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Carfentanyl

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Identification
Molecular formula
C24H30O3N
CAS number
59708-52-0
IUPAC name
ethyl 1-(4,4-diphenylbut-3-enyl)-4-phenyl-piperidine-4-carboxylate
State
State

At room temperature, Carfentanyl is in a solid state. It is typically handled as a powder, which can be highly potent and requires careful handling to avoid accidental exposure.

Melting point (Celsius)
166.00
Melting point (Kelvin)
439.20
Boiling point (Celsius)
580.70
Boiling point (Kelvin)
853.80
General information
Molecular weight
394.53g/mol
Molar mass
394.5340g/mol
Density
1.2239g/cm3
Appearence

Carfentanyl typically appears as a white to off-white powder. It can also be found in a crystalline form. The powder is usually fine and has no distinctive odor.

Comment on solubility

Solubility of Ethyl 1-(4,4-diphenylbut-3-enyl)-4-phenyl-piperidine-4-carboxylate

The solubility of ethyl 1-(4,4-diphenylbut-3-enyl)-4-phenyl-piperidine-4-carboxylate can be described as follows:

  • Polar vs. Non-Polar: Due to the presence of the bulky diphenyl and piperidine moieties, this compound tends to be more non-polar, which can affect its solubility in different solvents.
  • Solvent Compatibility: It is likely to exhibit greater solubility in organic solvents such as:
    • Toluene
    • Dichloromethane
    • Ethyl acetate
  • Water Solubility: Given its non-polar characteristics, the solubility of this compound in water is expected to be quite low. Water molecules cannot effectively interact with the large hydrophobic groups.

In conclusion, the solubility profile of ethyl 1-(4,4-diphenylbut-3-enyl)-4-phenyl-piperidine-4-carboxylate emphasizes the importance of selecting the right solvent for effective dissolution, particularly in organic chemical environments. As the saying goes, "Like dissolves like." Thus, understanding the solubility properties of this compound is crucial for its practical applications.

Interesting facts

Interesting Facts about Ethyl 1-(4,4-Diphenylbut-3-enyl)-4-Phenyl-Piperidine-4-Carboxylate

Ethyl 1-(4,4-diphenylbut-3-enyl)-4-phenyl-piperidine-4-carboxylate is a fascinating compound that belongs to the family of piperidine derivatives. As a chemist or a student delving into organic chemistry, you may find several remarkable aspects to explore:

  • Synthetic Applications: This compound is often studied for its potential applications in synthetic organic chemistry. Its unique structure allows for various transformations, making it a valuable intermediate in the synthesis of pharmaceuticals.
  • Biological Activities: There is evidence suggesting that compounds containing piperidine rings exhibit a variety of biological activities, including analgesic, anti-inflammatory, and antitumor properties. Researchers are continually exploring these attributes to unlock new therapeutic potential.
  • Structural Features: The presence of both phenyl and diphenyl groups in its structure contributes to the compound's unique properties, such as increased stability and possibly enhanced interactions with biological targets.
  • Research Significance: Compounds like ethyl 1-(4,4-diphenylbut-3-enyl)-4-phenyl-piperidine-4-carboxylate are often used as model compounds in drug design studies, offering insight into molecular interactions and aiding in the development of more effective therapeutics.

As you explore this compound further, consider how its structure influences its reactivity and potential uses in various fields such as medicinal chemistry and materials science. Its intriguing combination of chemical features exemplifies the complexity and beauty of organic compounds!