Rosefuran
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| Preferred IUPAC name
3-Methyl-2-(3-methylbut-2-en-1-yl)furan | |
| Other names
3-methyl-2-prenylfuran; 2-(3-Methyl-2-butenyl)-3-methylfuran
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C10H14O | |
| Molar mass | 150.221 g·mol−1 |
| Appearance | colorless liquid |
| Density | 0.9089 @30 °C |
| Boiling point | 103 to 104 °C (217 to 219 °F; 376 to 377 K) at 50 mmHg |
| Hazards | |
| Flash point | 62.22 °C; 144.00 °F; 335.37 K |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Rosefuran (3-methyl-2-prenylfuran) is an organic compound, classified as a terpenoid. It is a minor constituent of the aroma of the rose (Rosa damascene). Rosefuran is a 2,3-disubstituted furan (3-methyl-2-(3-methyl-2-buten-1-yl)furan). It has an odor threshold of 200 ppb and constitutes 0.16% of Bulgarian rose oil. Rosefuran has been established as a female sex pheromone of an acarid mite, Caloglyphus sp. Concentrations of less than 100 ng of synthetic rosefuran caused sexual excitation in males of the species.