[S(R)]-N-[(S)-(4-Methoxyphenyl)[2-(di-tert-butylphosphino)phenyl]methyl]-N,2-dimethyl-2-propanesulfinamide

95%

Reagent Code: #68854
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CAS Number 2561513-54-8

science Other reagents with same CAS 2561513-54-8

blur_circular Chemical Specifications

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Weight 475.7 g/mol
Formula C₂₇H₄₂NO₂PS
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description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions, enabling the synthesis of chiral molecules with high enantiomeric purity. Its sterically demanding and electronically tailored structure enhances selectivity and efficiency in forming complex organic compounds, making it valuable in pharmaceutical synthesis and fine chemical production. Additionally, it is employed in academic and industrial research to develop novel catalytic processes for constructing stereocenters in biologically active molecules.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,083.00
inventory 100mg
10-20 days ฿12,042.00
inventory 500mg
10-20 days ฿50,382.00

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[S(R)]-N-[(S)-(4-Methoxyphenyl)[2-(di-tert-butylphosphino)phenyl]methyl]-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions, enabling the synthesis of chiral molecules with high enantiomeric purity. Its sterically demanding and electronically tailored structure enhances selectivity and efficiency in forming complex organic compounds, making it valuable in pharma

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions, enabling the synthesis of chiral molecules with high enantiomeric purity. Its sterically demanding and electronically tailored structure enhances selectivity and efficiency in forming complex organic compounds, making it valuable in pharmaceutical synthesis and fine chemical production. Additionally, it is employed in academic and industrial research to develop novel catalytic processes for constructing stereocenters in biologically active molecules.

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