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Structure of 29681-43-4
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Methyl 4-methoxy-2-pyridinecarboxylate features a pyridine core with strategically positioned methoxy and ester groups, enabling efficient integration into heterocyclic synthesis. The electron-donating methoxy substituent enhances reactivity at the C4 position, while the methyl ester facilitates straightforward derivatization. This compound serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and bioactive nitrogen heterocycles.
Methyl 4-methoxy-2-pyridinecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyridine-based heterocycles. Its ester functionality facilitates nucleophilic substitution and reduction reactions, while the methoxy group enhances solubility and modulates electronic properties. The molecule exhibits good bench stability and is compatible with standard coupling and functionalization protocols, making it valuable for medicinal chemistry and process development workflows.
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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: