(S)-2-(2-((S)-(4-(tert-Butyl)phenyl)sulfinyl)phenyl)-4-phenyl-4,5-dihydrooxazole

98%

Reagent Code: #236846
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CAS Number 2242702-44-7

science Other reagents with same CAS 2242702-44-7

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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, enabling high enantioselectivity in catalytic reactions such as hydrogenation and C–C bond formation. Its rigid oxazoline structure and stereogenic centers make it effective in controlling stereochemistry during the synthesis of pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions where precise spatial arrangement is critical for desired product formation. Also utilized in the development of enantiopure compounds for medicinal chemistry and agrochemical research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,990.00
inventory 250mg
10-20 days ฿10,430.00
inventory 1g
10-20 days ฿29,280.00
(S)-2-(2-((S)-(4-(tert-Butyl)phenyl)sulfinyl)phenyl)-4-phenyl-4,5-dihydrooxazole
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Used as a chiral auxiliary or ligand in asymmetric synthesis, enabling high enantioselectivity in catalytic reactions such as hydrogenation and C–C bond formation. Its rigid oxazoline structure and stereogenic centers make it effective in controlling stereochemistry during the synthesis of pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions where precise spatial arrangement is critical for desired product formation. Also utilized in the development of enantiopure

Used as a chiral auxiliary or ligand in asymmetric synthesis, enabling high enantioselectivity in catalytic reactions such as hydrogenation and C–C bond formation. Its rigid oxazoline structure and stereogenic centers make it effective in controlling stereochemistry during the synthesis of pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions where precise spatial arrangement is critical for desired product formation. Also utilized in the development of enantiopure compounds for medicinal chemistry and agrochemical research.

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