191090-38-7

Basic information

• Product Name: (S)-(-)-5,5-DIPHENYL-4-BENZYL-2-OXZOLIDINONE
• Synonyms: (S)-4-(-)-BENZYL-5,5-DIPHENYL-2-OXAZOLIDINONE;(S)-(-)-5,5-DIPHENYL-4-BENZYL-2-OXZOLIDINONE;(S)-5,5-Diphenyl-4-benzyl-2-oxazolidinone;)-5,5-Diphenyl-4-benzyl-2-oxzolidinone;(s)-(-)-5,5-diphenyl-4-(phenylmethyl)-2-oxazolidinone;(4S)-4-Benzyl-5,5-diphenyl-2-oxazolidinone;(S)-4-Benzyl-5,5-diphenyloxazolidin-2-one;(S)-5,5-Diphenyl-4-benzyl-2-oxazolidinone,99%e.e.
• CAS NO: 191090-38-7
• Molecular Formula: C₂₂H₁₉NO₂
• Molecular Weight: 329.39
• Product Categories: Chiral Auxiliaries;Oxazolidinone Derivatives;Asymmetric Synthesis
• Mol File: 191090-38-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 250-254 °C(lit.)
• Boiling Point: 553 ºC at 760 mmHg
• Flash Point: 288.3 ºC
• Appearance: /
• Density: 1.187±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.616
• CAS DataBase Reference: (S)-(-)-5,5-DIPHENYL-4-BENZYL-2-OXZOLIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(-)-5,5-DIPHENYL-4-BENZYL-2-OXZOLIDINONE(191090-38-7)
• EPA Substance Registry System: (S)-(-)-5,5-DIPHENYL-4-BENZYL-2-OXZOLIDINONE(191090-38-7)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 191090-38-7(Hazardous Substances Data)

Usage

General Description

(S)-(-)-5,5-diphenyl-4-benzyl-2-oxazolidinone is a chemical compound that belongs to the oxazolidinone class of compounds. It is a chiral molecule with a specific stereoisomeric configuration. (S)-(-)-5,5-DIPHENYL-4-BENZYL-2-OXZOLIDINONE has potential applications in organic synthesis, medicinal chemistry, and materials science. Its unique structure and properties make it a valuable building block in the development of new pharmaceuticals and other important organic compounds. It is important to handle this compound with care and follow appropriate safety measures when working with it in a laboratory setting.

InChI:InChI=1/C22H19NO2/c24-21-23-20(16-17-10-4-1-5-11-17)22(25-21,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-15,20H,16H2,(H,23,24)/t20-/m0/s1

Upstream product

• 79868-78-3 (S)-(-)-2-amino-1,1,3-triphenyl-1-propanol 
• 503-38-8 trichloromethyl chloroformate 
• 100-58-3 phenylmagnesium bromide 
• 3081-24-1 H-Phe-OEt 
• 637330-69-9 (S)-3-(2'-benzyl-3'-phenylpropionyl)-4-benzyl-5,5-diphenyloxazolidin-2-one 

Downstream Products

• 1308428-46-7 C₂₆H₂₆N₂O₂ 
• 1386977-28-1 (S)-3-(6-amino-5-methylpyridin-3-yl)-4-benzyl-5,5-diphenyloxazolidin-2-one 
• 1174133-86-8 (S)-4-benzyl-3-(pentan-3-ylideneamino)-5,5-diphenyloxazolidin-2-one 
• 1361955-28-3 (4S)-3-[(4,5-dimethyl-2-(methylsulfanyl)-3,6-dihydro-2H-thiopyranyl)carbonyl]-4-benzyl-5,5-diphenyl-2-oxazolidinone 
• 1361955-16-9 C₂₅H₂₁NO₃S₂ 
• 1361955-40-9 (S)-4-benzyl-3-(2-chloroacetyl)-5,5-diphenyloxazolidin-2-one 
• 878194-06-0 (R)-pentafluorophenyl 2-phenylpropionate 
• 1257306-42-5 C₃₁H₂₇NO₃ 
• 1051911-48-8 (S)-3-amino-4-benzyl-5,5-diphenyloxazolidin-2-one 

Relevant articles and documents

Synthesis and application of N-3,5-dinitrobenzoyl and C3 symmetric diastereomeric chiral stationary phases

Three diastereomeric chiral compounds, namely, (R,R)-(+)-2-amino-1,2-diphenylethanol, (1S,2R)-(+)-2-amino-1,2-diphenylethanol, and (1R,2R)-(+)-1,2-diphenylethylenediamine were used as starting materials for preparing three N-3,5-dinitrobenzoyl derivative

Liquid Chromatographic Resolution of Racemic 2-Oxazolidinones and their Analogs on Seven Pirkle-Type Chiral Stationary Phases

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A short synthesis of (S)-α-(diphenylmethyl)alkyl amines from amino acids

A range of (S)-α-(diphenylmethyl)alkyl amines were prepared from the corresponding (S)-α-amino acid ester hydrochlorides. These amines were derived by direct hydrogenation of their precursor oxazolidinones.