89026-59-5 Usage
Description
4-(4-methoxyphenyl)piperazine-1-carboxamide is a chemical compound with a molecular formula of C12H16N2O2. It is a piperazine derivative featuring a methoxyphenyl group attached to the piperazine ring. 4-(4-methoxyphenyl)piperazine-1-carboxamide has garnered interest due to its potential applications in the treatment of neurological and psychiatric disorders, as well as for its antipsychotic and anti-inflammatory properties. Its ability to act as a serotonin receptor antagonist positions it as a promising candidate for further pharmacological and therapeutic research.
Uses
Used in Pharmaceutical Industry:
4-(4-methoxyphenyl)piperazine-1-carboxamide is utilized as a therapeutic agent for the treatment of neurological and psychiatric disorders. Its capacity to modulate the serotonin system in the brain makes it a valuable asset in managing conditions related to serotonin dysregulation.
Used in Research and Development:
In the field of scientific research, 4-(4-methoxyphenyl)piperazine-1-carboxamide serves as a key compound for studying the mechanisms of serotonin receptor antagonism. This research is crucial for developing a deeper understanding of the serotonin system's role in various mental health conditions and for identifying potential therapeutic targets.
Used in Drug Discovery:
4-(4-methoxyphenyl)piperazine-1-carboxamide is employed as a lead compound in drug discovery efforts. Its unique chemical structure and biological activity make it a promising starting point for the design and development of new medications aimed at treating a range of neurological and psychiatric disorders.
Used in Anti-inflammatory Applications:
Given its potential anti-inflammatory properties, 4-(4-methoxyphenyl)piperazine-1-carboxamide is used as an agent for exploring treatments that target inflammation-related aspects of neurological and psychiatric conditions. This can lead to the development of medications that not only address the primary symptoms but also the underlying inflammatory processes.
Check Digit Verification of cas no
The CAS Registry Mumber 89026-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,2 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89026-59:
(7*8)+(6*9)+(5*0)+(4*2)+(3*6)+(2*5)+(1*9)=155
155 % 10 = 5
So 89026-59-5 is a valid CAS Registry Number.
89026-59-5Relevant articles and documents
The Dehydration of Ureas by Two-Phase Dichlorocarbene Reaction, a Synthetic Access to Substituted Cyanamides
Schroth, W.,Kluge, H.,Frach, R.,Hodek, W.,Schaedler, H. D.
, p. 787 - 802 (2007/10/02)
A wide variety of N,N-disubstituted ureas are dehydrated in the CHCl3/NaOH catalytic two-phase system under mild conditions.The sequence of urea-transamidation and dehydration thus offers a profitable approach to aprotic cyanamides.Among various tested PT-catalysts tertiary amines prove to be the most efficient and favourable ones.Tertiary amines may also be used advantageously in the transformation of carboxylic amides and thioamides to the corresponding nitriles.The application of the same technique is less suitable in the case of N-mono-substituted ureas, N,N'-disubstituted ureas as well as N(dialkylaminomethylidene)ureas, because consequent reactions of the primarily formed cyanamides predominate.Problems concerning the dehydration mechanism are elucidated in terms of HMO-perturbation theory.
