4-Methoxyphenylboronic acid pinacol ester

CAS: 171364-79-7

Ref. 3D-FM25342

Produktinformation

• Name: 4-Methoxyphenylboronic acid pinacol ester
• Synonyme: 2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane4,4,5,5-Tetramethyl-2-(4-methoxyphenyl)-1,3,2-dioxaborolane4-Methoxy-1- (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 1,3,2-Dioxaborolane, 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-, 2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane, 4,4,5,5-Tetramethyl-2-(4-methoxyphenyl)-1,3,2-dioxaborolane, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-methoxybenzene, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole, 4-Methoxyphenyl(pinacolato)borane, 4-Methoxyphenylboronicacidpinacolester, p-(Pinacolboryl)anisole
• CAS: 171364-79-7

Beschreibung

4-Methoxyphenylboronic acid pinacol ester (MPBE) is a chemical compound that is used to synthesize 4-methoxyphenylboronic acid (MPBA). MPBE can be used as a dehydrogenation agent, which converts alcohols and other organic compounds into their corresponding boronate esters. MPBE has been shown to act as an endogenous peroxide sensor in MCF-7 cells by inducing the expression of genes involved in DNA repair and antioxidant mechanisms. In addition, MPBE relies on the presence of hydrogen peroxide for its reaction with organic substrates. The conversion of 4-methoxyphenylboronic acid (MPBA) to 4-methoxyphenylacetic acid (MPA) by MPBE was also demonstrated in this study. This conversion was followed by a second hydrolysis step and yielded MPA, which is an innovative chemical transformation.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 234.1 g/mol
• Formel: C₁₃H₁₉BO₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C13H19BO3/c1-12(2)13(3,4)17-14(16-12)10-6-8-11(15-5)9-7-10/h6-9H,1-5H3
• InChI Key: InChIKey=VFIKPDSQDNROGM-UHFFFAOYSA-N
• SMILES: COc1ccc(B2OC(C)(C)C(C)(C)O2)cc1