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Anthraquinone
SpectraBase Compound ID 9A26HDYigh7
InChI InChI=1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
InChIKey RZVHIXYEVGDQDX-UHFFFAOYSA-N
Mol Weight 208.22 g/mol
Molecular Formula C14H8O2
Exact Mass 208.052429 g/mol
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample U.S. Epa Repository, Research Triangle Park, North Carolina
Technique KBr WAFER
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Source of Sample Merck-Schuchardt Hohenbrunn
Technique KBr-Pellet
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Sample Bayer
Technique KBr pellet
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample James Hinton, Valparaiso, Florida
Technique KBr WAFER
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Source of Sample Spectrochem Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number 101223
Technique KBr1
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Source of Sample Tokyo Kasei Kogyo Company, Ltd., Tokyo, Japan
Solvent CDCl3; Reference=TMS; Temperature 297K
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Solvent CDCl3
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Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 331503
Solvent CDCl3
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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
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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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
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31466
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Dr. Rolf Kuehnle
Technique GC/MS
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Source of Sample Sigma-Aldrich Cat. #31466
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
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Source of Spectrum SRH-2022-10524-0
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Source of Spectrum HE-1986-1156-0
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Source of Spectrum HE-1982-0-0
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Source of Spectrum PG-1982-374-0
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Source of Spectrum QE-28-SM21-Anthraquinone (DOI: 10.1002/chem.202200005)
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Source of Spectrum HRC-20-112-9,10-anthracenedione (DOI: 10.1002/jhrc.1240200211)
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Source of Spectrum REC-6-6-3a (DOI: 10.1016/j.rechem.2023.100997)
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Source of Spectrum SRH-2022-3404-0
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Source of Spectrum SRH-2022-9424-0
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Source of Spectrum SRH-2022-9583-0
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Source of Spectrum AA-0-1478-1
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Source of Spectrum Va-0-0-0
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Source of Spectrum WS-1986-400-0
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Source of Spectrum TE-1992-932-0
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Source of Spectrum J-50-4460-4
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Source of Spectrum CJ-1992-0-0
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Source of Spectrum AD-0-2532-0
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Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample P. E. Hansen, O. K. Poulsen, A. Berg Org. Magn. Resonance 9, 649(1977)
Solvent Chloroform-d; Reference=TMS; Temperature=304 K Spectrometer= Varian XL-100
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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 331503
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent TOLUENE
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Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number 101223
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Source of Sample Spectrochem Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number 101223
Copyright Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number A90004
  • 9,10-Anthracenedione
  • 9,10-Anthraquinone
  • 9,10-ANTHRACHINON
  • ANTHRACHINONE
  • ANTHRAQUINONE;9,10-ANTHRACENEDIONE
  • 9,10-ANTHRACHINONE
  • CORBIT
  • MORKIT
  • 9,10-DIOXOANTHRACENE
  • ANTHRACENE, 9,10-DIHYDRO-9,10- DIOXO-,
  • Anthraquinone (8CI)
  • anthracene-9,10-dione
  • ANTHRACHINON
  • Doxepine-A
  • anthra-9,10-quinone
Title Journal or Book Year
Substituent-effect additivity in 1-X-, 2-X- and 1,2-di-X-9,10-anthraquinone series, a tool for13C NMR chemical shift assignment Magnetic Resonance in Chemistry 1995
Natural abundance17O NMR spectroscopic study of quinone methides Magnetic Resonance in Chemistry 1992
17O NMR studies on polycyclic quinones, hydroxyquinones and related cyclic ketones: Models for anthracycline intercalators Organic Magnetic Resonance 1984
Carbon-13 NMR of polycyclic aromatic compounds. 1—Methoxybenz[a]anthracene-7, 12-diones Organic Magnetic Resonance 1982
Carbon-13 nuclear magnetic resonance studies of anthraquinones. IV—correlation of substituent effects for 1-substituted anthraquinones Organic Magnetic Resonance 1981
Carbon-13 N.M.R. Studies of 1,4-Naphthoquinones and 9,10-Anthraquinones Australian Journal of Chemistry 1979
The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones and eight polymethoxyanthraquinones Organic Magnetic Resonance 1978

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