(3-(Tert-butoxy)-2',6'-diisopropyl-6-methoxy-[1,1'-biphenyl]-2-yl)dicyclohexylphosphane

97%

Reagent Code: #68611
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CAS Number 2489243-29-8

science Other reagents with same CAS 2489243-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 536.77 g/mol
Formula C₃₅H₅₃O₂P
inventory_2 Storage & Handling
Storage room temperature, dry, inert gas

description Product Description

This chemical is primarily utilized as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its bulky and electron-rich structure enhances the stability and reactivity of the metal catalyst, facilitating the formation of carbon-carbon and carbon-nitrogen bonds in complex organic synthesis. It is especially valuable in pharmaceutical and agrochemical industries for producing active ingredients and intermediates with high selectivity and efficiency. Additionally, its application extends to material science, where it aids in the development of advanced polymers and fine chemicals.

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Test Parameter Specification
Appearance White to Off-white Solid, Powder or Crystals
Purity (%) 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,630.00

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(3-(Tert-butoxy)-2',6'-diisopropyl-6-methoxy-[1,1'-biphenyl]-2-yl)dicyclohexylphosphane
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This chemical is primarily utilized as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its bulky and electron-rich structure enhances the stability and reactivity of the metal catalyst, facilitating the formation of carbon-carbon and carbon-nitrogen bonds in complex organic synthesis. It is especially valuable in pharmaceutical and agrochemical industries for producing active ingredients and intermediates wi

This chemical is primarily utilized as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its bulky and electron-rich structure enhances the stability and reactivity of the metal catalyst, facilitating the formation of carbon-carbon and carbon-nitrogen bonds in complex organic synthesis. It is especially valuable in pharmaceutical and agrochemical industries for producing active ingredients and intermediates with high selectivity and efficiency. Additionally, its application extends to material science, where it aids in the development of advanced polymers and fine chemicals.

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