BrettPhos AuNTf₂

Reagent Code: #154952
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CAS Number 1296269-97-0

science Other reagents with same CAS 1296269-97-0

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Weight 1014.9 g/mol
Formula C₃₇H₅₄AuF₆NO₆PS₂+
badge Registry Numbers
MDL Number MFCD22572681
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Widely used in palladium- and gold-catalyzed cross-coupling reactions, this reagent serves as a highly active precatalyst in forming carbon-carbon and carbon-heteroatom bonds. It is especially effective in coupling aryl halides with amines, alcohols, and other nucleophiles under mild conditions. Its phosphine ligand structure enhances catalyst stability and turnover, making it suitable for reactions involving sterically hindered substrates or electron-deficient partners. Commonly applied in pharmaceutical synthesis and materials science where high efficiency and selectivity are required. Also used in C–H functionalization transformations due to its ability to promote oxidative addition and reductive elimination steps with high fidelity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿31,900.00

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BrettPhos AuNTf₂
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Widely used in palladium- and gold-catalyzed cross-coupling reactions, this reagent serves as a highly active precatalyst in forming carbon-carbon and carbon-heteroatom bonds. It is especially effective in coupling aryl halides with amines, alcohols, and other nucleophiles under mild conditions. Its phosphine ligand structure enhances catalyst stability and turnover, making it suitable for reactions involving sterically hindered substrates or electron-deficient partners. Commonly applied in pharmaceutica

Widely used in palladium- and gold-catalyzed cross-coupling reactions, this reagent serves as a highly active precatalyst in forming carbon-carbon and carbon-heteroatom bonds. It is especially effective in coupling aryl halides with amines, alcohols, and other nucleophiles under mild conditions. Its phosphine ligand structure enhances catalyst stability and turnover, making it suitable for reactions involving sterically hindered substrates or electron-deficient partners. Commonly applied in pharmaceutical synthesis and materials science where high efficiency and selectivity are required. Also used in C–H functionalization transformations due to its ability to promote oxidative addition and reductive elimination steps with high fidelity.

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