104266-89-9

Basic information

• Product Name: 2-Oxazolidinone, 3-(phenylacetyl)-4-(phenylmethyl)-, (S)-
• CAS NO: 104266-89-9
• Molecular Formula: C18H17NO3
• Molecular Weight: 295.338
• Mol File: 104266-89-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-(phenylacetyl)-4-(phenylmethyl)-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-(phenylacetyl)-4-(phenylmethyl)-, (S)-(104266-89-9)
• EPA Substance Registry System: 2-Oxazolidinone, 3-(phenylacetyl)-4-(phenylmethyl)-, (S)-(104266-89-9)

Safety Data

• Hazardous Substances Data: 104266-89-9(Hazardous Substances Data)

Upstream product

• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 65-85-0 benzoic acid 
• 103-82-2 phenylacetic acid 
• 144-55-8 sodium hydrogencarbonate 
• 103-80-0 phenylacetyl chloride 
• 3282-30-2 pivaloyl chloride 
• 888329-89-3 (S)-4-benzyl-3-(2-phenylethynyl)oxazolidin-2-one 
• 536-74-3 phenylacetylene 

Downstream Products

• 253680-94-3 [7-(4-benzyl-2-oxo-oxazolidin-3-yl)-5,7-dioxo-6-phenyl-heptyl]-carbamic acid tert-butyl ester 
• 265656-11-9 (S)‐4‐benzyl‐3‐[(S)‐2‐phenylpent‐4‐enoyl]oxazolidin‐2‐one 
• 510730-52-6 (4S,2'R)-3-((2'-benzyloxymethyl)phenylacetyl)-4-(phenylmethyl)-2-oxazolidinone 
• 14441-08-8 (3S)-N-(benzyloxycarbonyl)-3-amino-3-phenylpropanoic acid 
• 245323-41-5 tert-butyl (3S)-N-(benzyloxycarbonyl)-3-amino-3-phenylpropanoate 
• 245323-38-0 (S)-4-(tert-butoxy)-4-oxo-2-phenylbutanoic acid 
• 235097-99-1 (S)-4-benzyl-3-(2-phenylpent-4-enoyl)-2-oxazolidinone 
• 104267-07-4 2S-(N,N'-bis-(t-butoxycarbonyl)hydrazino)phenylacetic acid, methyl ester 
• 104267-07-4 2R-(N,N'-bis-(t-butoxycarbonyl)hydrazino)-3-phenylacetic acid, methyl ester 
• 1225034-56-9 (S)-ethyl 4-((S)-4-benzyl-2-oxooxazolidin-3-yl)-4-oxo-3-phenylbutanoate 
• 875-74-1 (R)-phenylglycine 
• 113543-52-5 (R)-Azido-phenyl-acetic acid benzyl ester 
• 111525-67-8 (3(2S),4S)-3-(2-azido-2-phenyl-1-oxoethyl)-4-(phenylmethyl)-2-oxazolidinone 
• 113543-46-7 (3(2R),4S)-3-(2-azido-1-oxo-2-phenethyl)-4-(phenylmethyl)-2-oxazolidinone 

Relevant articles and documents

A method for synthesis of acylated oxazolidone

The invention discloses a method for synthesis of acylated oxazolidone. Synthesis method of the invention, comprising the following steps: in the non-protic organic solvent, the compound III and under the action of an acid, the compound I with compound II carries out amidation reaction, to obtain compound IV. The method of the invention can be conducted under mild conditions, high yield, high purity, and is suitable for industrial production requirements.

A green synthetic route to imides from terminal alkynes and amides by simple solid catalysts

An atom-efficient and green synthetic route to highly valuable imides (5492% yields) from terminal alkynes and amides has been developed. This new route is composed of two consecutive reactions, that is, (i) the reported Cu(OH)2-catalyzed cross-coupling o

Stereoselective rearrangement of β-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones

Zinc alkoxides of syn- or anti-β-hydroxy-N-acyloxazolidin-2-ones undergo stereoselective rearrangement to afford their corresponding syn- or anti-N-2-hydroxyethyl-1,3-oxazinane-2,4-diones in good yield.