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Structure of 108281-78-3
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6-Bromo-3-methyl-[1,2,4]triazolo[4,3-a]pyridine features a fused triazolopyridine core with bromine and methyl substituents at regioselective positions, enabling direct functionalization in cross-coupling reactions. The electron-deficient heteroaromatic system enhances reactivity in palladium-catalyzed transformations. This bench-stable scaffold integrates readily into complex molecular architectures for medicinal chemistry and materials applications.
6-Bromo-3-methyl-[1,2,4]triazolo[4,3-a]pyridine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the bromine site via Pd-catalyzed cross-coupling reactions. The triazolopyridine core exhibits favorable stability and orthogonal reactivity, supporting efficient incorporation into complex heterocyclic scaffolds. Its methyl group provides a handle for further derivatization, while the molecule's crystalline nature and clean purification profile enhance utility in high-throughput synthesis and process 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: