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. COA of Formula: C8H9BO4.
Zeng, Jialin;Torigoe, Takeru;Kuninobu, Yoichiro research published 《 Control of Site-Selectivity in Hydrogen Atom Transfer by Electrostatic Interaction: Proximal-Selective C(sp3)-H Alkylation of 2-Methylanilinium Salts Using a Decatungstate Photocatalyst》, the research content is summarized as follows. Site-selective C(sp3)-H alkylation of 2-methylanilinium salts via radical intermediates was developed. The anionic decatungstate photocatalyst ([W10O32]4-) interacts with the ammonium group of the substrate through electrostatic interaction and selectively abstracts a hydrogen atom from the proximal benzylic carbon atom under UV irradiation A variety of 2-methylanilinium salts reacted with electron-deficient alkenes R1CH=C(R2)(R3) (R1 = H, CN; R2 = H, SO2Ph, COOMe; R3 = CN, Ph, SO2Ph, etc.). The alkylated product such as Me 4-(2-amino-5-methylphenyl)-2-phenylbutanoate was successfully converted into an aryl iodide such as Me 4-(2-iodo-5-methylphenyl)-2-phenylbutanoate via cleavage of the C-N bond and a tetrahydrobenzoazepinone derivative such as 7-methyl-3-phenyl-1,3,4,5-tetrahydro-2H-benzo[b]azepin-2-one by intramol. cyclization. Mechanistic studies clearly show the existence of the interactions between [W10O32]4- and the ammonium group.
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., COA of Formula: C8H9BO4
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics