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Structure of 183483-29-6
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This pyridine-based carboxylic acid features a brominated heterocyclic moiety enabling direct functionalization in cross-coupling reactions. The acetic acid side chain provides polarity and handles well under standard conditions, facilitating integration into synthetic sequences requiring electron-deficient aryl linkages.
2-(2-Bromopyridin-4-yl)acetic acid serves as a versatile building block for constructing pyridine-containing scaffolds in medicinal chemistry. Its brominated pyridine moiety enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates derivatization via amide formation or esterification. The compound exhibits good bench stability and is readily purified by recrystallization, supporting its use in iterative synthesis campaigns targeting bioactive heterocycles.
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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: