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Structure of 849937-96-8
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5-Bromo-2,4-dichloropyridine features a pyridine core substituted with bromine at the 5-position and chlorine atoms at the 2- and 4-positions, creating a highly reactive electrophilic platform. This electron-deficient heterocycle facilitates efficient coupling reactions in cross-coupling and nucleophilic substitution processes. The molecule exhibits excellent stability under standard conditions, enabling reliable use in synthetic workflows requiring precise functional group manipulation.
5-Bromo-2,4-dichloropyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromo group facilitates selective C–C bond formation while the dichloro substitution pattern ensures compatibility with diverse reaction conditions. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for scalable synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: