[S(R)]-N-[(S)-[2-(Diphenylphosphino)phenyl](4-methoxyphenyl)methyl]-2-methyl-2-propanesulfinamide

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Reagent Code: #68859
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CAS Number 1616688-62-0

science Other reagents with same CAS 1616688-62-0

blur_circular Chemical Specifications

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Weight 501.6 g/mol
Formula C₃₀H₃₂NO₂PS
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This compound is widely used as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. It plays a crucial role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other key reactions where high enantiomeric purity is required. Its structural design allows for efficient coordination with transition metals, enabling the production of optically active compounds with high selectivity. This makes it valuable in the development of drugs, agrochemicals, and other biologically active molecules where chirality is critical for efficacy and safety. Additionally, it is employed in academic and industrial research to explore new catalytic processes and optimize existing methodologies.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,291.00
inventory 100mg
10-20 days ฿9,000.00
inventory 500mg
10-20 days ฿35,640.00

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[S(R)]-N-[(S)-[2-(Diphenylphosphino)phenyl](4-methoxyphenyl)methyl]-2-methyl-2-propanesulfinamide
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This compound is widely used as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. It plays a crucial role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other key reactions where high enantiomeric purity is required. Its structural design allows for efficient coordination with transition metals, enabling the production of optically active compounds with high selectivity. This makes it valuable in th

This compound is widely used as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. It plays a crucial role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other key reactions where high enantiomeric purity is required. Its structural design allows for efficient coordination with transition metals, enabling the production of optically active compounds with high selectivity. This makes it valuable in the development of drugs, agrochemicals, and other biologically active molecules where chirality is critical for efficacy and safety. Additionally, it is employed in academic and industrial research to explore new catalytic processes and optimize existing methodologies.

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