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(S)-(-)-(TRIFLUOROMETHYL)-OXIRANE

Compound with spectra: 2 NMR

(S)-(-)-(TRIFLUOROMETHYL)-OXIRANE
SpectraBase Compound ID 502KzSrfltG
InChI InChI=1S/C3H3F3O/c4-3(5,6)2-1-7-2/h2H,1H2/t2-/m1/s1
InChIKey AQZRARFZZMGLHL-UWTATZPHSA-N
Mol Weight 112.051 g/mol
Molecular Formula C3H3F3O
Exact Mass 112.013599 g/mol
Enantiomer InChIKey AQZRARFZZMGLHL-REOHCLBHSA-N
Racemate InChIKey AQZRARFZZMGLHL-UHFFFAOYSA-N

View Spectrum of (S)-(-)-(TRIFLUOROMETHYL)-OXIRANE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (S)-(-)-(TRIFLUOROMETHYL)-OXIRANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1,2-Epoxy-3,3,3-trifluoropropane
(R)-(+)-2-TRIFLUOROMETHYLOXIRANE
(S)-(-)-1,2-DIHYDROXY-3,3,3-TRIFLUORO-2-PROPANOL
3,3,3-trifluoropropane-1,2-diol
(S)-(-)-1-ETHOXY-3,3,3-TRIFLUORO-2-PROPANOL
1,1,1,3-TETRAFLUOROPROPAN-2-OL
1,1,1,3-TETRAFLUORO-2-PROPANOL
1,2-Epoxy-3-fluoropropane
(R)-(-)-1-BROMO-3,3,3-TRIFLUORO-2-PROPANOL
3-bromo-1,1,1-trifluoropropan-2-ol
Title Journal or Book Year
Chiral Synthesis via Organoboranes. 40. Selective Reductions. 55. A Simple One-Pot Synthesis of the Enantiomers of Trifluoromethyloxirane. A General Synthesis in High Optical Purities of .alpha.-Trifluoromethyl Secondary Alcohols via the Ring-Cleavage Reactions of the Epoxide The Journal of Organic Chemistry 1995

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