Aldahdooh, Mohammed K. team published research on Reactive & Functional Polymers in 2021 | 2576-47-8

Application In Synthesis of 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., 2576-47-8.

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Application In Synthesis of 2576-47-8.

Aldahdooh, Mohammed K.;Ali, Shaikh A. research published 《 Synthesis and application of alternate cyclopolymers of β-diallylaminoethyliminodiacetic acid with maleic acid and sulfur dioxide》, the research content is summarized as follows. Bis-cationic monomer β-diallylaminoethyliminodiacetic acid dihydrochloride (I) underwent alternate cyclocopolymns. with SO2 and maleic acid to give poly(bis-zwitterion) (PBZ) (± ±) II, and III, resp. The PBZs contained the chelating motifs of [NH+(CH2)2NH+(CH2CO2)2] embedded in the pyrrolidine ring of each repeating unit. Both the PBZs were water-insoluble, however they became water-soluble with assistance from salts like NaCl. PBZs II and III, having the point of zero charge at pH 2.4, became water soluble outside the pH-windows of 0.81-4.46 and 1.49-3.35, resp., whereby the electroneutral pH-responsive polymers become charge-imbalanced. The ‘apparent’ pKas of the protonated amine centers in II were found to be 5.18 and 9.92. As an antiscalant, PBZ III (2.5 ppm) demonstrated inhibition of CaSO4 scale formation with 99% efficacy for over 180 min, while at 1.5 ppm inhibition efficiency was found to be 98% for 50 min. PBZ II at concentrations of 20 and 10 ppm demonstrated CaCO3 scale inhibition of 98% for over 240 min and 95% for over 90 min, resp. A synergistic mixture of III (20 ppm) and KI (400 ppm) arrested corrosion of mild steel in 1 M HCl with a remarkable efficacy of 98% for 24 h at 60°C.

Application In Synthesis of 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., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary