Polyesters are important plastics, with monomers linked by ester moieties. Phosphoesters form the backbone of DNA molecules. 99769-19-4, formula is C8H9BO4, Name is 3-(Methoxycarbonyl)phenylboronic acid.Nitrate esters, such as nitroglycerin, are known for their explosive properties. Formula: C8H9BO4.
Xia, Hongyu;Wang, Ganghu;Zhao, Dongbo;Zhu, Chunyin research published 《 Visible Light Induced Aerobic Coupling of Arylboronic Acids Promoted by Hydrazone》, the research content is summarized as follows. A visible-light-induced oxidative coupling of arylboronic acids was developed for the synthesis of biaryls Ar1Ar2 [Ar1 = Ar2 = Ph, 4-MeC6H4, 4-FC6H4, etc.; Ar1 = 4-BrC6H4, 4-MeC6H4, 4-FC6H4, etc.; Ar2 = 4-H(O)CC6H4, 3-MeOC6H4, 4-AcC6H4, etc.]. The reaction that employed polydentate hydrazones as the bifunctional catalyst works smoothly under room temperature It was compatible with a wide range of functional group. The study of UV-Vis spectrum indicated that hydrazone and its complex with CuI show major absorptions upon visible-light, which secures the dual role of hydrazone as both ligand and photocatalyst in this reaction. Hence, the reaction was proposed to involve stepwise transmetallations, photo-induced oxidations, and reductive elimination.
Formula: C8H9BO4, 3-Methoxycarbonylphenylboronic acid is a useful research compound. Its molecular formula is C8H9BO4 and its molecular weight is 179.97 g/mol. The purity is usually 95%.
3-Methoxycarbonylphenylboronic acid is a reactanct that has been involved in a variety of applications. For instance, it has been used in Suzuki-Miyaura cross-coupling, Iterative cross-coupling of boronate building blocks, cross-coupling with aryl/ alkenyl sulfonates, synthesis of symmetrical biaryls via CuCl catalyzed homocoupling, trifluoromethylation, and cyanation just to name a few of its many uses.
3-Methoxycarbonylphenylboronic acid is a boronate ligand that has been shown to have an interaction with the nitrogen atoms in amines. This compound is used for the Suzuki coupling reaction, which is a chemical reaction between an organoboron compound and an organic electrophile. 3-Methoxycarbonylphenylboronic acid has a helical structure that can be seen by FTIR spectroscopy and it has potent inhibitory activity., 99769-19-4.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics