[S(R)]-N-[(R)-[2-(Diphenylphosphino)phenyl]-1-naphthalenylmethyl]-N,2-dimethyl-2-propanesulfinamide

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Reagent Code: #68842
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CAS Number 2565792-58-5

science Other reagents with same CAS 2565792-58-5

blur_circular Chemical Specifications

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Weight 535.7 g/mol
Formula C₃₄H₃₄NOPS
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It plays a crucial role in transition metal-catalyzed processes, such as hydrogenation, cross-coupling, and allylic substitution reactions, enabling the production of enantiomerically pure compounds. Its unique structure, featuring a diphenylphosphino group and a sulfinamide moiety, allows for effective coordination with metal centers, enhancing the stereochemical control of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing chiral drugs and intermediates with high optical purity. Additionally, it is employed in academic research to develop new methodologies in asymmetric catalysis.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿89,892.00
inventory 100mg
10-20 days ฿21,591.00

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[S(R)]-N-[(R)-[2-(Diphenylphosphino)phenyl]-1-naphthalenylmethyl]-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It plays a crucial role in transition metal-catalyzed processes, such as hydrogenation, cross-coupling, and allylic substitution reactions, enabling the production of enantiomerically pure compounds. Its unique structure, featuring a diphenylphosphino group and a sulfinamide moiety, allows for effective coordination with metal centers, enhancing th

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It plays a crucial role in transition metal-catalyzed processes, such as hydrogenation, cross-coupling, and allylic substitution reactions, enabling the production of enantiomerically pure compounds. Its unique structure, featuring a diphenylphosphino group and a sulfinamide moiety, allows for effective coordination with metal centers, enhancing the stereochemical control of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing chiral drugs and intermediates with high optical purity. Additionally, it is employed in academic research to develop new methodologies in asymmetric catalysis.

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