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Structure of 52605-96-6
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2-Chloro-3-methoxypyridine features a pyridine core with orthogonal chlorine and methoxy substituents, enabling selective functionalization in heterocyclic synthesis. This bench-stable, moisture-tolerant building block integrates readily into pharmaceutical intermediates and agrochemical scaffolds via cross-coupling or nucleophilic substitution reactions.
2-Chloro-3-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity at the C2 position. The methoxy group at C3 provides orthogonal functionality for selective transformations, while the chloropyridine moiety offers excellent bench stability and compatibility with standard synthetic workflows. This compound facilitates efficient construction of heterocyclic scaffolds commonly found in pharmaceutical development.
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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: