Ethers are a class of organic compounds that contain an ether groupâan oxygen atom connected to two alkyl or aryl groups. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid.They have the general formula RâOâRâ? where R and Râ?represent the alkyl or aryl groups. Quality Control of 122775-35-3.
Kurpik, Gracjan;Walczak, Anna;Gilski, Miroslaw;Harrowfield, Jack;Stefankiewicz, Artur R. research published ã?Effect of the nuclearity on the catalytic performance of a series of Pd(II) complexes in the Suzuki-Miyaura reactionã? the research content is summarized as follows. Development of well-defined multivalent systems with densely packed multiple functional groups located within a single mol. structure provides an excellent opportunity to generate catalysts of enhanced activity. A series of mono-, di- and trinuclear Pd(II) complexes based on polyketonate ligands allied with 2,2′-bipyridine was designed, synthesized and fully characterized in both solution and solid state. The mono-, di- and tritopic β-diketonate mols. serve as scaffolds for Pd(II) active sites which, in the two latter cases, are forced into close proximity. Application of the complexes as catalysts in Suzuki-Miyaura cross-coupling as a model reaction revealed significant differences in reaction yields and a trend in reactivity reflecting their nuclearity.
Quality Control of 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., 122775-35-3.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem