5-(Dicyclohexylphosphino)-1',3',5'-triphenyl-[1,4']-bi-1H-pyrazole

98%

Reagent Code: #68806
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CAS Number 1021176-69-1

science Other reagents with same CAS 1021176-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 558.7 g/mol
Formula C₃₆H₃₉N₄P
badge Registry Numbers
MDL Number MFCD11616511
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. It plays a significant role in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential in the synthesis of complex organic molecules. Its steric and electronic properties make it highly effective in stabilizing metal centers, enhancing reaction efficiency and selectivity. Additionally, it is employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular structure is crucial. Its application extends to asymmetric catalysis, enabling the production of enantiomerically pure compounds, which are vital in drug development and fine chemical synthesis.

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Test Parameter Specification
Appearance White to Light Yellow to Yellow Powder or Crystals or Granules or Chunks
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,424.00
inventory 250mg
10-20 days ฿5,211.00
inventory 50mg
10-20 days ฿1,530.00

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5-(Dicyclohexylphosphino)-1',3',5'-triphenyl-[1,4']-bi-1H-pyrazole
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This chemical is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. It plays a significant role in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential in the synthesis of complex organic molecules. Its steric and electronic properties make it highly effective in stabilizing metal centers, enhancing reaction efficiency and selectivity. Additionally, it is employed in the development of pharm

This chemical is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. It plays a significant role in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential in the synthesis of complex organic molecules. Its steric and electronic properties make it highly effective in stabilizing metal centers, enhancing reaction efficiency and selectivity. Additionally, it is employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular structure is crucial. Its application extends to asymmetric catalysis, enabling the production of enantiomerically pure compounds, which are vital in drug development and fine chemical synthesis.

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