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

98%

Reagent Code: #68639
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CAS Number 133545-24-1

science Other reagents with same CAS 133545-24-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 638.7133 g/mol
Formula C₄₂H₄₀O₂P₂
badge Registry Numbers
MDL Number MFCD09753006
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereoselectivity. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other key transformations where achieving high enantiomeric excess is essential. The ligand's structure, with its sterically demanding and electron-rich properties, enhances the efficiency and selectivity of the catalytic processes, making it a valuable tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,123.00
inventory 250mg
10-20 days ฿20,592.00
inventory 1g
10-20 days ฿51,480.00

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(R)-()-2,2'-Bis(di-p-tolylphosphino)-6,6'-dimethoxy-1,1'-biphenyl
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereoselectivity. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other key transformations where achieving high enantiomeric excess is essential. The ligand's structure, with its

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereoselectivity. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other key transformations where achieving high enantiomeric excess is essential. The ligand's structure, with its sterically demanding and electron-rich properties, enhances the efficiency and selectivity of the catalytic processes, making it a valuable tool in organic synthesis.

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