Chemistry Heterocyclic Building Blocks Piperazines
Piperazine is a type of organic compound characterized by a six-membered ring that contains two nitrogen atoms located at opposite positions within the ring. It appears in the form of tiny deliquescent crystals with an alkaline nature and a salty flavor.
Piperazine dissolves readily in water and ethylene glycol but does not dissolve in diethyl ether. It exhibits weak basicity with two pKb values of 5.35 and 9.73 at 25 °C. A 10% aqueous solution of piperazine has a pH range of 10.8-11.8.
Although piperazine has an extraordinary ability to dissolve uric acid and create a soluble urate outside of the body, its effectiveness in clinical settings has not been as impressive.
Piperazine, which is also known as hexahydropyrazine, is an anthelmintic medication that is utilized to treat intestinal roundworm infections in both humans and domestic animals (including poultry). It is also effective against pinworm infections in humans.
In 1953, Piperazine was initially presented as an anthelmintic. Its anthelmintic effect typically involves the paralysis of parasites, which enables the host body to expel or remove the invading organism with ease.
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Phenyl piperazine-1-carboxylate hydrochloride
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(R)-Piperazin-2-ylmethanol dihydrochloride
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Furan-2-yl(piperazin-1-yl)methanone hydrochloride
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2-(1-Piperazinyl)pyrimidine Dihydrochloride
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Piperazin-1-yl(quinoxalin-6-yl)methanone hydrochloride
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(S)-Piperazin-2-ylmethanol dihydrochloride
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2-(tert-Butyl)piperazine dihydrochloride
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1-(5-Bromo-3-methylpyridin-2-yl)piperazine
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1-(3-(Trifluoromethyl)pyridin-2-yl)piperazine
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Piperazin-1-yl(tetrahydrofuran-2-yl)methanone hydrobromide