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

Compound with spectra: 3 NMR

METHYL-(Z)-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;(Z)-ENAMINO-TAUTOMER
SpectraBase Compound ID L5mxaccqyBs
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/h4-7,17H,1-3H3/b11-8-
InChIKey DOGRCJPCNDLZQU-FLIBITNWSA-N
Mol Weight 289.25 g/mol
Molecular Formula C13H14F3NO3
Exact Mass 289.092578 g/mol

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

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • METHYL-3-(N-4-METHOXYPHENYL)-AMINO-2-METHYL-4,4,4-TRIFLUORO-2-BUTENOATE
METHYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-2-METHYL-2-BUTENOATE;Z-ENAMINO-TAUTOMER
BENZYL-3-(N-4-METHOXYPHENYL)-AMINO-4,4,4-TRIFLUORO-2-BUTENOATE
ISOPROPYL-4-CHLORO-4,4-DIFLUORO-3-(4-METHOXYANILINO)-2-BUTENOATE;(Z)-ENAMINO-TAUTOMER
2-METHYL-3-(4'-METHOXYANILINO)-CYCLOHEX-2-EN-1-ONE
SXOUQAZSEAPGTH-ZHACJKMWSA-N
SXOUQAZSEAPGTH-KHPPLWFESA-N
2H-thiopyran-3,5(4H,6H)-dione, 4-[1-[(4-methoxyphenyl)amino]ethylidene]-
2,2,2-trifluoro-N-(4-methoxyphenyl)-N'-(4-nitrophenyl)acetamidine
2-Methoxy-3-(4-methoxyanilino)-2H-furan-5-one
METHYL-4-[(4'-METHOXYPHENYL)-AMINO]-6-OXO-7,7,7-TRIFLUORO-4-HEPTENOATE
Title Journal or Book Year
New Strategy for the Stereoselective Synthesis of Fluorinated β-Amino Acids The Journal of Organic Chemistry 2002
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

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