2-Diphenylphosphino-2'-(N,N-dimethylamino)biphenyl

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Reagent Code: #68780
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CAS Number 240417-00-9

science Other reagents with same CAS 240417-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 381.45 g/mol
Formula C₂₆H₂₄NP
badge Registry Numbers
MDL Number MFCD03094578
thermostat Physical Properties
Melting Point 126-128 °C
inventory_2 Storage & Handling
Storage 2~8℃, dry, sealed

description Product Description

This chemical is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its unique structure, combining phosphine and amino groups, enhances the stability and reactivity of the catalyst, enabling efficient formation of carbon-carbon and carbon-nitrogen bonds. It is also employed in asymmetric synthesis, facilitating the production of chiral compounds in pharmaceuticals and fine chemicals. Additionally, it serves as a key component in the development of advanced materials and organic electronic devices due to its ability to modulate electronic properties.

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Test Parameter Specification
Melting point 122-127
Purity (GC) 96.5-100
Appearance White to yellow solid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿700.00
inventory 200mg
10-20 days ฿300.00
inventory 5g
10-20 days ฿2,490.00

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2-Diphenylphosphino-2'-(N,N-dimethylamino)biphenyl
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This chemical is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its unique structure, combining phosphine and amino groups, enhances the stability and reactivity of the catalyst, enabling efficient formation of carbon-carbon and carbon-nitrogen bonds. It is also employed in asymmetric synthesis, facilitating the production of chiral compounds in pharmaceuticals and fine chemicals. Additionally, it serv

This chemical is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its unique structure, combining phosphine and amino groups, enhances the stability and reactivity of the catalyst, enabling efficient formation of carbon-carbon and carbon-nitrogen bonds. It is also employed in asymmetric synthesis, facilitating the production of chiral compounds in pharmaceuticals and fine chemicals. Additionally, it serves as a key component in the development of advanced materials and organic electronic devices due to its ability to modulate electronic properties.

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