5-[Di(1-adaMantyl)phosphino](1,3,5-triphenyl-1H-pyrazol-4-yl)-1H-pyrazole

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Reagent Code: #120380
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CAS Number 1239478-87-5

science Other reagents with same CAS 1239478-87-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 662.84 g/mol
Formula C₄₄H₄₇N₄P
badge Registry Numbers
MDL Number MFCD22200502
thermostat Physical Properties
Melting Point 295-300°C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inflated

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 and pyrazole groups, enhances steric and electronic properties, making it effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. It is also employed in asymmetric synthesis, where its chiral environment aids in producing enantioselective products. Additionally, its stability under harsh reaction conditions makes it suitable for use in industrial-scale catalytic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,237.00
inventory 1g
10-20 days ฿16,839.00
inventory 5g
10-20 days ฿58,932.00

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5-[Di(1-adaMantyl)phosphino](1,3,5-triphenyl-1H-pyrazol-4-yl)-1H-pyrazole
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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 and pyrazole groups, enhances steric and electronic properties, making it effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. It is also employed in asymmetric synthesis, where its chiral environment aids in producing enantioselective products. Additionally, its stability under harsh reaction cond

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl and pyrazole groups, enhances steric and electronic properties, making it effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. It is also employed in asymmetric synthesis, where its chiral environment aids in producing enantioselective products. Additionally, its stability under harsh reaction conditions makes it suitable for use in industrial-scale catalytic applications.

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