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Structure of 1801422-13-8
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3-(Chloromethyl)-5-methoxypyridine hydrochloride features a reactive chloromethyl group positioned para to a methoxy-substituted pyridine ring, enabling efficient functionalization in synthetic workflows. The hydrochloride salt enhances solubility and stability under standard conditions, facilitating use in medicinal chemistry and heterocyclic derivatization.
3-(Chloromethyl)-5-methoxypyridine hydrochloride serves as a versatile electrophilic building block for pyridine-based heterocycles, enabling efficient functionalization via nucleophilic substitution. The chloromethyl group exhibits high reactivity under mild conditions, facilitating rapid incorporation into pharmaceutical intermediates and agrochemical scaffolds. Its bench-stable hydrochloride salt form ensures reliable handling and reproducible reaction outcomes in standard synthetic workflows.
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GHS Pictogram :
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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 : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: