5,6-dihydroxy-7,4'-dimethoxyflavone
Compound with spectra: 5 NMR, and 1 MS (GC)
| SpectraBase Compound ID | Fb3E6IFVDI3 |
|---|---|
| InChI | InChI=1S/C17H14O6/c1-21-10-5-3-9(4-6-10)12-7-11(18)15-13(23-12)8-14(22-2)16(19)17(15)20/h3-8,19-20H,1-2H3 |
| InChIKey | UUQJTIHOVGMQIH-UHFFFAOYSA-N |
| Mol Weight | 314.29 g/mol |
| Molecular Formula | C17H14O6 |
| Exact Mass | 314.079038 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|
| 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 | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | AJC-9-S427-3 |
- LADANEIN
- 7,4'-O-DIMETHYL-SCUTELLAREIN;5,6-DIHYDROXY-7,4'-DIMETHOXY-FLAVONE
- 7,4'-O-DIMETHYLSCUTELLAREIN
| 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 |
| Flavonoid glycosides from Colebrookea oppositifolia | Phytochemistry | 1996 |
| Three flavone glycosides from Gelonium multiflorum | Phytochemistry | 1993 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.