| Identification | Back Directory | [Name]
3’,4’,5’-Trihydroxy-6,7-dimethoxyflavone | [CAS]
29536-41-2 | [Synonyms]
Betuletol
Eupaletin
6,7-Dimethoxy-3,5,4'-trihydroxyflavone
3,5,4'-Trihydroxy-6,7-dimethoxyflavone
3’,4’,5’-Trihydroxy-6,7-dimethoxyflavone
3,5-Dihydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxychromen-4-one
3,5-Dihydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxy-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 3,5-dihydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxy- | [Molecular Formula]
C17H14O7 | [MDL Number]
MFCD09264650 | [MOL File]
29536-41-2.mol | [Molecular Weight]
330.29 |
| Chemical Properties | Back Directory | [Melting point ]
289-292℃ | [Boiling point ]
587.7±50.0 °C(Predicted) | [density ]
1.45 | [form ]
neat | [pka]
6.16±0.40(Predicted) | [BRN ]
1354525 | [InChI]
1S/C17H14O7/c1-22-11-7-10-12(14(20)17(11)23-2)13(19)15(21)16(24-10)8-3-5-9(18)6-4-8/h3-7,18,20-21H,1-2H3 | [InChIKey]
KWMAWXWUGIEVDG-UHFFFAOYSA-N | [SMILES]
O=C1C(O)=C(C2=CC=C(O)C=C2)OC3=CC(OC)=C(OC)C(O)=C31 |
| Hazard Information | Back Directory | [Uses]
Eupalitin, flavonol, is an active natural product. Eupalitin can be isolated from Eupatorium ligustrinum D.C[1]. | [References]
[1] L. Quijano, et al. The structures of eupalin and eupatolin. Two new flavonol rhamnosides isolated from Eupatorium ligustrinum D.C.,Tetrahedron,Volume 26, Issue 12,1970,Pages 2851-2859, ISSN 0040-4020. |
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