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4-Aminoanisole
SpectraBase Compound ID FqoEeVy2N8w
InChI InChI=1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
InChIKey BHAAPTBBJKJZER-UHFFFAOYSA-N
Mol Weight 123.15 g/mol
Molecular Formula C7H9NO
Exact Mass 123.068414 g/mol
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Copyright Copyright © 2018-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number A88255
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Source of Sample Tokyo Kasei Kogyo Company, Ltd., Tokyo, Japan
Solvent CDCl3; Reference=TMS; Temperature 297K
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Source of Sample MCB MANUFACTURING CHEMISTS, NORWOOD, OHIO
Solvent CDCl3
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Technique Cell
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Source of Sample Merck-Schuchardt Hohenbrunn
Technique KBr-Pellet
Copyright Copyright © 1989, 1990-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Sample Fluka
Technique KBr pellet
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample American Hoechst Corporation
Technique KBr WAFER
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample MCB MANUFACTURING CHEMISTS, NORWOOD, OHIO
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 2023-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany
Technique GC/MS
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Source of Spectrum H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany
Technique GC/MS
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2024-2025 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SRH-2022-1830-0
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Source of Spectrum SRH-2022-5718-0
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Source of Spectrum ASC-362-SM21-3e
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Source of Spectrum PG-1982-1646-0
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Source of Spectrum ACI-57-SM43-43-2 (DOI: 10.1002/anie.201805022)
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Source of Spectrum ACI-56-SM8-3c (DOI: 10.1002/anie.201705025)
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Source of Spectrum QE-24-SM11-11-2 (DOI: 10.1002/chem.201801942)
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Source of Spectrum QE-27-SM7-2i (DOI: 10.1002/chem.202003640)
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Source of Spectrum ADS-6-SM11-Table 2, entry 13 (DOI: 10.1002/advs.201802132)
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Source of Spectrum JOC-78-4541-Table 6, entry 4 (DOI: 10.1021/jo400556g)
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Source of Spectrum SRH-2022-2294-0
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Source of Spectrum CCC-11-SM6-S6-3
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Source of Spectrum CJC-39-SM10-2b
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Source of Spectrum AJO-11-SM9-Figure S8-b
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Source of Spectrum CN109731577A
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Source of Spectrum AD-0-2947-0
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Source of Spectrum NP-0-5643-0
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Source of Spectrum EP-7358-0-0
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Source of Spectrum PR-1066-0-0
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Source of Spectrum JZ-1992-824-0
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Source of Spectrum JZ-1992-4978-0
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Source of Spectrum EK-1999-331-0
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Source of Spectrum J-58-5623-3
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Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F9-1994-1748-2
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Source of Spectrum F-68-1718-21
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Source of Spectrum ACI-51-SMS2-Table1,entry9
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Source of Spectrum CCC-10-SM12-S12_6
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CSC-11-SM17-Table2Entry2
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Pfaltz & Bauer, Inc., Waterbury, Connecticut
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian HA-100/Digilab FT-NMR-3
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Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
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Solvent DMSO-D6
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Solvent THF
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Solvent CDCl3
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Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent THF
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Solvent CDCl3
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Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent THF
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent THF
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent THF
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Solvent CDCl3
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Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent THF
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Solvent CDCl3
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Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2015-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Forensic Spectral Research
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
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Solvent Neat liquid
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Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
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Solvent CDCl3
Copyright Copyright © 2008-2025 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Methanol
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Copyright Copyright © 2021-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number A88255
  • P-anisidine
  • 4-Methoxyaniline
  • 1-Methoxy-4-aminobenzene
  • para-Methoxyaniline
  • 4-AMINO-ANISOL;4-METHOXYBENZENAMINE
  • Benzenamine, 4-methoxy-
  • 4-Methoxy-phenylamine
  • para-Anisidine
  • p-Aminoanisole
  • Paracetamol HYME @
  • m-Ethoxyaniline
  • 4-Anisidine
  • 4-Methoxybenzenamine
  • p-Anisylamine
  • p-Dianisidine
  • p-Methoxyaniline
  • Anisole, p-amino-
  • Aniline, 4-methoxy-
  • Aniline, p-methoxy-
  • p-Methoxyphenylamine
  • 4-Methoxybenzeneamine
  • 1-Amino-4-methoxybenzene
  • 4-Methoxy-1-aminobenzene
  • p-anisidin
  • CCRIS 917
  • HSDB 1603
  • EINECS 203-254-2
  • NSC 7921
  • AI3-02392
  • Acetaminophen HYME
  • Bucetin-M (deethyl-) HYME
  • Phenacetin-M (deethyl-) HYME
  • 4-Aminophenol ME
  • Lactylphenetidine-M (deethyl-) HYME
Title Journal or Book Year
A robust method for determining1H-15N long-range correlations:15N optimized CIGAR-HMBC experiments Magnetic Resonance in Chemistry 2003
15N NMR: Substituent effect analysis inpara-andmeta-substituted phenylhydrazines Magnetic Resonance in Chemistry 1994
15N Nuclear Magnetic Resonance Spectra of Phenylacetanilides Australian Journal of Chemistry 1988
Resonance and solvent effects on absorption spectra. 6. Substituent solvation effects on nitrogen-15 chemical shifts of para-substituted anilines and para-substituted 2-nitroanilines The Journal of Organic Chemistry 1987
17O NMR Investigation of cyclic aromatic ethers Journal of Heterocyclic Chemistry 1987
17O Nuclear Magnetic Resonance Studies. V.17O Shieldings of Some Substituted Anisoles Bulletin of the Chemical Society of Japan 1979
Natural-abundance nitrogen-15 nuclear magnetic resonance spectroscopy. Electronic effects in benzenesulfonamides The Journal of Organic Chemistry 1978

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