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Structure of 1538440-91-3
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This triazolopyridine carboxylic acid features a fused heterocyclic core with a methyl-substituted triazole ring, delivering enhanced solubility and stability under standard conditions. The electron-deficient pyridine moiety enables efficient coupling reactions in medicinal chemistry, while the carboxylic acid group facilitates conjugation and salt formation for improved bioavailability.
2-Methyl-[1,2,4]triazolo[1,5-a]pyridine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its fused triazolopyridine core provides enhanced metabolic stability and improved solubility compared to simpler pyridine derivatives. The carboxylic acid functionality enables direct amidation, esterification, or coupling reactions, facilitating integration into complex molecular architectures. Bench-stable and readily purified by recrystallization, it functions efficiently in standard synthetic workflows involving amide bond formation, transition metal catalysis, or solid-phase synthesis.
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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 : H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: