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Structure of 1344046-12-3
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3-Bromoquinoline-5-carboxylic acid features a bromine substituent at the 3-position and a carboxylic acid group at the 5-position of the quinoline scaffold, enabling direct functionalization in cross-coupling reactions. This bifunctional architecture supports efficient derivatization for medicinal chemistry and materials applications, combining electronic modulation with synthetic accessibility.
3-Bromoquinoline-5-carboxylic acid serves as a versatile building block for the synthesis of quinoline-based pharmaceutical intermediates and functional materials. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates derivatization via amide formation or esterification. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for iterative synthetic strategies in medicinal chemistry and process development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: