2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl

98%

Reagent Code: #68779
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CAS Number 819867-23-7

science Other reagents with same CAS 819867-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.62 g/mol
Formula C₃₃H₃₇P
inventory_2 Storage & Handling
Storage 2~8℃, dry, sealed

description Product Description

2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. Its bulky structure enhances steric hindrance, improving the efficiency and selectivity of catalytic processes. This compound is especially valuable in palladium-catalyzed reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Its stability and electron-donating properties make it a preferred choice for synthesizing complex organic molecules in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in asymmetric catalysis to produce chiral compounds with high enantiomeric purity.

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Test Parameter Specification
Purity 97.5-100%
Appearance White solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿620.00
inventory 100g
10-20 days ฿28,200.00
inventory 250mg
10-20 days ฿360.00
inventory 5g
10-20 days ฿2,250.00
inventory 25g
10-20 days ฿9,300.00

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2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl
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2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. Its bulky structure enhances steric hindrance, improving the efficiency and selectivity of catalytic processes. This compound is especially valuable in palladium-catalyzed reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Its stability and electron-donating prop

2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. Its bulky structure enhances steric hindrance, improving the efficiency and selectivity of catalytic processes. This compound is especially valuable in palladium-catalyzed reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Its stability and electron-donating properties make it a preferred choice for synthesizing complex organic molecules in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in asymmetric catalysis to produce chiral compounds with high enantiomeric purity.

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