Chloro(1-t-butylindenyl)[2-(dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl]palladium(II)

98%

Reagent Code: #166761
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CAS Number 1779569-06-0

science Other reagents with same CAS 1779569-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 788.85 g/mol
Formula C₄₆H₆₃ClPPd
badge Registry Numbers
MDL Number MFCD29037169
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a highly active 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 and the development of complex organic molecules. Its bulky phosphine ligand enhances stability and reactivity, especially with sterically hindered substrates. Commonly employed in late-stage functionalization of drug candidates and in the preparation of functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,650.00

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Chloro(1-t-butylindenyl)[2-(dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl]palladium(II)
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Used as a highly active 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 and the development of complex organic molecules. Its bulky phosphine ligand enhances stability and reactivity, especially with sterically hindered substrates. Commonly employed in late-stage functionalization of drug candidates and in

Used as a highly active 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 and the development of complex organic molecules. Its bulky phosphine ligand enhances stability and reactivity, especially with sterically hindered substrates. Commonly employed in late-stage functionalization of drug candidates and in the preparation of functional materials.

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