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| | Phenylmagnesium chloride Basic information |
| | Phenylmagnesium chloride Chemical Properties |
| Melting point | 89-90℃ | | Boiling point | 230℃ (8 Torr) | | density | 0.98 g/mL at 20 °C | | Fp | 1 °F | | storage temp. | 2-8°C | | form | solution | | color | Yellow | | Water Solubility | It reacts violently with water. | | Sensitive | Air & Moisture Sensitive | | Merck | 14,7298 | | BRN | 3587900 | | InChI | InChI=1S/C6H5.ClH.Mg/c1-2-4-6-5-3-1;;/h1-5H;1H;/q;;+1/p-1 | | InChIKey | GQONLASZRVFGHI-UHFFFAOYSA-M | | SMILES | C1([Mg]Cl)C=CC=CC=1 | | CAS DataBase Reference | 100-59-4(CAS DataBase Reference) | | EPA Substance Registry System | Magnesium, chlorophenyl- (100-59-4) |
| | Phenylmagnesium chloride Usage And Synthesis |
| Chemical Properties | yellowish-brown to dark brown solution | | Uses | In organic synthesis, especially in the production of hydrocarbons, alcohols, ketones, organic acids, amines, silicones, boranes. | | Uses | Grignard reagent in greener solvent, 2-methyltetrahydrofuran (2-MeTHF)
2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry | | Uses | Phenylmagnesium chloride (PhMgCl) solution is a common Grignard reagent used in the synthesis of ()-phenserine and stephacidin B. It is employed in a variety of cross-coupling reactions. It can also be used as an electrolyte solution along with aluminium chloride (AlCl3) in the rechargeable magnesium batteries. | | Definition | ChEBI: Phenylmagnesium chloride is an arylmagnesium halide. | | General Description | This product has been enhanced for energy efficiency. | | reaction suitability | reaction type: Grignard Reaction |
| | Phenylmagnesium chloride Preparation Products And Raw materials |
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