4,5-Bis-(di-i-propylphosphinomethyl)acridine

98%

Reagent Code: #152524
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CAS Number 1101230-28-7

science Other reagents with same CAS 1101230-28-7

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inventory_2 Storage & Handling
Storage Room temperature, argon

description Product Description

Used as a highly effective ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its sterically bulky yet flexible phosphine groups enhance metal center stability and reactivity, improving catalytic efficiency and selectivity. Commonly applied in C–C and C–heteroatom bond formations, such as Suzuki–Miyaura and Buchwald–Hartwig aminations, where it supports high turnover numbers under mild conditions. Also employed in asymmetric synthesis when coordinated to chiral metal complexes, enabling enantioselective transformations in pharmaceutical and fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿5,660.00
inventory 50mg
10-20 days ฿23,120.00

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4,5-Bis-(di-i-propylphosphinomethyl)acridine
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Used as a highly effective ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its sterically bulky yet flexible phosphine groups enhance metal center stability and reactivity, improving catalytic efficiency and selectivity. Commonly applied in C–C and C–heteroatom bond formations, such as Suzuki–Miyaura and Buchwald–Hartwig aminations, where it supports high turnover numbers under mild conditions. Also employed in asymmetric synthesis when coordinated to chiral

Used as a highly effective ligand in homogeneous catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its sterically bulky yet flexible phosphine groups enhance metal center stability and reactivity, improving catalytic efficiency and selectivity. Commonly applied in C–C and C–heteroatom bond formations, such as Suzuki–Miyaura and Buchwald–Hartwig aminations, where it supports high turnover numbers under mild conditions. Also employed in asymmetric synthesis when coordinated to chiral metal complexes, enabling enantioselective transformations in pharmaceutical and fine chemical manufacturing.

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