93380-05-3

Basic information

• Product Name: Butanoic acid, 2-[[(4-methylphenyl)sulfonyl]amino]-, methyl ester, (S)-
• CAS NO: 93380-05-3
• Molecular Formula: C12H17NO4S
• Molecular Weight: 271.337
• Mol File: 93380-05-3.mol

Chemical Properties

• CAS DataBase Reference: Butanoic acid, 2-[[(4-methylphenyl)sulfonyl]amino]-, methyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 2-[[(4-methylphenyl)sulfonyl]amino]-, methyl ester, (S)-(93380-05-3)
• EPA Substance Registry System: Butanoic acid, 2-[[(4-methylphenyl)sulfonyl]amino]-, methyl ester, (S)-(93380-05-3)

Safety Data

• Hazardous Substances Data: 93380-05-3(Hazardous Substances Data)

Upstream product

• 109075-06-1 (S)-2-((4R,5R)-2,2-dimethyl-5-((S)-1-tosylaziridin-2-yl)-1,3-dioxolan-4-yl)-1-tosyl-aziridine 
• 109075-02-7 1,2,5,6-tetradeoxy-1,6-dimethyl-2,5-bis-3,4-O-(1-methylethylidene)-L-iditol 
• 93380-04-2 ester methylique de la N-tosyl β-iodo L-alanine 
• 186581-53-3 diazomethane 
• 109075-04-9 2(S)-butyric acid 
• 109075-03-8 1,2,5,6-tetradeoxy-1,6-dimethyl-2,5-bis-L-iditol 

Relevant articles and documents

Nucleophilic Opening of Chiral Bis(aziridines): A Route to Enantiomerically Pure α-Amino Aldehydes or Acids and Polysubstituted Piperidines

α-Amino aldehydes or acids can be obtained by nucleophilic opening of suitably protected chiral bis(aziridines) derived from D-mannitol.Nucleophiles consist of a wide range of organometallic and heteronucleophilic reagents.Reaction orientation toward bis-

DIASTEREOSPECIFIC SYNTHESIS OF DIAZIRIDINES FROM D-MANNITOL. ACCESS TO CHIRAL α-AMINOACIDS.

Nucleophilic opening of chiral diastereoisomeric diaziridines obtained from D-mannitol leads to precursors of D or L α-aminoacids (or aldehydes) and also provides a means of synthesizing polyhydroxylated piperidines.

LITHIUM DIORGANOCUPRATE REACTIONS WITH L-SERINE DERIVATIVES

The lithium diorganocuprate reactions with L-serine derivatives are studied.Retention of configuration, or at least a high enantiomeric excess (> 80percent) of the formed α-amino esters is observed in all cases.Attempts are made to restrict side-reactions.