2-[Bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]benzaldehyde

98%

Reagent Code: #68771
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CAS Number 1202865-21-1

science Other reagents with same CAS 1202865-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 574.77 g/mol
Formula C₃₇H₅₁O₃P
badge Registry Numbers
MDL Number MFCD15143663
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. It is effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its sterically hindered and electron-rich phosphine structure. The compound enhances the stability and activity of metal catalysts, improving reaction efficiency and selectivity. It is also employed in various synthetic applications, including the synthesis of pharmaceuticals and fine chemicals. Additionally, its application extends to materials science, where it is used in the development of advanced polymers and coordination complexes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,672.00
inventory 1g
10-20 days ฿42,372.00
inventory 100mg
10-20 days ฿6,318.00

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2-[Bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]benzaldehyde
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This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. It is effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its sterically hindered and electron-rich phosphine structure. The compound enhances the stability and activity of metal catalysts, improving reaction efficiency and selectivity. It is also employed in various synthetic applications, including the synthesis of pharmaceuticals an

This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. It is effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its sterically hindered and electron-rich phosphine structure. The compound enhances the stability and activity of metal catalysts, improving reaction efficiency and selectivity. It is also employed in various synthetic applications, including the synthesis of pharmaceuticals and fine chemicals. Additionally, its application extends to materials science, where it is used in the development of advanced polymers and coordination complexes.

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