(S)-4-Phenyl-2-(2-((S)-p-tolylsulfinyl)phenyl)-4,5-dihydrooxazole

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Reagent Code: #236959
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CAS Number 402755-64-0

science Other reagents with same CAS 402755-64-0

blur_circular Chemical Specifications

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Weight 361.46 g/mol
Formula C₂₂H₁₉NO₂S
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. Its structure enables high stereocontrol in reactions such as aldol additions, alkylations, and cycloadditions. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including drug intermediates where precise stereochemistry is critical. The sulfinyl and oxazoline groups work in tandem to coordinate with metal centers, enhancing enantioselectivity in transition-metal-catalyzed transformations. Also applied in the development of chiral catalysts for academic and industrial research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,580.00
inventory 250mg
10-20 days ฿10,040.00
inventory 1g
10-20 days ฿27,090.00

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(S)-4-Phenyl-2-(2-((S)-p-tolylsulfinyl)phenyl)-4,5-dihydrooxazole
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Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. Its structure enables high stereocontrol in reactions such as aldol additions, alkylations, and cycloadditions. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including drug intermediates where precise stereochemistry is critical. The sulfinyl and oxazoline groups work in tandem to coordinate with metal centers, enhancing enantioselectivity in transi

Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. Its structure enables high stereocontrol in reactions such as aldol additions, alkylations, and cycloadditions. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including drug intermediates where precise stereochemistry is critical. The sulfinyl and oxazoline groups work in tandem to coordinate with metal centers, enhancing enantioselectivity in transition-metal-catalyzed transformations. Also applied in the development of chiral catalysts for academic and industrial research.

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