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Isorocaine

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Identification
Molecular formula
C16H19ClN2O
CAS number
105536-99-8
IUPAC name
3-(4-chlorophenyl)-5-[2-(1-piperidyl)ethyl]isoxazole
State
State

At room temperature, Isorocaine is in a solid state.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
415.50
Boiling point (Kelvin)
688.65
General information
Molecular weight
290.79g/mol
Molar mass
290.7880g/mol
Density
1.2430g/cm3
Appearence

Isorocaine is typically a white to off-white powder.

Comment on solubility

Solubility Overview of 3-(4-chlorophenyl)-5-[2-(1-piperidyl)ethyl]isoxazole

The solubility of 3-(4-chlorophenyl)-5-[2-(1-piperidyl)ethyl]isoxazole can greatly influence its bioavailability and pharmacological properties. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely to be soluble in organics like dimethyl sulfoxide (DMSO) and ethanol, which are common solvents for many pharmaceuticals.
  • Water Solubility: Generally, isoxazole derivatives may display limited water solubility due to their non-polar characteristics. Thus, aqueous solubility may be low.
  • Influence of Structure: The presence of the 4-chlorophenyl and piperidyl groups can affect intermolecular interactions, potentially enhancing lipophilicity and altering solubility profiles.
  • pH Dependence: The solubility might also be influenced by pH changes, which can affect ionization states and hydrophilicity.

In summary, while the solubility characteristics can vary, it is essential to consider both the solvent environment and structural features of 3-(4-chlorophenyl)-5-[2-(1-piperidyl)ethyl]isoxazole to predict its behavior in different formulations. Understanding these solubility dynamics is crucial for optimizing its therapeutic applications.

Interesting facts

Interesting Facts About 3-(4-chlorophenyl)-5-[2-(1-piperidyl)ethyl]isoxazole

This compound, known for its unique structure and potential biological activity, holds significant interest in the fields of medicinal chemistry and pharmacology.

Key Features

  • Isoxazole Ring: The core structure features an isoxazole ring, a five-membered heterocyclic compound containing two different types of atoms (nitrogen and oxygen). Isoxazoles are noted for their diverse biological properties.
  • Chlorophenyl Substitution: The presence of a 4-chlorophenyl group is notable as halogen substitutions can influence the compound's reactivity and interaction with biological targets.
  • Piperidine Moiety: This compound also includes a piperidine group, a six-membered nitrogen-containing ring. The piperidine substituent often enhances pharmacological activity, making it common in drug design.

Applications and Potential

The unique combination of a piperidine and isoxazole moiety suggests that this compound may exhibit interesting pharmacological effects. Many similar compounds have been researched for:

  • Antidepressant effects
  • Antineoplastic properties
  • Neuroprotective activities

Researchers are particularly intrigued by the compound's potential to interact with neurotransmitter systems, which could pave the way for novel treatments for central nervous system disorders. As one researcher eloquently stated, "The future of pharmacotherapy lies in understanding and utilizing the complexities of molecular interactions."

Conclusion

Overall, 3-(4-chlorophenyl)-5-[2-(1-piperidyl)ethyl]isoxazole stands out as an exciting compound for scientists exploring new therapeutic avenues. Its structural characteristics and potential biological activities warrant further investigation, and it is a prime candidate for future studies in drug development.