[S(R)]-N-[(1S)-2-(Diphenylphosphino)-1-[2-(diphenylphosphino)-4,5-dimethoxyphenyl]ethyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #236105
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CAS Number 2565792-27-8

science Other reagents with same CAS 2565792-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 653.76 g/mol
Formula C₃₈H₄₁NO₃P₂S
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions. It is especially effective in the reduction of prochiral olefins, ketones, and imines, delivering high enantiomeric excess (ee) in the products. Its robust performance in creating stereocenters makes it valuable in the synthesis of pharmaceutical intermediates and fine chemicals where precise chirality is required. The presence of two diphenylphosphino groups and a sulfinamide moiety enhances metal coordination and stereocontrol, contributing to its efficiency and selectivity across a range of catalytic systems.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿820.00
inventory 100mg
10-20 days ฿11,020.00
inventory 25mg
10-20 days ฿3,740.00

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[S(R)]-N-[(1S)-2-(Diphenylphosphino)-1-[2-(diphenylphosphino)-4,5-dimethoxyphenyl]ethyl]-2-methyl-2-propanesulfinamide
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions. It is especially effective in the reduction of prochiral olefins, ketones, and imines, delivering high enantiomeric excess (ee) in the products. Its robust performance in creating stereocenters makes it valuable in the synthesis of pharmaceutical intermediates and fine chemicals where precise chiral

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions. It is especially effective in the reduction of prochiral olefins, ketones, and imines, delivering high enantiomeric excess (ee) in the products. Its robust performance in creating stereocenters makes it valuable in the synthesis of pharmaceutical intermediates and fine chemicals where precise chirality is required. The presence of two diphenylphosphino groups and a sulfinamide moiety enhances metal coordination and stereocontrol, contributing to its efficiency and selectivity across a range of catalytic systems.

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