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. Application In Synthesis of 99769-19-4.
Guchhait, Sankar Kumar;Saini, Meenu research published 《 Chan-Lam N-arylation and C-H amination with heteroaromatic ring-NH: an approach to access extended-fused imidazo[1,2-a]-pyridines/pyrazines》, the research content is summarized as follows. A di-amination strategy of areneboronic acids with heterocyclic azines via a tandem process of intermol. Chan-Lam N-arylation and intramol. arene C-H amination under copper(II)-mediated aerobic conditions was realized. It constructs a fused imidazole scaffold and affords a convenient route to access imidazo[1,2-a]-fused pyridine, pyrazine and other heterocycles.
Application In Synthesis 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