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Structure of 2093329-79-2
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2-Bromo-6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridine features a brominated pyridine core paired with a sterically hindered isopropyl-substituted triazole moiety, enabling robust coupling in transition-metal-catalyzed transformations. This bench-stable scaffold integrates readily into diverse heterocyclic architectures, offering enhanced solubility and predictable reactivity in medicinal chemistry applications.
2-Bromo-6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridine serves as a versatile building block for constructing nitrogen-rich heterocyclic scaffolds. The bromopyridine moiety enables palladium-catalyzed cross-coupling reactions, while the 4-isopropyl-1,2,4-triazole group offers enhanced stability and orthogonal reactivity. This compound facilitates the synthesis of biologically relevant triazolylpyridines with improved solubility and metabolic resistance, making it well-suited for medicinal chemistry campaigns requiring robust functional group compatibility and bench-stable intermediates.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318-H410
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: