2-((Di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine
98%
- Product Code: 68758
CAS:
863971-66-8
| Molecular Weight: | 322.47 g./mol | Molecular Formula: | C₁₉H₃₆N₂P |
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| EC Number: | MDL Number: | MFCD11656080 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.936 g/cm3 at 25 °C (lit.) | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring both phosphine and amine groups, makes it highly effective in stabilizing metal centers and enhancing catalytic activity. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its steric and electronic properties make it suitable for asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. The ligand’s robustness under various reaction conditions further expands its utility in industrial and academic research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,240.00 |
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2-((Di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine
This compound is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring both phosphine and amine groups, makes it highly effective in stabilizing metal centers and enhancing catalytic activity. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its steric and electronic properties make it suitable for asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. The ligand’s robustness under various reaction conditions further expands its utility in industrial and academic research settings.
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