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Structure of 107588-90-9
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4-(Chloromethyl)-3-methoxypyridine hydrochloride features a reactive chloromethyl group flanked by a methoxy-substituted pyridine ring, enabling efficient functionalization in synthetic transformations. This bench-stable salt form enhances solubility and handling while maintaining high reactivity for coupling and derivatization processes.
4-(Chloromethyl)-3-methoxypyridine hydrochloride serves as a versatile pyridyl alkylating agent, enabling efficient introduction of functionalized side chains in medicinal chemistry and process development. The chloromethyl group exhibits high reactivity in nucleophilic substitution reactions, facilitating the construction of complex heterocyclic scaffolds. Its stability under standard bench conditions and ease of purification make it a practical choice for multi-step syntheses requiring reliable functional group transformation.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: