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Structure of 2288708-87-0
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4-(Bromomethyl)-2-methoxypyridine hydrobromide features a reactive bromomethyl group flanked by an electron-rich pyridine ring and a methoxy substituent, enabling efficient coupling in nucleophilic substitution reactions. This bench-stable, moisture-tolerant reagent integrates seamlessly into synthetic workflows requiring selective alkylation under mild conditions.
4-(Bromomethyl)-2-methoxypyridine hydrobromide serves as a versatile electrophilic building block for C–H functionalization and nucleophilic substitution reactions. The bromomethyl group enables efficient coupling with amines, thiols, and carbon nucleophiles under mild conditions, while the pyridine ring provides enhanced solubility and stability in polar solvents. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for constructing complex heterocyclic scaffolds in medicinal chemistry and process development workflows.
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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#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314-H335
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Precautionary Statements : P260-P264-P270-P271-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: