Chlorodiphenylphosphine
| Names | |
|---|---|
| Preferred IUPAC name
Diphenylphosphinous chloride | |
| Other names
chlorodiphenylphosphine p-chlorodiphenylphosphine diphenyl phosphine chloride diphenylchlorophosphine | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.012.813 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C12H10ClP | |
| Molar mass | 220.63776 g mol−1 |
| Appearance | clear to light yellow liquid |
| Density | 1.229 g cm−3 |
| Boiling point | 320 ˚C |
| Reacts | |
| Solubility | Reacts with alcohols highly soluble in benzene, THF, and ethers |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H290, H302, H314, H412 | |
| P234, P260, P264, P270, P273, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P390, P404, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Chlorodiphenylphosphine is an organophosphorus compound with the formula (C6H5)2PCl, abbreviated Ph2PCl. It is a colourless oily liquid with a pungent odor that is often described as being garlic-like and detectable even in the ppb range. It is useful reagent for introducing the Ph2P group into molecules, which includes many ligands. Like other halophosphines, Ph2PCl is reactive with many nucleophiles such as water and easily oxidized even by air.