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Structure of 1401624-81-4
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2,6-Dibromo-[1,2,4]triazolo[1,5-a]pyridine features a rigid, electron-deficient heterocyclic core that integrates two bromine substituents at key positions, enabling direct functionalization in cross-coupling reactions. This bench-stable scaffold serves as a robust building block for advanced materials and pharmaceutical intermediates.
2,6-Dibromo-[1,2,4]triazolo[1,5-a]pyridine serves as a versatile building block for the synthesis of functionalized triazolopyridine scaffolds. Its bromine substituents enable palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and heteroaryl architectures with high regiocontrol. The molecule exhibits excellent bench stability and compatibility with diverse reaction conditions, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: