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| | Tris(4-fluorophenyl)phosphine Basic information |
| | Tris(4-fluorophenyl)phosphine Chemical Properties |
| Melting point | 79-83 °C(lit.) | | Boiling point | 160°C/0.1mmHg(lit.) | | storage temp. | Inert atmosphere,Room Temperature | | form | Crystalline Powder | | color | White to very slightly yellow | | Water Solubility | Insoluble in water. | | Sensitive | Air Sensitive | | BRN | 919838 | | InChIKey | GEPJPYNDFSOARB-UHFFFAOYSA-N | | CAS DataBase Reference | 18437-78-0(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29319090 |
| | Tris(4-fluorophenyl)phosphine Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powde | | Uses | Tris(4-fluorophenyl)phosphine (TFPP) and tris(2,2,2- trifluoroethyl) phosphite (TTFP) were used as flame-retarding additives in Li-ion battery clectrolytes.
Ligand for rhodium-catalyzed oxygenative addition to terminal alkynes for a greener synthesis esters, amides, and carboxylic acids. | | Uses | Tris(4-fluorophenyl)phosphine, is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. | | Uses | Ligand for rhodium-catalyzed oxygenative addition to terminal alkynes for a greener synthesis esters, amides, and carboxylic acids.
Rhodium-Catalyzed Oxygenative Addition to Terminal Alkynes for the Synthesis of Esters, Amides, and Carboxylic Acids | | Preparation | with 4-bromofluorobenzene, magnesium, and phosphorous (III) trichloride.3 Alternatively, reduction of tris(4-fluorophenyl)phosphine oxide with an iron catalyst. | | General Description | We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information. |
| | Tris(4-fluorophenyl)phosphine Preparation Products And Raw materials |
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