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Structure of 886365-28-2
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Methyl 5-bromo-2-chloroisonicotinate features a dual halogenated pyridine core with bromine at the 5-position and chlorine at the 2-position, enabling selective cross-coupling reactions. This bench-stable derivative integrates readily into complex heterocyclic architectures under standard conditions.
Methyl 5-bromo-2-chloroisonicotinate serves as a versatile building block for the synthesis of heterocyclic scaffolds and pharmaceutical intermediates. The ortho-halogenated pyridine core enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further functionalization. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient downstream transformations in medicinal chemistry and process development 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P501
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Lot numbers can be found on the outside label of a product: