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2-Hydroxyanthraquinone
SpectraBase Compound ID 76b1iBxv29z
InChI InChI=1S/C14H8O3/c15-8-5-6-11-12(7-8)14(17)10-4-2-1-3-9(10)13(11)16/h1-7,15H
InChIKey GCDBEYOJCZLKMC-UHFFFAOYSA-N
Mol Weight 224.21 g/mol
Molecular Formula C14H8O3
Exact Mass 224.047344 g/mol
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Technique KBr-Pellet
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample E. Sawicki, R. A. Taft Sanitary Engineering Center, Cincinnati, Ohio
Technique KBr WAFER
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Polysol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3_OR_DMSO-D6
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
  • 2-HYDROXY-9,10-ANTHRAQUINONE
  • 2-HYDROXY-9,10-ANTHRACHINON
  • GCDBEYOJCZLKMC-UHFFFAOYSA-N
  • ANTHRAQUINONE, 2-HYDROXY-,
  • 9,10-Anthracenedione, 2-hydroxy-
  • 2-Hydroxyanthra-9,10-quinone
Title Journal or Book Year
Halophenol Rearrangement in Lewis Acid-Catalyzed Friedel - Crafts Conditions: Evidence of Competitive Initial Protonation and Acylation Australian Journal of Chemistry 2008
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
Metal arene complexes in organic synthesis. Hydroxylation, trimethylsilylation, and carbethoxylation of some polycyclic aromatic hydrocarbons utilizing .eta.6-arene-chromium tricarbonyl complexes The Journal of Organic Chemistry 1992
Carbon-13 nuclear magnetic resonance studies of anthraquinones. Part III—correlation of substituent effects for 2-substituted anthraquinones Organic Magnetic Resonance 1981
The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones and eight polymethoxyanthraquinones Organic Magnetic Resonance 1978

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