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Structure of 389122-08-1
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5-Bromo-1H-1,2,4-triazol-3-amine features a brominated triazole core with a primary amine at the 3-position, enabling direct functionalization in heterocyclic synthesis. The electron-deficient triazole ring enhances reactivity in nucleophilic substitution and coupling processes. This bench-stable compound serves as a key intermediate for bioactive molecule construction.
5-Bromo-1H-1,2,4-triazol-3-amine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the triazol-3-amine functionality offers orthogonal reactivity for further derivatization. Its bench stability and compatibility with diverse reaction conditions facilitate efficient access to triazole-based 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 : 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: