130854-92-1

Basic information

• Product Name: Benzenesulfonamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-4-methyl-
• CAS NO: 130854-92-1
• Molecular Formula: C16H19NO4S
• Molecular Weight: 321.397
• Mol File: 130854-92-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-4-methyl-(130854-92-1)
• EPA Substance Registry System: Benzenesulfonamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-4-methyl-(130854-92-1)

Safety Data

• Hazardous Substances Data: 130854-92-1(Hazardous Substances Data)

Upstream product

• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 98-59-9 p-toluenesulfonyl chloride 
• 144-86-5 N-chloro-4-methylbenzenesulfonamide 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 855422-02-5 (2E)-3-phenyl-2-propenyl [(4-methylphenyl)sulfonyl] carbamic acid ester 

Downstream Products

• 167502-75-2 (1S,2S)-3-tert-butyldimethylsilyloxy-2-(4-methylphenyl)sulfonamido-1-phenyl1-propanol 

Relevant articles and documents

Efficient synthesis of chiral β- and γ-N-tosylaminoalcohols from 1-aryl-2-aminopropane-1,3-diols

(1S,2S)-1-Aryl-2-tozylaminopropan-1-ols were synthesized by cyclization of 1-aryl-2-aminopropane-1,3-diol to aryl(1-tosylaziridin-2-yl)methanols, followed by hydride reduction of the latter. Reduction of the aza-Payne rearrangement products of intermediat

Synthesis of optically pure 2-Aziridinemethanols: Versatile synthetic building blocks

Synthesis of three cis-trans pairs of N-sulfonylated-2-aziridinemethanols starting from (S)-threonine, (R)-allothreonine, a chiral 2-amino alcohol, or enantiomerically enriched 2,3-epoxy alcohols is described. A synthetic route to N-tosyl- and N-mesyl-2-a