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Structure of 1159812-31-3
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7-Bromo-2-methyl-[1,2,4]triazolo[1,5-a]pyridine features a rigid heterocyclic core with complementary electron-deficient and alkyl substituents. This scaffold enables direct incorporation into medicinal chemistry libraries, serving as a key building block for kinase inhibitors and bioactive small molecules. The bromo group facilitates late-stage functionalization via cross-coupling reactions.
7-Bromo-2-methyl-[1,2,4]triazolo[1,5-a]pyridine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates reliable C–H functionalization, while the methyl substituent enhances solubility and modulates electronic properties. Its bench-stable nature and compatibility with standard coupling conditions make it ideal for iterative synthesis of bioactive compounds.
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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: