Benzofuran
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| Benzofuran | |
|---|---|
| Image:Benzofuran chemical structure.png | |
| Other names | Coumarone, benzo[b]furan |
| Identifiers | |
| CAS number | |
| SMILES | C1(OC=C2)=C2C=CC=C1 |
| Properties | |
| Molecular formula | C8H6O |
| Molar mass | 118.13 g/mol |
| Melting point |
< -18 °C |
| Boiling point | 173 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. It is the parent of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants.
It is prepared by O-alkylation of salicylaldehyde with chloroacetic acid followed by dehydration of the resulting ether.[1]
References
- ↑ Albert W. Burgstahler and Leonard R. Worden “Coumarone” Organic Syntheses, Collected Volume 5, p.251 (1973). http://www.orgsyn.org/orgsyn/pdfs/CV5P0251.pdf
See also
- Furan, an analog without the fused benzene ring.
- Indole, an analog with a nitrogen instead of the oxygen atom.
- Simple aromatic ringsTemplate:Heterocyclic-stub
ar:بنزو فيوران de:Benzofuranfi:Bentsofuraani
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