[S(R)]-N-[(S)-[4-(1,1-Dimethylethyl)phenyl][5-(diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]methyl]-N,2-dimethyl-2-propanesulfinamide

95%

Reagent Code: #68855
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CAS Number 2374225-91-7

science Other reagents with same CAS 2374225-91-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 673.9 g/mol
Formula C₄₃H₄₈NO₂PS
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a xanthene backbone and a sulfinamide group, makes it highly effective in inducing enantioselectivity in organic transformations. It is often employed in asymmetric hydrogenation, C-C bond formation, and other stereoselective processes, enabling the production of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Its application is crucial in the pharmaceutical and fine chemical industries, where the synthesis of enantiomerically pure compounds is essential for drug efficacy and safety. Additionally, its stability and tunable steric and electronic properties make it a versatile tool in advanced synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿50,400.00
inventory 25mg
10-20 days ฿7,308.00
inventory 100mg
10-20 days ฿14,400.00

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[S(R)]-N-[(S)-[4-(1,1-Dimethylethyl)phenyl][5-(diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]methyl]-N,2-dimethyl-2-propanesulfinamide
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This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a xanthene backbone and a sulfinamide group, makes it highly effective in inducing enantioselectivity in organic transformations. It is often employed in asymmetric hydrogenation, C-C bond formation, and other stereoselective processes, enabling the production of chiral intermediates or active pharmaceutical ingredients (APIs) wi

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a xanthene backbone and a sulfinamide group, makes it highly effective in inducing enantioselectivity in organic transformations. It is often employed in asymmetric hydrogenation, C-C bond formation, and other stereoselective processes, enabling the production of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Its application is crucial in the pharmaceutical and fine chemical industries, where the synthesis of enantiomerically pure compounds is essential for drug efficacy and safety. Additionally, its stability and tunable steric and electronic properties make it a versatile tool in advanced synthetic chemistry.

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