Application of 1122-10-7, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 1122-10-7, Name is 3,4-Dibromo-1H-pyrrole-2,5-dione,introducing its new discovery.
Synthesis and biological evaluation of 4,4-dimethyl-5,5-di(1- methylethyl)-2,3,4,5-tetrahydro-1H-dipyrrolo[3,4-d:2,1-f] [1,2]azasiline-1,3- dione and other pyrrolediones as new antibacterial active agents
The UV-light induced photosubstitution of 3,4-dibromo-2,5-dihydro-1H- 2,5-pyrroledione (2) [1] with pyrrole derivatives leads to 3-mono- and 3,4- disubstituted pyrrolediones depending on the starting material. These pyrrole homologues of arcyriarubin A (1) are further processed by nucleophilic substitution of the remaining bromine substituent with pyrrolidine. Cleavage of the protecting group affords the free pyrrole substituents. By UV-light irradiation the azasiline, system (6) is accessible, and its structure was established by X-ray methods. The in vitro antibacterial activity of the pyrrolediones was evaluated, and a strong activity of the compounds 4, 7, 8 and 12 against the methicillin- and ciprofloxacin-resistant bacterium Staphylococcus aureus 134/94 was established.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1122-10-7, and how the biochemistry of the body works.Application of 1122-10-7
Reference£º
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem