Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Research Support, Non-U.S. Gov’t, Journal of the American Chemical Society called Alkyltriflones in the Ramberg-Backlund Reaction: An Efficient and Modular Synthesis of gem-Difluoroalkenes, Author is Maekawa, Yuuki; Nambo, Masakazu; Yokogawa, Daisuke; Crudden, Cathleen M., which mentions a compound: 4360-63-8, SMILESS is BrCC1OCCO1, Molecular C4H7BrO2, Synthetic Route of C4H7BrO2.
The unprecedented synthesis of gem-difluoroalkenes through the Ramberg-Backlund reaction of alkyl triflones was described. Structurally diverse, fully-substituted gem-difluoroalkenes that were difficult to prepare by other methods was easily prepared from readily available triflones by treatment with specific Grignard reagents. Exptl. and computational studies provided insight into the unique and critical role of Grignard reagent, which served both as a base to remove the alpha-proton, and as a Lewis acid to assist C-F bond activation.
There is still a lot of research devoted to this compound(SMILES：BrCC1OCCO1)Synthetic Route of C4H7BrO2, and with the development of science, more effects of this compound(4360-63-8) can be discovered.
Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem