Phenol, 2-(diphenylphosphinyl)-

≥95%

Reagent Code: #223303
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CAS Number 16522-52-4

science Other reagents with same CAS 16522-52-4

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scatter_plot Molecular Information
Weight 294.2843 g/mol
Formula C₁₈H₁₅O₂P
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MDL Number MFCD00417583
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key ligand in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its phosphine oxide group provides strong electron-withdrawing properties, enhancing catalyst stability and reactivity. Commonly employed in Suzuki, Heck, and Buchwald–Hartwig aminations for forming carbon-carbon and carbon-nitrogen bonds in pharmaceutical and agrochemical synthesis. Also utilized in the development of phosphorescent materials and as a building block in designing functional ligands for asymmetric catalysis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿48,000.00
inventory 100mg
10-20 days ฿64,000.00
inventory 250mg
10-20 days ฿120,000.00
inventory 1g
10-20 days ฿320,000.00

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Phenol, 2-(diphenylphosphinyl)-
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Used as a key ligand in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its phosphine oxide group provides strong electron-withdrawing properties, enhancing catalyst stability and reactivity. Commonly employed in Suzuki, Heck, and Buchwald–Hartwig aminations for forming carbon-carbon and carbon-nitrogen bonds in pharmaceutical and agrochemical synthesis. Also utilized in the development of phosphorescent materials and as a building block in designing functional l

Used as a key ligand in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its phosphine oxide group provides strong electron-withdrawing properties, enhancing catalyst stability and reactivity. Commonly employed in Suzuki, Heck, and Buchwald–Hartwig aminations for forming carbon-carbon and carbon-nitrogen bonds in pharmaceutical and agrochemical synthesis. Also utilized in the development of phosphorescent materials and as a building block in designing functional ligands for asymmetric catalysis.

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