Lidocaine hydrochloride
- 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
Identification
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.