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

97%, 99% e.e.

Reagent Code: #229238
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CAS Number 2757083-17-1

science Other reagents with same CAS 2757083-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.26 g/mol
Formula C₁₂H₁₅FN₂O
thermostat Physical Properties
Boiling Point 300.0±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structural features enable high selectivity in asymmetric synthesis, making it valuable for developing enantiomerically pure drugs. The oxazole ring and fluoropyridine moiety contribute to enhanced metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of kinase inhibitors and receptor modulators where stereochemistry plays a critical role in activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,340.00
inventory 250mg
10-20 days ฿22,650.00
(R)-4-(tert-Butyl)-2-(5-fluoropyridin-2-yl)-4,5-dihydrooxazole
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structural features enable high selectivity in asymmetric synthesis, making it valuable for developing enantiomerically pure drugs. The oxazole ring and fluoropyridine moiety contribute to enhanced metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of kinase inhibitors and receptor modulators whe

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structural features enable high selectivity in asymmetric synthesis, making it valuable for developing enantiomerically pure drugs. The oxazole ring and fluoropyridine moiety contribute to enhanced metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of kinase inhibitors and receptor modulators where stereochemistry plays a critical role in activity.

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