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N-methylaniline
SpectraBase Compound ID I0kVPhqX9Px
InChI InChI=1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3
InChIKey AFBPFSWMIHJQDM-UHFFFAOYSA-N
Mol Weight 107.16 g/mol
Molecular Formula C7H9N
Exact Mass 107.073499 g/mol
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Sample Merck-Schuchardt Hohenbrunn
Technique Cell
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Technique NEAT
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample The Matheson Company, Inc., East Rutherford, New Jersey
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Prof. Buback, University of Goettingen, Germany
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Prof. Buback, University of Goettingen, Germany
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
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Source of Sample Aldrich
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number M29304
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Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number M29304
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
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Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
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Source of Spectrum XW-10-1494-0
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Source of Spectrum NW-2074-0-0
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Source of Spectrum W5-1989-1385-0
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Source of Spectrum SRH-2022-9394-0
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Source of Spectrum F-54-8499-32
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Source of Spectrum EP-7347-0-0
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Source of Spectrum PR-1065-0-0
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Source of Spectrum MV-1986-10-0
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Source of Spectrum EK-1999-163-0
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Source of Spectrum EP-3093-0-0
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Source of Spectrum JZ-1992-585-0
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Source of Spectrum SO-0-1107-0
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Source of Spectrum F-62-6104-4
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Source of Spectrum ASC-359-SM27-2n
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Source of Spectrum SRH-2022-1448-0
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3
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Source of Sample The Matheson Company, Inc., East Rutherford, New Jersey
Solvent CCl4
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Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number M29304
Solvent CDCl3
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Source of Sample Eastman Organic Chemicals, Rochester, New York
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian HA-100/Digilab FT-NMR-3
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Solvent CDCL3
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Solvent CDCl3 chloroform-d
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Solvent Dioxane
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Solvent Acetone-D6
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Solvent CDCl3
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Solvent CHCl2F
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Solvent CHCl2F
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Solvent CH3OCH3
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Solvent C2D6SO dimethylsulfo
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Solvent Dioxane
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Solvent CH3OCH3
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Solvent Benzene-D6
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Solvent Acetone-D6
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Solvent CDCl3
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Solvent CHCl2F
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Solvent CHCl2F
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Solvent CH3OCH3
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Solvent CH3OCH3
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Solvent Benzene-D6
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Solvent CHCl2F
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Solvent CHCl2F
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Solvent CH3OCH3
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Solvent CH3OCH3
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Solvent CH3OCH3
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Solvent CH3OCH3
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Solvent CDCl3
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Solvent CHCl2F
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Solvent CHCl2F
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Solvent CH3OCH3
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Solvent CH3OCH3
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Solvent CDCl3
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Solvent CHCl2F
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Solvent CHCl2F
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Solvent CH3OCH3
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Solvent CH3OCH3
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Solvent Benzene-D6
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Solvent CH3OCH3
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Solvent Benzene-D6
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent DMSO-D6
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Solvent CDCl3
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Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number M29304
Solvent CDCl3
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Solvent Unknown
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Solvent CDCl3
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Solvent DMSO-D6;0.75M
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Solvent Neat liquid
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Source of Sample Aldrich
Catalog Number 236233
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Source of Sample Aldrich
Catalog Number M29304
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Catalog Number 236233
  • Monomethylaniline
  • N-Methylphenylamine
  • N-Methylaminobenzene
  • N-Methylbenzeneamine
  • Anilinomethane
  • ANILINE, N-METHYL-,
  • METHYLPHENYLAMINE
  • N-Methylbenzenamine
  • N-Methyl-N-phenylamine
  • METHYLPHENYLAMINE;N-METHYLANILINE
  • AFBPFSWMIHJQDM-UHFFFAOYSA-N
  • N-METHYLANILIN
  • N-METHYLANILINE (PRACT.)
  • Benzenamine, N-methyl-
  • Methylaniline
Title Journal or Book Year
A study of the 15 N NMR chemical shifts in substituted anilines and phenylhydrazines, and their derivatives Magnetic Resonance in Chemistry 2008
NMR spectra of nitrogen-containing compounds. Correlations between experimental and GIAO calculated data Magnetic Resonance in Chemistry 1999
Substituent effect treatment of interactions between contiguous functionalities G-X. 2. Remote response to polar-inductive and mesomeric influence of X on G = -O- and -NH- The Journal of Organic Chemistry 1980
The Journal of Organic Chemistry 1980
A nitrogen-15 nuclear magnetic resonance study of N-aryl phosphoramidates and phosphorimidates Canadian Journal of Chemistry 1980
13C substituent effects in monosubstituted benzenes Organic Magnetic Resonance 1979
NMR spectral studies—XII Tetrahedron 1975

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