Synthesis and biological properties of heterylalkylamides of 4-substituted piperazin-1-ylacetic acids was written by Vartanyan, S. O.;Avakyan, A. S.;Sargsyan, A. B.;Arutyunyan, S. A.;Gukasyan, T. G.;Tsatinyan, A. S.;Noravyan, O. S.;Markaryan, I. A.. And the article was included in Hayastani Kimiakan Handes in 2010.Related Products of 21867-64-1 This article mentions the following:
Reaction of chloroacetyl chloride with 1,4-benzodioxan-2-yl or isochroman-1-yl-containing aliphatic amines gave the corresponding N-substituted chloroacetamides. Subsequent treatment of the latter with monosubstituted piperazines afforded the corresponding substituted piperazineacetamides. The biol. properties of these compounds have been investigated. In the experiment, the researchers used many compounds, for example, 1-Propylpiperazine (cas: 21867-64-1Related Products of 21867-64-1).
1-Propylpiperazine (cas: 21867-64-1) belongs to piperazine derivatives. Piperazine was first introduced as an anthelmintic in 1953. Piperazine compounds mediate their anthelmintic action by generally paralyzing parasites, allowing the host body to easily remove or expel the invading organism. Outside the body, piperazine has a remarkable power to dissolve uric acid and producing a soluble urate, but in clinical experience it has not proved equally successful. Related Products of 21867-64-1
Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics