Skip to main content

Flupirtine

ADVERTISEMENT
Identification
Molecular formula
C15H21ClFN2O
CAS number
56995-20-1
IUPAC name
2-[2-(4-fluorobenzoyl)pyrrol-1-yl]ethyl-dimethyl-ammonium;chloride
State
State

At room temperature, Flupirtine appears as a solid compound, typically obtained as a powder. This physical form allows it to be handled and manufactured into various pharmaceutical formulations for medicinal use.

Melting point (Celsius)
113.00
Melting point (Kelvin)
386.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
338.84g/mol
Molar mass
338.8370g/mol
Density
1.3000g/cm3
Appearence

Flupirtine is usually found in the form of a crystalline powder. This compound is white to off-white in color and is odorless.

Comment on solubility

Solubility of 2-[2-(4-fluorobenzoyl)pyrrol-1-yl]ethyl-dimethyl-ammonium; chloride

The solubility of 2-[2-(4-fluorobenzoyl)pyrrol-1-yl]ethyl-dimethyl-ammonium; chloride is primarily influenced by its ionic nature due to the presence of the chloride ion. Here are some noteworthy points regarding its solubility:

  • Ionic Compounds: As an ionic compound, the solubility in water is expected to be relatively high because ions often dissolve well in polar solvents.
  • Polar Functional Groups: The solubility may also be enhanced by the presence of polar groups which promote interactions with water molecules.
  • Environmental Conditions: Factors such as temperature, pH, and the presence of other ions in solution can significantly affect solubility.

It's worth noting that while the chloride ion typically aids in solubility, structural factors of the organic component may also play a role in solubility behavior. As a result, actual solubility can vary and may need experimental verification in different media.

In summary, expect soluble behavior due to:

  1. Ion-Dipole Interactions: The ionic nature facilitates interactions with water.
  2. Hydrogen Bonding Potential: Any polar groups present can further enhance solvation.
  3. Temperature Dependence: Solubility might increase with a rise in temperature.

These characteristics highlight the interplay between chemical structure and solubility. Understanding these aspects can be essential for applications in various fields, such as pharmaceuticals.

Interesting facts

Interesting Facts about 2-[2-(4-fluorobenzoyl)pyrrol-1-yl]ethyl-dimethyl-ammonium Chloride

This compound, known for its intricate chemical structure, plays a significant role in various fields of chemistry and biology. Here are several intriguing aspects:

  • Biological Activity: The presence of the 4-fluorobenzoyl moiety suggests potential applications in medicinal chemistry, especially in the design of therapeutics targeting specific biological pathways.
  • Structure-Activity Relationship: The pyrrol ring within the compound adds to its structural complexity, allowing chemists to explore a wide range of derivatives that could affect its biological activity.
  • Quaternary Ammonium Compound: The presence of the dimethylammonium group indicates that this compound can behave as a surfactant or ionic liquid, which makes it interesting for applications in material science.
  • Potential Applications: Given its unique attributes, this compound could be a candidate for:
    • Antimicrobial agents
    • Pharmaceutical development
    • Industrial applications as a surfactant
  • Research Opportunities: The distinctive combination of the pyrrol and benzoyl functional groups opens a pathway for chemists to conduct further studies on:
    • Reactivity with various nucleophiles
    • Syntheses of new derivatives for enhanced properties

In summary, 2-[2-(4-fluorobenzoyl)pyrrol-1-yl]ethyl-dimethyl-ammonium chloride serves as a fascinating study subject for scientists focused on understanding and leveraging its unique chemical properties for future applications.

Synonyms
1-(2-(Dimethylamino)ethyl)-2-(p-fluorobenzoyl)pyrrole monohydrochloride
14927-35-6
KETONE, 1-(2-(DIMETHYLAMINO)ETHYL)PYRROL-2-YL p-FLUOROPHENYL, HYDROCHLORIDE