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N1-(4-METHOXYPHENYL)-1-CHLORO-2,2-DIFLUORO-4-PENTEN-1-IMINE

Compound with spectra: 4 NMR

N1-(4-METHOXYPHENYL)-1-CHLORO-2,2-DIFLUORO-4-PENTEN-1-IMINE
SpectraBase Compound ID 9mj5M9DZQJV
InChI InChI=1S/C12H12ClF2NO/c1-3-8-12(14,15)11(13)16-9-4-6-10(17-2)7-5-9/h3-7H,1,8H2,2H3/b16-11-
InChIKey XLTWRLIJEKCKKN-WJDWOHSUSA-N
Mol Weight 259.68 g/mol
Molecular Formula C12H12ClF2NO
Exact Mass 259.057548 g/mol

View Spectrum of N1-(4-METHOXYPHENYL)-1-CHLORO-2,2-DIFLUORO-4-PENTEN-1-IMINE

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

View Spectrum of N1-(4-METHOXYPHENYL)-1-CHLORO-2,2-DIFLUORO-4-PENTEN-1-IMINE

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

View Spectrum of N1-(4-METHOXYPHENYL)-1-CHLORO-2,2-DIFLUORO-4-PENTEN-1-IMINE

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

View Spectrum of N1-(4-METHOXYPHENYL)-1-CHLORO-2,2-DIFLUORO-4-PENTEN-1-IMINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
4-Methoxy-N-(1,1,1-trifluoroheptan-2-ylidene)aniline
[N-(p-Methoxyphenyl)(trifluoroacetimidoyl)]trimethylsilane
2,2,2-trifluoro-N-(4-methoxyphenyl)-N'-prop-2-enylethanimidamide
2,2,2-trifluoro-N'-(4-methoxyphenyl)-N-(propan-2-ylideneamino)ethanimidamide
N,N'-bis[4'-(Octyloxy)phenyl]-oxa-diimidoyl Dichloride
(1E,3Z)-3-AMINO-1-(4-METHOXYPHENYL)-2-METHYL-4-(METHYLSULFONYL)-1-AZABUTA-1,3-DIENE
(4-Methoxy-phenyl)-[2-[1-triethylsilanyl-meth-(Z)-ylidene]-hex-(E)-ylidene]-amine
indophenol, acetate
N,N'-Bis(4-methoxyphenyl)ethanimidamide
benzenamine, N-[(E)-(5-bromo-2-thienyl)methylidene]-4-methoxy-
Title Journal or Book Year
Diastereoselective Synthesis of Fluorinated, Seven-Membered β-Amino Acid Derivatives via Ring-Closing Metathesis Organic Letters 2003
Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis:  Intramolecular π-Stacking Interactions as a Source of Stereocontrol Organic Letters 2001
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