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6-Bromo-2-naphthol features a naphthalene core, a fused two-ring aromatic structure well-known for its stability and resonance. On this framework, a hydroxyl group (-OH) sits at the 2-position, while a bromine atom (Br) resides at the 6-position. These substituents imbue the molecule with significant reactivity, allowing it to serve as a versatile building block in cross-coupling and substitution reactions.
This dual function—electrophilic at the bromine site and nucleophilic at the hydroxyl—makes the compound attractive for orthogonal chemical modifications.
This dual function—electrophilic at the bromine site and nucleophilic at the hydroxyl—makes the compound attractive for orthogonal chemical modifications.