(R)-2,2'-Bis(di-p-tolylphosphino)-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

98%

Reagent Code: #37400
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CAS Number 1365531-81-2

science Other reagents with same CAS 1365531-81-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 698.7700 g/mol
Formula C₄₄H₄₄O₄P₂
badge Registry Numbers
MDL Number MFCD19443623
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its sterically demanding and electron-rich structure enhances the selectivity and efficiency of the catalytic process, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals. Additionally, it is employed in the development of advanced materials and organic compounds with specific stereochemical requirements.

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inventory 100mg
10-20 days ฿7,191.00

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(R)-2,2'-Bis(di-p-tolylphosphino)-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its sterically demanding and electron-rich structure enhances the selectivity and efficiency of the catalytic process, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals. Addition

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its sterically demanding and electron-rich structure enhances the selectivity and efficiency of the catalytic process, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals. Additionally, it is employed in the development of advanced materials and organic compounds with specific stereochemical requirements.

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