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Structure of 18471-99-3
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1-Methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid features a fused quinoline core with a methylated nitrogen and a carboxylic acid at C3, enabling direct integration into bioactive scaffolds. The electron-deficient dihydroquinoline ring facilitates conjugation in medicinal chemistry applications, while the bench-stable carboxylic acid group supports straightforward derivatization under standard conditions.
1-Methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid serves as a versatile scaffold for medicinal chemistry and synthetic organic research. Its conjugated quinolinone core enables reliable functionalization at C3 and C4 positions, facilitating coupling reactions and derivatization under mild conditions. The carboxylic acid group supports direct amidation or esterification, while the methyl substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by recrystallization, it functions as a key building block in the synthesis of heterocyclic APIs and bioactive molecules.
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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: