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Rolicyclidine

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Identification
Molecular formula
C19H27ClN2O2
CAS number
2201-22-3
IUPAC name
[2-(1-piperidyl)cyclohexyl] N-(2-chloro-6-methyl-phenyl)carbamate
State
State

Rolicyclidine is typically found as a solid at room temperature. Due to its synthetic nature, its precise state can vary based on preparation and storage conditions.

Melting point (Celsius)
98.50
Melting point (Kelvin)
371.65
Boiling point (Celsius)
350.45
Boiling point (Kelvin)
623.60
General information
Molecular weight
330.89g/mol
Molar mass
330.8500g/mol
Density
1.1832g/cm3
Appearence

Rolicyclidine appears as a white powdery solid. It is a synthetic compound and its exact appearance can vary based on purity and form, but in its pure state, it generally appears as a crystalline or powder form.

Comment on solubility

Solubility Characteristics of [2-(1-piperidyl)cyclohexyl] N-(2-chloro-6-methyl-phenyl)carbamate

The solubility of [2-(1-piperidyl)cyclohexyl] N-(2-chloro-6-methyl-phenyl)carbamate is influenced by various factors such as the nature of the functional groups, polarity, and intermolecular interactions. This compound can exhibit both polar and non-polar characteristics due to its unique structure.

Key Factors Affecting Solubility:

  • Polarity: The presence of the carbamate group introduces polar characteristics, which typically enhances solubility in polar solvents.
  • Hydrophobic Regions: The cyclohexyl and piperidyl groups provide hydrophobic portions that can limit solubility in water but enhance it in organic solvents.
  • Intermolecular Interactions: Hydrogen bonding potential from the carbamate may allow for some solubility in protic solvents.

Overall, one might expect the compound to have limited solubility in water while being more soluble in organic solvents such as methanol or ethanol. As emphasized in the realm of chemistry, "the structure dictates the solubility" — understanding these relationships aids in predicting the behavior of chemical compounds in various environments.

Interesting facts

Interesting Facts About [2-(1-piperidyl)cyclohexyl] N-(2-chloro-6-methyl-phenyl)carbamate

This compound, known for its complex structure and interesting properties, belongs to the class of carbamates that are renowned for their efficacy in various applications.

Key Features:

  • Biological Activity: This compound has been studied for its potential biological activities, particularly its role as a pharmacological agent. Researchers are investigating its effects on neurotransmitter systems, making it a candidate for therapeutic exploration.
  • Synthetic Pathways: The synthesis of this compound often involves intricate organic reactions, showcasing the creativity and problem-solving skills essential in organic chemistry. Its multi-step synthesis can serve as a learning tool for students exploring advanced organic reactions.
  • Structural Insights: The presence of both a piperidyl ring and a cyclohexyl group in its structure contributes to its unique conformational dynamics. Understanding these dynamics plays a crucial role in predicting the compound’s reactivity and potential interactions with biological targets.
  • Applications: Beyond academic interest, compounds with similar structures are often utilized in drug formulation, emphasizing the importance of studying such molecules. They may offer insights into drug design and development processes.

Research Implications:

The investigation into [2-(1-piperidyl)cyclohexyl] N-(2-chloro-6-methyl-phenyl)carbamate opens doors for future research. As chemists continue to unravel the complexities of such compounds, they not only expand the existing knowledge base but also contribute to the advancement of medicinal chemistry. As one researcher noted, "The potential for discovering new therapeutic agents lies in our willingness to explore the unknown."


As you dive deeper into the study of organic compounds, keep an eye on such interesting candidates. They serve not only as prosaic examples of chemistry principles but also as possible future innovations in drug discovery and development.