(R)-4-(tert-Butyl)-2-(2-(pyridin-2-yl)propan-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #232287
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CAS Number 2757083-51-3

science Other reagents with same CAS 2757083-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.35 g/mol
Formula C₁₅H₂₂N₂O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its oxazoline core acts as a directing group in asymmetric synthesis, enabling selective formation of carbon-carbon bonds. Commonly employed in catalysis and medicinal chemistry for building complex molecules with high enantiomeric purity. Also serves as a ligand in transition metal-catalyzed reactions, enhancing reaction efficiency and stereoselectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,610.00
inventory 250mg
10-20 days ฿10,500.00
inventory 1g
10-20 days ฿32,870.00
(R)-4-(tert-Butyl)-2-(2-(pyridin-2-yl)propan-2-yl)-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its oxazoline core acts as a directing group in asymmetric synthesis, enabling selective formation of carbon-carbon bonds. Commonly employed in catalysis and medicinal chemistry for building complex molecules with high enantiomeric purity. Also serves as a ligand in transition metal-catalyzed reactions, enhancing reaction efficien

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its oxazoline core acts as a directing group in asymmetric synthesis, enabling selective formation of carbon-carbon bonds. Commonly employed in catalysis and medicinal chemistry for building complex molecules with high enantiomeric purity. Also serves as a ligand in transition metal-catalyzed reactions, enhancing reaction efficiency and stereoselectivity.

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