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Oxepin

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Oxepin
Skeletal formula of oxepin
Ball-and-stick model of the oxepin molecule
Names
IUPAC name
Oxepine
Other names
Oxacycloheptatriene
Benzene oxide
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C6H6O/c1-2-4-6-7-5-3-1/h1-6H ☒N
    Key: ATYBXHSAIOKLMG-UHFFFAOYSA-N ☒N
  • InChI=1/C6H6O/c1-2-4-6-7-5-3-1/h1-6H
    Key: ATYBXHSAIOKLMG-UHFFFAOYAS
  • C1=CC=COC=C1
Properties
C6H6O
Molar mass 94.11 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Oxepin 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. The oxepin–benzene oxide equilibrium is affected by the ring substituents.[1] A related dimethyl derivative exists mainly as the oxepin isomer, an orange liquid.[2]

Formation and selected reactions of benzene oxide.

Oxepin is an intermediate in the oxidation of benzene by the cytochrome P450.[3] Other arene oxides are metabolites of the parent arene.

References

  1. ^ E. Vogel, H. Günther (1967). "Benzene Oxide-Oxepin Valence Tautomerism". Angewandte Chemie International Edition in English. 6 (5): 385–401. doi:10.1002/anie.196703851.
  2. ^ "2,7-Dimethyloxepin". Org. Synth. 49: 62. 1969. doi:10.15227/orgsyn.049.0062. {{cite journal}}: Unknown parameter |authors= ignored (help)
  3. ^ R. Snyder, G. Witz, and B. D. Goldstein (1993). "The Toxicology of Benzene". Environmental Health Perspectives. 100: 293–306. doi:10.1289/ehp.93100293. JSTOR 3431535. PMC 1519582. PMID 8354177.{{cite journal}}: CS1 maint: multiple names: authors list (link)