Phenanthrenequinone
| File:9,10-Phenanthrenedione.svg | |
| Names | |
|---|---|
| Systematic IUPAC name
9,10-Phenanthrenequinone[1] | |
| Identifiers | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.001.377 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C14H8O2 | |
| Molar mass | 208.216 g·mol−1 |
| Appearance | Orange solid |
| Odor | Odorless |
| Melting point | 209 °C (408 °F; 482 K) |
| Boiling point | 360 °C (680 °F; 633 K) |
| Slightly soluble (7.5 mg L−1) | |
| Hazards | |
| GHS labelling: | |
 
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| Warning | |
| H315, H319, H400 | |
| P264, P273, P280, P302+P352, P305+P351+P338, P332+P313, P337+P313, P362, P391, P501 | |
| NFPA 704 (fire diamond) | |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Phenanthrenedione is a cytotoxic derivative of the polycyclic aromatic hydrocarbon phenanthrene.[2]
References
- ^ " 84-11-7|Phenanthrenequinone|Toxnet|". nih.gov.
- ^ Robert A. Kanaly; Natsuko Hamamura (September 2013). "9,10-Phenanthrenedione biodegradation by a soil bacterium and identification of transformation products by LC/ESI-MS/MS". Chemosphere. 92 (11): 1442–1449. doi:10.1016/j.chemosphere.2013.03.054. Retrieved 8 March 2016.
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