Phenalene
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| Names | |||
|---|---|---|---|
| Preferred IUPAC name 1H-Phenalene | |||
| Other names 1-Benzonaphthene; 1H-Benzonaphthene; Perinaphthene; Perinaphthindene; peri-Naphthindene | |||
| Identifiers | |||
| 3D model (JSmol) | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.005.371 | ||
| PubChem CID | |||
| UNII | |||
| CompTox Dashboard (EPA) | |||
| 
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| Properties | |||
| C13H10 | |||
| Molar mass | 166.22 g/mol | ||
| Appearance | white solid | ||
| Density | 1.139 g/cm3 | ||
| Melting point | 159–160 °C (318–320 °F; 432–433 K) | ||
| Acidity (pKa) | 18.1 (in DMSO) | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
1H-Phenalene, often called simply phenalene is a polycyclic aromatic hydrocarbon (PAH). Like many PAHs, it is an atmospheric pollutant formed during the combustion of fossil fuels. It is the parent compound for the phosphorus-containing phosphaphenalenes.
The name was proposed by German chemists in 1922 as a contraction of periphenonaphthalene.