Hydrochloride of Esterified 4-Phenylpiperidine
- Molecular formula
- C23H30ClNO3
- CAS Number
- 746-21-0
- IUPAC Name
- ethyl 1-(3-hydroxy-3-phenyl-propyl)-4-phenyl-piperidine-4-carboxylate;hydrochloride
- Molecular Weight
- 345.88g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1430g/cm3
- Synonyms
- Phenoperidine hydrochloride
Identification
Intriguing Insights on Ethyl 1-(3-Hydroxy-3-phenyl-propyl)-4-phenyl-piperidine-4-carboxylate Hydrochloride
Ethyl 1-(3-hydroxy-3-phenyl-propyl)-4-phenyl-piperidine-4-carboxylate hydrochloride is a fascinating compound in the realm of organic chemistry, offering a unique structure that is of significant interest to researchers in medicinal chemistry and pharmacology. This compound belongs to the class of piperidine derivatives, which are known for their diverse biological activities.
Key Characteristics:
- Pharmacological Relevance: The presence of the piperidine ring in its structure is linked to several pharmacological functions, including potential analgesic and anti-inflammatory effects.
- Synthetic Versatility: This compound can serve as an intermediate in the synthesis of various pharmaceuticals, particularly those that target the central nervous system.
- Structural Complexity: Its intricate arrangement of functional groups enhances its interaction potential with biological systems, making it an interesting subject for drug development.
Furthermore, the compound combines multiple functionalities, such as a hydroxyl group and an ester moiety, which can influence its solubility and reactivity. One of the standout features is its stereochemistry, which could be crucial for determining its biological activity. As noted by many in the field, "the efficacy of a compound is often determined by the precise arrangement of its atoms."
The hydrochloride salt form enhances its stability and solubility in aqueous solutions, further facilitating experimental studies and applications in drug formulation. Researchers continually explore the implications of such compounds, seeking to unlock their full potential in therapeutic contexts.
This compound not only represents a noteworthy example of structural innovation in organic chemistry but also serves as a testament to the ongoing exploration and optimization of compounds that could lead to groundbreaking advancements in medical science.