Xia, Guang-Da team published research in Chemical Communications (Cambridge, United Kingdom) in 2022 | 122775-35-3

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Quality Control of 122775-35-3

Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Quality Control of 122775-35-3.

Xia, Guang-Da;He, Yuan-Yuan;Zhang, Jing;Liu, Zi-Kui;Gao, Yang;Hu, Xiao-Qiang research published 《 Deoxygenative gem-difluorovinylation of aliphatic alcohols》, the research content is summarized as follows. An unprecedented deoxygenative gem-difluorovinylation of aliphatic alcs. R1OH (R1 = 3-(4-methoxyphenyl)propyl, cyclopentyl, 3-hydroxy-3-methylbutyl, etc.) using α-trifluoromethyl alkenes R2C(=CH2)(CF3) (R2 = Ph, naphthalen-2-yl, 2H-1,3-benzodioxol-5-yl, etc.) was achieved under photocatalytic conditions. Inexpensive Ph3 P acts as an efficient O-atom transfer reagent to facilitate the deoxygenation of alcs. for the generation of reactive alkyl radical species. Remarkable features of this reaction include mild conditions, simple operation and broad scope. The synthetic utility of this reaction was validated by the success of two-step one-pot reactions, scale-up synthesis and chemoselective monodeoxygenation of diols.

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Quality Control of 122775-35-3

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