Chen, Hao team published research on European Journal of Medicinal Chemistry in 2021 | 122775-35-3

HPLC of Formula: 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.

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. HPLC of Formula: 122775-35-3.

Chen, Hao;Wang, Ke;Yang, Yang;Huang, Xupeng;Dai, Xinyan;Feng, Zhiqiang research published 《 Design, synthesis, and structure-activity relationship of programmed cell death-1/programmed cell death-ligand 1 interaction inhibitors bearing a benzo[d]isothiazole scaffold》, the research content is summarized as follows. A novel series of compounds such as I [R = CH2NHCHCO2HCH2OH, CH2(N-piperidin-3-ol), CH2(N-pyrrolidin-3-ol), etc.] bearing a benzo[d]isothiazole scaffold were developed, among which compound I [R = CH2NHCHCO2HCH2OH] exhibited promising activity, with an IC50 value of 8.5 nM. Further cell-based PD-1/PD-L1 blockade bioassays indicated that compound I [R = CH2NHCHCO2HCH2OH] could inhibit the PD-1/PD-L1 interaction at the cellular level, with an EC50 value of 5.6μM compound I [R = CH2NHCHCO2HCH2OH] could had better potency in restoring the activity of effector cells, as the maximal luminescence values (RLUmax) of compound I [R = CH2NHCHCO2HCH2OH] were equivalent to those of PD-L1 mAbs. The docking anal. of compound I [R = CH2NHCHCO2HCH2OH] with the PD-L1 dimer complex (PDB ID: 6R3K) confirmed that I [R = CH2NHCHCO2HCH2OH] was a promising lead compound for the development of inhibitors of the PD-1/PD-L1 interaction. The preliminary structure-activity relationship was investigated in this paper, with the aim of future drug development.

HPLC of Formula: 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