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Structure of 17295-11-3
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Methyl 6-hydroxy-2-naphthoate features a hydroxyl group at the 6-position and a methyl ester at the 2-position on a naphthalene core. This configuration enables direct participation in coupling reactions and facilitates derivatization for fluorescent probes or pharmaceutical intermediates. The phenolic functionality enhances solubility and reactivity under standard conditions.
Methyl 6-hydroxy-2-naphthoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to naphthalene-based scaffolds. The ortho-hydroxyl and ester functionalities provide complementary handles for selective derivatization, including etherification, ester hydrolysis, and transition-metal-catalyzed coupling reactions. Its bench-stable nature and straightforward purification make it well-suited for use in medicinal chemistry campaigns and the construction of functionalized heterocycles.
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Lot numbers can be found on the outside label of a product: