Di(1-adamantyl)-1-piperidinylphenylphosphine

≥95%

Reagent Code: #121140
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CAS Number 1237588-13-4

science Other reagents with same CAS 1237588-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 461.66 g/mol
Formula C₃₁H₄₄NP
badge Registry Numbers
MDL Number MFCD28053539
thermostat Physical Properties
Melting Point 225-230 ℃
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups, enhances steric bulk and electron density, making it effective in stabilizing metal complexes and improving catalytic efficiency. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its robust nature allows for use in challenging reaction conditions, including high temperatures and strong bases, making it valuable in pharmaceutical and fine chemical synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,996.00
inventory 250mg
10-20 days ฿4,707.00

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Di(1-adamantyl)-1-piperidinylphenylphosphine
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This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups, enhances steric bulk and electron density, making it effective in stabilizing metal complexes and improving catalytic efficiency. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its r

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups, enhances steric bulk and electron density, making it effective in stabilizing metal complexes and improving catalytic efficiency. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its robust nature allows for use in challenging reaction conditions, including high temperatures and strong bases, making it valuable in pharmaceutical and fine chemical synthesis.

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