Cas no 16015-70-6 (1-(3-Methoxyphenyl)piperazine hydrochloride)

1-(3-Methoxyphenyl)piperazine hydrochloride is a chemical compound commonly used as an intermediate in pharmaceutical and biochemical research. Its structure features a piperazine ring substituted with a 3-methoxyphenyl group, conferring reactivity suitable for further derivatization. The hydrochloride salt form enhances stability and solubility, facilitating handling in synthetic applications. This compound is particularly valuable in medicinal chemistry for the development of serotonin receptor ligands and other CNS-active molecules. Its well-defined purity and consistent performance make it a reliable choice for exploratory synthesis and pharmacological studies. Proper storage under controlled conditions ensures long-term usability.
1-(3-Methoxyphenyl)piperazine hydrochloride structure
16015-70-6 structure
Product Name:1-(3-Methoxyphenyl)piperazine hydrochloride
CAS No:16015-70-6
MF:C11H17ClN2O
MW:228.718481779099
CID:844869
PubChem ID:12645572
Update Time:2025-06-08

1-(3-Methoxyphenyl)piperazine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-(3-Methoxyphenyl)piperazine hydrochloride
    • 4-(3-methoxyphenyl) piperazine hydrochloride
    • UI3G4CVQ3Z
    • 3-Meopp HCl
    • N-(3-Methoxyphenyl)piperazine hydrochloride
    • QOQLPYRYJCBRNU-UHFFFAOYSA-N
    • NSC66266
    • 68M769
    • Piperazine, 1-(3-methoxyphenyl)-, monohydrochloride
    • Piperazine, 1-(m-methoxyphenyl)-, monohydrochloride
    • Piperazine, 1-(3-methoxyphenyl)-, hydrochloride (1:1)
    • Piperazine, 1-(3-methoxyphenyl)-, hydrochloride
    • SR-01000641477-1
    • UNII-UI3G4CVQ3Z
    • DB-190416
    • NSC-66266
    • Q27291086
    • CS-B1530
    • AKOS025149812
    • 1-(3-methoxyphenyl)piperazine;hydrochloride
    • AS-75574
    • C13174
    • UYZISVLMMYHXMS-UHFFFAOYSA-N
    • 16015-70-6
    • 1-(3-Methoxyphenyl)piperazine HCl
    • SCHEMBL1706127
    • Inchi: 1S/C11H16N2O.ClH/c1-14-11-4-2-3-10(9-11)13-7-5-12-6-8-13;/h2-4,9,12H,5-8H2,1H3;1H
    • InChI Key: QOQLPYRYJCBRNU-UHFFFAOYSA-N
    • SMILES: Cl.O(C)C1=CC=CC(=C1)N1CCNCC1

Computed Properties

  • Exact Mass: 228.1029409g/mol
  • Monoisotopic Mass: 228.1029409g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 2
  • Complexity: 169
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 24.5

1-(3-Methoxyphenyl)piperazine hydrochloride Pricemore >>

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Additional information on 1-(3-Methoxyphenyl)piperazine hydrochloride

1-(3-Methoxyphenyl)Piperazine Hydrochloride: A Comprehensive Overview

1-(3-Methoxyphenyl)piperazine hydrochloride (CAS No. 16015-70-6) is a versatile compound with significant applications in the fields of pharmaceuticals, neuroscience, and chemical research. This compound, also known as MOPP, is a derivative of piperazine and features a methoxyphenyl group, which imparts unique pharmacological properties. In this detailed overview, we will explore the chemical structure, synthesis, pharmacological effects, and potential therapeutic applications of 1-(3-Methoxyphenyl)piperazine hydrochloride.

Chemical Structure and Synthesis:

The molecular formula of 1-(3-Methoxyphenyl)piperazine hydrochloride is C12H17N2O·HCl, with a molecular weight of approximately 239.73 g/mol. The compound consists of a piperazine ring attached to a 3-methoxyphenyl group. The methoxy group at the para position of the phenyl ring enhances the lipophilicity and stability of the molecule, contributing to its biological activity.

The synthesis of 1-(3-Methoxyphenyl)piperazine hydrochloride can be achieved through various methods. One common approach involves the reaction of 3-methoxybenzaldehyde with piperazine in the presence of an acid catalyst, followed by hydrochloric acid treatment to form the hydrochloride salt. This method is widely used due to its simplicity and high yield.

Pharmacological Properties:

1-(3-Methoxyphenyl)piperazine hydrochloride exhibits a range of pharmacological effects, primarily due to its interaction with serotonin receptors. It acts as a serotonin receptor agonist, particularly at the 5-HT1A, 5-HT2A, and 5-HT2C receptors. This property makes it a valuable tool in studying serotonin-mediated pathways and their role in various neurological disorders.

In addition to its serotonergic activity, MOPP also interacts with dopamine receptors, particularly D2. This dual action on serotonin and dopamine receptors suggests potential applications in treating conditions such as depression, anxiety, and schizophrenia. Recent studies have shown that MOPP-like compounds can modulate neurotransmitter systems in ways that may offer therapeutic benefits without the side effects associated with traditional antidepressants and antipsychotics.

Clinical Applications:

The potential therapeutic applications of 1-(3-Methoxyphenyl)piperazine hydrochloride are an active area of research. Preclinical studies have demonstrated its efficacy in animal models of depression and anxiety. For instance, administration of MOPP has been shown to reduce depressive-like behaviors in rodents through its modulation of serotonin and dopamine systems.

In the context of schizophrenia, MOPP-like compounds have been investigated for their ability to improve cognitive function and reduce positive symptoms. Clinical trials are currently underway to evaluate the safety and efficacy of these compounds in human patients. Preliminary results are promising, suggesting that MOPP-based therapies may offer a novel approach to treating psychiatric disorders.

Toxicology and Safety: strong>

The safety profile of 1-(3-Methoxyphenyl)piperazine hydrochloride strong> is an important consideration for its potential therapeutic use. Preclinical toxicology studies have generally shown that it is well-tolerated at therapeutic doses. However, like many psychoactive compounds, it can produce side effects such as dizziness, nausea, and changes in blood pressure at higher doses.

To ensure safe use in clinical settings, ongoing research is focused on optimizing dosing regimens and identifying patient populations most likely to benefit from treatment with < strong>MOPP strong>. Additionally, efforts are being made to develop analogs with improved safety profiles while retaining the desired pharmacological properties. p > < p >< strong >Conclusion: strong > p > < p >< strong >1-(3-Methoxyphenyl)piperazine hydrochloride strong > (CAS No. 16015-70-6) is a promising compound with diverse applications in pharmaceutical research and development. Its unique chemical structure and pharmacological properties make it a valuable tool for studying neurotransmitter systems and developing new therapies for psychiatric disorders. As research continues to advance our understanding of this compound, it holds significant potential for improving patient outcomes in various clinical settings. p > article > response >

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