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Structure of 192642-85-6
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5-Bromo-2-pyridineacetic acid features a bromine substituent at the 5-position of the pyridine ring, enhancing electrophilic reactivity and enabling diverse functionalization. The carboxylic acid group provides a robust handle for amide coupling and conjugation, while the pyridine core offers favorable solubility and coordination properties. This structure supports applications in medicinal chemistry and materials synthesis.
5-Bromo-2-pyridineacetic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation of brominated pyridine motifs into target molecules. Its carboxylic acid functionality facilitates amide coupling and esterification under standard conditions, while the bromine substituent supports palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for iterative synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: