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Structure of 24202-74-2
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4-(Methoxycarbonyl)nicotinic acid features a pyridine ring bearing both carboxylic acid and methoxycarbonyl groups at para positions, enabling direct conjugation in heterocyclic synthesis. This electron-deficient scaffold integrates readily into bioactive molecules, offering enhanced solubility and stability under standard conditions.
4-(Methoxycarbonyl)nicotinic acid serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to pyridine-based pharmacophores. Its dual functionality—carboxylic acid and ester groups—facilitates selective derivatization, including amidation, hydrolysis, and coupling reactions. The molecule exhibits excellent bench stability and is compatible with standard peptide coupling protocols, making it ideal for constructing 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: