Although transition metallacyclopropenes have been extensively explored for more than 40 years, their analogues of rare-earth metals have remained elusive. Herein, we report the synthesis of three isolable scandacyclopropenes, thus representing the first well-defined rare-earth metallacyclopropenes. Structural characterization and DFT calculations revealed a delocalized three-center two-electron (3c-2e) aromatic system. When scandacyclopropenes were treated with phenylacetylene or TMSN3, the scandium complex of bis-phenylacetylide or bis-azide was obtained, respectively. The reaction of scandacyclopropene with phenazine could provide the binuclear ring-opening scandium complex via 1,4-insertion of phenazine into one Sc-C bond and subsequent metathesis reaction. However, insertion of TMSNCO or N2O into one Sc-C bond of scandacyclopropenes gave a five- or six-membered scandacycle. In addition, scandacyclopropenes can serve as a two-electron reductive agent for PhSSPh and PhNNPh. These results show that scandacyclopropenes exhibit diversified and unique reactivity toward small molecules because of the strongly nucleophilic alkenediyl dianion and highly strained three-membered ring.