrahydropyran-4(2H)-carboxaldehyde 

Downstream Products

• 179238-92-7 (2R,3R)-2-Methyl-1-(4-phenylsulfanyl-3,4,5,6-tetrahydro-(2H)-pyran-4-yl)propane-1,3-diol 

Relevant articles and documents

Stereochemically controlled synthesis of 1,8-dioxaspiro[4.5]decanes and 1-oxa-8-thiaspiro[4.5]decanes by phenylsulfanyl migration

Single enantiomers and diastereoisomers of 2- and 3-alkyl-3-phenylsulfanyl-1,8-dioxa- and 1-oxa-8-thiaspiro-[4.5]decanes can be prepared in good yield by acid-catalysed phenylsulfanyl (PhS-) migration. Either the syn-or anti-stereochemistry can be controlled by aldol reactions or by reduction of hydroxy-ketones. The Royal Society of Chemistry 2000.