(R)-N-((S)-(5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl)(phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide

95%

Reagent Code: #229500
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CAS Number 2757083-10-4

science Other reagents with same CAS 2757083-10-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 617.78 g/mol
Formula C₃₉H₄₀NO₂PS
badge Registry Numbers
MDL Number MFCD33401727
thermostat Physical Properties
Boiling Point 709.5±70.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

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 highly effective in the synthesis of chiral amines, amino acids, and other pharmaceutical intermediates where high enantiomeric excess is required. Due to its rigid xanthene backbone and well-defined chiral environment, it enhances stereocontrol in C–H activation and cross-coupling reactions. Its sulfinamide and phosphine functional groups allow for strong coordination to transition metals, making it valuable in industrial and academic research for developing enantiopure drugs and fine chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,810.00
inventory 100mg
10-20 days ฿11,650.00
inventory 250mg
10-20 days ฿24,970.00

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(R)-N-((S)-(5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl)(phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide
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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 highly effective in the synthesis of chiral amines, amino acids, and other pharmaceutical intermediates where high enantiomeric excess is required. Due to its rigid xanthene backbone and well-defined chiral environment, it enhances stereocontrol in C–H activation and cross-coupling reactions.

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 highly effective in the synthesis of chiral amines, amino acids, and other pharmaceutical intermediates where high enantiomeric excess is required. Due to its rigid xanthene backbone and well-defined chiral environment, it enhances stereocontrol in C–H activation and cross-coupling reactions. Its sulfinamide and phosphine functional groups allow for strong coordination to transition metals, making it valuable in industrial and academic research for developing enantiopure drugs and fine chemicals.

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