Phanquinone
Chemical compound
From Wikipedia, the free encyclopedia
Phanquinone is an organic compound with the formula C12H6N2O2. It is derived by oxidation of 4,7-phenanthroline.
| Names | |
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| Other names
4,7-phenanthroline-5,6-dione | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.001.378 |
| EC Number |
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| 365810 | |
| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C12H6N2O2 | |
| Molar mass | 210.192 g·mol−1 |
| Appearance | yellow solid |
| Melting point | 295 °C (563 °F; 568 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H302, H312, H332, H412 | |
| P261, P264, P270, P271, P273, P280, P301+P317, P302+P352, P304+P340, P317, P321, P330, P362+P364, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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It has been investigated as both antiprotozoal agent and for its bactericidal activity .[1] It has an extensive role as a ligand in coordination chemistry.[2][3]
