136620-74-1

Basic information

• Product Name: methyl(4S,5R)-5-phenyl-2-thioxooxazolidine-4-carboxylate
• Synonyms: methyl(4S,5R)-5-phenyl-2-thioxooxazolidine-4-carboxylate
• CAS NO: 136620-74-1
• Molecular Weight: 237.279
• Mol File: 136620-74-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl(4S,5R)-5-phenyl-2-thioxooxazolidine-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl(4S,5R)-5-phenyl-2-thioxooxazolidine-4-carboxylate(136620-74-1)
• EPA Substance Registry System: methyl(4S,5R)-5-phenyl-2-thioxooxazolidine-4-carboxylate(136620-74-1)

Safety Data

• Hazardous Substances Data: 136620-74-1(Hazardous Substances Data)

Upstream product

• 21055-37-8 methyl isothiocyanatoacetate 
• 100-52-7 benzaldehyde 
• 851402-42-1 3-(2-isothiocyanato-acetyl)-oxazolidin-2-one 
• 67-56-1 methanol 
• 109-88-6 magnesium methanolate 
• 104324-23-4 (S)-4-Benzyl-3-((4S,5R)-5-phenyl-2-thioxo-oxazolidine-4-carbonyl)-oxazolidin-2-one 

Downstream Products

• 136620-84-3 (2R,3S)-2-((tert-butoxycarbonyl)amino)-3-((4-methylbenzyl)thio)-3-phenylpropionic acid 
• 136620-76-3 methyl (2S,3R)-2-((tert-butoxycarbonyl)amino)-3-((methanesulfonyl)oxy)-3-phenylpropionate 
• 136620-77-4 methyl (2R,3S)-3-(acetylthio)-2-((tert-butoxycarbonyl)amino)-3-phenylpropionate 
• 136620-75-2 methyl (2S,3R)-2-((tert-butyloxycarbonyl)amino)-3-hydroxy-3-phenylpropionate 
• 136642-82-5 methyl (4S,5R)-3-N-tert-butoxycarbonyl-5-phenyl-1,3-oxazolidin-2-oxo-4-carboxylate 
• 136620-78-5 methyl(2R,3S)-2-((tert-butyloxycarbonyl)amino)-3-mercapto-3-phenylpropionate 
• 141394-65-2 (4S,5R)-2-Oxo-5-phenyl-oxazolidine-4-carboxylic acid methyl ester 
• 63658-17-3 methyl 2-(tert-butoxycarbonylamino)-3-phenylacrylate 
• 88422-03-1 (4S,5R)-5-Phenyl-2-thioxo-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-methyl ester 

Relevant articles and documents

Catalytic enantioselective aldol additions of α-isothiocyanato imides to aldehydes

Highly enantioselective organocatalytic aldol additions of α-isothiocyanato imides to aldehydes are reported. These reactions provide convenient access to enantiomerically enriched and protected β-hydroxy-α-amino acids with catalyst loadings as low as 1 m

Cyclic anti-aggregatory peptides

This invention relates to compounds of the formula: STR1 wherein: A' is absent, Asn, Gln, Ala or Abu; A is absent or a D- or L-amino acid chosen from Arg, HArg, (Me2)Arg, (Et2)Arg, Abu, Ala, Gly, His, Lys, or an α-R' substituted deri