[S(R)]-N-[(S)-[2-(Dicyclohexylphosphanyl)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide

≥95%

Reagent Code: #236128
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CAS Number 2565792-82-5

science Other reagents with same CAS 2565792-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 527.75 g/mol
Formula C₃₁H₄₆NO₂PS
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

This chiral phosphine-sulfinamide compound serves as a specialized ligand in asymmetric catalysis. It is directly employed in enantioselective transition metal-catalyzed reactions, such as iridium-catalyzed hydrogenation of imines to chiral amines and other stereoselective transformations. These applications are essential in the pharmaceutical industry for synthesizing single-enantiomer compounds, including chiral amines and alcohols. The compound's inherent stereochemistry provides high enantioselectivity in hydrogenation and cross-coupling reactions, making it invaluable in research and process chemistry for building complex organic molecules with precise stereocenters.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿1,770.00
inventory 25mg
10-20 days ฿7,850.00
inventory 100mg
10-20 days ฿25,110.00

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[S(R)]-N-[(S)-[2-(Dicyclohexylphosphanyl)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide
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This chiral phosphine-sulfinamide compound serves as a specialized ligand in asymmetric catalysis. It is directly employed in enantioselective transition metal-catalyzed reactions, such as iridium-catalyzed hydrogenation of imines to chiral amines and other stereoselective transformations. These applications are essential in the pharmaceutical industry for synthesizing single-enantiomer compounds, including chiral amines and alcohols. The compound's inherent stereochemistry provides high enantioselectivi

This chiral phosphine-sulfinamide compound serves as a specialized ligand in asymmetric catalysis. It is directly employed in enantioselective transition metal-catalyzed reactions, such as iridium-catalyzed hydrogenation of imines to chiral amines and other stereoselective transformations. These applications are essential in the pharmaceutical industry for synthesizing single-enantiomer compounds, including chiral amines and alcohols. The compound's inherent stereochemistry provides high enantioselectivity in hydrogenation and cross-coupling reactions, making it invaluable in research and process chemistry for building complex organic molecules with precise stereocenters.

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