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5,6,7-TRIHYDROXY-4'-METHOXYFLAVONE

Compound with spectra: 3 NMR

5,6,7-TRIHYDROXY-4'-METHOXYFLAVONE
SpectraBase Compound ID AqyYE5Rct13
InChI InChI=1S/C16H12O6/c1-21-9-4-2-8(3-5-9)12-6-10(17)14-13(22-12)7-11(18)15(19)16(14)20/h2-7,18-20H,1H3
InChIKey XVMMEYCPXZYLAI-UHFFFAOYSA-N
Mol Weight 300.27 g/mol
Molecular Formula C16H12O6
Exact Mass 300.063388 g/mol

View Spectrum of 5,6,7-TRIHYDROXY-4'-METHOXYFLAVONE

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 5,6,7-TRIHYDROXY-4'-METHOXYFLAVONE

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 5,6,7-TRIHYDROXY-4'-METHOXYFLAVONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 5,6,7-TRIHYDROXY-4'-METHOXY-FLAVONE;SCUTELLAREIN-4'-METHYLETHER
SCUTELLAREIN
6-IODOACACETIN
6-METHYLAPIGENIN
6-Chloranyl-2-(4-hydroxyphenyl)-5,7-bis(oxidanyl)chromen-4-one
FIYPYRNWAKRRIU-UHFFFAOYSA-N
ISOSCUTELLAREIN
2-(3,4-dimethoxyphenyl)-5,7-bis(oxidanyl)chromen-4-one
Diosmetin
Chrysoeriol
VELUTIN;7,3'-DI-O-METHYLTRICETIN
Title Journal or Book Year
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
13C NMR spectral assignment of the A-ring of polyoxygenated flavones Phytochemistry 1998

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