Interesting facts
Interesting Facts about 1-(1-Naphthyl)piperazine
1-(1-Naphthyl)piperazine, often abbreviated as NPP, is a fascinating compound that has gained considerable attention within the fields of chemistry and neuroscience. Here are some intriguing aspects of this compound:
- Structure and Function: The compound features a piperazine ring, which contributes to its psychopharmacological properties, along with a naphthyl group that enhances its ability to interact with various receptors in the brain.
- Research Applications: It is frequently utilized in scientific research as a tool to study neurotransmitter systems, particularly those involving serotonin and dopamine. This makes it a valuable compound in the development of new medications for mental health disorders.
- Potential in Pharmacology: NPP has shown promising results in various studies regarding its potential as an antidepressant and anxiolytic agent. Its unique structural properties allow it to bind effectively to serotonin receptors, which are crucial for mood regulation.
- Derivative of Piperazine: As a derivative of piperazine, NPP shares the biological and chemical characteristics of piperazine compounds, often resulting in diverse pharmacological effects.
- Legacy in Literature: The significance of 1-(1-Naphthyl)piperazine extends beyond its practical applications. It has been mentioned in various scholarly articles, drawing interest from chemists and pharmacologists alike. One quote from a notable study states, "The exploration of naphthyl derivatives has opened new pathways for developing effective therapeutic agents."
In summary, 1-(1-Naphthyl)piperazine stands out for its diverse applications in research and potential therapeutic benefits. As scientists continue to explore its capabilities, NPP keeps illuminating new pathways in the quest for understanding mental health and drug development.
Synonyms
57536-86-4
1-(1-Naphthyl)piperazine
1-Naphthylpiperazine
1-(naphthalen-1-yl)piperazine
1-naphthalen-1-ylpiperazine
Piperazine, 1-(1-naphthalenyl)-
1-Naphthalen-1-yl-piperazine
MFCD00600021
N-(1-naphthyl)piperazine
CHEMBL277120
FJ7MR37A24
GTPL3
Lopac-S-003
1-alpha-Naphthylpiperazine
4-(1-naphthyl)piperazine
Biomol-NT_000100
N-(1- naphthyl)piperazine
N-(1-naphthyl) piperazine
N-(1-naphthyl)-piperazine
1-(naphth-1-yl)piperazine
4-(1-naphthyl) piperazine
UNII-FJ7MR37A24
Lopac0_001181
Oprea1_621306
1-(1-naphthalenyl)piperazine
SCHEMBL240244
BPBio1_001387
1-(naphthalene-1-yl)piperazine
DTXSID30973071
CHEBI:108599
VNICFCQJUVFULD-UHFFFAOYSA-N
4-Naphthalen-1-yl-piperazin-1-ium
AC8505
BDBM50007407
PDSP1_000930
PDSP2_000916
AKOS003591178
CCG-205255
FN65693
SDCCGSBI-0051148.P002
NCGC00015905-01
NCGC00015905-02
NCGC00015905-03
NCGC00015905-04
NCGC00162360-01
NCGC00162360-02
1-naphthalen-1-yl-piperazine, AldrichCPR
1-naphthalen-1-ylpiperazine hydrochloride
PD047820
SY265026
CS-0188376
AT-057/41429159
L001113
BRD-K05977380-001-01-7
Q15409372
Solubility of 1-(1-naphthyl)piperazine
1-(1-naphthyl)piperazine, with the chemical formula C14H16N2, exhibits some notable characteristics regarding its solubility.
Typically, the solubility of this compound in various solvents can be summarized as follows:
In summary, while 1-(1-naphthyl)piperazine is not particularly soluble in water, it finds better solubility in organic solvents, making it useful for applications in various organic chemistry contexts. Its solubility characteristics highlight the importance of selecting appropriate solvents when working with this compound.