1-{[5-(2-Chlorophenyl)thiophen-2-yl]methyl}piperazine
CAS No.:
1000932-50-2
M. Wt:
292.83
M. Fa:
C15H17ClN2S
InChI Key:
UHAWGGVIXJROMY-UHFFFAOYSA-N
Names and Identifiers of 1000932-50-2
CAS Number |
1000932-50-2 |
|---|---|
IUPAC Name |
1-[[5-(2-chlorophenyl)thiophen-2-yl]methyl]piperazine |
InChI |
InChI=1S/C15H17ClN2S/c16-14-4-2-1-3-13(14)15-6-5-12(19-15)11-18-9-7-17-8-10-18/h1-6,17H,7-11H2 |
InChIKey |
UHAWGGVIXJROMY-UHFFFAOYSA-N |
Canonical SMILES |
C1CN(CCN1)CC2=CC=C(S2)C3=CC=CC=C3Cl |
Physical and chemical properties of 1000932-50-2
Molecular Formula |
C15H17ClN2S |
|---|---|
Molecular Weight |
292.83 |
Applications of 1000932-50-2
1-{[5-(2-Chlorophenyl)thiophen-2-yl]methyl}piperazine has potential applications in various fields:
- Medicinal Chemistry: As a lead compound for developing new antidepressants or anticancer agents.
- Material Science: Due to its unique electronic properties, it may find use in organic electronics or as a precursor for functional materials.
- Pharmaceutical Research: Its activity profile makes it suitable for further exploration in drug development programs targeting neurological disorders.
Interaction Studies of 1000932-50-2
Interaction studies are crucial for understanding how 1-{[5-(2-Chlorophenyl)thiophen-2-yl]methyl}piperazine interacts with biological targets:
- Receptor Binding Assays: These studies evaluate the affinity of the compound for various receptors, such as serotonin or dopamine receptors, providing insights into its potential therapeutic effects.
- Enzyme Inhibition Studies: Investigating whether the compound can inhibit specific enzymes involved in disease pathways can reveal its mechanism of action and therapeutic potential.
Biological Activity of 1000932-50-2
Research indicates that compounds containing piperazine and thiophene moieties often exhibit significant biological activities, including:
- Antidepressant Effects: Some studies suggest that piperazine derivatives can act as serotonin receptor modulators, potentially influencing mood and anxiety.
- Antitumor Activity: Compounds with similar structures have shown promise in inhibiting cancer cell proliferation through various mechanisms, including apoptosis induction.
- Antimicrobial Properties: The presence of heteroatoms in the thiophene ring may enhance antimicrobial activity against certain pathogens.