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Structure of 892874-34-9
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7-Bromoquinoline-3-carboxylic acid features a bromine substituent at the 7-position and a carboxylic acid group at the 3-position of the quinoline scaffold. This electron-deficient heterocycle integrates readily into synthetic routes requiring halogenation or coupling reactions. The polar carboxylic acid moiety enhances solubility in polar solvents and facilitates derivatization. Its bench-stable, moisture-tolerant structure supports reliable handling under standard laboratory conditions.
7-Bromoquinoline-3-carboxylic acid serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization at the quinoline core via Pd-catalyzed cross-coupling reactions. The bromo group facilitates efficient Suzuki, Stille, or Negishi transformations, while the carboxylic acid provides a handle for amide coupling, esterification, or metal complexation. Its stability under standard synthetic conditions and compatibility with diverse reaction environments make it a practical choice for constructing bioactive heterocycles and conjugated systems.
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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: