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Structure of 874-46-4
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This [1,2,4]Triazolo[1,5-a]pyridin-2-amine features a rigid, electron-deficient heterocyclic core that enables robust integration into pharmaceutical scaffolds. Its nitrogen-rich architecture supports strong hydrogen bonding and π-stacking interactions, enhancing target affinity in kinase inhibition studies. The amine functionality offers direct handle for derivatization under mild conditions, facilitating rapid library expansion. Bench-stable and moisture-tolerant, it simplifies handling in synthetic workflows.
[1,2,4]Triazolo[1,5-a]pyridin-2-amine serves as a versatile heterocyclic building block in medicinal chemistry, enabling rapid access to bioactive scaffolds. Its fused triazolopyridine core exhibits favorable bench stability and functional group tolerance, facilitating downstream derivatization via nucleophilic substitution or transition-metal-catalyzed coupling. The molecule functions effectively as a hydrogen-bond donor and π-system in target-directed synthesis, particularly in kinase inhibitor and CNS-targeted compound 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-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: