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Fentanyl

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Identification
Molecular formula
C22H28N2O
CAS number
437-38-7
IUPAC name
N-[2-(4-benzoyl-1-piperidyl)-2-oxo-1-phenyl-ethyl]-3-carbamimidoyl-benzamide
State
State

At room temperature, fentanyl is typically found in a solid state. It can be converted into powder or tablet for various applications, especially medicinal purposes. However, it is often encountered in illicit drug trafficking in different forms such as powder or spiked on papers.

Melting point (Celsius)
87.50
Melting point (Kelvin)
360.65
Boiling point (Celsius)
698.98
Boiling point (Kelvin)
972.13
General information
Molecular weight
336.47g/mol
Molar mass
336.4710g/mol
Density
1.1800g/cm3
Appearence

Fentanyl typically appears as a white to off-white powder, although it can also be found in pill, tablet, spiked on blotter paper, or dissolved in liquid form. Its appearance may vary depending on the form in which it is illicitly distributed.

Comment on solubility

Solubility of N-[2-(4-benzoyl-1-piperidyl)-2-oxo-1-phenyl-ethyl]-3-carbamimidoyl-benzamide

The solubility of the compound N-[2-(4-benzoyl-1-piperidyl)-2-oxo-1-phenyl-ethyl]-3-carbamimidoyl-benzamide (C22H28N2O) can be characterized by several key factors:

  • Polarity: As a molecule with both amide and carbonyl functional groups, it may exhibit moderate polarity, which can influence its interactions with solvents.
  • Solvent Compatibility: The solubility is likely to be enhanced in organic solvents such as acetone and ethanol, while being less soluble in water due to its larger hydrophobic aromatic structures.
  • Temperature Dependence: Solubility can be temperature-dependent; generally, an increase in temperature can lead to higher solubility in many organic solvents.

In summary, understanding the solubility properties of this compound is essential for its applications in various chemical contexts. It is important to conduct empirical solubility tests to determine its behavior in practical scenarios.

Interesting facts

Interesting Facts About N-[2-(4-benzoyl-1-piperidyl)-2-oxo-1-phenyl-ethyl]-3-carbamimidoyl-benzamide

N-[2-(4-benzoyl-1-piperidyl)-2-oxo-1-phenyl-ethyl]-3-carbamimidoyl-benzamide is a fascinating compound notable for several reasons. Here's a closer look:

  • Structure: This compound features a complex structure that includes multiple functional groups, particularly the piperidine ring, which is essential in medicinal chemistry for its biological activity.
  • Biological Significance: Compounds with piperidine derivatives often demonstrate significant pharmacological properties. They are prevalent in the development of drugs, targeting various diseases, especially in pain management and neuropharmacology.
  • Research Interest: Due to its unique structure, it has garnered attention in research environments studying anti-cancer and neuroprotective properties. Its potential roles are of particular interest in developing new therapies.
  • Synthesis: The synthesis of such compounds typically requires advanced organic chemistry techniques, often involving multiple reaction steps and careful manipulation of functional groups, demonstrating the creativity and complexity inherent in modern organic synthesis.
  • Applications: This compound may find applications beyond pharmaceuticals, potentially extending to areas such as materials science by influencing the design of new biological sensors or catalysts.

As a scientist or student delving into the world of chemical compounds, understanding the multifaceted nature of such molecules, like N-[2-(4-benzoyl-1-piperidyl)-2-oxo-1-phenyl-ethyl]-3-carbamimidoyl-benzamide, opens up exciting avenues for exploration in drug design and beyond. Its rich structure serves as an excellent example of the intricate relationship between chemistry and biology.

Synonyms
SCHEMBL3487100