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Resveratrol

Compound with spectra: 14 NMR, 2 FTIR, 1 Raman, and 9 MS (GC)

Resveratrol
SpectraBase Compound ID 2jYog6CfLSw
InChI InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+
InChIKey LUKBXSAWLPMMSZ-OWOJBTEDSA-N
Mol Weight 228.25 g/mol
Molecular Formula C14H12O3
Exact Mass 228.078644 g/mol

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FTIR Spectrum
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Biomol International, L.P.
Source of Spectrum Forensic Spectral Research
Catalog Number FR-104
Technique KBr1 0.61mg

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ATR-IR Spectrum
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Biomol International, L.P.
Source of Spectrum Forensic Spectral Research
Catalog Number FR-104

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1H NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-d6

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

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

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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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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6

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

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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Raman Spectrum
Copyright Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Biomol International, L.P.
Source of Spectrum Forensic Spectral Research
Catalog Number FR-104

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MS (GC) Spectrum
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 Adams' Essential Oil Components (GC-MS), Version 4

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MS (GC) Spectrum
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 Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y1-41-2397-1

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum ASC-359-992-2d

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-62-4825-4

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum X4-21-739-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum X2-50-295-1

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y4-81-161-4
  • 5-(2-(4-Hydroxyphenyl)ethenyl)-1,3-benzenediol, (E)-
  • 1,3-Benzenediol, 5-(2-(4-hydroxyphenyl)ethenyl)-, (E)-
  • LUKBXSAWLPMMSZ-OWOJBTEDSA-N
  • TRANS-RESVERATROL
  • TRANS-3,4',5-TRIHYDROXYSTILBENE;TRANS-RESVERATROL
  • (E)-RESVERATROL;(E)-3,4',5-TRIHYDROXYSTILBENE
  • (E)-RESVERATROL;1-(4'-HYDROXYBENZYL)-2-(3,5-DIHYDROXY-BENZYL)-ETHENE
  • (TRANS)-3,5,4'-TRIHYDROXY-ESTILBENE
  • 3,4',5-TRIHYDROXY-STILBENE
  • TRANS-RESVERATROL;(E)-3,5,4'-TRIHYDROXY-STILBENE;(E)-5-[2-(4-HYDROXYPHENYL)-ETHENYL]-BENZENE-1,3-DIOL
  • trans-Resveratol [(E)-3,5,4'-trihydroxystilbene]
  • (E)-1-(4-hydroxyphenyl)-2-(3,5-dihydroxyphenyl)ethene
  • 1,3-Benzenediol, 5-[(1E)-2-(4-hydroxyphenyl)ethenyl]-
cis-Resveratrol
3,5-DIHYDROXYSTILBENE-(Z)
3,5-DIHYDROXYSTILBENE-PINOSYLVIN
E-3-HYDROXYSTILBEN
4-Hydroxy-4'-nitrostilbene
QKMYQGPZABXECA-ONEGZZNKSA-N
1,3-Dimethyl-5-[(E)-2-(4-methylphenyl)ethenyl]benzene
Heptacyclo[12.12.8.2(6,9).2(19,22).2(29,32).1(3,25).1(12,16)]dotetraconta-1,3(37),4,6,8,10,12,14,16(40),17,19,21,23,25,27,29,31,33,35,38,41-heneicosaene
4-Bromo-3',5'-dimethylstilbene
4-(4-Methoxy-styryl)-pyridine
Title Journal or Book Year
Chemical Constituents from <i>Caesalpinia férrea</i>: Identification and <sup>1</sup>H and <sup>13</sup>C Resonance Assignment American Journal of Analytical Chemistry 2014
Phytochemical Constituents and Determination of Resveratrol from the Roots of <i>Arachis hypogea</i> L. American Journal of Plant Sciences 2013
Identification and Characterization of Process Related Impurities of Trans-Resveratrol Scientia Pharmaceutica 2013
Comparison of the phytoestrogentrans-resveratrol (3,4′,5-trihydroxystilbene) structures from x-ray diffraction and solution NMR Magnetic Resonance in Chemistry 2005
Phenolic Constituents of the Rhizomes of the Thai Medicinal Plant Belamcanda chinensis with Proliferative Activity for Two Breast Cancer Cell Lines Journal of Natural Products 2005
On the Chemistry of the Resveratrol Diastereomers Monatshefte f�r Chemie / Chemical Monthly 2003
Constituents of the Bark and Twigs of Artocarpus dadah with Cyclooxygenase Inhibitory Activity Journal of Natural Products 2002
Tyrosinase Inhibitors from Artocarpus gomezianus Planta Medica 2000
Homoisoflavanones and stilbenoids from Scilla nervosa Phytochemistry 1999
Anti-leukaemic compounds derived from stilbenes in Picea abies bark Phytochemistry 1993
An Antiplatelet Principle ofVeratrum formosanum Planta Medica 1992

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