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Structure of 13472-84-9
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3-Chloro-2-methoxypyridine features a pyridine ring functionalized with chlorine at the 3-position and methoxy at the 2-position, delivering enhanced reactivity in cross-coupling and nucleophilic substitution processes. The electron-withdrawing chlorine and electron-donating methoxy groups create a balanced electronic profile, enabling selective transformations under mild conditions. This bench-stable heterocycle serves as a key building block for pharmaceutical intermediates and agrochemical scaffolds.
3-Chloro-2-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive C–Cl bond and ortho-methoxy directing group. The methoxy substituent enhances solubility and stabilizes the pyridine ring toward nucleophilic attack, while the chlorine facilitates functionalization under mild conditions. Its bench-stable nature and compatibility with diverse reaction partners make it ideal for constructing complex heterocyclic scaffolds in API 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: