Archives for Chemistry Experiments of 4-Amino-3-nitrobenzoic acid

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 1588-83-6 help many people in the next few years. Application In Synthesis of 4-Amino-3-nitrobenzoic acid.

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 1588-83-6, Name is 4-Amino-3-nitrobenzoic acid, formurla is C7H6N2O4. In a document, author is Ahmed, N. S., introducing its new discovery. Application In Synthesis of 4-Amino-3-nitrobenzoic acid.

Synthesis of 1,8-Naphthyridine Derivatives under Ultrasound Irradiation and Cytotoxic Activity against HepG2 Cell Lines

Novel pyrazole derivatives 3a,b, 5, 1,3,4-oxadiazole 6, 1,3,4-thiadiazole 8, and 1,2,4-triazole 9a-c incorporated into 1,8-naphthyridine have been synthesized using the versatile synthon 2-(2,7-dimethyl-1,8-naphthyridin-4-yloxy) acetohydrazide 1. An improvement in rates and yields was observed when the reactions were carried out under ultrasonic irradiation compared with the classical synthesis. The newly synthesized compounds were evaluated for HepG2 cell growth inhibition. The results obtained revealed that the tested compounds possess inhibitory effect on the growth of HepG2 liver cancer cells. The results were compared to doxorubicin (DOX) as a reference drug (IC50 : 0.04 M). Compounds 9b showed the highest inhibition activity against HepG2 cell line (IC50 : 0.048 M) among all tested compounds.

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 1588-83-6 help many people in the next few years. Application In Synthesis of 4-Amino-3-nitrobenzoic acid.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem