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Structure of 117934-34-6
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3-(Chloromethyl)-2-methoxypyridine hydrochloride features a reactive chloromethyl group flanked by a methoxy-substituted pyridine ring, enabling efficient functionalization in medicinal chemistry. This bench-stable, moisture-tolerant reagent integrates readily into late-stage derivatization workflows, delivering direct access to biologically relevant heterocyclic scaffolds under standard conditions.
3-(Chloromethyl)-2-methoxypyridine hydrochloride serves as a versatile electrophilic building block in medicinal chemistry, enabling efficient installation of pyridylmethyl linkages via nucleophilic substitution. The chloromethyl group exhibits high reactivity toward amines, thiols, and other soft nucleophiles under mild conditions, while the methoxy substituent provides moderate electron-donating character and enhances solubility. Bench-stable and readily purified by recrystallization, it functions effectively in the synthesis of heterocyclic scaffolds and targeted bioactive molecules.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: