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Structure of 1805506-21-1
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6-Bromo-2-hydroxynicotinic acid features a bromine substituent at the 6-position and a hydroxyl group at the 2-position of the pyridine ring, delivering enhanced reactivity for cross-coupling and functionalization. This electron-deficient scaffold enables direct incorporation into bioactive heterocycles and serves as a key intermediate in medicinal chemistry.
6-Bromo-2-hydroxynicotinic acid serves as a versatile building block in the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-hydroxyl and bromine substituents enable direct functionalization via palladium-catalyzed cross-coupling and cyclization reactions. The molecule exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: