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(2S,4S,5R)-2-(4-fluorophenyl)-4-methyl-5-phenyl-1,3-oxazolidine

Compound with spectra: 1 NMR

(2S,4S,5R)-2-(4-fluorophenyl)-4-methyl-5-phenyl-1,3-oxazolidine
SpectraBase Compound ID 3APp29jfje6
InChI InChI=1S/C16H16FNO/c1-11-15(12-5-3-2-4-6-12)19-16(18-11)13-7-9-14(17)10-8-13/h2-11,15-16,18H,1H3/t11-,15-,16-/m0/s1
InChIKey OJPFEHYUYKODBF-UVBJJODRSA-N
Mol Weight 257.31 g/mol
Molecular Formula C16H16FNO
Exact Mass 257.121592 g/mol
Enantiomer InChIKey OJPFEHYUYKODBF-HFBAOOFYSA-N

View Spectrum of (2S,4S,5R)-2-(4-fluorophenyl)-4-methyl-5-phenyl-1,3-oxazolidine

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3;0.2M
(2R,4R,5R)-2-(4-fluorophenyl)-4-methyl-5-phenyl-1,3-oxazolidine
(2R,4S,5R)-2-(4-fluorophenyl)-4-methyl-5-phenyl-1,3-oxazolidine
(2S,4R,5R)-2-(4-fluorophenyl)-4-methyl-5-phenyl-1,3-oxazolidine
GUTLRLZWWAASMM-JQFCIGGWSA-N
GUTLRLZWWAASMM-COXVUDFISA-N
GUTLRLZWWAASMM-RRQGHBQHSA-N
GUTLRLZWWAASMM-XOKHGSTOSA-N
AZXOTROCWLZHAP-UVBJJODRSA-N
AZXOTROCWLZHAP-RLCCDNCMSA-N
AZXOTROCWLZHAP-KNXALSJPSA-N
Title Journal or Book Year
Substituent Influences on the Stability of the Ring and Chain Tautomers in 1,3-O,N-Heterocyclic Systems:  Characterization by 13C NMR Chemical Shifts, PM3 Charge Densities, and Isodesmic Reactions The Journal of Organic Chemistry 2001

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