(Acetonitrile)[(2-biphenyl)di-tert-butylphosphine]gold(I) hexafluoroantimonate

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Reagent Code: #134877
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CAS Number 866641-66-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 772.17 g/mol
Formula C₂₂H₃₀AuF₆NPSb
badge Registry Numbers
MDL Number MFCD11045449
thermostat Physical Properties
Melting Point 198-203 °C (D)
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas storage

description Product Description

Used as a highly active catalyst in cross-coupling reactions, particularly in the formation of carbon–carbon and carbon–heteroatom bonds. It is especially effective in gold-catalyzed transformations such as alkyne functionalization, cyclization reactions, and C–H activation under mild conditions. The presence of the bulky di-tert-butylphosphine ligand enhances catalyst stability and reactivity, while the acetonitrile ligand allows for easy displacement to initiate catalysis. The hexafluoroantimonate counterion contributes to high solubility in polar organic solvents, making it suitable for use in homogeneous catalytic systems. Commonly employed in pharmaceutical and fine chemical synthesis where high selectivity and efficiency are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,550.00
inventory 250mg
10-20 days ฿10,310.00
inventory 1g
10-20 days ฿31,330.00

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(Acetonitrile)[(2-biphenyl)di-tert-butylphosphine]gold(I) hexafluoroantimonate
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Used as a highly active catalyst in cross-coupling reactions, particularly in the formation of carbon–carbon and carbon–heteroatom bonds. It is especially effective in gold-catalyzed transformations such as alkyne functionalization, cyclization reactions, and C–H activation under mild conditions. The presence of the bulky di-tert-butylphosphine ligand enhances catalyst stability and reactivity, while the acetonitrile ligand allows for easy displacement to initiate catalysis. The hexafluoroantimonate coun

Used as a highly active catalyst in cross-coupling reactions, particularly in the formation of carbon–carbon and carbon–heteroatom bonds. It is especially effective in gold-catalyzed transformations such as alkyne functionalization, cyclization reactions, and C–H activation under mild conditions. The presence of the bulky di-tert-butylphosphine ligand enhances catalyst stability and reactivity, while the acetonitrile ligand allows for easy displacement to initiate catalysis. The hexafluoroantimonate counterion contributes to high solubility in polar organic solvents, making it suitable for use in homogeneous catalytic systems. Commonly employed in pharmaceutical and fine chemical synthesis where high selectivity and efficiency are required.

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