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. Electric Literature of 99769-19-4.
Li, Yang;Sun, Ning;Hao, Meng;Zhang, Cai-Lin;Li, Hong;Zhu, Wen-Qing research published 《 Nanopalladium-Catalyzed Oxidative Heck Reaction of Fluorinated Olefins: H2O2 as a Green Oxidant》, the research content is summarized as follows. Pd-based nanocatalysts were prepared through immobilization of Pd(OAc)2/phenanthroline on nanocarbon materials and subsequent pyrolysis. The catalysts were characterized by X-ray diffraction (XRD), XPS and electron microscopy (TEM). Pd-based nanocatalysts can efficiently catalyze the oxidative Heck reaction of 2,3,3,3-tetrafuoroprop-1-ene by using H2O2 as a green oxidant and generate (Z)-β-fluoro-β-(trifluoromethyl)styrenes RCH=C(F)CF3 (R = 4-methylphenyl, 3-methoxyphenyl, 2H-1,3-benzodioxol-5-yl, etc.) in excellent yield. The yield and Z/E selectivity of the titled reaction remained higher than 90% after four reaction cycles.
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., Electric Literature of 99769-19-4
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics