(R)-N-((R)-(3,5-Di-tert-butyl-4-methoxyphenyl)(2-(diphenylphosphanyl)-4,5-dimethoxyphenyl)methyl)-2-methylpropane-2-sulfinamide
95%
- Product Code: 231354
CAS:
2565792-47-2
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Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
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.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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25mg | 10-20 days | ฿5,110.00 |
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100mg | 10-20 days | ฿15,940.00 |
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(R)-N-((R)-(3,5-Di-tert-butyl-4-methoxyphenyl)(2-(diphenylphosphanyl)-4,5-dimethoxyphenyl)methyl)-2-methylpropane-2-sulfinamide
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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