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Structure of 677702-58-8
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5-Bromo-4-methylnicotinic acid features a bromine substituent at the 5-position and a methyl group at the 4-position on the nicotinic acid scaffold. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a key building block for bioactive molecules in medicinal chemistry and materials science.
5-Bromo-4-methylnicotinic acid serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid and methyl functionalities offer orthogonal handles for further functionalization. The compound exhibits good bench stability and facilitates efficient derivatization in standard synthetic 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: