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METHYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;IMINO-TAUTOMER

Compound with spectra: 3 NMR

METHYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;IMINO-TAUTOMER
SpectraBase Compound ID 8T2yqxsRvHM
InChI InChI=1S/C13H14F3NO3/c1-8(12(18)20-3)11(13(14,15)16)17-9-4-6-10(19-2)7-5-9/h4-8H,1-3H3/b17-11+
InChIKey VFJKGNMKAVJRBZ-GZTJUZNOSA-N
Mol Weight 289.25 g/mol
Molecular Formula C13H14F3NO3
Exact Mass 289.092578 g/mol

View Spectrum of METHYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;IMINO-TAUTOMER

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

View Spectrum of METHYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;IMINO-TAUTOMER

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

View Spectrum of METHYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;IMINO-TAUTOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • METHYL-3-(N-4-METHOXYPHENYL)-IMINO-2-METHYL-4,4,4-TRIFLUOROBUTANOATE
METHYL-(Z)-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;IMINO-TAUTOMER
ISOPROPYL-4-CHLORO-4,4-DIFLUORO-3-(4-METHOXYANILINO)-2-BUTENOATE;IMINO-TAUTOMER
N-(1-(4-Chlorophenyl)-2,2,2-trifluoroethylidene)-4-methoxyaniline
4-Methoxy-N-(2,2,2-trifluoro-1-(p-tolyl)ethylidene)aniline
N(2)-(4-METHOXYPHENYL)-3-(2-PYRROLIDINYLIDENE)-1,1,1-TRIFLUORO-2-PROPANIMINE
N-(p-Methoxyphenyl)-3,3-difluoro-1-trimethylsilylpent-4-ene-2-imine
BENZYL-S-[1-[(N-4-METHOXYPHENYL)-IMINO]-2,2,2-TRIFLUOROETHYL]-THIOGLYCOLATE
METHYL-S-[1-[(N-4-METHOXYPHENYL)-IMINO]-2,2,2-TRIFLUOROETHYL]-THIOLACTATE
benzene, 1-methoxy-4-[[(E)-2,2,2-trifluoro-1-[2-[(phenylamino)carbonyl]hydrazino]ethylidene]amino]-
(Z)-3-METHYL-4-[(TETRAHYDRO-2'-H-PYRAN-2'-YL)-OXY]-2-BUTEN-1-YL-N-(PARA-METHOXYPHENYL)-TRIFLUOROACETIMIDATE
Title Journal or Book Year
A Trial toward the Synthesis of γ-Fluorinated β-Amino-α-thiohydroxyamino Acid:  A Finding of Desulfurizative C−C Bond Formation in Thio-Wittig-Type Rearrangement of S-(N-Aryltrifluoroacetimidoyl)thioglycolates The Journal of Organic Chemistry 2001
First Highly Diastereoselective Synthesis of syn α-Methyl β-Fluoroalkyl β-Amino Esters Organic Letters 1999

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