tBuBrettPhos Pd G3

95%

Reagent Code: #146521
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CAS Number 1536473-72-9

science Other reagents with same CAS 1536473-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 854.4299999999999 g/mol
Formula C₄₄H₆₂NO₅PPdS
badge Registry Numbers
MDL Number MFCD25976528
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used in palladium-catalyzed cross-coupling reactions, especially in Buchwald–Hartwig aminations and Suzuki–Miyaura couplings. It enables efficient C–N and C–C bond formation under mild conditions, making it ideal for synthesizing complex molecules such as pharmaceuticals and agrochemicals. The catalyst is highly active with sterically hindered substrates and heteroaromatic systems, offering excellent functional group tolerance and high yields. Its stability and reactivity reduce the need for excess ligands or harsh reaction conditions, streamlining process development in drug discovery and industrial-scale synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿180.00
100mg
10-20 days ฿500.00
250mg
10-20 days ฿1,100.00
1g
10-20 days ฿2,990.00
5g
10-20 days ฿12,840.00
25g
10-20 days ฿56,700.00
tBuBrettPhos Pd G3
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Widely used in palladium-catalyzed cross-coupling reactions, especially in Buchwald–Hartwig aminations and Suzuki–Miyaura couplings. It enables efficient C–N and C–C bond formation under mild conditions, making it ideal for synthesizing complex molecules such as pharmaceuticals and agrochemicals. The catalyst is highly active with sterically hindered substrates and heteroaromatic systems, offering excellent functional group tolerance and high yields. Its stability and reactivity reduce the need for exces

Widely used in palladium-catalyzed cross-coupling reactions, especially in Buchwald–Hartwig aminations and Suzuki–Miyaura couplings. It enables efficient C–N and C–C bond formation under mild conditions, making it ideal for synthesizing complex molecules such as pharmaceuticals and agrochemicals. The catalyst is highly active with sterically hindered substrates and heteroaromatic systems, offering excellent functional group tolerance and high yields. Its stability and reactivity reduce the need for excess ligands or harsh reaction conditions, streamlining process development in drug discovery and industrial-scale synthesis.

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