(S)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis(di-2-furylphosphine)

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Reagent Code: #68665
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CAS Number 145214-59-1

science Other reagents with same CAS 145214-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.4555 g/mol
Formula C₃₀H₂₄O₆P₂
badge Registry Numbers
MDL Number MFCD09753004
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 stereochemical precision. It facilitates reactions such as hydrogenation, carbon-carbon bond formation, and other transformations where achieving high enantioselectivity is essential. Additionally, it is employed in research and development to explore new catalytic processes and optimize existing ones for better efficiency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,786.00
inventory 250mg
10-20 days ฿12,771.00
inventory 1g
10-20 days ฿39,717.00

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(S)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis(di-2-furylphosphine)
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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 stereochemical precision. It facilitates reactions such as hydrogenation, carbon-carbon bond formation, and other transformations where achieving high enantioselectivity is essential. Additionally, it is employed in

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 stereochemical precision. It facilitates reactions such as hydrogenation, carbon-carbon bond formation, and other transformations where achieving high enantioselectivity is essential. Additionally, it is employed in research and development to explore new catalytic processes and optimize existing ones for better efficiency and selectivity.

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