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Etonitazene

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Identification
Molecular formula
C22H28N2O3
CAS number
126-80-1
IUPAC name
2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate
State
State

At room temperature, etonitazene is typically a solid.

Melting point (Celsius)
206.50
Melting point (Kelvin)
479.65
Boiling point (Celsius)
400.20
Boiling point (Kelvin)
673.35
General information
Molecular weight
394.48g/mol
Molar mass
394.5010g/mol
Density
1.4238g/cm3
Appearence

Etonitazene typically appears as a crystalline solid. Its color may vary from white to off-white or slightly yellowish, depending on purity and form.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate can be quite intriguing due to its complex structure, which influences its interaction with solvents. Understanding solubility is essential for various applications in chemistry, especially in pharmaceuticals and material science. Here are some key points to consider:

  • Polar vs. Nonpolar Solvents: This compound may exhibit varying solubility in polar and nonpolar solvents. Generally, compounds with extensive hydrophobic (nonpolar) regions tend to have low solubility in water but may dissolve better in organic solvents like ethanol or dichloromethane.
  • pH Dependence: The solubility may vary significantly with changes in pH, making it crucial for applications involving biological systems, where pH can fluctuate.
  • Temperature Effects: Solubility usually increases with temperature for most solid solutes, which might be applicable for this compound as well. Thus, heating the solvent can enhance solubility.
  • Complex Formation: The ability to form complexes with other solutes or solvents might also play a role in enhancing solubility, showcasing potential interactions due to the presence of functional groups.

In summary, the solubility of 2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate is highly influenced by its molecular structure, solvent choice, pH, and temperature. It's essential for researchers to consider these factors carefully in their endeavors to utilize this compound effectively.

Interesting facts

Interesting Facts about 2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate

The compound 2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate is a fascinating example of organic chemistry, specifically in the realm of pharmaceutical compounds. Here are some key highlights:

  • Pharmaceutical Relevance: This compound contains a piperidine ring, which is known for its presence in various biologically active molecules. Piperidine derivatives often exhibit important medicinal properties, making them a significant area of research in drug development.
  • Carbamate Functionality: The carbamate functional group is notable for its role in various chemical reactions. It's commonly found in pesticides, herbicides, and pharmaceuticals, showcasing its versatility in synthetic chemistry.
  • Bioactivity: Many compounds featuring the benzyloxyphenyl group demonstrate activity in treating a range of conditions, including inflammation and cancer. The structural similarities to other known bioactive compounds suggest that this molecule could also offer therapeutic potential.
  • Complex Structure: The compound’s structure combines multiple functional groups that can interact synergistically, enhancing the overall activity and specificity of the compound. This makes it a compelling subject for study in medicinal chemistry.
  • Synthesis Strategies: Creating this compound involves a variety of synthetic strategies that may include reactions such as nucleophilic substitutions and coupling reactions. Understanding these mechanisms is crucial for chemists aiming to optimize synthesis.

In summary, 2-(1-piperidyl)ethyl N-(4-benzyloxyphenyl)carbamate represents a rich intersection of medicinal chemistry and organic synthesis, highlighting the importance of structure in determining activity and the potential for innovative therapeutic applications.