(R)-4-(tert-Butyl)-2-(1,8-naphthyridin-2-yl)-4,5-dihydrooxazole

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Reagent Code: #231386
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CAS Number 2757082-56-5

science Other reagents with same CAS 2757082-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.32 g/mol
Formula C₁₅H₁₇N₃O
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in pharmaceutical research as a chiral intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Its rigid oxazole-naphthyridine framework enhances binding selectivity to certain enzyme targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide motifs while offering improved metabolic stability. Also applied in asymmetric synthesis where the (R)-configuration plays a critical role in enantioselective reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,740.00
inventory 250mg
10-20 days ฿6,540.00
(R)-4-(tert-Butyl)-2-(1,8-naphthyridin-2-yl)-4,5-dihydrooxazole
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Used in pharmaceutical research as a chiral intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Its rigid oxazole-naphthyridine framework enhances binding selectivity to certain enzyme targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide motifs while offering improved metabolic stability. Also applied in asymmetric synthesis where the (R)-configuration plays a

Used in pharmaceutical research as a chiral intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Its rigid oxazole-naphthyridine framework enhances binding selectivity to certain enzyme targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide motifs while offering improved metabolic stability. Also applied in asymmetric synthesis where the (R)-configuration plays a critical role in enantioselective reactions.

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