Flavone
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| Names | |
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| IUPAC name
Flavone[1]
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| Systematic IUPAC name
2-Phenyl-4H-1-benzopyran-4-one 2-Phenyl-4H-chromen-4-one | |
| Identifiers | |
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3D model (JSmol)
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| 157598 | |
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| 1224858 | |
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PubChem CID
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| Properties | |
| C15H10O2 | |
| Molar mass | 222.243 g·mol−1 |
| Appearance | white solid |
| Melting point | 96–97 °C (205–207 °F; 369–370 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Template:Chembox Footer/trackingTemplate:Short description
Flavone is an organic compound with the formula Page Module:Chem2/styles.css has no content.C6H4OC3H(Ph)O. A white solid, flavone is a derivative of chromone with a phenyl (Ph) substituent adjacent to the ether group. The compound is of little direct practical importance, but substituted derivatives, the flavones and flavonoids are a large class of nutritionally important natural products.[2] Flavone can be prepared in the laboratory by cyclization of 2-hydroxacetophenone.[3] Isomeric with flavone is isoflavone, where the phenyl group is adjacent to the ketone.
References
- ^ https://iupac.qmul.ac.uk/flavonoid/index.html#Flv321
- ^ Page Module:Citation/CS1/styles.css has no content.Gaspar, Alexandra; Matos, Maria João; Garrido, Jorge; Uriarte, Eugenio; Borges, Fernanda (2014). "Chromone: A Valid Scaffold in Medicinal Chemistry". Chemical Reviews. 114 (9): 4960–4992. doi:10.1021/cr400265z.
- ^ Page Module:Citation/CS1/styles.css has no content.T. S. Wheeler (1952). "Flavone". Organic Syntheses. 32: 72. doi:10.15227/orgsyn.032.0072.
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