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Structure of 1823775-69-4
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Methyl 2-aminoquinoline-6-carboxylate features a quinoline core with strategically positioned amino and ester functionalities. This electron-rich scaffold integrates readily into heterocyclic syntheses, serving as a key intermediate in medicinal chemistry. The para-amino group enhances reactivity for derivatization, while the methyl ester enables controlled hydrolysis under standard conditions.
Methyl 2-aminoquinoline-6-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinoline-based scaffolds. Its amino and ester functionalities offer orthogonal reactivity for derivatization via coupling, alkylation, or cyclization reactions. The compound exhibits good bench stability and facilitates purification by standard chromatographic methods, making it well-suited for iterative synthesis campaigns in API development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: