Jumal, Juliana et al. published their research in AIP Conference Proceedings in 2018 |CAS: 34413-35-9

5,6,7,8-Tetrahydroquinoxaline(cas:34413-35-9) belongs to quinoxaline. The antitumoral properties of quinoxaline compounds have been of interest. Recently, quinoxaline and its analogs have been investigated as the catalyst’s ligands. Related Products of 34413-35-9

On June 5, 2018, Jumal, Juliana; Ayomide, Adetunji Fridaos published an article.Related Products of 34413-35-9 The title of the article was Synthesis and radical scavenging activity of 6-hydroxyl-4-methylcoumarin and its derivatives. And the article contained the following:

Four compounds of coumarin derivatives namely 6-hydroxyl-4-methylcoumarin (I), 6-hydroxyl-4-methyl-5-(p-nitrophenyl azocoumarin) (II), 6-hydroxyl-4-methyl-5,7-(bis-p-nitrophenyl azocoumarin) (III) and 6-hydroxyl-4-methyl-5,7-(bis-p-chlorophenyl azocoumarin) (IV) were successfully synthesized. These compounds were prepared by reacting hydroquinone with ethylacetoacetate and selected anilines which are chloro and nitro aniline. All synthesized compounds were characterized by CHN micro-elemental anal., 1H NMR (NMR) and Fourier Transform IR (FTIR) spectroscopic methods. The IR spectra of these compounds exhibited five important stretching vibrations: (-OH), (C=O), (C=C), (C-O) and (C-N) at 3441-3359 cm-1, 1604-1632 cm-1, 1581-1496 cm-1, 1331-1225 cm-1, 1251-1109 cm-1, resp. 1H NMR spectra of these compounds show the presence of proton aromatic, proton Me and proton pyrone ring with the chem. shift at δH 7.00-8.70 ppm, δH 2.20-2.50 ppm and δH 6.10-6.90 ppm, resp. CHN anal. results of all compounds are in good agreement with the calculated values. All the synthesized compounds were evaluated for their antioxidant activity using DPPH method and ascorbic acid used as the standard UV-Vis spectroscopic technique was used to investigate the absorbance of these compounds Compound (II) shows high antioxidant activities compared to compound (I), (III) and (IV) which show moderate to low activities. The experimental process involved the reaction of 5,6,7,8-Tetrahydroquinoxaline(cas: 34413-35-9).Related Products of 34413-35-9

5,6,7,8-Tetrahydroquinoxaline(cas:34413-35-9) belongs to quinoxaline. The antitumoral properties of quinoxaline compounds have been of interest. Recently, quinoxaline and its analogs have been investigated as the catalyst’s ligands. Related Products of 34413-35-9

Referemce:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider