(R)-N-((R)-(3,5-Di-tert-butyl-4-methoxyphenyl)(2-(diphenylphosphanyl)-4,5-dimethoxyphenyl)methyl)-2-methylpropane-2-sulfinamide

95%

Reagent Code: #231354
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CAS Number 2565792-47-2

science Other reagents with same CAS 2565792-47-2

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Widely used as a chiral ligand precursor in asymmetric catalysis, this compound plays a key role in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Its sterically hindered structure and well-defined stereochemistry make it especially effective in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions, where high enantioselectivity is critical. It is commonly employed in the transformation of prochiral olefins, ketones, and imines, enabling efficient production of chiral intermediates for drugs and biologically active molecules. Due to its stability and modularity, it is also utilized in the development of new catalytic systems for asymmetric C–C bond formation and other stereoselective transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿5,110.00
100mg
10-20 days ฿15,940.00
(R)-N-((R)-(3,5-Di-tert-butyl-4-methoxyphenyl)(2-(diphenylphosphanyl)-4,5-dimethoxyphenyl)methyl)-2-methylpropane-2-sulfinamide
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Widely used as a chiral ligand precursor in asymmetric catalysis, this compound plays a key role in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Its sterically hindered structure and well-defined stereochemistry make it especially effective in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions, where high enantioselectivity is critical. It is commonly employed in the transformation of prochiral olefins, ketones, and imines, enabling efficient production of c

Widely used as a chiral ligand precursor in asymmetric catalysis, this compound plays a key role in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Its sterically hindered structure and well-defined stereochemistry make it especially effective in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions, where high enantioselectivity is critical. It is commonly employed in the transformation of prochiral olefins, ketones, and imines, enabling efficient production of chiral intermediates for drugs and biologically active molecules. Due to its stability and modularity, it is also utilized in the development of new catalytic systems for asymmetric C–C bond formation and other stereoselective transformations.

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