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Structure of 41668-13-7
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5-Bromo-6-hydroxynicotinic acid features a bromine substituent at the 5-position and a hydroxyl group at the 6-position of the nicotinic acid core. This combination imparts enhanced polarity and reactivity, enabling direct incorporation into synthetic scaffolds for medicinal chemistry applications. The molecule exhibits bench-stable behavior under standard conditions and offers site-specific functionalization potential.
5-Bromo-6-hydroxynicotinic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the pyridine ring for downstream derivatization. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the hydroxyl and carboxylic acid functionalities offer sites for selective protection or conjugation. Its bench-stable crystalline form supports straightforward handling, purification, and integration into standard heterocyclic 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: