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Structure of 26557-90-4
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3-Bromo-5-methyl-1H-1,2,4-triazole features a brominated triazole core with a methyl group at the 5-position, offering enhanced reactivity in cross-coupling and functionalization workflows. The electron-deficient triazole ring facilitates nucleophilic substitution, while the methyl substituent improves solubility and stability under standard conditions. This compound serves as a key intermediate in medicinal chemistry and agrochemical synthesis.
3-Bromo-5-methyl-1H-1,2,4-triazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances solubility and modulates electronic properties. Its stability under standard bench conditions facilitates straightforward handling and purification. Functions effectively in Suzuki-Miyaura, Sonogashira, and Buchwald-Hartwig transformations to construct complex triazolyl scaffolds relevant to pharmaceutical 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: