Ester is a chemical compound derived from an oxoacid (organic or inorganic) in which at least one –OH hydroxyl group is replaced by an –O– alkyl (alkoxy) group, 99769-19-4, formula is C8H9BO4, Name is 3-(Methoxycarbonyl)phenylboronic acid. as in the substitution reaction of a carboxylic acid and an alcohol. Computed Properties of 99769-19-4.
Luo, Bingcai;Zhang, Yubao;Chen, Ying;Huo, Jianqiang research published 《 Photocatalytic conversion of arylboronic acids to phenols by a new 2D donor-acceptor covalent organic framework》, the research content is summarized as follows. In this research, synthesized a two-dimensional (2D) D-A type COF (BTT-BTDDA-COF) based on alternating connections of benzotrithiophene (BTT) and 4,4′-(2,1,3-benzothiadiazole-4,7-diyl)dianiline (BTDDA) units, with a wide visible light absorption range and good photoelec. response characteristics was reported. In the photocatalytic conversion of arylboronic acid to phenol, BTT-BTDDA-COF exhibits high catalytic activity, wide substrate applicability and good recoverability. The high-efficiency photocatalytic activity of BTT-BTDDA-COF was reasonably attributed to the electron push-pull effect between the donor and acceptor units, which significantly improves the transfer and separation of carriers, which leads to the expansion of the visible light absorption range. The above results show the practicability of COFs material design and provide a new idea for the application of the new D-A COF catalyst in photocatalytic organic conversion.
Computed Properties of 99769-19-4, 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