[S(R)]-N-[(R)-[2-(Diphenylphosphino)phenyl]phenylmethyl]-N,2-dimethyl-2-propanesulfinamide

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Reagent Code: #68845
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CAS Number 2222798-18-5

science Other reagents with same CAS 2222798-18-5

blur_circular Chemical Specifications

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Weight 485.6 g/mol
Formula C₃₀H₃₂NOPS
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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 crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of enantiomerically pure compounds, which are essential for producing active pharmaceutical ingredients (APIs) with high stereochemical precision. Additionally, it is employed in academic research to develop new synthetic methodologies and explore novel catalytic processes. Its unique structure and stereochemical properties make it a valuable tool for achieving high selectivity and efficiency in complex organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,472.00
inventory 500mg
10-20 days ฿26,073.00

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[S(R)]-N-[(R)-[2-(Diphenylphosphino)phenyl]phenylmethyl]-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 crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of enantiomerically pure compounds, which are essential for producing active pharmaceutical ingredients (APIs) with high stereochemical pr

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of enantiomerically pure compounds, which are essential for producing active pharmaceutical ingredients (APIs) with high stereochemical precision. Additionally, it is employed in academic research to develop new synthetic methodologies and explore novel catalytic processes. Its unique structure and stereochemical properties make it a valuable tool for achieving high selectivity and efficiency in complex organic syntheses.

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