4-Chloro-7-(3,5-dimethylisoxazol-4-yl)-6-methoxyquinoline-3-carboxamide

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Reagent Code: #47222
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CAS Number 1300031-57-5

science Other reagents with same CAS 1300031-57-5

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Weight 331.7537 g/mol
Formula C₁₆H₁₄ClN₃O₃
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. It is particularly significant in the development of kinase inhibitors, which are essential for targeting specific enzymes involved in cellular signaling pathways. These inhibitors have potential applications in treating diseases such as cancer, inflammatory disorders, and autoimmune conditions. Additionally, its structural features, including the quinoline and isoxazole moieties, make it a valuable scaffold for designing novel therapeutic agents with improved efficacy and selectivity. Researchers also explore its use in creating fluorescent probes for biochemical studies due to its unique photophysical properties.

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inventory 100mg
10-20 days ฿14,652.00

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4-Chloro-7-(3,5-dimethylisoxazol-4-yl)-6-methoxyquinoline-3-carboxamide
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. It is particularly significant in the development of kinase inhibitors, which are essential for targeting specific enzymes involved in cellular signaling pathways. These inhibitors have potential applications in treating diseases such as cancer, inflammatory disorders, and autoimmune conditions. Additionally, its structural features, including the quinol

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. It is particularly significant in the development of kinase inhibitors, which are essential for targeting specific enzymes involved in cellular signaling pathways. These inhibitors have potential applications in treating diseases such as cancer, inflammatory disorders, and autoimmune conditions. Additionally, its structural features, including the quinoline and isoxazole moieties, make it a valuable scaffold for designing novel therapeutic agents with improved efficacy and selectivity. Researchers also explore its use in creating fluorescent probes for biochemical studies due to its unique photophysical properties.

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