928007-62-9

Basic information

• Product Name: Benzenesulfonamide, N-[(3R)-3-hydroxy-3-phenylpropyl]-4-methyl-
• CAS NO: 928007-62-9
• Molecular Formula: C16H19NO3S
• Molecular Weight: 305.398
• Mol File: 928007-62-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[(3R)-3-hydroxy-3-phenylpropyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[(3R)-3-hydroxy-3-phenylpropyl]-4-methyl-(928007-62-9)
• EPA Substance Registry System: Benzenesulfonamide, N-[(3R)-3-hydroxy-3-phenylpropyl]-4-methyl-(928007-62-9)

Safety Data

• Hazardous Substances Data: 928007-62-9(Hazardous Substances Data)

Upstream product

• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 928007-58-3 [1-(4-methylphenylsulfonyl)aziridin-2-yl]phenylmethanol 
• 40435-14-1 (S)-1-phenyl-2-(tosyloxy)ethanol 
• 73627-97-1 (R)-3-phenyl-3-hydroxypropanenitrile 
• 25779-13-9 (S)-1-phenyl-1,2-ethanediol 
• 21210-43-5 (S)-Methyl mandelate 
• 98-59-9 p-toluenesulfonyl chloride 
• 138750-31-9 (1R)-3-amino-1-phenyl-1-propanol 
• 936011-91-5 (S)-2-phenyl-1-tosylazetidine 
• 928007-60-7 (1S,2S)-2,3-epoxy-N-(4-methylphenylsulfonyl)-3-phenylpropan-1-amine 
• 928007-54-9 (1S,2S)-2-(4-methylphenylsulfonylamino)-3-(4-methylphenylsulfonyloxy)-1-phenylpropan-1-ol 

Relevant articles and documents

Lewis acid mediated SN2-type nucleophilic ring opening followed by [4+2] cycloaddition of N-tosylazetidines with aldehydes and ketones: synthesis of chiral 1,3-oxazinanes and 1,3-amino alcohols

A highly efficient strategy for Cu(OTf)2 mediated SN2-type nucleophilic ring opening followed by [4+2] cycloaddition reactions of enantiopure 2-phenyl-N-tosylazetidines with various aldehydes and ketones afforded a variety of substit

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