2-(Diphenylphosphino)benzonitrile

98%

Reagent Code: #80765
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CAS Number 34825-99-5

science Other reagents with same CAS 34825-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.3 g/mol
Formula C₁₉H₁₄NP
badge Registry Numbers
MDL Number MFCD05864011
inventory_2 Storage & Handling
Storage room temperature, in an inert gas

description Product Description

2-(Diphenylphosphino)benzonitrile is used as a bidentate P,N-ligand in catalytic processes, particularly in transition metal-catalyzed reactions such as cross-coupling (e.g., Suzuki-Miyaura, Heck) and hydrogenation. The phosphine group and nitrile functionality coordinate with metal centers, enhancing catalytic activity, selectivity, and stability of complexes. Commonly employed in organic synthesis to facilitate the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the development of pharmaceuticals and fine chemicals due to its ability to improve reaction efficiency in Pd- and Ni-based catalysis.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,170.00
inventory 50mg
10-20 days ฿1,110.00

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2-(Diphenylphosphino)benzonitrile
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2-(Diphenylphosphino)benzonitrile is used as a bidentate P,N-ligand in catalytic processes, particularly in transition metal-catalyzed reactions such as cross-coupling (e.g., Suzuki-Miyaura, Heck) and hydrogenation. The phosphine group and nitrile functionality coordinate with metal centers, enhancing catalytic activity, selectivity, and stability of complexes. Commonly employed in organic synthesis to facilitate the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the development

2-(Diphenylphosphino)benzonitrile is used as a bidentate P,N-ligand in catalytic processes, particularly in transition metal-catalyzed reactions such as cross-coupling (e.g., Suzuki-Miyaura, Heck) and hydrogenation. The phosphine group and nitrile functionality coordinate with metal centers, enhancing catalytic activity, selectivity, and stability of complexes. Commonly employed in organic synthesis to facilitate the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the development of pharmaceuticals and fine chemicals due to its ability to improve reaction efficiency in Pd- and Ni-based catalysis.

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