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Structure of 107512-34-5
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4-Chloro-3-methoxy-2-methylpyridine features a strategically positioned chloro group and methoxy substituent on a pyridine core, enabling selective coupling reactions. The methyl group enhances electron density at C2, facilitating functionalization under mild conditions. This scaffold offers robust stability and compatibility with diverse reaction environments.
4-Chloro-3-methoxy-2-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine functionality. The methoxy and methyl groups provide orthogonal sites for further functionalization, while the compound exhibits excellent bench stability and ease of purification—ideal for modular synthesis of heterocyclic scaffolds and API intermediates.
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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: