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Structure of 7470-88-4
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1-(6-Aminonaphthalen-2-yl)ethan-1-one features a naphthalene core with an electron-rich amino group at the 6-position and a ketone at the 2-position, enabling direct conjugation and synthetic versatility. This scaffold integrates readily into fluorescent probes and pharmaceutical intermediates due to its planar structure and reactive carbonyl functionality.
1-(6-Aminonaphthalen-2-yl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling the synthesis of naphthalene-based scaffolds through standard amide coupling and electrophilic substitution reactions. Its amino and ketone functionalities offer orthogonal reactivity for downstream derivatization, including reductive amination and condensation processes. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in API development.
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Lot numbers can be found on the outside label of a product: