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Structure of 205448-65-3
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Methyl 7-methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylate features a fused quinoline core with electron-rich methoxy and carbonyl functionalities, enabling direct integration into synthetic routes for bioactive heterocycles. The methyl ester group supports convenient derivatization under standard conditions. This bench-stable compound serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and antimicrobial agents.
Methyl 7-methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylate serves as a versatile scaffold for the synthesis of quinoline-based heterocycles and bioactive molecules. Its ortho-quinone-like reactivity enables efficient palladium-catalyzed cross-couplings, while the methoxy and ester groups provide orthogonal handles for further functionalization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: