(R)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

98%

Reagent Code: #68652
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CAS Number 1365531-84-5

science Other reagents with same CAS 1365531-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1186.64 g/mol
Formula C₄₈H₂₈F₂₄O₄P₂
badge Registry Numbers
MDL Number MFCD19443625
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring electron-withdrawing trifluoromethyl groups and methoxy substituents, enhances its effectiveness in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other key synthetic processes where high enantiomeric purity is required. The ligand’s steric and electronic properties make it highly selective, enabling the production of chiral intermediates and active pharmaceutical ingredients (APIs) with exceptional precision. Its application is critical in the pharmaceutical and fine chemical industries, where achieving specific stereochemistry is essential for the efficacy and safety of the final products.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,958.00
inventory 250mg
10-20 days ฿14,094.00
inventory 1g
10-20 days ฿45,621.00

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(R)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring electron-withdrawing trifluoromethyl groups and methoxy substituents, enhances its effectiveness in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other key synthetic processes where high enantiomeric purity is required. The ligand’s steric and electronic properties

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring electron-withdrawing trifluoromethyl groups and methoxy substituents, enhances its effectiveness in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other key synthetic processes where high enantiomeric purity is required. The ligand’s steric and electronic properties make it highly selective, enabling the production of chiral intermediates and active pharmaceutical ingredients (APIs) with exceptional precision. Its application is critical in the pharmaceutical and fine chemical industries, where achieving specific stereochemistry is essential for the efficacy and safety of the final products.

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