Application In Synthesis of 4′-Hydroxyacetophenone. In 2019.0 CR CHIM published article about KETONES in [Kiss, Laszlo; Kunsagi-Mate, Sandor] Univ Pecs, Dept Gen & Phys Chem, Ifjusag St 6, H-7624 Pecs, Hungary; [Kiss, Laszlo; Kunsagi-Mate, Sandor] Janos Szentagothai Res Ctr, Ifjusag St 20, H-7624 Pecs, Hungary; [Kunsagi-Mate, Sandor] Univ Pecs, Dept Pharmaceut Chem, Rokus St 2, H-7624 Pecs, Hungary in 2019.0, Cited 9.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.
The voltammetric oxidation of five para-substituted acetophenone derivatives (containing nitro, chloro, bromo, methyl and hydroxyl groups as substituents) and that of benzophenone was studied on a platinum and glassy carbon electrode in acetonitrile media. Electrode passivation was observed in the case when all selected compounds are on a glassy carbon electrode; an oxidation peak appeared between 2.5 and 3 V. The voltammograms of 4′-hydroxyacetophenone showed an additional peak around 2 V, which may be associated with the oxidation of the phenol moiety. In the case of a platinum electrode, no relevant peaks appeared on the voltammograms, reflecting the absence of passivation. The use of a redox probe 1,4-dihydroxybenzene showed that the glassy carbon electrode, after cyclization in the solutions of the outlined compounds, has higher sensitivity towards the oxidation product (1,4-benzoquinone) of this compound. (C) 2019 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.
Application In Synthesis of 4′-Hydroxyacetophenone. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Kiss, L; Kunsagi-Mate, S or concate me.
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