Feuerstein, Wolfram team published research in Chemistry – A European Journal in 2020 | 244205-40-1

COA of Formula: C6H6BBrO2, 2-Bromophenylboronic Acid is used as an inhibitor of the hormone sensitive lipase.
2-Bromophenylboronic acid, also known as 2-Bromophenylboronic acid, is a useful research compound. Its molecular formula is C6H6BBrO2 and its molecular weight is 200.83 g/mol. The purity is usually 95%.
2-Bromophenylboronic acid is a glucose monitoring agent that has a ruthenium complex with an acidic environment. The nitro group and the amines are in close proximity to the boron center, and this proximity leads to a high nucleophilic character of the molecule. This reactivity allows 2-bromophenylboronic acid to be used as a fluorescence probe for acidic environments. 2-Bromophenylboronic acid also inhibits secretase enzymes, which are involved in Alzheimer’s disease and other neurodegenerative disorders. It is an inhibitor of γ-secretase, which is responsible for cleaving the amyloid precursor protein (APP), and it has shown efficacy against biphenyl, an anticancer drug that binds to benzodiazepine receptors. 2-Bromophenylboronic acid is also an enantiopure compound because all four substituents are different from each other., 244205-40-1.

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 244205-40-1, formula is C6H6BBrO2, Name is (2-Bromophenyl)boronic acid. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. COA of Formula: C6H6BBrO2.

Feuerstein, Wolfram;Holzer, Christof;Gui, Xin;Neumeier, Lilly;Klopper, Wim;Breher, Frank research published ã€?Synthesis of New Donor-Substituted Biphenyls: Pre-ligands for Highly Luminescent (CĈD̂) Gold(III) Pincer Complexesã€? the research content is summarized as follows. The authors herein report on new synthetic strategies for the preparation of pyridine and imidazole substituted 2,2′-dihalo biphenyls. These structures are pre-ligands suitable for the preparation of resp. stannoles. The latter can successfully be transmetalated to K[AuCl4] forming nonpalindromic [(CĈD̂)Au(III)] pincer complexes featuring a lateral pyridine (D = N) or N-heterocyclic carbene (NHC, D = C’) donor. The latter is the 1st report on a pincer complex with two formally anionic sp2 and one carbenic C donor. The [(CĈD̂)Au(III)] complexes show intense phosphorescence in solution at room temperature The developed multistep strategy and touch upon synthetic challenges are discussed. The prepared complexes were fully characterized including x-ray diffraction anal. The Au(III) complexes’ photophys. properties were studied by absorption and emission spectroscopy as well as quantum chem. calculations on the quasi-relativistic two-component TD-DFT and GW/Bethe-Salpeter level including spin-orbit coupling. Thus, the authors shed light on the electronic influence of the nonpalindromic pincer ligand and reveal nonradiative relaxation pathways of the different ligands employed.

COA of Formula: C6H6BBrO2, 2-Bromophenylboronic Acid is used as an inhibitor of the hormone sensitive lipase.
2-Bromophenylboronic acid, also known as 2-Bromophenylboronic acid, is a useful research compound. Its molecular formula is C6H6BBrO2 and its molecular weight is 200.83 g/mol. The purity is usually 95%.
2-Bromophenylboronic acid is a glucose monitoring agent that has a ruthenium complex with an acidic environment. The nitro group and the amines are in close proximity to the boron center, and this proximity leads to a high nucleophilic character of the molecule. This reactivity allows 2-bromophenylboronic acid to be used as a fluorescence probe for acidic environments. 2-Bromophenylboronic acid also inhibits secretase enzymes, which are involved in Alzheimer’s disease and other neurodegenerative disorders. It is an inhibitor of γ-secretase, which is responsible for cleaving the amyloid precursor protein (APP), and it has shown efficacy against biphenyl, an anticancer drug that binds to benzodiazepine receptors. 2-Bromophenylboronic acid is also an enantiopure compound because all four substituents are different from each other., 244205-40-1.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary