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Structure of 1227502-89-7
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2-Chloro-5-hydroxy-4-methylpyridine features a reactive chloro group flanked by a hydroxyl and methyl substituent on the pyridine ring, enabling selective functionalization in synthetic pathways. This electron-deficient heterocycle integrates readily into medicinal chemistry scaffolds and serves as a key intermediate in agrochemical and pharmaceutical development under standard conditions.
2-Chloro-5-hydroxy-4-methylpyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds. The hydroxyl group facilitates direct derivatization or protection, while the chloro and methyl substituents provide orthogonal reactivity for cross-coupling and functionalization. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for modular synthesis workflows in API development.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: