Interesting facts
Interesting Facts about Ethyl 1-(3-oxobutyl)-4-phenyl-piperidin-1-ium-4-carboxylate; Chloride
Ethyl 1-(3-oxobutyl)-4-phenyl-piperidin-1-ium-4-carboxylate; chloride is a fascinating compound with numerous implications in both medicinal and chemical research. Here are some intriguing aspects:
- Structural Complexity: This compound features a piperidinium core, which is typically associated with various pharmacologically active compounds. The presence of both ethyl and oxobutyl groups contributes to its structural diversity.
- Potential Biological Activity: Compounds like this one may exhibit interesting biological properties. Researchers often investigate similar piperidinium derivatives for their potential use as analgesics or in the treatment of neurodegenerative diseases.
- Quaternary Ammonium Nature: As a quaternary ammonium compound, its ionized form plays a critical role in interactions with biological membranes, potentially affecting its biological activity.
- Research Applications: The synthesis and modification of compounds with piperidin-1-ium structures can lead to valuable insights into drug design and development. Scientists often use such compounds to explore structure-activity relationships.
- Emerging Interests: With the rise in popularity of synthetic methods in organic chemistry, there is a growing interest in creating novel derivatives of complex compounds like this one to explore new therapeutic avenues.
This compound exemplifies the interplay between complex organic chemistry and potential real-world applications, making it a significant topic of study for chemists and pharmacologists alike.
Synonyms
16036-86-5
1-(3-Oxobutyl)-4-phenylisonipecotic acid ethyl ester hydrochloride
VUFB2809
ISONIPECOTIC ACID, 1-(3-OXOBUTYL)-4-PHENYL-, ETHYL ESTER, HYDROCHLORIDE
Solubility of Ethyl 1-(3-oxobutyl)-4-phenyl-piperidin-1-ium-4-carboxylate;chloride
The solubility of ethyl 1-(3-oxobutyl)-4-phenyl-piperidin-1-ium-4-carboxylate;chloride can be influenced by several factors:
Overall, while the CH3 ethyl group tends to favor solubility in organic solvents, the CH4 carboxylate and chloride functionalities can enhance water solubility. Thus, evaluating the solubility characteristics of this compound in various solvents would provide more precise insights into its behavior in both laboratory and industrial environments.