Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Organic compounds having carbon bonded to bromine are called organic bromides. Related Products of 2576-47-8.
Gerschel, Philipp;Battistella, Beatrice;Siegmund, Daniel;Ray, Kallol;Apfel, Ulf-Peter research published 《 Electrochemical CO2 Reduction – The Effect of Chalcogenide Exchange in Ni-Isocyclam Complexes》, the research content is summarized as follows. Among the numerous homogeneous electrochem. CO2 reduction catalysts, [Ni(cyclam)]2+ is known as one of the most potent catalysts. Likewise, [Ni(isocyclam)]2+ is reported to enable the electrochem. CO2 conversion but received significantly less attention. However, for both catalysts, a purposeful substitution of a single N donor group by chalcogen atoms was never reported. The authors report isocyclam based Ni complexes with {ON3}, {SN3}, {SeN3} as well as {N4} moieties and studied the influence of N/chalcogen substitution on the electrochem. CO2 reduction While [Ni(isocyclam)]2+ showed the highest selectivity toward CO2 reduction within this series with a FE of 86% for the generation of CO at an overpotential of -1.20 V and acts as a homogeneous catalyst, the O- and S-containing Ni complexes revealed comparable catalytic activities at ∼0.3 V milder overpotential but tend to form deposits on the electrode acting as precursors for a heterogeneous catalysis. Also, the heterogeneous species generated from the O- and S-containing complexes enable a catalytic hydride transfer to MeCN, giving acetaldehyde. The incorporation of Se, however, resulted in loss of CO2RR activity mainly leading to H generation that is also catalyzed by a heterogeneous electrodeposit.
2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., Related Products of 2576-47-8
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary