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| Names | |||
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Preferred IUPAC name
1-Benzofuran
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| Other names
Benzofuran
Coumarone Benzo[b]furan |
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| Identifiers | |||
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271-89-6 |
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| 3D model (Jmol) | Interactive image | ||
| ChEBI |
CHEBI:35260 |
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| ChEMBL |
ChEMBL363614 |
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| ChemSpider |
8868 |
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| DrugBank |
DB04179 |
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| ECHA InfoCard | 100.005.439 | ||
| KEGG |
C14512 |
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| PubChem | 9223 | ||
| UNII |
LK6946W774 |
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| Properties | |||
| C8H6O | |||
| Molar mass | 118.14 g·mol−1 | ||
| Melting point | −18 °C (0 °F; 255 K) | ||
| Boiling point | 173 °C (343 °F; 446 K) | ||
| Hazards | |||
| Lethal dose or concentration (LD, LC): | |||
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LD50 (median dose)
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500 mg/kg (mice). | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |||
Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar. Benzofuran is the "parent" of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants.
Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.
Benzofurans can be prepared by various methods in the laboratory. Notable examples include: