(S)-2,2'-Bis[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

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Reagent Code: #37998
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CAS Number 1365531-94-7

science Other reagents with same CAS 1365531-94-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 874.9800 g/mol
Formula C₅₂H₆₀O₈P₂
badge Registry Numbers
MDL Number MFCD19443626
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. Its structure, featuring electron-rich phosphine groups and methoxy substituents, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is critical. The ligand’s steric and electronic properties enhance the selectivity and efficiency of the catalytic process, making it a valuable tool in organic synthesis and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,752.00

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(S)-2,2'-Bis[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-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. Its structure, featuring electron-rich phosphine groups and methoxy substituents, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is critical. The ligand’s steric a

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring electron-rich phosphine groups and methoxy substituents, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is critical. The ligand’s steric and electronic properties enhance the selectivity and efficiency of the catalytic process, making it a valuable tool in organic synthesis and industrial applications.

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