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Structure of 179555-11-4
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6-Amino-4-methylnicotinic acid features a pyridine core functionalized with an amino group at C6 and a methyl substituent at C4, delivering enhanced solubility and stability under standard conditions. This electron-rich scaffold integrates readily into bioactive molecule synthesis, particularly in medicinal chemistry campaigns targeting kinase inhibitors and metabolic pathway modulators.
6-Amino-4-methylnicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted nicotinamide derivatives and heterocyclic scaffolds. Its amino and carboxylic acid functionalities offer orthogonal reactivity for peptide coupling, amidation, and cyclization reactions. The methyl group enhances metabolic stability and provides a site for further functionalization. Bench-stable and readily purified by recrystallization, it facilitates scalable synthesis of API intermediates and bioactive compounds.
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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: