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PCP analogue

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Identification
Molecular formula
C21H32ClNO5
CAS number
.
IUPAC name
(4-piperidin-1-ium-1-ylcyclohexyl) 3,4,5-trimethoxybenzoate;chloride
State
State

The compound is typically in a solid state at room temperature.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
355.87g/mol
Molar mass
355.8700g/mol
Density
1.2000g/cm3
Appearence

The compound typically appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of (4-piperidin-1-ium-1-ylcyclohexyl) 3,4,5-trimethoxybenzoate;chloride

The solubility of this intriguing compound, (4-piperidin-1-ium-1-ylcyclohexyl) 3,4,5-trimethoxybenzoate;chloride, is influenced by its unique structural characteristics. A few key points to consider regarding its solubility include:

  • Polarity: The presence of the charged piperidinium moiety suggests that the compound may exhibit a degree of hydrophilicity, enhancing its solubility in polar solvents such as water.
  • Functional Groups: The three methoxy groups on the benzoate may contribute to solubility in organic solvents, promoting interactions in non-polar environments.
  • Solvent Interactions: Its solubility can notably change depending on the solvent system utilized. It may dissolve more readily in alcohols or acetone in contrast to less polar solvents like hexane.
  • Temperature and pH: Solubility can also be affected by temperature and the pH of the solution, altering the ionization state of the compound which impacts its solubility behavior.

Overall, this compound exemplifies the intricate relationship between molecular structure and solubility. Its behavior illustrates how functional groups and charge can significantly influence how substances interact with various solvents, making it a compelling subject for further exploration in the realm of solubility studies.

Interesting facts

Interesting Facts about (4-piperidin-1-ium-1-ylcyclohexyl) 3,4,5-trimethoxybenzoate;chloride

This intriguing compound is a member of a class of chemicals known for their unique interactions and applications in various fields. Here are some fascinating aspects of this compound:

  • Unique Structure: The piperidin-1-ium moiety contributes to its properties, making it particularly interesting in medicinal chemistry.
  • Potential Uses: Compounds like this one are often explored for their potential as pharmaceutical agents, especially in relation to their ability to interact with certain biological receptors.
  • Research Relevance: Researchers are actively investigating this compound's behavior in biological systems, which could lead to advancements in drug development.
  • Electrophilic Character: The presence of chloride enhances the electrophilicity of the compound, potentially allowing it to participate in various organic reactions.
  • Cyclic Elements: The cyclohexyl group can impart considerable conformational flexibility, which is crucial for the biological activity of compounds in interactions with enzymes and receptors.

In summary, the compound (4-piperidin-1-ium-1-ylcyclohexyl) 3,4,5-trimethoxybenzoate;chloride has a complex structure that opens up multiple avenues for research, particularly in the realms of pharmacology and organic synthesis. As we continue to delve deeper into chemical innovation, the understanding and applications of such compounds hold significant promise.

Synonyms
3,4,5-Trimethoxybenzoic acid 4-piperidinocyclohexyl ester hydrochloride
1532-13-4
BENZOIC ACID, 3,4,5-TRIMETHOXY-, 4-PIPERIDINOCYCLOHEXYL ESTER, HYDROCHLORIDE
Estere 3,4,5-trimetossibenzoico del 4-piperidino-cicloesanolo clorohydrato [Spanish]
Estere 3,4,5-trimetossibenzoico del 4-piperidino-cicloesanolo clorohydrato