(S)-N,N'-[1,1'-Binaphthalene]-2,2'-diylbis[2-(diphenylphosphino)benzamide]

≥98%,≥99% e.e.

Reagent Code: #65669
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CAS Number 879505-38-1

science Other reagents with same CAS 879505-38-1

blur_circular Chemical Specifications

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Weight 860.9 g/mol
Formula C₅₈H₄₂N₂O₂P₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, derived from binaphthalene and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The ligand's ability to coordinate with metals like rhodium, palladium, or iridium enhances the efficiency and selectivity of catalytic processes, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and agrochemicals. Its application is critical in producing enantiomerically pure compounds, which are essential in drug development and other industries requiring high stereochemical control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,640.00
inventory 250mg
10-20 days ฿11,690.00
inventory 1g
10-20 days ฿34,970.00

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(S)-N,N'-[1,1'-Binaphthalene]-2,2'-diylbis[2-(diphenylphosphino)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, derived from binaphthalene and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The ligand's ability to coordinate with metals like rhodium, palladium, or iridium enhances the efficiency and selectivi

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, derived from binaphthalene and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The ligand's ability to coordinate with metals like rhodium, palladium, or iridium enhances the efficiency and selectivity of catalytic processes, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and agrochemicals. Its application is critical in producing enantiomerically pure compounds, which are essential in drug development and other industries requiring high stereochemical control.

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