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Structure of 101990-70-9
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5-(Chloromethyl)-2-methoxypyridine features a reactive chloromethyl group appended to a methoxypyridine scaffold, enabling efficient coupling in nucleophilic substitution reactions. The electron-rich pyridine ring enhances regioselective functionalization, while the methoxy substituent stabilizes intermediates under standard conditions. This compound serves as a key synthon in medicinal chemistry for constructing bioactive heterocycles.
5-(Chloromethyl)-2-methoxypyridine serves as a versatile synthetic building block for pyridine-based heterocycles, enabling efficient functionalization at the 5-position via nucleophilic substitution. The chloromethyl group exhibits high reactivity toward amines, thiols, and carbanions, facilitating rapid access to diverse pharmacophores. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for medicinal chemistry campaigns requiring rapid scaffold diversification.
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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 : H302+H312-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P405-P501
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Lot numbers can be found on the outside label of a product: