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(S)-(-)-1-AMINO-3,3,3-TRIFLUORO-2-PROPANOL

Compound with spectra: 2 NMR

(S)-(-)-1-AMINO-3,3,3-TRIFLUORO-2-PROPANOL
SpectraBase Compound ID ABpq0xBIQWP
InChI InChI=1S/C3H6F3NO/c4-3(5,6)2(8)1-7/h2,8H,1,7H2/t2-/m0/s1
InChIKey RISHBQWFBUTROQ-REOHCLBHSA-N
Mol Weight 129.08 g/mol
Molecular Formula C3H6F3NO
Exact Mass 129.040148 g/mol
Enantiomer InChIKey RISHBQWFBUTROQ-UWTATZPHSA-N
Racemate InChIKey RISHBQWFBUTROQ-UHFFFAOYSA-N

View Spectrum of (S)-(-)-1-AMINO-3,3,3-TRIFLUORO-2-PROPANOL

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)-(-)-1-AMINO-3,3,3-TRIFLUORO-2-PROPANOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
3-amino-1,1,1-trifluoropropan-2-ol
1,1,1,3-TETRAFLUORO-2-PROPANOL
1,1,1,3-TETRAFLUOROPROPAN-2-OL
3,3,3-trifluoropropane-1,2-diol
(S)-(-)-1,2-DIHYDROXY-3,3,3-TRIFLUORO-2-PROPANOL
(R)-(-)-1-BROMO-3,3,3-TRIFLUORO-2-PROPANOL
3-bromo-1,1,1-trifluoropropan-2-ol
(S)-(+)-1-AZIDO-3,3,3-TRIFLUORO-2-PROPANOL
3,3,3-TRIFLUORO-2-BROMOPROPYLAMINE
TRIFLUOROACETALDEHYDE-HYDRATE
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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