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. Safety of 3-(Methoxycarbonyl)phenylboronic acid.
Lu, Zhiwu;Hu, Xu-Dong;Zhang, Hui;Zhang, Xiao-Wen;Cai, Jinhui;Usman, Muhammad;Cong, Hengjiang;Liu, Wen-Bo research published 《 Enantioselective Assembly of Cycloenones with a Nitrile-Containing All-Carbon Quaternary Center from Malononitriles Enabled by Ni Catalysis》, the research content is summarized as follows. Herein, an enantioselective nickel-catalyzed desymmetrization of malononitriles for the generation of nitrile-containing all-carbon quaternary stereocenters was reported. This protocol involved a nickel-catalyzed addition of aryl boronic acids to alkynes, followed by a selective nitrile insertion, provided unprecedented access to enantioenriched 5-7-membered α-cyano-substituted cyclic enones I [X = O, N; Y = (CH2)n; n = 0, 1, 2; Ar = Ph, 3-thienyl, 3-furanyl, etc.; R1 = Me, Ph, 2-thienyl, etc.; R2 = Me, CH2CH=CH2, Bn, etc.] with a fully substituted olefin from a broad range of substrates. The synthetic utility of these nitrile products I was demonstrated by gram-scale synthesis and conversion to several useful functional groups.
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