[S(R)]-N-[(S)-[(3-(Benzyloxy)-2-(dicyclohexylphosphino)phenyl)phenylmethyl]-N,2-dimethyl-2-propanesulfinamide

≥95%

Reagent Code: #236127
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CAS Number 2565792-76-7

science Other reagents with same CAS 2565792-76-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 603.85 g/mol
Formula C₃₇H₅₀NO₂PS
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its sterically bulky dicyclohexylphosphino group and chiral sulfinamide moiety enhance enantioselectivity, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Commonly employed in palladium- and rhodium-complexed catalysts for forming chiral centers with high optical purity.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿1,750.00
inventory 100mg
10-20 days ฿25,070.00
inventory 25mg
10-20 days ฿6,460.00

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[S(R)]-N-[(S)-[(3-(Benzyloxy)-2-(dicyclohexylphosphino)phenyl)phenylmethyl]-N,2-dimethyl-2-propanesulfinamide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its sterically bulky dicyclohexylphosphino group and chiral sulfinamide moiety enhance enantioselectivity, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Commonly employed in palladium- and rhodium-complexed catalysts for forming chiral centers with high optical purity.

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its sterically bulky dicyclohexylphosphino group and chiral sulfinamide moiety enhance enantioselectivity, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Commonly employed in palladium- and rhodium-complexed catalysts for forming chiral centers with high optical purity.

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