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Structure of 18677-43-5
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2,4-Dimethoxypyridine features two methoxy groups at the 2- and 4-positions of the pyridine ring, enhancing electron density and directing electrophilic substitution. This bench-stable, moisture-tolerant heterocycle integrates readily into cross-coupling reactions and serves as a key scaffold in medicinal chemistry and agrochemical synthesis.
2,4-Dimethoxypyridine serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds. Its ortho-dialkoxy substitution pattern enhances electrophilic aromatic substitution reactivity while providing stable, bench-ready functionality for subsequent transformations. The molecule functions effectively in cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive compounds and pharmaceutical candidates.
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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: