2-((Di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine

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Reagent Code: #68758
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CAS Number 863971-66-8

science Other reagents with same CAS 863971-66-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.47 g/mol
Formula C₁₉H₃₆N₂P
badge Registry Numbers
MDL Number MFCD11656080
inventory_2 Storage & Handling
Density 0.936 g/cm3 at 25 °C (lit.)
Storage room temperature, inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,240.00

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2-((Di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine
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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 ma

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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