Zhang, Yang et al. published their research in Chemical Engineering Research and Design in 2022 | CAS: 70458-96-7

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine is a fairly basic compound and is an amine solvent. Two common salts in the form of which piperazine is usually prepared for pharmaceutical or veterinary purposes are the citrate, 3C4H10N2.2C6H8O7 (i.e. containing 3 molecules of piperazine to 2 molecules of citric acid), and the adipate, C4H10N2.C6H10O4 (containing 1 molecule each of piperazine and adipic acid).Synthetic Route of C16H18FN3O3

A novel amorphous porous biochar for adsorption of antibiotics: Adsorption mechanism analysis via experiment coupled with theoretical calculations was written by Zhang, Yang;Cheng, Long;Ji, Yuanhui. And the article was included in Chemical Engineering Research and Design in 2022.Synthetic Route of C16H18FN3O3 The following contents are mentioned in the article:

High-performance activated carbons are crucial for adsorbing antibiotics in water environment. In this work, amorphous porous biochars (APBCs) with high sp. surface area (935 m2·g-1) were achieved by using sesame straw. Compared with the conventional biochars precursor, sesame straw with the advantages of rich resources and low price is more economical and environmentally friendly. Moreover, KOH and Ca(OH)2 were selected as co-activators, which characterization results revealed that co-activators significantly increased the coarseness of activated carbon surface and enlarged pore structure. In addition, the adsorption mechanism of norfloxacin (NOR), ciprofloxacin (CIP) and enrofloxacin (ENR) on APBCs were further investigated by experiments and d. functional theory (DFT) calculations The results discovered that pseudo second-order kinetics and Sips model followed the adsorption experiment data, implying that the adsorption process was heterogeneous and multilayer. And the interactions between APBCs and antibiotics were electrostatic interaction, hydrogen bond and π-π interaction, which were conducive to chem. adsorption. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Synthetic Route of C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine is a fairly basic compound and is an amine solvent. Two common salts in the form of which piperazine is usually prepared for pharmaceutical or veterinary purposes are the citrate, 3C4H10N2.2C6H8O7 (i.e. containing 3 molecules of piperazine to 2 molecules of citric acid), and the adipate, C4H10N2.C6H10O4 (containing 1 molecule each of piperazine and adipic acid).Synthetic Route of C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics