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(2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

Compound with spectra: 6 NMR

(2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL
SpectraBase Compound ID D2d6GLHpWDT
InChI InChI=1S/C12H16F3NO2/c1-8(7-17)11(12(13,14)15)16-9-3-5-10(18-2)6-4-9/h3-6,8,11,16-17H,7H2,1-2H3/t8-,11-/m0/s1
InChIKey GEWXXDMCKYFTMH-KWQFWETISA-N
Mol Weight 263.26 g/mol
Molecular Formula C12H16F3NO2
Exact Mass 263.113313 g/mol
Enantiomer InChIKey GEWXXDMCKYFTMH-LDYMZIIASA-N

View Spectrum of (2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

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

View Spectrum of (2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

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

View Spectrum of (2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

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

View Spectrum of (2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

View Spectrum of (2S,3S)-3-(4-METHOXYPHENYLAMINO)-4,4,4-TRIFLUORO-2-METHYLBUTAN-1-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (2R*,3R*)-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-1-BUTANOL
  • (-)-(2S,3S)-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYLBUTAN-1-OL
(+)-(2R,3R)-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYLBUTAN-1-OL
N-(4-METHOXYPHENYL)-N-[3-METHYL-1-(TRIFLUOROMETHYL)-3-BUTENYL]-AMINE
(2R,3R)-2-methyl-3-(p-anisidino)butyric acid methyl ester
5-(4-Methoxy-phenylamino)-octan-4-ol
N-(4-Methoxyphenyl)-N-[1-phenylpropyl]amine
(R)-3,3,3-trifluoro-2-((4-methoxyphenyl)amino)-2-methylpropanenitrile
Ethyl 2-(4-methoxyanilino)butanoate
N-(4-Methoxyphenyl)-1-(2-phenylethyl)piperidin-4-amine
trans-4-(p-anisidino)cyclohexanecarboxylic acid, methyl ester
cis-4-(p-anisidino)cyclohexanecarboxylic acid, methyl ester
Title Journal or Book Year
Highly Enantioselective Synthesis of Fluorinated γ-Amino Alcohols through Proline-Catalyzed Cross-Mannich Reaction Organic Letters 2005
New Strategy for the Stereoselective Synthesis of Fluorinated β-Amino Acids The Journal of Organic Chemistry 2002
First Highly Diastereoselective Synthesis of syn α-Methyl β-Fluoroalkyl β-Amino Esters Organic Letters 1999

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