Bis[2-[(oxo)diphenylphosphino]phenyl] Ether

≥99%(HPLC), sublimation and purification

Reagent Code: #128393
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CAS Number 808142-23-6

science Other reagents with same CAS 808142-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 570.55 g/mol
Formula C₃₆H₂₈O₃P₂
thermostat Physical Properties
Melting Point 280 °C
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a specialized ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its rigid ether-linked bisphosphine structure enhances metal complex stability and improves catalytic efficiency in transformations such as Suzuki-Miyaura and Buchwald-Hartwig aminations. The compound’s steric and electronic properties promote high selectivity and turnover in the synthesis of biaryl and nitrogen-containing compounds, which are key intermediates in pharmaceuticals and agrochemicals. Also employed in the development of novel catalysts for asymmetric synthesis due to its tunable coordination geometry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,700.00

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Bis[2-[(oxo)diphenylphosphino]phenyl] Ether
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Used as a specialized ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its rigid ether-linked bisphosphine structure enhances metal complex stability and improves catalytic efficiency in transformations such as Suzuki-Miyaura and Buchwald-Hartwig aminations. The compound’s steric and electronic properties promote high selectivity and turnover in the synthesis of biaryl and nitrogen-containing compounds, which are key intermediates in pharmaceuticals and agroc

Used as a specialized ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its rigid ether-linked bisphosphine structure enhances metal complex stability and improves catalytic efficiency in transformations such as Suzuki-Miyaura and Buchwald-Hartwig aminations. The compound’s steric and electronic properties promote high selectivity and turnover in the synthesis of biaryl and nitrogen-containing compounds, which are key intermediates in pharmaceuticals and agrochemicals. Also employed in the development of novel catalysts for asymmetric synthesis due to its tunable coordination geometry.

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