Loperamide hydrochloride

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Identification

Molecular formula
C29H31Cl2FNO2
CAS Number
34552-83-5
IUPAC Name
1-[4-(4-fluorophenyl)-4-oxo-butyl]-4-piperidin-1-ium-1-yl-piperidin-1-ium-4-carboxamide;dichloride
Molecular Weight
513.51g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4500g/cm3
Synonyms
Propitan
Interesting facts

Interesting Facts about 1-[4-(4-fluorophenyl)-4-oxo-butyl]-4-piperidin-1-ium-1-yl-piperidin-1-ium-4-carboxamide; Dichloride

This compound, known for its complex structure, showcases the fascinating intersection of organic chemistry and pharmacology. Here are some intriguing aspects:

  • Structural Complexity: The compound features multiple functional groups which can play significant roles in its biological activity. The presence of piperidine rings suggests potential neuroactive properties.
  • Fluorine Substitution: The incorporation of a fluorinated aromatic group (4-fluorophenyl) is notable as fluorine can enhance metabolic stability and lipophilicity. This often results in compounds that are more effective in pharmaceutical applications.
  • Potential Applications: Due to its structure, this compound could be investigated as a candidate for therapeutic applications, particularly in the treatment of neurological disorders or pain management.
  • Ionization Properties: As a piperidin-1-ium derivative, this compound may exhibit interesting ionization characteristics that can influence its pharmacokinetics and interaction with biological systems.
  • Research Significance: Compounds of this nature are often explored in medicinal chemistry for their potential as drug candidates, contributing to the understanding of structure-activity relationships (SAR).

In summary, 1-[4-(4-fluorophenyl)-4-oxo-butyl]-4-piperidin-1-ium-1-yl-piperidin-1-ium-4-carboxamide; dichloride exemplifies the rich potential within synthetic organic compounds, particularly those designed for specific biological activity. It's a prime example of how chemical synthesis can lead to novel entities that pave the way for advancements in medicinal chemistry.

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