Tris[3,5-bis(trifluoromethyl)phenyl]phosphine
98.0%(GC)
- Product Code: 68882
Alias:
Tris[N,N-bis(trimethylsilyl)amine]phosphine; Tris[3,4-bis(trifluoromethyl)phenyl]phosphine
CAS:
175136-62-6
| Molecular Weight: | 670.27 g./mol | Molecular Formula: | C₂₄H₉F₁₈P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00042428 | |
| Melting Point: | 95 °C | Boiling Point: | 128-130°C 0,5mm |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a ligand in catalytic processes, especially in transition metal-catalyzed reactions. Its electron-deficient nature, due to the trifluoromethyl groups, makes it highly effective in stabilizing metal centers and enhancing the reactivity of catalysts. It is commonly employed in cross-coupling reactions, such as Suzuki and Heck couplings, where it improves yield and selectivity. Additionally, it finds application in asymmetric synthesis, where its steric bulk and electronic properties help control the stereochemistry of the reaction. It is also utilized in the synthesis of pharmaceuticals and fine chemicals, where precise catalytic activity is crucial. Its stability under harsh reaction conditions further broadens its utility in industrial and laboratory settings.
Product Specification:
| Test | Specification |
|---|---|
| PURITY GC | 98 100% |
| Appearance | Yellow-brown |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿850.00 |
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| 0.250 | 10-20 days | ฿1,820.00 |
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| 1.000 | 10-20 days | ฿6,240.00 |
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| 5.000 | 10-20 days | ฿23,580.00 |
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Tris[3,5-bis(trifluoromethyl)phenyl]phosphine
This chemical is primarily used as a ligand in catalytic processes, especially in transition metal-catalyzed reactions. Its electron-deficient nature, due to the trifluoromethyl groups, makes it highly effective in stabilizing metal centers and enhancing the reactivity of catalysts. It is commonly employed in cross-coupling reactions, such as Suzuki and Heck couplings, where it improves yield and selectivity. Additionally, it finds application in asymmetric synthesis, where its steric bulk and electronic properties help control the stereochemistry of the reaction. It is also utilized in the synthesis of pharmaceuticals and fine chemicals, where precise catalytic activity is crucial. Its stability under harsh reaction conditions further broadens its utility in industrial and laboratory settings.
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