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Structure of 892874-49-6
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7-Chloro-3-quinolinecarboxylic acid features a chlorinated quinoline core with a carboxylic acid group at the 3-position, enabling direct conjugation in synthetic transformations. This electron-deficient scaffold integrates readily into bioactive molecule frameworks, offering enhanced metabolic stability and targeted binding affinity in medicinal chemistry applications.
7-Chloro-3-quinolinecarboxylic acid serves as a versatile building block for the synthesis of quinoline-based pharmaceuticals and agrochemicals. Its carboxylic acid functionality enables direct coupling reactions, while the chloro substituent at the 7-position provides a handle for palladium-catalyzed cross-coupling transformations. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and scale-up processes.
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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: