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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
State
State
At room temperature, 3-phenyl-5-(1-piperidin-1-ylethyl)isoxazole chloride is typically in a solid state.
Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
298.81g/mol
Molar mass
298.8100g/mol
Density
1.0743g/cm3
Appearence
The compound is typically seen as a solid crystalline powder. It may appear white or slightly off-white depending on the purity and specific conditions under which it was produced.
Comment on solubility

Solubility of 3-phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole; chloride

The solubility of 3-phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole; chloride can be influenced by various factors. Notably, this compound contains both an isoxazole ring and a piperidinium moiety, which play significant roles in its solubility properties:

  • Polarity: The presence of the charged piperidinium group contributes to the molecule's overall polarity, enhancing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The potential for hydrogen bonding between the ionic groups and water molecules can further facilitate solubility.
  • Organic Solvents: In addition to its solubility in polar solvents, this compound may also exhibit some degree of solubility in organic solvents due to the hydrophobic character of the phenyl group.

In conclusion, while 3-phenyl-5-(1-piperidin-1-ium-1-ylethyl)isoxazole; chloride may dissolve readily in aqueous solutions due to its ionic nature, it is also important to consider the solvent environment, as solubility can vary with different solvents.

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.

Synonyms
3-Phenyl-5-(1-piperidinoethyl)isoxazole hydrochloride
14716-61-1
ISOXAZOLE, 3-PHENYL-5-(1-PIPERIDINOETHYL)-, HYDROCHLORIDE