tion of the structure shown for chorismic acid was obtained by examination of a deuterium oxide solution of barium chorismate by nuclear-magneticresonance spectroscopy (Gibson & Jackman, 1963). Chorismic acid can be formulated as the 3-enolpyruvic ether of tran8-3,4-dihydroxycyclohexa-1,5dienecarboxylic acid. SUMMARY 1. Chorismic acid, a new intermediate in aromatic biosynthesis, is the 3-enolpyruvic ether of trans-3,4-dihydroxycyclohexa-1 ,5-dienecarboxylic acid. 2. Although chorismic acid itself is a fairly labile compound the barium salt is readily isolated and has been examined. 3. The ultraviolet-and infrared-absorption spectra of chorismate are given together with details of chromatography. 4. Chorismate is readily converted, by warming, into a mixture of prephenate and 4-hydroxybenzoate. Under acid conditions the prephenic acid is further converted into phenylpyruvic acid.