(R)-4-Benzyl-2-(5-fluoropyridin-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #229438
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CAS Number 2757083-18-2

science Other reagents with same CAS 2757083-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.27 g/mol
Formula C₁₅H₁₃FN₂O
thermostat Physical Properties
Boiling Point 385.9±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazole core and fluoropyridine moiety enhance binding selectivity to certain neuronal receptors, making it valuable in developing neuroprotective agents. The (R)-enantiomer shows higher efficacy in modulating ion channel activity compared to the racemic form. It is also employed in structure-activity relationship studies for optimizing drug candidates with improved metabolic stability and blood-brain barrier penetration.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,890.00
250mg
10-20 days ฿15,830.00
(R)-4-Benzyl-2-(5-fluoropyridin-2-yl)-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazole core and fluoropyridine moiety enhance binding selectivity to certain neuronal receptors, making it valuable in developing neuroprotective agents. The (R)-enantiomer shows higher efficacy in modulating ion channel activity compared to the racemic form. It is also employed in structure-activity relationship studies for optimizing drug candida
Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazole core and fluoropyridine moiety enhance binding selectivity to certain neuronal receptors, making it valuable in developing neuroprotective agents. The (R)-enantiomer shows higher efficacy in modulating ion channel activity compared to the racemic form. It is also employed in structure-activity relationship studies for optimizing drug candidates with improved metabolic stability and blood-brain barrier penetration.
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