Oxepine
Chemical compound
From Wikipedia, the free encyclopedia
Oxepine is an oxygen-containing heterocycle consisting of a seven-membered ring with three double bonds. The parent C6H6O exists as an equilibrium mixture with benzene oxide.

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| Names | |||
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| Preferred IUPAC name
Oxepine | |||
| Other names
Oxacycloheptatriene | |||
| Identifiers | |||
3D model (JSmol) |
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PubChem CID |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| C6H6O | |||
| Molar mass | 94.113 g·mol−1 | ||
| Related compounds | |||
Related compounds |
Cyclohexene oxide Oxonane | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The oxepin–benzene oxide equilibrium is affected by the ring substituents.[1] A related dimethyl derivative exists mainly as the oxepine isomer, an orange liquid.[2]
In nature, oxepine is an intermediate in the oxidation of benzene by the cytochrome P450 (CYP).[3] Other arene oxides are metabolites of the parent arene.
Benzene oxides are produced in the laboratory from dehydrohalogenation of the corresponding dihaloepoxide:[4]


