Sodium 2′-dicyclohexylphosphino-2,6-dimethoxy-1,1′-biphenyl-3-sulfonate hydrate

95%

Reagent Code: #68787
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CAS Number 1049726-96-6

science Other reagents with same CAS 1049726-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 512.57(anhydrous basis) g/mol
Formula C₂₆H₃₄NaO₅PSH₂O
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MDL Number MFCD07781994
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description Product Description

Widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its water-soluble nature makes it valuable in aqueous-phase catalytic processes, enhancing reaction efficiency and enabling easier separation of products. Commonly employed in pharmaceutical synthesis for constructing complex organic molecules. Its stability and effectiveness in challenging reaction conditions make it a preferred choice for industrial and academic research applications.

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Test Parameter Specification
Purity 95-100%
Appearance White to Yellow Solid; Powder or Crystals
Phosphorus NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿380.00
inventory 500mg
10-20 days ฿2,230.00
inventory 100mg
10-20 days ฿880.00

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Sodium 2′-dicyclohexylphosphino-2,6-dimethoxy-1,1′-biphenyl-3-sulfonate hydrate
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Widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its water-soluble nature makes it valuable in aqueous-phase catalytic processes, enhancing reaction efficiency and enabling easier separation of products. Commonly employed in pharmaceutical synthesis for constructing complex organic molecules. Its stability and effectiveness in challenging reaction conditions make it a preferred choice for industrial and

Widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its water-soluble nature makes it valuable in aqueous-phase catalytic processes, enhancing reaction efficiency and enabling easier separation of products. Commonly employed in pharmaceutical synthesis for constructing complex organic molecules. Its stability and effectiveness in challenging reaction conditions make it a preferred choice for industrial and academic research applications.

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