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Names | |
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Preferred IUPAC name
1,7-Dihydroxy-9H-xanthen-9-one | |
Other names
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Identifiers | |
3D model (
JSmol)
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3DMet | |
207044 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
KEGG | |
PubChem
CID
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CompTox Dashboard (
EPA)
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Properties | |
C13H8O4 | |
Molar mass | 228.203 g·mol−1 |
Melting point | 240 °C (464 °F; 513 K) |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Euxanthone is a naturally occurring xanthonoid, an organic compound with the molecular formula C13H8O4. It can be synthesized from gentisic acid, β-resorcylic acid, and acetic anhydride. [1] It occurs naturally in many plant species. Commercial production is from purified root extract of Polygala tenuifolia. [2] It has been investigated for bioactive properties. [3] [4]
![]() | |
Names | |
---|---|
Preferred IUPAC name
1,7-Dihydroxy-9H-xanthen-9-one | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
3DMet | |
207044 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
KEGG | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C13H8O4 | |
Molar mass | 228.203 g·mol−1 |
Melting point | 240 °C (464 °F; 513 K) |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Euxanthone is a naturally occurring xanthonoid, an organic compound with the molecular formula C13H8O4. It can be synthesized from gentisic acid, β-resorcylic acid, and acetic anhydride. [1] It occurs naturally in many plant species. Commercial production is from purified root extract of Polygala tenuifolia. [2] It has been investigated for bioactive properties. [3] [4]