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Structure of 156094-63-2
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2-(Bromomethyl)-6-methoxypyridine features a reactive bromomethyl group flanked by a methoxy-substituted pyridine ring, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring selective alkylation or chain extension under mild conditions.
2-(Bromomethyl)-6-methoxypyridine serves as a versatile synthetic building block for the installation of pyridylmethyl linkages in medicinal chemistry and catalysis research. The bromomethyl group enables efficient SN₂ functionalization, while the 6-methoxypyridine core provides a stable, electron-deficient heterocyclic scaffold compatible with palladium-catalyzed cross-coupling reactions. Its bench-stable nature and straightforward purification support reliable use in multi-step synthesis.
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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 : 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: