2-(Di-tert-butylphosphino)-1-phenyl-1H-indole
98%
- Product Code: 68774
CAS:
740815-37-6
| Molecular Weight: | 337.44 g./mol | Molecular Formula: | C₂₂H₂₈NP |
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| EC Number: | MDL Number: | MFCD06798302 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This chemical is primarily used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. It facilitates the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in organic synthesis for producing pharmaceuticals, agrochemicals, and fine chemicals. Its sterically demanding structure enhances selectivity and efficiency in catalytic processes, especially in palladium-catalyzed reactions like Suzuki-Miyaura and Buchwald-Hartwig couplings. Additionally, it is employed in the development of advanced materials and polymers, where precise control over molecular structure is critical. Its stability and electron-donating properties make it a preferred choice in challenging catalytic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,602.00 |
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| 0.250 | 10-20 days | ฿3,204.00 |
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2-(Di-tert-butylphosphino)-1-phenyl-1H-indole
This chemical is primarily used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. It facilitates the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in organic synthesis for producing pharmaceuticals, agrochemicals, and fine chemicals. Its sterically demanding structure enhances selectivity and efficiency in catalytic processes, especially in palladium-catalyzed reactions like Suzuki-Miyaura and Buchwald-Hartwig couplings. Additionally, it is employed in the development of advanced materials and polymers, where precise control over molecular structure is critical. Its stability and electron-donating properties make it a preferred choice in challenging catalytic transformations.
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