473554-13-1

Basic information

• Product Name: (2S,4R,5S)-N-tosyl-4-methyl-5-phenyl-1,2,3-oxathiazolidine-2-oxide
• Synonyms: (2S,4R,5S)-N-tosyl-4-methyl-5-phenyl-1,2,3-oxathiazolidine-2-oxide
• CAS NO: 473554-13-1
• Molecular Weight: 351.447
• Mol File: 473554-13-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,4R,5S)-N-tosyl-4-methyl-5-phenyl-1,2,3-oxathiazolidine-2-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4R,5S)-N-tosyl-4-methyl-5-phenyl-1,2,3-oxathiazolidine-2-oxide(473554-13-1)
• EPA Substance Registry System: (2S,4R,5S)-N-tosyl-4-methyl-5-phenyl-1,2,3-oxathiazolidine-2-oxide(473554-13-1)

Safety Data

• Hazardous Substances Data: 473554-13-1(Hazardous Substances Data)

Upstream product

• 861821-87-6 Cyclohexanesulfinic acid (1S,2R)-1-phenyl-2-(toluene-4-sulfonylamino)-propyl ester 
• 58107-41-8 N-[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]-4-methylbenzenesulfonamide 

Downstream Products

• 1011794-46-9 N-(furan-2-yl-methylene)-2,4,6-trimethylbenzenesulfinamide 
• 1011794-47-0 N-(3-phenyl-allylidene)-2,4,6-trimethylphenylsulfinamide 
• 1011794-45-8 N-(4-nitro-benzylidene)-2,4,6-trimethylbenzenesulfinamide 
• 1011794-43-6 (R_S,E)-N-benzylidene-2,4,6-trimethylbenzenesulfinamide 
• 1011794-44-7 N-(4-methoxy-benzylidene)-2,4,6-trimethylbenzenesulfinamide 
• 1011794-49-2 N-(hexylidene)-2,4,6-trimethylphenylsulfinamide 
• 1011794-48-1 N-(cyclohexylmethylene)-2,4,6-trimethylphenylsulfinamide 
• 1011794-50-5 C₂₅H₂₉NO₄S₂ 
• 58107-41-8 N-[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]-4-methylbenzenesulfonamide 
• 229639-56-9 (R)-N-{1-[1-(4-Chlorophenyl)cyclobutyl]-3-methylbutyl}amine 
• 861821-87-6 Cyclohexanesulfinic acid (1S,2R)-1-phenyl-2-(toluene-4-sulfonylamino)-propyl ester 

Relevant articles and documents

Practical and highly stereoselective technology for preparation of enantiopure sulfoxides and sulfinamides utilizing activated and functionally differentiated N-sulfonyl-1,2,3-oxathiazolidine-2-oxide derivatives

A simple, general, and practical technology to prepare enantiopure 1,2,3-oxathiazolidine-2-oxide derivatives using chiral aryl N-sulfonyl aminoalcohol derivatives and thionyl chloride is reported. The versatility of these novel chiral building blocks (MIOO and TMPOO), was exemplified by the expedient production of a variety of unique chiral sulfoxides and valuable chiral sulfinamides in excellent yields and enantiopurities.