N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine

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Reagent Code: #218886
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CAS Number 321155-13-9

science Other reagents with same CAS 321155-13-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.45 g/mol
Formula C₂₅H₂₆NP
badge Registry Numbers
MDL Number MFCD16251547
thermostat Physical Properties
Melting Point 116-120 °C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a ligand in transition metal-catalyzed coupling reactions, particularly in palladium-catalyzed cross-coupling processes such as Suzuki-Miyaura and Heck reactions. Its phosphine group coordinates effectively with palladium, enhancing catalytic activity and stability. The rigid structure and steric bulk contribute to improved selectivity and yield in asymmetric synthesis. Commonly employed in the development of pharmaceuticals and fine chemicals where precise stereochemical control is required. Also utilized in the design of homogeneous catalysts for industrial applications due to its tunable electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,840.00
inventory 500mg
10-20 days ฿11,070.00

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N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine
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Used as a ligand in transition metal-catalyzed coupling reactions, particularly in palladium-catalyzed cross-coupling processes such as Suzuki-Miyaura and Heck reactions. Its phosphine group coordinates effectively with palladium, enhancing catalytic activity and stability. The rigid structure and steric bulk contribute to improved selectivity and yield in asymmetric synthesis. Commonly employed in the development of pharmaceuticals and fine chemicals where precise stereochemical control is required. Als

Used as a ligand in transition metal-catalyzed coupling reactions, particularly in palladium-catalyzed cross-coupling processes such as Suzuki-Miyaura and Heck reactions. Its phosphine group coordinates effectively with palladium, enhancing catalytic activity and stability. The rigid structure and steric bulk contribute to improved selectivity and yield in asymmetric synthesis. Commonly employed in the development of pharmaceuticals and fine chemicals where precise stereochemical control is required. Also utilized in the design of homogeneous catalysts for industrial applications due to its tunable electronic properties.

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