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Structure of 27032-63-9
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5-Chloro-2-hydrazinylpyridine features a reactive hydrazino group positioned ortho to a chlorine-bearing pyridine ring, enabling selective coupling reactions in heterocyclic synthesis. This bench-stable scaffold integrates readily into bioactive molecule design, particularly for targeting electron-deficient aromatic systems.
5-Chloro-2-hydrazinylpyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyridazine and triazine scaffolds via cyclization reactions. The hydrazinyl group facilitates regioselective coupling with carbonyl compounds and electrophiles, while the chloropyridine moiety supports palladium-catalyzed cross-coupling transformations. Bench-stable and compatible with common protecting groups, it functions effectively in multi-step synthetic sequences for medicinal chemistry applications.
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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: