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Structure of 95881-83-7
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3-Chloro-5-methoxypyridine features a pyridine core with complementary electron-withdrawing chlorine and electron-donating methoxy substituents, enabling selective functionalization in cross-coupling reactions. This ortho-directing combination enhances regiocontrol in palladium-catalyzed transformations, delivering complex heterocyclic architectures under standard conditions.
3-Chloro-5-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine functionality. The methoxy group enhances solubility and modulates electronic properties, while the molecule exhibits excellent bench stability and compatibility with diverse functional groups. Its predictable reactivity facilitates efficient synthesis of substituted heterocycles and advanced intermediates for 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: