| Names | |
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IUPAC name
Diphenylditelluide
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| Other names
Phenylditelluride
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| Identifiers | |
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3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.046.332 |
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PubChem CID
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| Properties | |
| C12H10Te2 | |
| Molar mass | 409.42 g/mol |
| Appearance | Orange powder |
| Density | 2.23 g/cm3 |
| Melting point | 66 to 67 °C (151 to 153 °F; 339 to 340 K) |
| Boiling point | decomposes |
| Insoluble | |
| Solubility in other solvents | Dichloromethane |
| Structure | |
| 90° at Se C2 symmetry |
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| 0 D | |
| Hazards | |
| Main hazards | Toxic |
| R-phrases (outdated) | 20/21/22-36/37/38 |
| S-phrases (outdated) | 26-36 |
| Related compounds | |
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Related compounds
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Ph2S2, Ph2Se2 |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Diphenylditelluride is the chemical compound with the formula (C6H5Te)2, abbreviated Ph2Te2 This orange-coloured solid is the oxidized derivative of the unstable benzenetellurol, PhTeH. Ph2Te2 is used as a source of the PhTe unit in organic synthesis.
Ph2Te2 is prepared by the oxidation of tellurophenolate, which is generated via the Grignard reagent:
The molecule has C2 symmetry.