Phenyllithium
| Names | |
|---|---|
| Systematic IUPAC name Phenyllithium | |
| Other names Lithiobenzene | |
| Identifiers | |
| 3D model (JSmol) | |
| Abbreviations | LiPh, PhLi | 
| 506502 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.008.838 | 
| EC Number | 
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| 2849 | |
| MeSH | phenyllithium | 
| PubChem CID | |
| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C6H5Li | |
| Molar mass | 84.045 g/mol | 
| Appearance | Colorless crystals | 
| Density | 0.828 g/cm3 | 
| Boiling point | 140 to 143 °C (284 to 289 °F; 413 to 416 K) | 
| Reacts | |
| Thermochemistry | |
| Std enthalpy of formation (ΔfH⦵298) | 48.3 to 52.5 kJ/mol | 
| Hazards | |
| GHS labelling: | |
| Danger | |
| H226, H250, H261, H302, H312, H314, H332 | |
| P210, P222, P231+P232, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P334, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P363, P370+P378, P402+P404, P403+P235, P405, P422, P501 | |
| Safety data sheet (SDS) | External MSDS | 
| Related compounds | |
| Related compounds | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Phenyllithium is an organometallic agent with the empirical formula C6H5Li. It is most commonly used as a metalating agent in organic syntheses and a substitute for Grignard reagents for introducing phenyl groups in organic syntheses. Crystalline phenyllithium is colorless; however, solutions of phenyllithium are various shades of brown or red depending on the solvent used and the impurities present in the solute.