Ethyl 5-(Tert-Butyl)Oxazole-4-Carboxylate

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Reagent Code: #185474
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CAS Number 714273-89-9

science Other reagents with same CAS 714273-89-9

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Weight 197.23 g/mol
Formula C₁₀H₁₅NO₃
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Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential antiviral and anticancer properties. Its oxazole core contributes to enhanced metabolic stability and binding affinity in drug candidates. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies. Also utilized in agrochemical research for designing novel pesticides due to its favorable electronic and steric properties. Suitable for combinatorial chemistry and high-throughput screening protocols owing to its reactivity and stability under various coupling conditions.

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inventory 100mg
10-20 days ฿6,080.00

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Ethyl 5-(Tert-Butyl)Oxazole-4-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential antiviral and anticancer properties. Its oxazole core contributes to enhanced metabolic stability and binding affinity in drug candidates. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies. Also utilized in agrochemical research for designing novel pesticides due to its favorable electronic and steric prope

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential antiviral and anticancer properties. Its oxazole core contributes to enhanced metabolic stability and binding affinity in drug candidates. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies. Also utilized in agrochemical research for designing novel pesticides due to its favorable electronic and steric properties. Suitable for combinatorial chemistry and high-throughput screening protocols owing to its reactivity and stability under various coupling conditions.

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