Cao, Haijie’s team published research in Chemical Engineering Journal (Amsterdam, Netherlands) in 2021 | CAS: 150-19-6

m-Methoxyphenol(cas: 150-19-6) may be used in synthesis of:C(4) symmetric calix[4]resorcinarene, 2-nitroso-5-methoxyphenol, 6-methoxy-2(3H)-benzoxazoloneRelated Products of 150-19-6

Cao, Haijie; Wang, Kuikui; Yang, Zhengqiang; Wu, Shijie; Han, Dandan published an article in 2021. The article was titled 《Quantum chemical study on the ozonolysis mechanism of guaiacol and the structure-reactivity relationship of phenols with hydroxyl, methoxy, and methyl substituents》, and you may find the article in Chemical Engineering Journal (Amsterdam, Netherlands).Related Products of 150-19-6 The information in the text is summarized as follows:

Quantum chem. calculations with the M06-2X method were performed to uncover the ozonolysis mechanism of guaiacol and several hydroxylated, methoxylated, and methylated phenols to improve the understanding of the ozone-induced attenuation of phenolic compounds The detailed kinetic properties were obtained by the transition state theory (TST) and the Rice – Ramsperger – Kassel – Marcus (RRKM) theory. Results confirm that the primary ozonides originated from guaiacol occupy considerably long retention time than the short-lived primary ozonides formed from vinyl-type compounds in the air. The TST rate constant of guaiacol ozonolysis is calculated with a value of 8.81 x 10-20 cm3 mol.-1 s-1 at room temperature The RRKM results prove that the rate constant is pos. dependent on temperature but shows no relation with pressure. The reactivity of substituted phenols exhibits a strong correlation with the ozone affinity of carbon atoms and the orbital energy difference (ELo-Hac) between the LUMO of O3 and the HOMO of phenols. The substituents can reduce the value of ELo-Hac and improve the phenols’ reactivity, especially when they locate at the ortho- and para-position. The substituents also improve the ozone affinity of carbon atoms due to the electron-withdrawing effect. The Me group delivers a moderate impact on the reactivity compared to hydroxyl and methoxy groups. The results came from multiple reactions, including the reaction of m-Methoxyphenol(cas: 150-19-6Related Products of 150-19-6)

m-Methoxyphenol(cas: 150-19-6) may be used in synthesis of:C(4) symmetric calix[4]resorcinarene, 2-nitroso-5-methoxyphenol, 6-methoxy-2(3H)-benzoxazoloneRelated Products of 150-19-6

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem