3-phenyl-5-(1-piperidin-1-ylethyl)isoxazole chloride
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- Molecular formula
- C16H22ClN2O
- CAS Number
- .
- IUPAC Name
- 3-phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole;chloride
- Molecular Weight
- 298.81g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0743g/cm3
- Synonyms
- 3-Phenyl-5-(1-piperidinoethyl)isoxazole hydrochloride
Identification
Interesting facts
Interesting Facts about 3-Phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole; Chloride
The compound 3-phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole; chloride is a fascinating member of the isoxazole family, which is known for its diverse biological activities. Here are some intriguing highlights about this compound:
- Bioactivity: Isoxazole derivatives are often studied for their neuroactive properties. They may play crucial roles in drug development, particularly in treating conditions such as depression, anxiety, and other cognitive disorders.
- Functional Groups: The presence of the piperidine ring enhances the compound's pharmacological profile, providing opportunities for binding to various receptors in the nervous system.
- Design Versatility: This compound illustrates the creativity in organic synthesis, showcasing how chemists can manipulate substituents to explore new chemical behaviors and interactions.
- Research Applications: Due to its unique structure, researchers may investigate its potential as a scaffold for developing new therapeutics, especially in the field of central nervous system medicines.
- Chloride Ion Influence: The chloride anion can have implications for solubility and stability, which are crucial factors in biological systems and pharmacokinetics.
In conclusion, the study of compounds like 3-phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole; chloride opens up vast avenues for understanding neuronal signaling and developing new therapeutic agents.