Ethyl 3-(4-nitrophenyl)isoxazole-5-carboxylate

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Reagent Code: #180719
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CAS Number 370848-42-3

science Other reagents with same CAS 370848-42-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.21 g/mol
Formula C₁₂H₁₀N₂O₅
badge Registry Numbers
MDL Number MFCD02999452
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports derivatization for targeted drug design, especially in oncology research. Also employed in organic synthesis to build complex heterocyclic systems due to the reactivity of the isoxazole ring and ester functionality. The nitro group allows further transformation, such as reduction to an amine, enabling conjugation or incorporation into larger bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,450.00
inventory 250mg
10-20 days ฿10,960.00
inventory 1g
10-20 days ฿29,560.00

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Ethyl 3-(4-nitrophenyl)isoxazole-5-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports derivatization for targeted drug design, especially in oncology research. Also employed in organic synthesis to build complex heterocyclic systems due to the reactivity of the isoxazole ring and ester functionality. The nitro group allows further transformation, such as reduction to an amine, enabling conjugation or incorporation into
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports derivatization for targeted drug design, especially in oncology research. Also employed in organic synthesis to build complex heterocyclic systems due to the reactivity of the isoxazole ring and ester functionality. The nitro group allows further transformation, such as reduction to an amine, enabling conjugation or incorporation into larger bioactive molecules.
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