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Structure of 160233-76-1
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6-Bromo-4-quinolinecarboxylic acid features a bromine substituent at the 6-position and a carboxylic acid group at the 4-position of the quinoline core. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions, serving as a key building block for bioactive heterocycles and pharmaceutical intermediates.
6-Bromo-4-quinolinecarboxylic acid serves as a versatile building block for medicinal chemistry and materials science, enabling direct incorporation into pharmaceutical scaffolds via standard coupling reactions. Its bromine substituent facilitates palladium-catalyzed cross-coupling, while the carboxylic acid group supports amide formation and derivatization. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it ideal for reproducible synthesis 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: