[S(R)]-N-[(S)-[3,5-Bis(1,1-dimethylethyl)-4-methoxyphenyl][2-(diphenylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide

95%

Reagent Code: #68853
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CAS Number 1616688-63-1

science Other reagents with same CAS 1616688-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 613.8 g/mol
Formula C₃₈H₄₈NO₂PS
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure drugs, where the specific spatial arrangement of atoms can significantly influence the drug's efficacy and safety. Additionally, it finds application in the synthesis of complex organic molecules, enabling the creation of compounds with precise stereochemistry for use in advanced materials and fine chemicals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
500mg
10-20 days ฿43,200.00
25mg
10-20 days ฿7,875.00
100mg
10-20 days ฿10,800.00
[S(R)]-N-[(S)-[3,5-Bis(1,1-dimethylethyl)-4-methoxyphenyl][2-(diphenylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide
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This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure drugs, where the specific spatial arrangement of atoms can significantly influence the drug's efficac

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure drugs, where the specific spatial arrangement of atoms can significantly influence the drug's efficacy and safety. Additionally, it finds application in the synthesis of complex organic molecules, enabling the creation of compounds with precise stereochemistry for use in advanced materials and fine chemicals.

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