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

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Reagent Code: #68848
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CAS Number 2374225-98-4

science Other reagents with same CAS 2374225-98-4

blur_circular Chemical Specifications

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Weight 617.8 g/mol
Formula C₃₉H₄₀NO₂PS
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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. Its unique structure, featuring a diphenylphosphino group and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, enabling the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Its steric and electronic properties enhance the catalytic efficiency and selectivity of metal complexes, making it a valuable tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,185.00
inventory 500mg
10-20 days ฿46,800.00
inventory 25mg
10-20 days ฿6,201.00

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[S(R)]-N-[(S)-(2-methylphenyl)[5-(diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]methyl]-2-methyl-2-propanesulfinamide
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a diphenylphosphino group and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, enabling the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Its

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a diphenylphosphino group and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, enabling the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Its steric and electronic properties enhance the catalytic efficiency and selectivity of metal complexes, making it a valuable tool in organic synthesis.

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