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| Names | |
|---|---|
| IUPAC name 
trans-4,7-Dioxadispiro[4.0.46.25]dodeca-1,9-diene-3,8-dione | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
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PubChem CID
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| Properties | |
| C10H8O4 | |
| Molar mass | 192.17 g·mol−1 | 
| Appearance | Colourless, odourless solid | 
| Density | 1.45g/cm3 | 
| Melting point | 158 °C (316 °F; 431 K) | 
| Boiling point | 535.7 °C (996.3 °F; 808.9 K) @ 760mmHg | 
| low | |
| Solubility in chloroform | soluble | 
| Hazards | |
| Flash point | 300.7 °C (573.3 °F; 573.8 K) | 
| Lethal dose or concentration (LD, LC): | |
| 
LD50 (median dose) | 150 mg·kg−1 (mouse, i. p.) | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
|  (what is   ?) | |
| Infobox references | |
Anemonin is a compound found in plants of the buttercup family (Ranunculaceae). It is the dimerization product of the toxin protoanemonin and is easily hydrolysed to a dicarboxylic acid.
The name of the substance comes from the plant genus Anemone, from which it was first identified.Antispasmodic and analgetic properties have been described.