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Structure of 118791-14-3
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6-Chloro-3-quinolinecarboxylic acid features a chlorinated quinoline core with a carboxylic acid group at the 3-position, enabling direct conjugation or derivatization. This electron-deficient scaffold integrates readily into synthetic routes for pharmaceutical intermediates, offering enhanced reactivity and metabolic stability in bioactive molecule design.
6-Chloro-3-quinolinecarboxylic acid serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling direct functionalization at the C-3 position via coupling reactions. Its chloro substituent facilitates nucleophilic aromatic substitution, while the carboxylic acid group supports amide formation, esterification, or metal complexation. The molecule exhibits good bench stability and compatibility with standard purification techniques, making it well-suited for iterative synthesis of quinoline-based pharmaceuticals and agrochemical scaffolds.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: