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

95%

Reagent Code: #236957
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CAS Number 396094-85-2

science Other reagents with same CAS 396094-85-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.46 g/mol
Formula C₂₂H₁₉NO₂S
inventory_2 Storage & Handling
Storage 2-8°C, 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 carbon-carbon bond-forming reactions, such as aldol or Diels-Alder reactions. Commonly employed in pharmaceutical synthesis where precise chirality is critical. The sulfinyl and oxazoline groups coordinate with metal centers, enhancing reactivity and selectivity in transition-metal-catalyzed transformations. Also applied in the development of chiral catalysts for industrial and academic research settings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,160.00
inventory 250mg
10-20 days ฿20,960.00
inventory 1g
10-20 days ฿70,660.00

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(S)-4-Phenyl-2-(2-((R)-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 carbon-carbon bond-forming reactions, such as aldol or Diels-Alder reactions. Commonly employed in pharmaceutical synthesis where precise chirality is critical. The sulfinyl and oxazoline groups coordinate with metal centers, enhancing reactivity and selectivity in transition-metal-catalyzed transformations. Also applied in the development of chiral catalys

Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. Its structure enables high stereocontrol in carbon-carbon bond-forming reactions, such as aldol or Diels-Alder reactions. Commonly employed in pharmaceutical synthesis where precise chirality is critical. The sulfinyl and oxazoline groups coordinate with metal centers, enhancing reactivity and selectivity in transition-metal-catalyzed transformations. Also applied in the development of chiral catalysts for industrial and academic research settings.

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