Tri(2-furyl)phosphine
98%
- Product Code: 68875
Alias:
Tris(2-furyl)phosphine
CAS:
5518-52-5
| Molecular Weight: | 232.17 g./mol | Molecular Formula: | C₁₂H₉O₃P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151857 | |
| Melting Point: | 59-64 °C(lit.) | Boiling Point: | 136 °C4 mm Hg(lit.) |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Tri(2-furyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is particularly valuable in the synthesis of organometallic compounds, where it facilitates the stabilization of metal centers and enhances catalytic activity. This compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. Its unique electronic properties make it effective in asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. Additionally, tri(2-furyl)phosphine is utilized in the development of materials science, particularly in the creation of metal-organic frameworks (MOFs) and other advanced materials. Its versatility and ability to modify metal reactivity make it a key component in both academic research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 61 64? |
| PurityGC | 98 100% |
| APPEARANCE | White to off-white powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿540.00 |
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| 1.000 | 10-20 days | ฿1,020.00 |
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| 5.000 | 10-20 days | ฿2,860.00 |
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| 25.000 | 10-20 days | ฿10,580.00 |
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Tri(2-furyl)phosphine
Tri(2-furyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is particularly valuable in the synthesis of organometallic compounds, where it facilitates the stabilization of metal centers and enhances catalytic activity. This compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. Its unique electronic properties make it effective in asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. Additionally, tri(2-furyl)phosphine is utilized in the development of materials science, particularly in the creation of metal-organic frameworks (MOFs) and other advanced materials. Its versatility and ability to modify metal reactivity make it a key component in both academic research and industrial applications.
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