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Structure of 122851-69-8
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3-Bromo-2-(chloromethyl)pyridine features a pyridine core functionalized with bromo and chloromethyl groups at adjacent positions, enabling selective cross-coupling and nucleophilic substitution reactions. This bifunctional scaffold facilitates the assembly of complex heterocyclic architectures in medicinal chemistry and materials science.
3-Bromo-2-(chloromethyl)pyridine serves as a versatile bifunctional building block in medicinal chemistry and process development. The chloromethyl group enables nucleophilic substitution reactions, while the bromopyridine moiety supports palladium-catalyzed cross-coupling transformations. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient synthesis of complex heterocyclic scaffolds and targeted API intermediates.
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GHS Pictogram :
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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-P363-P405-P501
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Lot numbers can be found on the outside label of a product: