Panova, Valeria A. et al. published their research in Bioorganic Chemistry in 2021 | CAS: 16588-16-2

Ethyl 4-chloro-3-nitrobenzoate (cas: 16588-16-2) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Synthetic Route of C9H8ClNO4

Investigation of pyrazolo[1,5-a]quinoxalin-4-ones as novel monoamine oxidase inhibitors was written by Panova, Valeria A.;Filimonov, Sergey I.;Chirkova, Zhanna V.;Kabanova, Mariya V.;Shetnev, Anton A.;Korsakov, Mikhail K.;Petzer, Anel;Petzer, Jacobus P.;Suponitsky, Kyrill Yu. And the article was included in Bioorganic Chemistry in 2021.Synthetic Route of C9H8ClNO4 This article mentions the following:

The present study synthesized a series of pyrazolo[1,5-a]quinoxalin-4-one derivatives I [R1 = H, Me, MeO, Cl; R2 = NH2, CN, Me(CO)NH, Et(O)OC; R3 = H, HO, acetyloxidanyl, (2-ethoxy-2-oxoethyl)oxidanyl] and evaluated them as potential inhibitors of human MAO-A and MAO-B. The results showed that derivatives I [R1 = H, MeO, Cl; R2 = NH2, Me(CO)NH; R3 = H, HO, acetyloxidanyl] inhibited MAO-A, and derivatives I [R1 = Me, MeO; R2 = CN; R3 = H, (2-ethoxy-2-oxoethyl)oxidanyl] inhibited MAO-B with IC50 values in the submicromolar range (<1μM). The most potent MAO-A inhibitor, I [R1 = Cl, R2 = MeC(O)NH, R3 = acetyloxidanyl], exhibited an IC50 value of 0.028μM and displayed 50-fold selectivity for MAO-A over MAO-B. The most potent MAO-B inhibitor, I [R1 = Me, R2 = CN, R3 = H], exhibited an IC50 value of 0.617μM and displayed 8-fold selectivity for MAO-B. This was the first reported MAO inhibition by pyrazolo[1,5-a]quinoxalin-4-one derivatives, I and this study concluded that these compounds I were suitable lead for the future development of MAO inhibitors, particularly of the MAO-A isoform. In the experiment, the researchers used many compounds, for example, Ethyl 4-chloro-3-nitrobenzoate (cas: 16588-16-2Synthetic Route of C9H8ClNO4).

Ethyl 4-chloro-3-nitrobenzoate (cas: 16588-16-2) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Synthetic Route of C9H8ClNO4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics