1-(Dicyclohexylphosphino)-2-(2-methoxyphenyl)-1H-indole

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Reagent Code: #68728
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CAS Number 947402-60-0

science Other reagents with same CAS 947402-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 419.54 g/mol
Formula C₂₇H₃₄NOP
badge Registry Numbers
MDL Number MFCD15144752
thermostat Physical Properties
Melting Point 131.1-132.5°C
Boiling Point 561.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a ligand in transition metal-catalyzed reactions. Its unique structure, featuring a dicyclohexylphosphino group and a methoxyphenyl-substituted indole, makes it highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. These reactions are crucial for constructing complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, its steric and electronic properties enhance the stability and reactivity of the metal-ligand complex, improving the efficiency and selectivity of catalytic processes. It is also explored in asymmetric catalysis for synthesizing chiral compounds, which are vital in the production of enantiomerically pure drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,420.00

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1-(Dicyclohexylphosphino)-2-(2-methoxyphenyl)-1H-indole
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This compound is primarily utilized in the field of organic synthesis, particularly as a ligand in transition metal-catalyzed reactions. Its unique structure, featuring a dicyclohexylphosphino group and a methoxyphenyl-substituted indole, makes it highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. These reactions are crucial for constructing complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additiona

This compound is primarily utilized in the field of organic synthesis, particularly as a ligand in transition metal-catalyzed reactions. Its unique structure, featuring a dicyclohexylphosphino group and a methoxyphenyl-substituted indole, makes it highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. These reactions are crucial for constructing complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, its steric and electronic properties enhance the stability and reactivity of the metal-ligand complex, improving the efficiency and selectivity of catalytic processes. It is also explored in asymmetric catalysis for synthesizing chiral compounds, which are vital in the production of enantiomerically pure drugs.

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