[S(R)]-N-[(1S)-1-[2-(Dicyclohexylphosphino)phenyl]-2,2-dimethylpropyl]-N,2-dimethyl-2-propanesulfinamide

95%

Reagent Code: #68823
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CAS Number 2253984-98-2

science Other reagents with same CAS 2253984-98-2

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Weight 477.7 g/mol
Formula C₂₈H₄₈NOPS
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description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its structure, featuring a dicyclohexylphosphine group and a sulfinamide moiety, allows for precise control over stereochemistry, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals. Additionally, its stability and selectivity make it a preferred choice in research and industrial applications where high enantiomeric purity is essential.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,892.00
inventory 100mg
10-20 days ฿27,801.00

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[S(R)]-N-[(1S)-1-[2-(Dicyclohexylphosphino)phenyl]-2,2-dimethylpropyl]-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its structure, featuring a dicyclohexylphosphine group and a sulfinamide moiety, allows for precise control over stereochemistry, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals.

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its structure, featuring a dicyclohexylphosphine group and a sulfinamide moiety, allows for precise control over stereochemistry, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals. Additionally, its stability and selectivity make it a preferred choice in research and industrial applications where high enantiomeric purity is essential.

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