Description General description Methyl 6-bromo-2-naphthoate undergoes aromatic Finkelstein reaction followed by hydrolysis to afford 6-iodo-2-naphthoic acid. Application Methyl 6-bromo-2-naphthoate may be used to synthesize: • 6-vinyl-2-naphthalencarbaldehyde • methyl 6-(3-tert-butyl-4-methoxyphenyl)-2-naphthoate • methyl 6-[3-tert-butyl-4-[(tert-butyldiethylsilyl)oxy]-phenyl]-2-naphthoate • methyl 6-[3-(1-adamantyl)-4-[(tert-butyldimethylsilyl)-oxy]phenyl]-2-naphthoate • methyl 6-[3-(1-adamantyl)-4-[[(2,3-dimethyl-1,3-dioxolan-4-yl)methylloxy]phenyl]-2-naphthoate • 2-bromo-6-(bromomethyl)naphthalene Packaging 5, 25 g in glass bottle