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Structure of 145934-89-0
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2-Chloro-5-hydrazinylpyridine features a reactive hydrazino group positioned ortho to a chloropyridine moiety, enabling selective coupling reactions in heterocyclic synthesis. This bifunctional scaffold integrates readily into advanced intermediates for pharmaceuticals and agrochemicals. The compound exhibits enhanced stability under standard bench conditions and facilitates efficient derivatization through nucleophilic substitution or condensation pathways.
2-Chloro-5-hydrazinylpyridine serves as a versatile building block in medicinal chemistry, enabling direct substitution at the pyridine ring to access functionalized heterocycles. Its hydrazinyl group facilitates coupling reactions and cyclization pathways, while the chloro substituent offers orthogonal reactivity for cross-coupling or nucleophilic displacement. The compound exhibits good bench stability and compatibility with standard purification techniques, making it well-suited for iterative synthesis of API-relevant scaffolds.
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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-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: