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
Molecular Weight
323.23g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1350g/cm3
Synonyms
20229-01-0
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.

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