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Structure of 16830-24-3
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2-Methyl-4-pyridinecarboxylic acid methyl ester features a pyridine ring bearing a methyl substituent at the 2-position and a carboxylate ester at the 4-position. This configuration imparts enhanced solubility in organic solvents while maintaining stability under standard bench conditions. The molecule serves as a key intermediate in the synthesis of bioactive heterocycles, particularly in medicinal chemistry applications targeting kinase inhibitors and antimicrobial agents.
2-Methyl-4-pyridinecarboxylic acid methyl ester serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyridine-based heterocycles and pharmaceutical intermediates. Its methyl ester functionality facilitates straightforward hydrolysis or nucleophilic substitution, while the 2-methyl substituent enhances regioselectivity in electrophilic and transition-metal-catalyzed coupling reactions. The compound exhibits excellent bench stability and compatibility with standard purification protocols, making it well-suited for scalable synthesis and medicinal chemistry campaigns.
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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: