Bis(4-fluorophenyl)phosphine

95%

Reagent Code: #154413
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CAS Number 25186-17-8

science Other reagents with same CAS 25186-17-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.18 g/mol
Formula C₁₂H₉F₂P
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MDL Number MFCD23701667
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a ligand in transition metal-catalyzed reactions, particularly in palladium-catalyzed cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig aminations. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of the metal complex, improving catalytic efficiency and selectivity. Also employed in the synthesis of pharmaceuticals and agrochemicals where fine-tuned ligand properties are required. Suitable for applications in materials science, especially in the development of organic electronic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,480.00
inventory 250mg
10-20 days ฿13,950.00

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Bis(4-fluorophenyl)phosphine
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Used as a ligand in transition metal-catalyzed reactions, particularly in palladium-catalyzed cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig aminations. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of the metal complex, improving catalytic efficiency and selectivity. Also employed in the synthesis of pharmaceuticals and agrochemicals where fine-tuned ligand properties are required. Suitable for applications in materials science, especially in t

Used as a ligand in transition metal-catalyzed reactions, particularly in palladium-catalyzed cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig aminations. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of the metal complex, improving catalytic efficiency and selectivity. Also employed in the synthesis of pharmaceuticals and agrochemicals where fine-tuned ligand properties are required. Suitable for applications in materials science, especially in the development of organic electronic materials.

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