174840-02-9

Basic information

• Product Name: 4-Oxazolidinecarboxylicacid,2,2-dimethyl-,methylester,(4S)-(9CI)
• Synonyms: 4-Oxazolidinecarboxylicacid,2,2-dimethyl-,methylester,(4S)-(9CI)
• CAS NO: 174840-02-9
• Molecular Formula: C7H13NO3
• Molecular Weight: 159.18
• Product Categories: CARBOXYLICESTER
• Mol File: 174840-02-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Oxazolidinecarboxylicacid,2,2-dimethyl-,methylester,(4S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Oxazolidinecarboxylicacid,2,2-dimethyl-,methylester,(4S)-(9CI)(174840-02-9)
• EPA Substance Registry System: 4-Oxazolidinecarboxylicacid,2,2-dimethyl-,methylester,(4S)-(9CI)(174840-02-9)

Safety Data

• Hazardous Substances Data: 174840-02-9(Hazardous Substances Data)

Upstream product

• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 67-64-1 acetone 
• 117833-99-5 N-benzyloxycarbonyl 4(S)-(1'-methoxycarbonyl)-2,2-dimethyl-1,3-oxazolidine 

Relevant articles and documents

IOOC route to substituted chiral pyrrolidines. Potential glycosidase inhibitors

Branched-chain five-membered ring aza-sugar analogues, synthesized from amino acids by an intramolecular oxime-olefin cycloaddition reaction, the IOOC route, were found to be selective glycosidase inhibitors. The derivative 2,4(S)-di(hydroxymethyl)-3(S)-aminopyrrolidine, obtained from D-serine, was about 1 order of potency more active than its enantiomer obtained from L- serine.