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Structure of 1142191-66-9
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5-Bromo-3-methoxypicolinic acid features a bromine substituent at the 5-position and a methoxy group at the 3-position of the picolinic acid scaffold, delivering enhanced electron-withdrawing character and improved solubility in organic media. This combination facilitates efficient coupling reactions in synthetic medicinal chemistry, particularly in the construction of heterocyclic scaffolds and bioactive molecules.
5-Bromo-3-methoxypicolinic acid serves as a versatile building block in synthetic medicinal chemistry, enabling direct functionalization at the pyridine core. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the methoxy and carboxylic acid functionalities offer orthogonal handles for derivatization. Its bench-stable solid form and compatibility with standard reaction conditions make it well-suited for iterative synthesis of heterocyclic scaffolds 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: