5,6-DIHYDROXY-4',7-DIMETHOXYISOFLAVONE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | HRGPWSMcGzp |
|---|---|
| InChI | InChI=1S/C17H14O6/c1-21-10-5-3-9(4-6-10)11-8-23-12-7-13(22-2)16(19)17(20)14(12)15(11)18/h3-8,19-20H,1-2H3 |
| InChIKey | IUNDYZBBARECMK-UHFFFAOYSA-N |
| Mol Weight | 314.29 g/mol |
| Molecular Formula | C17H14O6 |
| Exact Mass | 314.079038 g/mol |
| 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 |
- 5,6-DIHYDROXY-7,4'-DIMETHOXY-ISOFLAVONE
7-METHOXY-5,6,4'-TRIHYDROXYISOFLAVONE
IRISOLIDONE
5-HYDROXY-7,3',4'-TRIMETHOXYISOFLAVONE
3-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-chromone
6-Acetoxy-4',7-dimethoxy-isoflavone
GENISTEIN-7-ACETYLFERULIC-ACID
Afromosine -acetate
5,7,3',4-Tetramethoxyisoflavone
GENISTEIN-4'-O-ALPHA-L-RHAMNOPYRANOSIDE
5,4'-DIHYDROXY-7,2'-DIMETHOXYISOFLAVONE
| 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 |
| Studies of the Selective O-Alkylation and Dealkylation of Flavonoids.XX. A Convenient Method for Synthesizing 5,6,7-Trihydroxyisoflavones and 5,6-Dihydroxy-7-methoxyisoflavones. | Chemical and Pharmaceutical Bulletin | 1996 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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