PCC (1-(1-Piperidinyl)cyclohexyl N-(2-chlorophenyl)carbamate)

Identification

Molecular formula

C₁₈H₂₅ClN₂O₂

CAS number

23820-74-4

IUPAC name

[2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate

State

The compound is in a solid state at room temperature. It is not volatile and is mostly stable under normal atmospheric conditions, but precautions for handling chemical solids should be taken.

Melting point (Celsius)

116.00

Melting point (Kelvin)

389.00

Boiling point (Celsius)

370.00

Boiling point (Kelvin)

643.00

General information

Molecular weight

320.86g/mol

Molar mass

320.8220g/mol

Density

1.2700g/cm³

Appearence

The compound is typically a crystalline solid. It may appear as a white to off-white powder, depending on its purity and form. The compound is generally stable under normal conditions but should be protected from moisture and light to avoid degradation.

Comment on solubility

Solubility of [2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate

The solubility of [2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate is an intriguing aspect of this compound, influenced by its unique structure. Understanding its solubility can provide insights into its behavior in various solvents and its potential applications. Here are some key points regarding its solubility:

Polar vs. Non-Polar Solvents: The presence of polar functional groups in the molecule, like the carbamate group, suggests that this compound may be more soluble in polar solvents, such as water and alcohols.
Hydrophobic Interactions: The cyclohexyl and piperidine components contribute hydrophobic characteristics, likely decreasing solubility in polar solvents.
Temperature Dependency: Solubility can also vary with temperature; generally, increasing temperature enhances the solubility of many organic compounds.
Influence of pH: As a carbamate, the solubility may be affected by pH changes, potentially leading to different solubility profiles in acidic or basic environments.

In summary, the solubility of [2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate is expected to be moderate in polar solvents while showing reduced solubility in apolar solvents. Its behavior in various environments warrants consideration when assessing its potential uses in pharmaceuticals and chemical applications.

Interesting facts

Interesting Facts about [2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate

[2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate is a fascinating compound that belongs to the class of carbamate derivatives. These compounds are known to exhibit a range of biological activities, making them of interest in pharmaceutical research and development. Here are some notable facts about this intriguing compound:

Pharmacological Potential: Compounds like this one are explored for their potential therapeutic effects, including anti-inflammatory and analgesic properties. This makes them promising candidates in the development of new pain relief medications.
Chemical Structure: The presence of the piperidyl group allows for unique interactions within biological systems. The cyclical nature of cyclohexyl provides structural stability, which can enhance the efficacy and duration of action of the compound.
Mechanism of Action: While specific mechanisms for this carbamate may vary, carbamates generally function by inhibiting certain enzymes in the body, such as acetylcholinesterase, leading to prolonged effects of neurotransmitters.
Synthetic Pathways: The synthesis of [2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate involves intricate organic chemistry techniques, showcasing the versatility of carbamate chemistry in synthetic applications.
Research Interest: Due to its structural components, researchers explore analogs of this compound to better understand structure-activity relationships and to optimize its therapeutic benefits.

In conclusion, [2-(1-piperidyl)cyclohexyl] N-(2-chlorophenyl)carbamate exemplifies the complexity and potential of carbamate derivatives in medicinal chemistry. Its unique chemical structure opens avenues for further exploration, and researchers are keen to uncover more about its biological activities and applications in drug development.