Methanesulfonato(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II)

98%

Reagent Code: #210206
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CAS Number 1599466-87-1

science Other reagents with same CAS 1599466-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 794.29 g/mol
Formula C₄₀H₅₀NO₅PPdS
badge Registry Numbers
MDL Number MFCD29905053
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

description Product Description

Widely used as a highly active and air-stable palladium catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. It enables efficient carbon–nitrogen and carbon–carbon bond formation under mild conditions, making it valuable in pharmaceutical synthesis, agrochemicals, and materials science. Its electron-rich ligand system enhances reactivity with sterically hindered and electronically deactivated substrates. Commonly employed in late-stage functionalization where functional group tolerance and high selectivity are critical. Suitable for both laboratory-scale research and industrial applications due to its reliability and ease of handling.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿480.00
inventory 250mg
10-20 days ฿1,020.00
inventory 1g
10-20 days ฿2,880.00
inventory 5g
10-20 days ฿11,600.00
inventory 25g
10-20 days ฿50,260.00

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Methanesulfonato(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II)
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Widely used as a highly active and air-stable palladium catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. It enables efficient carbon–nitrogen and carbon–carbon bond formation under mild conditions, making it valuable in pharmaceutical synthesis, agrochemicals, and materials science. Its electron-rich ligand system enhances reactivity with sterically hindered and electronically deactivated substrates. Commonly employed in late-stage functionaliz

Widely used as a highly active and air-stable palladium catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. It enables efficient carbon–nitrogen and carbon–carbon bond formation under mild conditions, making it valuable in pharmaceutical synthesis, agrochemicals, and materials science. Its electron-rich ligand system enhances reactivity with sterically hindered and electronically deactivated substrates. Commonly employed in late-stage functionalization where functional group tolerance and high selectivity are critical. Suitable for both laboratory-scale research and industrial applications due to its reliability and ease of handling.

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