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(4R,5S)-(+)-cis-4,5-Diphenyl-2-oxazolidinone, 98%, ee: 98%|339256|86286-50-2

(4R,5S)-(+)-cis-4,5-Diphenyl-2-oxazolidinone, 98%, ee: 98%

Cat. No JK339256_500_MG
J&K Chemical

Product Information

Product Name
(4R,5S)-(+)-cis-4,5-Diphenyl-2-oxazolidinone, 98%, ee: 98%
Brand Name
J&K
Product Number
339256
CAS
86286-50-2
Molecular Formula
C15H13NO2
Molecular Weight
239.27
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
10868374
IUPAC Name
(4R,5S)-4,5-diphenyl-1,3-oxazolidin-2-one
InChI Key
LTENIVFVXMCOQI-KGLIPLIRSA-N
SMILES
C1=CC=C(C=C1)C@@H2C@@H(OC(=O)N2)C3=CC=CC=C3

Properties

Melting Point
229
Optical Activity
+57° to +61° (C=2, MeOH)

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Catalytic Kinetic Resolution and Desymmetrization of Amines
Publication Name: Synlett
Publication Date: 2022-04-13
DOI: 10.1055/a-1790-3230

From Geminal Dibromoalkenes
Publication Name: Science of Synthesis
Publication Date: 2015

Racemic and enantioselective total synthesis of heliespirones A & C
Publication Name: Science China Chemistry
Publication Date: 2011-01-08
DOI: 10.1007/s11426-010-4173-y

Allenyl Amides by Base-Catalyzed Rearrangement
Publication Name: Science of Synthesis
Publication Date: 2008

Reaction with Organic Dicarbonates
Publication Name: Science of Synthesis
Publication Date: 2005

(4R,5S)-(+)-cis-4,5-Diphenyl-2-oxazolidinone, 98%, ee: 98%

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