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Structure of 1234616-36-4
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This triazolopyridine carboxylic acid features a rigid, electron-deficient heteroaromatic core that enhances binding affinity in medicinal chemistry applications. The carboxylic acid group enables direct conjugation or salt formation, facilitating integration into bioactive molecules. Bench-stable and moisture-tolerant, it serves as a strategic scaffold for targeted compound libraries.
[1,2,4]Triazolo[1,5-a]pyridine-8-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science, enabling efficient access to fused triazole-pyridine scaffolds. The carboxylic acid functionality facilitates direct derivatization via amide coupling, esterification, or metal-catalyzed cross-coupling reactions. Its high thermal stability and compatibility with diverse functional groups make it suitable for multi-step synthesis and scale-up applications in API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: