Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 99769-19-4, formula is C8H9BO4, Name is 3-(Methoxycarbonyl)phenylboronic acid. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. SDS of cas: 99769-19-4.
Lu, Xiao-Yu;Yan, Lu-Yu;Li, Jin-Song;Li, Jia-Mei;Zhou, Hai-pin;Jiang, Run-Chuang;Liu, Chuang-Chuang;Lu, Ran;Hu, Rong research published 《 Base-free Ni-catalyzed Suzuki-type cross-coupling reactions of epoxides with boronic acids》, the research content is summarized as follows. A Ni-catalyzed Suzuki-type cross-coupling of boronic acids with epoxides without an exogenous base and with broad substrate scope was developed. The product selectivity of styrenyl epoxides is different from that of previous work. This methodol. uses readily available starting materials to access a range of substituted alcs., which are valuable feedstock chems.
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., SDS of cas: 99769-19-4
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Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics