A protecting group-free divergent synthesis of natural benzofurans via one-pot synthesis of 2-bromo-6-hydroxybenzofurans was written by Sivaraman, Aneesh;Harmalkar, Dipesh S.;Kang, Jiyoon;Choi, Yongseok;Lee, Kyeong. And the article was included in Organic & Biomolecular Chemistry in 2019.HPLC of Formula: 365564-07-4 This article mentions the following:
The first one-pot strategy for the efficient synthesis of 2-bromo-6-hydroxybenzofurans was reported. The present protocol provided shorter routes for the synthesis of moracins M, N, O and P; gramniphenols F and G; and morunigrol C using a protecting group-free approach. In the experiment, the researchers used many compounds, for example, 2-(3,5-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 365564-07-4HPLC of Formula: 365564-07-4).
2-(3,5-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 365564-07-4) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive. At room temperature, ethers are pleasant-smelling colourless liquids. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.HPLC of Formula: 365564-07-4
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem