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Structure of 52605-97-7
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2,3-Dimethoxypyridine features two methoxy groups at adjacent positions on the pyridine ring, enhancing electron density and reactivity in cross-coupling processes. This bench-stable heterocycle serves as a key scaffold in medicinal chemistry and catalytic synthesis, offering improved solubility and compatibility with transition metal systems.
2,3-Dimethoxypyridine serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient functionalization at the C2 and C3 positions. Its ortho-dimethoxy substitution pattern enhances electrophilic aromatic substitution reactivity while providing robust bench stability and compatibility with standard coupling protocols. The molecule functions as a key scaffold for heterocyclic synthesis and facilitates the construction of complex APIs through directed metallation and cross-coupling reactions.
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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: