Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 99769-19-4, formula is C8H9BO4, Name is 3-(Methoxycarbonyl)phenylboronic acid. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Safety of 3-(Methoxycarbonyl)phenylboronic acid.
Lakshmidevi, Jangam;Vakati, Venkateswarlu;Ramesh Naidu, Bandameeda;Raghavender, M.;Rao, K. S. V. Krishna;Venkateswarlu, Katta research published 《 Pd(5%)-KIT-6, Pd(5%)-SBA-15 and Pd(5%)-SBA-16 catalysts in water extract of pomegranate ash: A case study in heterogenization of Suzuki-Miyaura reaction under external base and ligand free conditions》, the research content is summarized as follows. Real heterogenization of Suzuki-Miyaura cross-coupling (SMC) is arduous quest owing to unavoidable homogeneous mechanism of heterogeneous catalysts. This article reports a study of heterogenization of SMC using mesoporous silica supported Pd-nanoparticles (Pd-NPs) under ligand and external base free conditions. Pd-mesoporous silica catalysts such as Pd-KIT-6, Pd (5%)-SBA-16 and Pd (5%)-SBA-15 were synthesized and studied for SMC in water extract of pomegranate ash (WEPA). Pd (5%)-KIT-6 was the best amongst, and successful reusability of Pd (5%)-KIT-6 and hot-filtration experiments indicated its high stability, conveys pure heterogenous mechanism over inevitable homogenous mechanism. The large choice of substrates, high stability of the catalyst in green and renewable medium & base systems, and absence of ligands are the luminary potencies of this inquest.
Safety of 3-(Methoxycarbonyl)phenylboronic acid, 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