(R)-2-(5-Fluoropyridin-2-yl)-4-isopropyl-4,5-dihydrooxazole

97%, 99% e.e.

Reagent Code: #229442
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CAS Number 2828433-61-8

science Other reagents with same CAS 2828433-61-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.23 g/mol
Formula C₁₁H₁₃FN₂O
thermostat Physical Properties
Boiling Point 291.6±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±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 make it valuable in asymmetric synthesis, where the oxazole ring and fluoropyridine moiety contribute to binding selectivity and metabolic stability. Commonly employed in the development of kinase inhibitors and receptor modulators due to its ability to enhance potency and pharmacokinetic properties. Also utilized in agrochemical research for designing novel active ingredients with improved environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,670.00
inventory 250mg
10-20 days ฿18,120.00

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(R)-2-(5-Fluoropyridin-2-yl)-4-isopropyl-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 make it valuable in asymmetric synthesis, where the oxazole ring and fluoropyridine moiety contribute to binding selectivity and metabolic stability. Commonly employed in the development of kinase inhibitors and receptor modulators due to its ability to enhance potency and pharmacokinetic properties. Also utilized in agroc

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable in asymmetric synthesis, where the oxazole ring and fluoropyridine moiety contribute to binding selectivity and metabolic stability. Commonly employed in the development of kinase inhibitors and receptor modulators due to its ability to enhance potency and pharmacokinetic properties. Also utilized in agrochemical research for designing novel active ingredients with improved environmental profiles.

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