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Structure of 38896-30-9
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Methyl quinoline-6-carboxylate features a quinoline core with a methyl ester at the 6-position, offering a rigid, electron-deficient heteroaromatic scaffold. This configuration enhances stability and facilitates integration into synthetic routes for pharmaceutical intermediates and ligand development. The compound exhibits favorable solubility in organic solvents and maintains integrity under standard bench conditions.
Methyl quinoline-6-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to quinoline-based pharmaceutical scaffolds. Its carboxylate functionality facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions, while the quinoline core offers inherent stability and favorable pharmacokinetic properties. The compound exhibits excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for iterative synthesis in 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: