(t-Bu)PhCPhos

98%

Reagent Code: #68744
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CAS Number 1660153-91-2

science Other reagents with same CAS 1660153-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 404.53 g/mol
Formula C₂₆H₃₃N₂P
badge Registry Numbers
MDL Number MFCD29905429
thermostat Physical Properties
Melting Point 112 °C
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig reactions, due to its strong electron-donating properties and steric bulk, which enhance catalytic activity and selectivity. It is a highly effective ligand for palladium-catalyzed processes, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability under reaction conditions and ability to facilitate challenging transformations make it valuable in industrial and academic research. Additionally, it is employed in the development of new catalytic systems for C-C and C-N bond formation, contributing to advancements in synthetic organic chemistry.

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Test Parameter Specification
Appearance White to Light Yellow Solid
Purity (%) 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,022.00

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(t-Bu)PhCPhos
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Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig reactions, due to its strong electron-donating properties and steric bulk, which enhance catalytic activity and selectivity. It is a highly effective ligand for palladium-catalyzed processes, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability under reaction conditions and ability to facilitate challenging transformations make it valuable in industrial a

Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig reactions, due to its strong electron-donating properties and steric bulk, which enhance catalytic activity and selectivity. It is a highly effective ligand for palladium-catalyzed processes, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability under reaction conditions and ability to facilitate challenging transformations make it valuable in industrial and academic research. Additionally, it is employed in the development of new catalytic systems for C-C and C-N bond formation, contributing to advancements in synthetic organic chemistry.

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