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

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Reagent Code: #233525
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CAS Number 2757083-54-6

science Other reagents with same CAS 2757083-54-6

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 serotonin or dopamine modulators. The stereochemistry supports high enantioselectivity in drug candidates, improving efficacy and reducing side effects. Also employed in asymmetric synthesis and medicinal chemistry research for optimizing lead compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,350.00
inventory 250mg
10-20 days ฿19,900.00
inventory 1g
10-20 days ฿59,640.00

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(S)-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 serotonin or dopamine modulators. The stereochemistry supports high enantioselectivity in drug candidates, improving efficacy and reducing side effects. Also employed in asymmetric synthesis and medicinal chemistry re

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 serotonin or dopamine modulators. The stereochemistry supports high enantioselectivity in drug candidates, improving efficacy and reducing side effects. Also employed in asymmetric synthesis and medicinal chemistry research for optimizing lead compounds.

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