Dibenzodioxin
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| Dibenzo-p-dioxin | |
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| IUPAC name | Dibenzo-1,4-dioxin |
| Other names | Dibenzodioxin, Dibenzo-p-dioxin, Oxanthrene |
| Identifiers | |
| CAS number | [262-12-4] |
| Properties | |
| Molecular formula | C12H8O2 |
| Molar mass | 184.20 g/mol |
| Appearance | White crystals |
| Melting point |
122 °C (395 K) |
| Boiling point |
283.5 °C (556.5 K) |
| Related compounds | |
| Related compounds | dioxin 1,4-dioxin polychlorinated dibenzodioxins |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Dibenzodioxin, C12H8O2, is an organic heterocyclic compound in which two benzene rings are attached to a dioxin ring.
The name generally refers to the dibenzo-p-dioxin, as no detailed information is available on the dibenzo-o-dioxin isomer, expected to be highly unstable with peroxidelike characteristics.
Dibenzo-1,4-dioxin can be prepared by cycloaddition, namely by the Diels-Alder reaction[1]
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[edit] References
- ^ J. Chem. Soc., Perkin Trans. 1, 1994, 927 - 931, Effect of ring strain on the formation and pyrolysis of some Diels–Alder adducts of 2-sulfolene (2,3-dihydrothiophene 1,1-dioxide) and maleic anhydride with 1,3-dienes and products derived therefrom.
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