280128-43-0

Basic information

• Product Name: tert-butyl N-[(1R,R_S)-1-phenyl-2-p-tolylsulfinylethyl]carbamate
• Synonyms: tert-butyl N-[(1R,R_S)-1-phenyl-2-p-tolylsulfinylethyl]carbamate
• CAS NO: 280128-43-0
• Molecular Weight: 359.489
• Mol File: 280128-43-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tert-butyl N-[(1R,R_S)-1-phenyl-2-p-tolylsulfinylethyl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl N-[(1R,R_S)-1-phenyl-2-p-tolylsulfinylethyl]carbamate(280128-43-0)
• EPA Substance Registry System: tert-butyl N-[(1R,R_S)-1-phenyl-2-p-tolylsulfinylethyl]carbamate(280128-43-0)

Safety Data

• Hazardous Substances Data: 280128-43-0(Hazardous Substances Data)

Upstream product

• 280128-26-9 (S)-N-[(2R,R_S)-1-phenyl-2-p-tolylsulfinylethyl]-p-toluenesulfinamide 
• 67341-01-9 (R)-N-(tert-butoxycarbonyl)phenylglycinol 
• 350479-90-2 (S,E)-N-benzylidene-4-methylbenzenesulfinamide 
• 1519-39-7 (R)-methyl p-tolyl sulfoxide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 280128-39-4 (1R,R_S)-1-phenyl-2-p-tolylsulfinylethylamine 

Downstream Products

• 56613-80-0 D-2-phenylglycinol 
• 67341-01-9 (R)-N-(tert-butoxycarbonyl)phenylglycinol 

Relevant articles and documents

Sulfenate substitution as a complement and alternative to sulfoxidation in the diastereoselective preparation of chiral β-substituted β-amino sulfoxides

Building from a previous communication, the reaction of sulfenate anions with chiral N-Boc-protected β-substituted β-amino iodides was evaluated as a conceptually different synthetic approach to chiral β-substituted β-amino sulfoxides. Using arenesulfenat

Additions of Enantiopure α-Sulfinyl Carbanions to (S)-N-Sulfinimines: Asymmetric Synthesis of β-Amino Sulfoxides and β-Amino Alcohols

The addition of the lithium anions derived from (R)- and (S)-methyl and -ethyl p-tolyl sulfoxides to (S)-N-benzylidene-p-toluenesulfinamide provides an easy access route to enantiomerically pure β-(N-sulfinyl)amino sulfoxides. Stereoselectivity can be ach