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Structure of 114527-53-6
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This tetrahydroquinoline scaffold delivers a rigid, electron-rich aromatic core ideal for medicinal chemistry applications. The carboxylic acid functionality enables direct conjugation or salt formation, enhancing solubility and enabling downstream derivatization. Designed for synthetic accessibility and structural integrity under standard conditions.
1,2,3,4-Tetrahydroquinoline-3-carboxylic acid serves as a versatile scaffold in medicinal chemistry, enabling the synthesis of bioactive heterocycles through standard functionalization at the carboxylic acid and nitrogen sites. Its bench-stable nature and compatibility with common coupling reactions facilitate efficient derivatization, while the fused ring system provides structural rigidity beneficial for target engagement in CNS-directed compounds.
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Lot numbers can be found on the outside label of a product: