N-[(1S)-2-(Diphenylphosphino)-1-phenylethyl]-3,5-bis(trifluoromethyl)-benzamide

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Reagent Code: #68816
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CAS Number 1853342-57-0

science Other reagents with same CAS 1853342-57-0

blur_circular Chemical Specifications

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Weight 545.5 g/mol
Formula C₂₉H₂₂F₆NOP
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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 diphenylphosphine and trifluoromethyl groups, makes it highly effective in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond-forming reactions, and other processes where high enantiomeric purity is desired. The ligand's ability to coordinate with metals like rhodium or iridium enhances the selectivity and efficiency of the catalytic system, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and other complex organic molecules. Its steric and electronic properties are tailored to optimize performance in challenging asymmetric syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,168.00
inventory 500mg
10-20 days ฿50,400.00

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N-[(1S)-2-(Diphenylphosphino)-1-phenylethyl]-3,5-bis(trifluoromethyl)-benzamide
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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 diphenylphosphine and trifluoromethyl groups, makes it highly effective in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond-forming reactions, and other processes where high enantiomeric purity is desired. The ligand's ability to coordinate with metals like rhodium or iridium enhance

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring diphenylphosphine and trifluoromethyl groups, makes it highly effective in facilitating enantioselective transformations. It is commonly employed in hydrogenation, carbon-carbon bond-forming reactions, and other processes where high enantiomeric purity is desired. The ligand's ability to coordinate with metals like rhodium or iridium enhances the selectivity and efficiency of the catalytic system, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and other complex organic molecules. Its steric and electronic properties are tailored to optimize performance in challenging asymmetric syntheses.

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