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. Synthetic Route of 99769-19-4.
Li, Zhong-Yuan;Chaminda Lakmal, Hetti Handi;Cui, Xin research published 《 Enabling Catalytic Arene C-H Amidomethylation via Bis(tosylamido)methane as a Sustainable Formaldimine Releaser》, the research content is summarized as follows. 2-Arylpyridines and aryl N-heterocycles such as 2-phenylpyridine underwent regioselective directed tosylaminomethylation with bis(tosylamino)methane as the formaldimine source in the presence of [Ru(p-cymene)Cl2]2, NaOAc, and Na2CO3 in 1,4-dioxane to yield mono(tosylaminomethyl)aryl pyridines such as I. Using the method, a dihydrobenzonaphthyridine and a dihydropyridobenzazepine were prepared
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., Synthetic Route of 99769-19-4
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics