A unique rippled nanographene constituted by 52 fused rings is presented in which six out‐of‐plane motifs are fully fused into a triangular aromatic surface of ca. 2.5 nm size. Three units of an unprecedented fully lateral π‐extended octabenzo[5]helicene together with three units of saddle‐shaped heptagonal rings are combined in a single structure leading to a well‐soluble warped nanographene. The two pairs of possible enantiomers have been isolated and their linear, non‐linear and chiroptical properties evaluated, revealing an outstanding quantum yield and brightness values at low energy together with good chiroptical responses both in the absorption and emission.