1,1'-[(1R)-6,6'-Dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis[1,1-di-2-naphthalenylphosphine]

98%

Reagent Code: #65721
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CAS Number 256390-46-2

science Other reagents with same CAS 256390-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 782.8 g/mol
Formula C₅₄H₄₀O₂P₂
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 unique structure, featuring a biphenyl backbone and naphthyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and cross-coupling reactions. It is especially effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs) with high specificity and reduced side effects. Additionally, it finds applications in organic synthesis for constructing complex molecular architectures with precise chiral control.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿20,502.00
inventory 10mg
10-20 days ฿5,184.00

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1,1'-[(1R)-6,6'-Dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis[1,1-di-2-naphthalenylphosphine]
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a biphenyl backbone and naphthyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and cross-coupling reactions. It is especially effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs)

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a biphenyl backbone and naphthyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and cross-coupling reactions. It is especially effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs) with high specificity and reduced side effects. Additionally, it finds applications in organic synthesis for constructing complex molecular architectures with precise chiral control.

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