A new application about 2213-63-0

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 2213-63-0, help many people in the next few years.Recommanded Product: 2213-63-0

Recommanded Product: 2213-63-0, New research progress on 2213-63-0 in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a Article,once mentioned of 2213-63-0

Some heterocyclic systems namely cholest-5-en-7-thiazolo[4,5-b]quinoxaline-2-yl-hydrazone] were synthesized by the reaction of cholest-5-en-7-one-thiosemicarbazone with 2,3-dichloroquinoxaline at 80 C in high yield. The thiosemicarbazone derivatives were obtained by the condensation of the thiosemicarbazide with steroidal ketones. All the compounds have been characterized by means of elemental analyses, IR, 1H NMR and mass spectroscopic data. The in vitro antibacterial activity was evaluated by disk diffusion method and then the minimum inhibitory concentration (MIC) of compounds was determined against the culture of Escherichia coli. The results were compared with the standard drug chloramphenicol. The results showed that compounds 7 and 8 are better antibacterial agents as compared to chloramphenicol.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 2213-63-0, help many people in the next few years.Recommanded Product: 2213-63-0

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1400 | ChemSpider