SALVIGENIN
Compound with spectra: 9 NMR, and 3 MS (GC)
| SpectraBase Compound ID | DVFzu6HO6rg |
|---|---|
| InChI | InChI=1S/C18H16O6/c1-21-11-6-4-10(5-7-11)13-8-12(19)16-14(24-13)9-15(22-2)18(23-3)17(16)20/h4-9,20H,1-3H3 |
| InChIKey | QCDYOIZVELGOLZ-UHFFFAOYSA-N |
| Mol Weight | 328.32 g/mol |
| Molecular Formula | C18H16O6 |
| Exact Mass | 328.094688 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| 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 | CDCl3 |
| 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 © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | W5-29341-0-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | Y5-61-427-1 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | Y1-38-1010-0 |
- 5-HYDROXY-6,7,4'-TRIMETHOXYFLAVONE
- SALVIGENIN;5-HYDROXY-6,7,4'-TRIMETHOXY-FLAVONE;REFERENCE-9
- SALVIGENIN;5-HYDROXY-6,7,4'-TRIMETHOXY-FLAVONE
- 4H-1-Benzopyran-4-one, 5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-
CIRSIMARITIN
5-Hydroxy-6,7-dimethoxy-flavone
AMYRISIN_B;5,7-DIHYDROXY-2-(4-((2-HYDROXY-3-METHYLBUT-3-EN-1-YL)-OXY)-PHENYL)-6-METHOXY-4-H-CHROMEN-4-ONE
EUPAFOLIN
2-(3,5-dihydroxy-4-methoxy-phenyl)-5,7-dihydroxy-6-methoxy-chromen-4-one
BAICALEIN-6-ACETATE
5,7,4'-Trihydroxy-6,3',5'-trimethoxy-flavone
6-HYDROXY-5,7,4'-TRIMETHOXYFLAVONE
7-Hydroxy-5,6-dimethoxy-flavone
5,7,8-trimethoxy-2-phenyl-1-benzopyran-4-one
| 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 |
| Constituents of the EgyptianCentaurea scoparia; III. Phenolic Constituents of the Aerial Parts | Planta Medica | 1995 |
| Three flavone glycosides from Gelonium multiflorum | Phytochemistry | 1993 |
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