RockPhos Pd G3

98%

Reagent Code: #230594
label
Alias RockPhos-G3-cyclo-palladium complex, [(2-di-tert-butylphosphine-3-methoxy-6-methyl-2',4',6'-triisopropyl-1,1'-biphenyl)-2-(2-aminobiphenyl)] Palladium methanesulfonate (II)
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CAS Number 2009020-38-4

science Other reagents with same CAS 2009020-38-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 838.43 g/mol
Formula C₄₄H₆₂NO₄PPdS
badge Registry Numbers
MDL Number MFCD27952542
thermostat Physical Properties
Melting Point 220-250 °C
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used as a highly active palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Effective for forming carbon-carbon and carbon-nitrogen bonds in complex molecule synthesis, including pharmaceuticals and agrochemicals. Performs well under mild conditions and often provides high yields with low catalyst loading. Suitable for substrates that are sterically hindered or electronically deactivated, making it valuable in late-stage functionalization.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,000.00
250mg
10-20 days ฿5,420.00
1g
10-20 days ฿15,600.00
5g
10-20 days ฿64,240.00
RockPhos Pd G3
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Used as a highly active palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Effective for forming carbon-carbon and carbon-nitrogen bonds in complex molecule synthesis, including pharmaceuticals and agrochemicals. Performs well under mild conditions and often provides high yields with low catalyst loading. Suitable for substrates that are sterically hindered or electronically deactivated, making it valuable in late-stage functionalization.

Used as a highly active palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Effective for forming carbon-carbon and carbon-nitrogen bonds in complex molecule synthesis, including pharmaceuticals and agrochemicals. Performs well under mild conditions and often provides high yields with low catalyst loading. Suitable for substrates that are sterically hindered or electronically deactivated, making it valuable in late-stage functionalization.

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