The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 3,3-Bis(3,5-dibromo-4-hydroxy-2-methylphenyl)-3H-benzo[c][1,2]oxathiole 1,1-dioxide, is researched, Molecular C21H14Br4O5S, CAS is 76-60-8, about Removal of Bromocresol Green from aqueous solution by electro-Fenton and electro-Fenton-like processes with different catalysts: laboratory and kinetic model investigation, the main research direction is bromocresol green aqueous solution kinetic model.Synthetic Route of C21H14Br4O5S.
This study presents the removal of triarylmethane dye Bromocresol Green from aqueous solution by the electro-Fenton process. As catalysts five different cations were used: Fe2+, Ce3+, Ni2+, Mn2+, and Co2+. They play crucial roles in the whole process because they react with H2O2 producing hydroxyl radicals that are capable of breaking down dye mols. Based on this, a comparison of catalytic activity of these cations in the electro-Fenton process is made for Bromocresol Green degradation A simple and universal kinetic model is also applied to study the catalytic activity of investigated catalysts. Due to its multidimensionality it is fitted to exptl. data using a genetic algorithm. The procedure of fitting using a genetic algorithm is thoroughly described and demonstrated. The activity of utilized catalysts is compared based on both exptl. and model data revealing that for Bromocresol Green removal all alternative catalysts (Ni2+, Co2+, Ce3+, Mn2+) are better than the typical one (Fe2+, 51.83% degradation). The best catalyst is Co2+ with 78.35% degradation efficiency. Moreover, the adopted kinetic model proved its universality and outlined different interactions between catalysts and dye mols.
There is still a lot of research devoted to this compound(SMILES：CC1=C(Br)C(O)=C(Br)C=C1C2(C3=CC(Br)=C(O)C(Br)=C3C)C4=CC=CC=C4S(O2)(=O)=O)Synthetic Route of C21H14Br4O5S, and with the development of science, more effects of this compound(76-60-8) can be discovered.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles