1,8-Naphthalenediol [569-42-6], mp 144℃, is produced by caustic fusion of naphthosultone or naphthosultam, and by acid desulfonation of 1,8-dihydroxynaphthalene-4-sulfonic acid. It is oxidized to juglone by chromium(VI) oxide; gives a dark green color with iron(III) chloride; undergoes amination at 300℃ to give 1,8-naphthalenediamine; and couples with diazotized anilines in the 4- position.
ChEBI: Naphthalene-1,8-diol is a member of the class of naphthalenediols that is naphthalene in which the hydrogens at positions 1 and 8 are replaced by hydroxy groups. It has a role as a fungal metabolite.
