Bis(4-methoxyphenyl)phosphine
95%
- Product Code: 68943
CAS:
84127-04-8
| Molecular Weight: | 246.24 g./mol | Molecular Formula: | C₁₄H₁₅O₂P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15143653 | |
| Melting Point: | 36-40 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
Used as a ligand in coordination chemistry, it facilitates the formation of metal complexes, particularly in catalytic processes. Its electron-donating methoxy groups enhance the reactivity and stability of these complexes, making it valuable in organic synthesis, including cross-coupling reactions like Suzuki-Miyaura and Heck reactions. Additionally, it finds application in the development of phosphorescent materials and organic light-emitting diodes (OLEDs) due to its ability to modify electronic properties. In pharmaceutical research, it serves as a building block for synthesizing compounds with potential biological activity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Beige Flakes, Powder or Solid |
| PURITY | 94.5-100 |
| PROTON NMR SPECTRUM | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,670.00 |
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| 0.500 | 10-20 days | ฿16,330.00 |
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Bis(4-methoxyphenyl)phosphine
Used as a ligand in coordination chemistry, it facilitates the formation of metal complexes, particularly in catalytic processes. Its electron-donating methoxy groups enhance the reactivity and stability of these complexes, making it valuable in organic synthesis, including cross-coupling reactions like Suzuki-Miyaura and Heck reactions. Additionally, it finds application in the development of phosphorescent materials and organic light-emitting diodes (OLEDs) due to its ability to modify electronic properties. In pharmaceutical research, it serves as a building block for synthesizing compounds with potential biological activity.
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