[S(R)]-N-((1S)-1-(2-(Diphenylphosphino)phenyl)-2,2-dimethylpropyl)-N,2-dimethyl-2-propanesulfinamide

95%

Reagent Code: #68836
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CAS Number 2454167-14-5

science Other reagents with same CAS 2454167-14-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 465.6 g/mol
Formula C₂₈H₃₆NOPS
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description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure enables it to effectively induce chirality, making it valuable in the production of enantiomerically pure compounds. It is often employed in asymmetric hydrogenation, where it helps achieve high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in cross-coupling reactions, contributing to the efficient formation of carbon-carbon and carbon-heteroatom bonds. Its role in these processes is critical for developing optically active intermediates used in drug discovery and agrochemical production.

Available Sizes & Pricing

Size Availability Unit Price Quantity
500mg
10-20 days ฿116,982.00
100mg
10-20 days ฿24,093.00
25mg
10-20 days ฿8,334.00
[S(R)]-N-((1S)-1-(2-(Diphenylphosphino)phenyl)-2,2-dimethylpropyl)-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure enables it to effectively induce chirality, making it valuable in the production of enantiomerically pure compounds. It is often employed in asymmetric hydrogenation, where it helps achieve high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in cross-coupling reactions, contributing to the

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure enables it to effectively induce chirality, making it valuable in the production of enantiomerically pure compounds. It is often employed in asymmetric hydrogenation, where it helps achieve high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in cross-coupling reactions, contributing to the efficient formation of carbon-carbon and carbon-heteroatom bonds. Its role in these processes is critical for developing optically active intermediates used in drug discovery and agrochemical production.

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