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4-Methyl-quinoline N-oxide

Compound with spectra: 4 NMR, and 2 MS (GC)

4-Methyl-quinoline N-oxide
SpectraBase Compound ID 16jR4SK6Ftj
InChI InChI=1S/C10H9NO/c1-8-6-7-11(12)10-5-3-2-4-9(8)10/h2-7H,1H3
InChIKey BKKKHCJYHYPKBC-UHFFFAOYSA-N
Mol Weight 159.19 g/mol
Molecular Formula C10H9NO
Exact Mass 159.068414 g/mol

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13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample J. A. Su, E. Siew, E. V. Brown Org. Magn. Resonance 11, 565(1978)
Solvent Chloroform-d; Reference=TMS; Temperature=319 K Spectrometer= Varian CFT-20

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13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

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

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17O NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH3CN

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-8773-0-0

View Spectrum of 4-Methyl-quinoline N-oxide

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum T-68-1743-0
  • 4-METHYLQUINOLIN-N-OXID
  • Lepidine, 1-oxide
  • QUINOLINE, 4-METHYL-, 1-OXIDE
1,4-dimethylquinolinium iodide
2-Chlorolepidine
2(1H)-Quinolinethione, 4-methyl-
2-Fluoro-4-methylquinoline
4-Quinolineacetonitrile
Quinoline, 4-propyl-
3,4-Dimethyl-quinoline
4-(Methoxymethyl)quinoline
4-Quinolylaldoxime
6-chlorolepidine
Title Journal or Book Year
Natural abundance17O NMR spectroscopy of heterocyclicN-oxides and DiN-oxides. Structural effects Journal of Heterocyclic Chemistry 1985
Carbon-13 NMR studies of quinolines and isoquinolines. II. Chlorine-nitrogen interactions andN-oxide effects Organic Magnetic Resonance 1978
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