Tris(4-fluorophenyl)phosphine
98%
- Product Code: 68866
Alias:
Tris(4-fluorophenyl)phosphine
CAS:
18437-78-0
| Molecular Weight: | 316.26 g./mol | Molecular Formula: | FC₆H₄₃P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00013553 | |
| Melting Point: | 79-83 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Tris(4-fluorophenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis, particularly in transition metal-catalyzed reactions. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. It also finds application in the synthesis of organic semiconductors and optoelectronic materials due to its ability to modify electronic properties. Additionally, it serves as a precursor in the preparation of phosphine-based polymers and advanced materials for use in sensors and coatings. Its role in asymmetric catalysis further highlights its importance in producing chiral compounds for pharmaceuticals and fine chemicals.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 79 83? |
| PurityGC | 98 100% |
| APPEARANCE | WHITE TO OFF-WHITE OR LIGHT YELLOW POWDER OR CRYSTALS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,232.23 |
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| 5.000 | 10-20 days | Ft7,003.17 |
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| 25.000 | 10-20 days | Ft32,214.58 |
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| 100.000 | 10-20 days | Ft121,747.42 |
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Tris(4-fluorophenyl)phosphine
Tris(4-fluorophenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis, particularly in transition metal-catalyzed reactions. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. It also finds application in the synthesis of organic semiconductors and optoelectronic materials due to its ability to modify electronic properties. Additionally, it serves as a precursor in the preparation of phosphine-based polymers and advanced materials for use in sensors and coatings. Its role in asymmetric catalysis further highlights its importance in producing chiral compounds for pharmaceuticals and fine chemicals.
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