Lidocaine hydrochloride

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Identification

Molecular formula
C14H23ClN2O
CAS Number
73-78-9
IUPAC Name
N-(2-methyl-1-phenyl-2-piperidin-1-ium-1-yl-propylidene)acetamide;chloride
Molecular Weight
270.80g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0060g/cm3
Synonyms
N-(alpha-(1-Methyl-1-piperidinoethyl)benzylidene)acetamide monohydrochloride
Interesting facts

Interesting Facts about N-(2-methyl-1-phenyl-2-piperidin-1-ium-1-yl-propylidene)acetamide;chloride

N-(2-methyl-1-phenyl-2-piperidin-1-ium-1-yl-propylidene)acetamide;chloride, commonly known in the scientific community for its intriguing structural features, is a fascinating compound that plays a significant role in various fields of research.

Structural Insights

This compound boasts a complex molecular architecture that includes:

  • Piperidine Ring: A six-membered ring that enhances its basicity and allows for various interactions with biological targets.
  • Phenyl Group: This aromatic structure contributes to the compound's unique electronic properties and the potential for π-π stacking interactions.
  • Acetamide Functionality: Provides linked reactivity, enabling various transformations and biological activities.

Biological Relevance

Researchers have taken a keen interest in this compound due to its:

  • Potential as a pharmacological agent: Some derivatives exhibit promising activity in neuropharmacology.
  • Influence in studying neurotransmitter systems: Exploring its interactions can unveil mechanisms related to cognition and mood regulation.

Synthesis and Applications

The synthesis of N-(2-methyl-1-phenyl-2-piperidin-1-ium-1-yl-propylidene)acetamide;chloride involves innovative techniques that showcase modern organic chemistry methodologies. Notably:

  • The synthesis typically employs multi-step reactions to assemble its structure carefully.
  • Its derivatives have potential applications in developing therapeutic agents, particularly in treating neurological disorders.

In essence, N-(2-methyl-1-phenyl-2-piperidin-1-ium-1-yl-propylidene)acetamide;chloride stands as a symbol of innovation and discovery in chemical research, highlighting the intersections of organic synthesis, biological activity, and pharmacological advancements.

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