On September 24, 2020, Kilic, Ahmet; Beyazsakal, Levent; Findik, Bahar Tuba; Incebay, Hilal published an article.Application In Synthesis of N-(3-Aminopropyl)-imidazole The title of the article was Synthesis and electrochemical investigation of chiral amine bis(phenolate)-boron complexes: In vitro antibacterial activity screening of boron compounds. And the article contained the following:
A new class of low-cost, easily-synthesizable and modifiable chiral amine bis(phenolate) ligand (L), its chiral boron complex (LB), and five different salen groups (1-(3-Aminopropyl) imidazole (LB1), N,N-Diethyl-p-phenylenediamine (LB2), 2-Picolylamine (LB3), 4′-Aminoacetophenone (LB4), and 4-Amino-2,2,6,6-tetramethyl piperidine (LB5)) containing chiral boron complexes were synthesized. These newly synthesized chiral compounds were fully characterized by 1H and 13C NMR, FTIR, UV-visible, and LC-MS/MS spectroscopy, m.p., elemental anal., and cyclic voltammetry techniques. The in vitro antibacterial activity of the synthesized different chiral boron complexes was tested against four pathogenic bacteria strains using the resazurin-based broth microdilution method, and the MIC values of each boron complex were determined Based on the overall results, the N, N-Diethyl-p-phenylenediamine group containing chiral boron complex (LB2) showed the highest activity against all bacterial strains, with the lowest MIC value of 4μg/mL which is nearly in the range of values for com. antibacterial drugs. The experimental process involved the reaction of N-(3-Aminopropyl)-imidazole(cas: 5036-48-6).Application In Synthesis of N-(3-Aminopropyl)-imidazole
The Article related to preparation boron chiral amine phenolate complex, cyclic voltammetry boron chiral amine phenolate complex, antimicrobial activity boron chiral amine phenolate complex, Inorganic Chemicals and Reactions: Coordination Compounds and other aspects.Application In Synthesis of N-(3-Aminopropyl)-imidazole
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem