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7-HYDROXY-4',5,6-TRIMETHOXYISOFLAVONE

Compound with spectra: 4 NMR

7-HYDROXY-4',5,6-TRIMETHOXYISOFLAVONE
SpectraBase Compound ID JJOg26SO2ZT
InChI InChI=1S/C18H16O6/c1-21-11-6-4-10(5-7-11)12-9-24-14-8-13(19)17(22-2)18(23-3)15(14)16(12)20/h4-9,19H,1-3H3
InChIKey CHDLFAIVPUPGAT-UHFFFAOYSA-N
Mol Weight 328.32 g/mol
Molecular Formula C18H16O6
Exact Mass 328.094688 g/mol

View Spectrum of 7-HYDROXY-4',5,6-TRIMETHOXYISOFLAVONE

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

View Spectrum of 7-HYDROXY-4',5,6-TRIMETHOXYISOFLAVONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 7-HYDROXY-4',5,6-TRIMETHOXYISOFLAVONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 7-HYDROXY-4',5,6-TRIMETHOXYISOFLAVONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 7-HYDROXY-5,6,4'-TRIMETHOXY-ISOFLAVONE
7-O-METHYLTECTORIGENIN
5-HYDROXY-7,8-DIMETHOXY-3-(4'-METHOXYPHENYL)-4H-1-BENZOPYRAN-4-ONE
Irilone
4'-METHOXY-3',5,6,7-TETRAHYDROXYISOFLAVONE
5,7,4'-TRIHYDROXY-6,8-DIMETHOXYISOFLAVONE
3'-METHOXY-4',5,6,7-TETRAHYDROXYISOFLAVONE
4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-6-(3-methylbutenyl)-
5,8-DIHYDROXY-6,7-DIMETHOXYISOFLAVONE
ISOGACAONIN-C;5,7,4'-TRIHYDROXY-6-[1-HYDROXY-2-METHYLBUTEN-2-YL]-ISOFLAVONE
OLIBERGIN-B
Title Journal or Book Year
A New Isoflavonoid from Seeds of Lepidium sativum L. and Its Protective Effect on Hepatotoxicity Induced by Paracetamol in Male Rats Molecules 2014
Chemical Constituents of the Bark of Dipteryx alata Vogel, an Active Species against Bothrops jararacussu Venom Molecules 2010
Isoflavonoid Glycosides from the Roots of Baphia bancoensis Journal of Natural Products 2008
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XXIV. A Convenient Method for Synthesizing 6- and 8-Methoxylated 5,7-Dihydroxyisoflavones. Chemical and Pharmaceutical Bulletin 1998
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