(S)-4-(tert-Butyl)-2-(quinolin-8-yl)-4,5-dihydrooxazole

97%

Reagent Code: #236833
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CAS Number 220629-00-5

science Other reagents with same CAS 220629-00-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.33 g/mol
Formula C₁₆H₁₈N₂O
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis of pharmaceutical intermediates. Its structure enables high stereocontrol in transition metal-catalyzed reactions such as hydrogenation and C–C bond formation. Commonly employed in research settings to achieve high enantiomeric excess in the production of bioactive molecules. Also utilized in the development of catalysts for fine chemicals where precise spatial arrangement is critical. Shows stability under various reaction conditions, making it suitable for use in both academic and industrial synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,680.00
inventory 250mg
10-20 days ฿9,050.00
inventory 1g
10-20 days ฿29,200.00

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(S)-4-(tert-Butyl)-2-(quinolin-8-yl)-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis of pharmaceutical intermediates. Its structure enables high stereocontrol in transition metal-catalyzed reactions such as hydrogenation and C–C bond formation. Commonly employed in research settings to achieve high enantiomeric excess in the production of bioactive molecules. Also utilized in the development of catalysts for fine chemicals where precise spatial arrangement is critical. Shows stability under variou

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis of pharmaceutical intermediates. Its structure enables high stereocontrol in transition metal-catalyzed reactions such as hydrogenation and C–C bond formation. Commonly employed in research settings to achieve high enantiomeric excess in the production of bioactive molecules. Also utilized in the development of catalysts for fine chemicals where precise spatial arrangement is critical. Shows stability under various reaction conditions, making it suitable for use in both academic and industrial synthetic routes.

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