191090-40-1

Basic information

• Product Name: (R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDINONE
• Synonyms: (R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDINONE;(R)-(+)-4-BENZYL-5,5-DIPHENYL-2-OXAZOLIDINONE;(R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDIN INONE, 98%;(4R)-5,5-Diphenyl-4-benzyl-2-oxazolidinone;(R)-4-Benzyl-5,5-diphenyloxazolidin-2-one;(R)-(+)-5,5-Diphenyl-4-benzyl-2-oxazolidinone, ee: 98%;(R)-5,5-Diphenyl-4-benzyl-2-oxazolidinone,99%e.e.;(4R)-4-benzyl-5,5-diphenyl-1,3-oxazolidin-2-one
• CAS NO: 191090-40-1
• Molecular Formula: C₂₂H₁₉NO₂
• Molecular Weight: 329.39
• Product Categories: Asymmetric Synthesis;Chiral Auxiliaries;Oxazolidinone Derivatives
• Mol File: 191090-40-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 250-254 °C(lit.)
• Boiling Point: 553 ºCat 760 mmHg
• Flash Point: 288.3 ºC
• Appearance: /
• Density: 1.187±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 2.83E-12mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: (R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDINONE(191090-40-1)
• EPA Substance Registry System: (R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDINONE(191090-40-1)

Safety Data

• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 191090-40-1(Hazardous Substances Data)

Usage

Chemical Properties

White power

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-/m1/s1

Downstream Products

• 1361955-29-4 (4S)-3-[(4,5-dimethyl-2-(methylsulfanyl)-3,6-dihydro-2H-thiopyranyl)carbonyl]-4-benzyl-5,5-diphenyl-2-oxazolidinone 
• 1361955-17-0 C₂₅H₂₁NO₃S₂ 

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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