Mechanism of monoreduction by variable valency metal salts in unsymmetrical heterocycle-containing dinitrobenzenes was written by Begunov, R. S.;Demidova, N. Yu.;Brodskii, I. I.;Orlov, V. Yu.. And the article was included in Izvestiya Vysshikh Uchebnykh Zavedenii, Khimiya i Khimicheskaya Tekhnologiya in 2004.SDS of cas: 188604-99-1 The following contents are mentioned in the article:
The behavior of nitrogroups in 1-substituted saturated heterocycle-containing 2,4-dinitrobenzenes under Sn(II) and Ti(III) monoredn. has been investigated. A model of the process explaining the mechanism of conversion has been suggested. This study involved multiple reactions and reactants, such as 2-(4-Methylpiperidin-1-yl)-5-nitroaniline (cas: 188604-99-1SDS of cas: 188604-99-1).
2-(4-Methylpiperidin-1-yl)-5-nitroaniline (cas: 188604-99-1) belongs to piperazine derivatives. The piperazine scaffold is often found in biologically active compounds in different therapeutic areas. These therapeutic areas include antifungals, antidepressants, antivirals, and serotonin receptor (5-HT) antagonists/agonists. Piperazines are very broad chemical group, covering a wide range of drugs from antidepressants to antihistamines. The connecting property of all these chemicals is the presence of a piperazine functional group.SDS of cas: 188604-99-1
Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics