[S(R)]-N-[(1S)-1-[2-(Di-tert-butylphosphanyl)phenyl]phenylmethyl]-N,2-dimethyl-2-propanesulfinamide

95%

Reagent Code: #68821
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CAS Number 2253984-99-3

science Other reagents with same CAS 2253984-99-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 445.6 g/mol
Formula C₂₆H₄₀NOPS
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description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a di-tert-butylphosphanyl group and a sulfinamide moiety, makes it highly effective in controlling stereochemistry during the synthesis of complex organic molecules. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where high enantiomeric purity is required. Its application is significant in the pharmaceutical industry for the production of chiral drugs and intermediates, ensuring the desired biological activity and reducing unwanted side effects. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereochemical outcomes in organic synthesis.

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Test Parameter Specification
Appearance White to off-white solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 100mg
10-20 days ฿12,980.00

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[S(R)]-N-[(1S)-1-[2-(Di-tert-butylphosphanyl)phenyl]phenylmethyl]-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a di-tert-butylphosphanyl group and a sulfinamide moiety, makes it highly effective in controlling stereochemistry during the synthesis of complex organic molecules. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where high enantiomeric purity is required. Its application is signif

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a di-tert-butylphosphanyl group and a sulfinamide moiety, makes it highly effective in controlling stereochemistry during the synthesis of complex organic molecules. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where high enantiomeric purity is required. Its application is significant in the pharmaceutical industry for the production of chiral drugs and intermediates, ensuring the desired biological activity and reducing unwanted side effects. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereochemical outcomes in organic synthesis.

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