Phenethyldiphenylphosphine

98%

Reagent Code: #227831
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CAS Number 5952-49-8

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.34 g/mol
Formula C₂₀H₁₉P
badge Registry Numbers
MDL Number MFCD31630445
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Widely used as a ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Negishi couplings. Its electron-rich phosphine group enhances catalyst stability and reactivity, making it effective in forming carbon-carbon bonds in pharmaceutical and fine chemical synthesis. It is also employed in the development of transition metal complexes for asymmetric catalysis, where its steric and electronic properties can be tuned to improve selectivity and yield. Due to its solubility in organic solvents, it is well-suited for use in non-aqueous reaction systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿10,530.00
250mg
10-20 days ฿17,900.00
1g
10-20 days ฿59,270.00
Phenethyldiphenylphosphine
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Widely used as a ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Negishi couplings. Its electron-rich phosphine group enhances catalyst stability and reactivity, making it effective in forming carbon-carbon bonds in pharmaceutical and fine chemical synthesis. It is also employed in the development of transition metal complexes for asymmetric catalysis, where its steric and electronic properties can be tuned to improve selectivity and

Widely used as a ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Negishi couplings. Its electron-rich phosphine group enhances catalyst stability and reactivity, making it effective in forming carbon-carbon bonds in pharmaceutical and fine chemical synthesis. It is also employed in the development of transition metal complexes for asymmetric catalysis, where its steric and electronic properties can be tuned to improve selectivity and yield. Due to its solubility in organic solvents, it is well-suited for use in non-aqueous reaction systems.

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