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Structure of 83004-10-8
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2-Bromo-6-(bromomethyl)pyridine features a bromomethyl group at the pyridine ring's 6-position, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The pendant bromide offers orthogonal reactivity, facilitating sequential derivatization. This bifunctional architecture supports modular synthesis of complex heterocyclic scaffolds under mild conditions.
2-Bromo-6-(bromomethyl)pyridine serves as a versatile dihalogenated building block for constructing complex heterocyclic scaffolds. The bromomethyl group enables efficient functionalization via nucleophilic substitution, while the pyridine ring provides a stable platform for further derivatization. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions make it well-suited for synthetic routes in medicinal chemistry and materials science.
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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-H314
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Precautionary Statements : P260-P264-P270-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: