3-phenyl-5-(1-piperidin-1-ylethyl)isoxazole chloride

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Identification

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
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.

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