Fraxin
Names | |
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IUPAC name 8-(β-D-Glucopyranosyloxy)-7-hydroxy-6-methoxy-2H-1-benzopyran-2-one | |
Systematic IUPAC name 7-Hydroxy-6-methoxy-8-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-1-benzopyran-2-one | |
Identifiers | |
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3D model (JSmol) |
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ChEBI |
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ChemSpider |
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ECHA InfoCard | 100.007.597 |
PubChem CID |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C16H18O10 |
Molar mass | 370.310 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Fraxin is a glucoside of fraxetin.[1] Fraxin extracted from ash bark exhibits florescence in aqueous solution.[2] A blue/green luminescence can be observed by soaking ash twigs in hot water.
Bibliography
- ^ Hirsch, Anne-Marie; Longeon, Arlette; Guyot, Michèle (January 2002). "Fraxin and esculin: two coumarins specific to Actinidia chinensis and A. deliciosa (kiwifruit)". Biochemical Systematics and Ecology. 30 (1): 55–60. doi:10.1016/S0305-1978(01)00064-3.
- ^ Meikle, R. D. (1958). British Trees and Shrubs (Kew Series) (1st ed.). UK: Eyre & Spottiswoode. pp. 129–132.
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Types of coumarins
- Aesculetin
- Ferujol
- Umbelliferone
O-Methylated |
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Furanocoumarins |
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This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
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