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4-ACETYL-PYRIDINE-1-OXIDE
SpectraBase Compound ID CNmuSZpv1D4
InChI InChI=1S/C7H7NO2/c1-6(9)7-2-4-8(10)5-3-7/h2-5H,1H3
InChIKey GUHDDRZAZNIQJB-UHFFFAOYSA-N
Mol Weight 137.14 g/mol
Molecular Formula C7H7NO2
Exact Mass 137.047678 g/mol
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample S. A. Sojka, F. J. Dinan J. Org. Chem. 44, 307(1979)
Solvent Chloroform-d; Reference=TMS; Temperature=309 K Spectrometer= Varian XL-100
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent H2O
  • 4-ACETOXY-PYRIDINE-1-OXIDE
  • 4-ACETYLPYRIDINE-N-OXIDE;1-(4-PYRIDINYL)-ETHANONE-N-OXIDE
  • METHYL 4-PYRIDYL KETONE, N-OXIDE
  • KETONE, METHYL 4-PYRIDYL, N-OXIDE
  • 4-Acetylpyridine-N-oxide
Title Journal or Book Year
Substituent Effects on15N and17O NMR Chemical Shifts in 4′-Substitutedtrans-NNO-Azoxybenzenes Bulletin of the Chemical Society of Japan 1990
Dual resonance functionality in pyridine 1-oxides. A double multinuclear NMR approach The Journal of Organic Chemistry 1988
A 17O NMR study. Substituent chemical shifts of 4-substituted pyridine 1-oxides in DMSO: Importance of dual enhanced resonance contributions with PI-donor and PI-acceptor substituents Tetrahedron Letters 1986
17O NMR spectroscopy of 4-substituted pyridineN-oxides: Substituent and solvent effects Magnetic Resonance in Chemistry 1985

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