Machine Learning in Chemistry about 56621-48-8

In addition to the literature in the link below, there is a lot of literature about this compound(4-(Piperazin-1-yl)phenol)Name: 4-(Piperazin-1-yl)phenol, illustrating the importance and wide applicability of this compound(56621-48-8).

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 4-(Piperazin-1-yl)phenol( cas:56621-48-8 ) is researched.Name: 4-(Piperazin-1-yl)phenol.Andonova, Lily; Zheleva-Dimitrova, Dimitrina; Georgieva, Maya; Zlatkov, Alexander published the article 《Synthesis and antioxidant activity of some 1-aryl/aralkyl piperazine derivatives with xanthine moiety at N4》 about this compound( cas:56621-48-8 ) in Biotechnology & Biotechnological Equipment. Keywords: piperazine aryl aralkyl xanthine preparation antioxidant; 1-aryl/aralkyl piperazines; antioxidant activity; xanthine. Let’s learn more about this compound (cas:56621-48-8).

Six new aryl/aralkyl substituted piperazine derivatives, containing methylxanthine moiety I (R = Bn, 4-FC6H4, 4-HOC6H4, etc.) were synthesized. All compounds were in vitro screened for their activity as antioxidants using DPPH (2,2′-Diphenyl-1-picrylhydrazyl), ABTS (2,2′-azinobis-(3-ethylbenzothiazine-6-sulfonic acid)) and FRAP (ferric reducing/antioxidant power) methods. The antioxidant activity of the studied compounds against lipid peroxidation was also measured. The highest antioxidant activity was demonstrated by compound I (R = 4-HOC6H4). It is obvious that the presence of a hydroxyl group in the structure is essential for the antioxidant properties and should be taken into consideration in further design of structures with potential antioxidant properties.

In addition to the literature in the link below, there is a lot of literature about this compound(4-(Piperazin-1-yl)phenol)Name: 4-(Piperazin-1-yl)phenol, illustrating the importance and wide applicability of this compound(56621-48-8).

Reference:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem