834898-11-2

Basic information

• Product Name: 4-Oxazolidinepentanoic acid, 2-(1,1-dimethylethyl)-5-oxo-3-[(phenylmethoxy)carbonyl]-, methyl ester, (2S,4S)-
• CAS NO: 834898-11-2
• Molecular Formula: C21H29NO6
• Molecular Weight: 391.464
• Mol File: 834898-11-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-Oxazolidinepentanoic acid, 2-(1,1-dimethylethyl)-5-oxo-3-[(phenylmethoxy)carbonyl]-, methyl ester, (2S,4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Oxazolidinepentanoic acid, 2-(1,1-dimethylethyl)-5-oxo-3-[(phenylmethoxy)carbonyl]-, methyl ester, (2S,4S)-(834898-11-2)
• EPA Substance Registry System: 4-Oxazolidinepentanoic acid, 2-(1,1-dimethylethyl)-5-oxo-3-[(phenylmethoxy)carbonyl]-, methyl ester, (2S,4S)-(834898-11-2)

Safety Data

• Hazardous Substances Data: 834898-11-2(Hazardous Substances Data)

Upstream product

• 14273-85-9 methyl 4-iodobutanoate 
• 163084-89-7 benzyl (2S,4S)-2-(tert-butyl)-4-isobutyl-5-oxooxazolidine-3-carboxylate 

Downstream Products

• 26630-55-7 (2S)-L-α-Aminopimelic acid 
• 47312-26-5 (S)-2-Benzyloxycarbonylamino-heptanedioic acid 7-methyl ester 

Relevant articles and documents

Practical and efficient enantioselective synthesis of α-amino acids in aqueous media

Enantiomerically pure natural and unnatural α-amino acids have been synthesized from a chiral melhyleneoxazolidinone by means of a highly diastereoselective 1,4-conjugate addition of alkyl iodides in aqueous media. The zinc-copper conjugate addition reaction exhibits high chemoselectivity, with the possibility of using functionalized iodides, to afford a single diastereomer in short reaction times and with good yields.