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Structure of 1211515-68-2
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3-Bromo-5-methylpicolinic acid features a brominated pyridine core with a methyl group at the 5-position, enabling direct functionalization in cross-coupling reactions. The carboxylic acid moiety provides a robust anchor for peptide coupling and conjugation workflows. This bench-stable derivative offers enhanced reactivity compared to unsubstituted analogs, facilitating efficient access to complex heterocyclic architectures under standard conditions.
3-Bromo-5-methylpicolinic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation of bromo and methyl groups into heterocyclic scaffolds. Its ortho-brominated pyridine core facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid group supports facile derivatization via amide or ester formation. The compound exhibits excellent bench stability and is compatible with standard purification protocols, making it well-suited for modular synthesis of bioactive molecules and API intermediates.
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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: