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Eperisone hydrochloride

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Identification
Molecular formula
C20H27ClN2O2Cl
CAS number
56839-43-1
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(2-chlorophenyl)carbamate;chloride
State
State

At room temperature, eperisone hydrochloride is usually a solid. It is often provided in crystalline form for pharmaceutical applications.

Melting point (Celsius)
167.00
Melting point (Kelvin)
440.15
Boiling point (Celsius)
301.40
Boiling point (Kelvin)
574.55
General information
Molecular weight
323.23g/mol
Molar mass
323.2300g/mol
Density
1.1350g/cm3
Appearence

Eperisone hydrochloride is typically found as a white or almost white crystalline powder. It is known for being odorless or having a faint characteristic odor, and it is soluble in water.

Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(2-chlorophenyl)carbamate; chloride

The solubility of 2-piperidin-1-ium-1-ylethyl N-(2-chlorophenyl)carbamate; chloride can be quite intriguing due to its unique chemical structure. This compound, containing a piperidinium ion, suggests certain characteristics about its solubility in various solvents.

Characteristics Influencing Solubility:

  • Polarity: The presence of a charged piperidinium group typically enhances the solubility of the compound in polar solvents, such as water.
  • Hydrophobic Effects: The chlorophenyl group may introduce hydrophobic features, potentially reducing solubility in highly polar solvents.
  • Hydrogen Bonding: The carbamate moiety can engage in hydrogen bonding, which might facilitate solubility in solvents capable of hydrogen bonding.

Overall, one might observe the compound to be:

  • Soluble in water: Due to its ionic characteristics.
  • Less soluble in non-polar solvents: Due to the hydrophobic nature of the chlorophenyl segment.

As a result, the solubility profile of this compound can emphasize its versatility in various chemical environments, lending it valuable properties for applications in diverse fields.

Interesting facts

Interesting Facts about 2-Piperidin-1-ium-1-ylethyl N-(2-chlorophenyl)carbamate; Chloride

2-Piperidin-1-ium-1-ylethyl N-(2-chlorophenyl)carbamate; chloride is a fascinating compound that showcases the interplay of organic chemistry and pharmacology. Here are some standout facts:

  • Quaternary Ammonium Compound: This compound is a quaternary ammonium salt, meaning it has a positively charged nitrogen atom that is bonded to four organic groups. This property plays a crucial role in its behavior and interaction within biological systems.
  • Pharmacological Relevance: The carbamate moiety in the compound suggests potential enzyme inhibition, which can be crucial in medicinal chemistry and drug design. Compounds with similar structures are often studied for their effects on the nervous system.
  • Chlorine Substitution: The presence of the 2-chlorophenyl group may influence the compound's lipophilicity and overall pharmacokinetic profile. Chlorine atoms can enhance biological activity and modify interactions with receptors.
  • Potential Applications: As with many derivatives of piperidine, this compound may find applications in developing novel therapeutic agents, especially for neurodegenerative diseases or as insecticides in agriculture.
  • Complex Synthesis: The synthesis of such compounds typically involves multiple reaction steps, demonstrating the intricacies of creating specialized organic molecules. Understanding these pathways can be critical for advancing compound optimization in drug design.

In summary, 2-piperidin-1-ium-1-ylethyl N-(2-chlorophenyl)carbamate; chloride is a compound that combines structural complexity and potential biological significance, making it a subject of interest for scientists exploring new areas in pharmacology and organic synthesis.

Synonyms
20229-01-0
2-Piperidinoethyl 2-chlorcarbanilate hydrochloride
K 492
CARBANILIC ACID, 2-CHLORO-, 2-PIPERIDINOETHYL ESTER, MONOHYDROCHLORIDE