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Licarbazepine

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Identification
Molecular formula
C15H27ClNO2
CAS number
29331-92-8
IUPAC name
2-(6-chloro-1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium;chloride
State
State

At room temperature, licarbazepine is typically a solid.

Melting point (Celsius)
97.00
Melting point (Kelvin)
370.15
Boiling point (Celsius)
239.00
Boiling point (Kelvin)
512.15
General information
Molecular weight
299.22g/mol
Molar mass
299.2180g/mol
Density
1.2030g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-(6-chloro-1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium;chloride

The solubility of 2-(6-chloro-1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium;chloride is an interesting topic due to its unique chemical structure. Understanding the solubility characteristics of this compound can provide valuable insights for its potential applications.

Key Points on Solubility

  • Polarity: The presence of the piperidin-1-ium moiety indicates a cationic nature, which typically enhances solubility in polar solvents.
  • Solvent Effects: This compound is likely to be more soluble in:
    • Water, due to its ionic nature.
    • Alcohols, which can stabilize ionic species.
    • Other polar organic solvents.
  • Ionic Interactions: The chloride ion may further enhance solubility through electrostatic interactions with polar solvents.

Because of its structural features, we can generally expect that 2-(6-chloro-1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium;chloride will exhibit good solubility in aqueous solutions, making it relevant for various chemical and pharmaceutical applications.

Interesting facts

Interesting Facts about 2-(6-chloro-1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium;chloride

This compound is a fascinating example of a polycyclic structure, showcasing the intricate relationships between its various fused rings. Compounds like this one often exhibit unique and potent biological activity, making them of great interest in medicinal chemistry.

Key Highlights:

  • Complex Structure: The name indicates a spirocyclic structure which can lead to interesting stereochemical properties. Spiro compounds often have distinctive three-dimensional conformations.
  • Biological Relevance: Compounds featuring piperidinium moieties have been explored for their potential as pharmaceuticals, particularly in the realms of antipsychotic and anti-inflammatory agents.
  • Chlorine Substitution: The presence of chlorine within the structure can significantly influence the compound’s reactivity and lipophilicity, enhancing its biological activity.
  • Dioxaspiro Framework: The dioxaspiro segment of the molecule suggests the possibility of interesting electronic characteristics which might play a role in interaction with biological targets.

Moreover, the study of such compounds extends beyond academic interest; they may serve as valuable templates for drug design due to their potential ability to interact with various biological systems. Understanding these compounds can open doors to developing novel therapeutic agents that improve patient outcomes.

As researchers continue to explore the vast chemical landscape, compounds like this one remind us of the importance of structure in determining function, and highlight the continually evolving nature of organic and medicinal chemistry.

Synonyms
beta-6-Chloro-2-(2-piperidyl)-1,4-dioxaspiro(4.5)decane hydrochloride
1,4-DIOXASPIRO(4.5)DECANE, 6-CHLORO-2-(2-PIPERIDYL)-, HYDROCHLORIDE, beta-
7538-23-0