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Structure of 33021-53-3
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3-Acetylquinoline features a quinoline core functionalized with an acetyl group at the 3-position, delivering enhanced solubility and reactivity in synthetic transformations. This electron-deficient heterocycle serves as a key scaffold for pharmaceutical intermediates and ligand development.
3-Acetylquinoline serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the quinoline ring via electrophilic substitution or transition-metal-catalyzed coupling reactions. The acetyl group provides a handle for selective transformations, including enolization, oxidation to carboxylic acid derivatives, and participation in Claisen-type condensations. Its bench-stable nature and compatibility with common protecting group strategies make it suitable for use in medicinal chemistry and heterocyclic scaffold development.
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Lot numbers can be found on the outside label of a product: