Methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II)

98%

Reagent Code: #61144
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Alias XPhos Pd G4;XPhos Palladacycle Gen. 4
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CAS Number 1599466-81-5

science Other reagents with same CAS 1599466-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 860.48 g/mol
Formula C₄₇H₆₄NO₃PPdS
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

This chemical is primarily used as a highly efficient catalyst in cross-coupling reactions, particularly in the synthesis of complex organic molecules. It plays a crucial role in facilitating the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its application is particularly notable in Buchwald-Hartwig amination reactions, where it enables the coupling of aryl halides with amines to form aryl amines, a key step in drug development. The catalyst's stability and selectivity make it valuable in industrial and academic research for creating structurally diverse and biologically active compounds.

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Test Parameter Specification
APPEARANCE Light brown to gray Solid
Purity(NMR)(%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,930.00
inventory 500mg
10-20 days ฿7,100.00
inventory 1g
10-20 days ฿11,870.00

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Methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II)
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This chemical is primarily used as a highly efficient catalyst in cross-coupling reactions, particularly in the synthesis of complex organic molecules. It plays a crucial role in facilitating the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its application is particularly notable in Buchwald-Hartwig amination reactions, where it enables the coupling of aryl halides with amines to form aryl amines, a key step in drug development. The catalyst's stability and selectivity make it valuable in industrial and academic research for creating structurally diverse and biologically active compounds.
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