Kim, Hyeji team published research in Helvetica Chimica Acta in 2022 | 3900-89-8

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., Application In Synthesis of 3900-89-8

The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Their wide structural variety and divergent chemical properties lead to a broad range of named reactions and applications. Application In Synthesis of 3900-89-8.

Kim, Hyeji;Choi, Kyoungmin;Jang, Dongseok;Um, Hyun-Suk;Kim, Yeehwan;Lee, Chulbom research published ã€?Rhodium-Catalyzed Tandem Addition-Cyclization of 1,5-Enynes with Organoboronic Acids for the Synthesis of Alkylidene-Cyclobutanesã€? the research content is summarized as follows. Described here is the rhodium(I)-catalyzed tandem addition-cyclization of 1,5-enynes with aryl- and alkenylboronic acids. In the presence of triethylamine and catalytic [Rh(OH)(COD)]2 in methanol, both the terminal and internal alkyne substrates possessing an electron-deficient alkene undergo inter- and intramol. C-C bond formations to yield alkylidene-cyclobutane products. The reaction proceeds through a series of processes involving generation of an aryl or alkenyl rhodium from the organoboronic acid, 1,2-syn-carbometalation of the alkyne and 4-exo-type-cyclization of the resulting alkenyl rhodium intermediate with the tethered, carbonyl-conjugated alkene. Thus, the reaction enables a net R,H-addition across the 1,5-enyne π-system – hydroarylation and hydroalkenylation – under mild rhodium catalysis while achieving 4-membered ring formation. Preliminary studies show that the reaction can also be rendered enantioselective by employing a chiral diene ligand for the rhodium catalyst.

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., Application In Synthesis of 3900-89-8

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics