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Structure of 1227516-75-7
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5-Bromo-3-(bromomethyl)-2-methoxypyridine features a reactive bromomethyl group flanked by electron-withdrawing bromine and methoxy substituents, enabling selective functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable pyridine derivative integrates readily into complex molecular architectures under standard conditions.
5-Bromo-3-(bromomethyl)-2-methoxypyridine serves as a versatile bifunctional building block in medicinal chemistry and cross-coupling synthesis. The bromomethyl group enables efficient alkylation or Suzuki-Miyaura coupling, while the C5-bromo substituent supports palladium-catalyzed transformations. Its bench-stable nature and orthogonal reactivity facilitate modular construction of complex heterocyclic scaffolds, particularly in kinase inhibitor and API development workflows.
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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: