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3-(3-piperidin-1-ylpropyl)-5-phenylisoxazolium chloride

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Identification
Molecular formula
C17H23ClN2O
CAS number
,620=4576
IUPAC name
3-phenyl-5-(3-piperidin-1-ium-1-ylpropyl)isoxazole;chloride
State
State
This compound is typically found as a solid at room temperature.
Melting point (Celsius)
198.00
Melting point (Kelvin)
471.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
307.82g/mol
Molar mass
307.8270g/mol
Density
1.2000g/cm3
Appearence

The compound is a crystalline powder that appears white to off-white in color. Depending on the grade and purity, coloration might slightly vary within this range.

Comment on solubility

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

The solubility of 3-phenyl-5-(3-piperidin-1-ium-1-ylpropyl)isoxazole;chloride can be quite notable, mainly due to its ionic nature and the presence of the piperidinium group. Here are some key points regarding its solubility characteristics:

  • Water Solubility: The chloride salt form suggests that it is likely to be soluble in water. Ionic compounds typically dissolve well in polar solvents, making water a favorable medium.
  • Influence of Temperature: Like many salts, its solubility may increase with temperature, allowing for more effective dissolution in heated water.
  • Solvent Compatibility: In addition to water, it may also show some degree of solubility in various organic solvents, particularly those with polar characteristics.
  • Ionic Species: The presence of the quaternary ammonium ion can enhance solubility by stabilizing the solute-solvent interactions.
  • pH Dependence: The solubility can also be pH-dependent, which is crucial for its behavior in biological systems and pharmaceutical applications.

In summary, the solubility profile of 3-phenyl-5-(3-piperidin-1-ium-1-ylpropyl)isoxazole;chloride suggests that it is favorable for applications requiring aqueous solutions, particularly owing to its ionic nature. As with many such compounds, experimental determination under varied conditions is recommended to fully understand its solubility attributes.

Interesting facts

Interesting Facts about 3-phenyl-5-(3-piperidin-1-ium-1-ylpropyl)isoxazole;chloride

The compound 3-phenyl-5-(3-piperidin-1-ium-1-ylpropyl)isoxazole;chloride belongs to a fascinating class of organic compounds known as isoxazoles. These compounds are characterized by their unique five-membered heterocyclic ring containing nitrogen and oxygen. Here are some intriguing aspects of this compound:

  • Chemical Structure: The structure features a phenyl group, which is aromatic, providing significant stability and chemical reactivity in various environments. The presence of a piperidinium moiety suggests potential pharmacological activity, making this compound noteworthy in medicinal chemistry.
  • Biological Importance: Compounds derived from isoxazoles, like this one, have shown promise in various biological applications, including anti-inflammatory and anti-cancer activities. They present a rich field for drug development.
  • Ionization: The phenyl group and the piperidin-1-ium group contribute to the compound's ionization characteristics, which can affect solubility and interaction with biological targets.
  • Applications: Due to its structural features, this compound might be explored as a potential lead in developing therapeutic agents targeting specific diseases or conditions, particularly those involving neurological pathways.

In summary, 3-phenyl-5-(3-piperidin-1-ium-1-ylpropyl)isoxazole;chloride showcases a rich tapestry of structural complexity and potential utility that fascinates chemists and pharmacologists alike. The study of such compounds allows for understanding mechanisms of action in biological systems, shedding light on new avenues for drug discovery.

Synonyms
3-Phenyl-5-(3-piperidinopropyl)isoxazole hydrochloride
1090-85-3
ISOXAZOLE, 3-PHENYL-5-(3-PIPERIDINOPROPYL)-, HYDROCHLORIDE