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

97%, 99% e.e.

Reagent Code: #229229
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CAS Number 2757083-32-0

science Other reagents with same CAS 2757083-32-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.18 g/mol
Formula C₁₅H₁₃BrN₂O
thermostat Physical Properties
Boiling Point 428.2±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.46±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 pharmaceutical agents, particularly in the development of kinase inhibitors. Its structural features enable selective binding in biological systems, making it valuable in drug discovery for oncology and inflammatory diseases. The bromopyridine moiety allows for further functionalization via cross-coupling reactions, facilitating rapid diversification during medicinal chemistry optimization. Its oxazole core contributes to metabolic stability and improved pharmacokinetic profiles in lead compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,880.00
250mg
10-20 days ฿16,460.00
(R)-4-Benzyl-2-(5-bromopyridin-2-yl)-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its structural features enable selective binding in biological systems, making it valuable in drug discovery for oncology and inflammatory diseases. The bromopyridine moiety allows for further functionalization via cross-coupling reactions, facilitating rapid diversification during medicinal chemistry optimization. Its oxazole core contributes to metabolic stability and improved

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its structural features enable selective binding in biological systems, making it valuable in drug discovery for oncology and inflammatory diseases. The bromopyridine moiety allows for further functionalization via cross-coupling reactions, facilitating rapid diversification during medicinal chemistry optimization. Its oxazole core contributes to metabolic stability and improved pharmacokinetic profiles in lead compounds.

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