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Structure of 1092394-15-4
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6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine features a fused triazolopyridine core with a methoxy group at the 6-position and a primary amine at C2. This electron-rich heterocycle integrates readily into medicinal chemistry scaffolds, offering enhanced solubility and metabolic stability. The pendant amine enables direct coupling in peptide or small-molecule conjugation workflows under standard conditions.
6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine serves as a versatile heterocyclic building block in medicinal chemistry, enabling rapid access to triazolopyridine scaffolds prevalent in kinase inhibitors and CNS-targeted agents. Its methoxy group enhances solubility and modulates electronic properties, while the amine functionality facilitates straightforward derivatization via acylation, alkylation, or coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for high-throughput synthesis and lead optimization 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: