Benzocyclobutadiene
Not to be confused with benzocyclobutene.
 | |
| Names | |
|---|---|
| IUPAC name
Bicyclo[4.2.0]octa-1,3,5,7-tetraene | |
| Identifiers | |
4026-23-7  | |
| ChemSpider | 70373 |
| Jmol interactive 3D | Image |
| PubChem | 77987 |
| |
| |
| Properties | |
| C8H6 | |
| Molar mass | 102.14 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is  ?) | |
| Infobox references | |
Benzocyclobutadiene is the simplest polycyclic aromatic hydrocarbon, being composed of a benzene ring fused to a cyclobutadiene ring. It has chemical formula C8H6. Though the benzene ring is stabilized by aromaticity, the cyclobutadiene portion has a destabilizing effect. For this reason, benzocyclobutadiene will readily dimerize or polymerize and it reacts as a dienophile in Diels-Alder reactions.[1]
See also
References
- ↑ Carey, Francis A.; Sundberg, Richard J.; (1984). Advanced Organic Chemistry Part A Structure and Mechanisms (2nd ed.). New York N.Y.: Plenum Press. ISBN 0-306-41198-9.
This article is issued from Wikipedia - version of the Thursday, August 20, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.