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Structure of 1268882-60-5
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2-Bromo-5-hydrazinylpyridine features a hydrazinyl group flanked by a bromine substituent on a pyridine scaffold, enabling direct functionalization in transition-metal-catalyzed coupling reactions. The electron-deficient pyridine ring enhances reactivity toward nucleophilic attack, while the hydrazine moiety serves as a bifunctional handle for conjugation and cyclization processes under mild conditions.
2-Bromo-5-hydrazinylpyridine serves as a versatile building block in medicinal chemistry, enabling the construction of pyridine-based heterocycles through palladium-catalyzed cross-coupling and hydrazine-mediated cyclization. Its bromo group facilitates Suzuki, Stille, and Negishi reactions, while the hydrazinyl moiety participates in condensation and ring-forming transformations. The compound exhibits bench stability and compatibility with diverse functional groups, making it valuable for rapid scaffold diversification in API 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: