2-(Di-tert-butylphosphino)-1-phenyl-1H-indole

98%

Reagent Code: #68774
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CAS Number 740815-37-6

science Other reagents with same CAS 740815-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.44 g/mol
Formula C₂₂H₂₈NP
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MDL Number MFCD06798302
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,204.00
inventory 100mg
10-20 days ฿1,602.00

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2-(Di-tert-butylphosphino)-1-phenyl-1H-indole
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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

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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