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N-(azepan-1-yl)-1-(2-thienyl)methanimine

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Identification
Molecular formula
C12H17NS
CAS number
7153-01-7
IUPAC name
N-(azepan-1-yl)-1-(2-thienyl)methanimine
State
State

At room temperature, N-(azepan-1-yl)-1-(2-thienyl)methanimine is generally in a liquid state. It may become more viscous as temperatures decrease but is predominantly non-viscous at ambient conditions.

Melting point (Celsius)
-78.00
Melting point (Kelvin)
195.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
207.34g/mol
Molar mass
207.3200g/mol
Density
1.1500g/cm3
Appearence

N-(azepan-1-yl)-1-(2-thienyl)methanimine typically appears as a clear to pale yellow liquid. Its viscosity can vary slightly but remains relatively low, consistent with many amine compounds.

Comment on solubility

Solubility of N-(azepan-1-yl)-1-(2-thienyl)methanimine

N-(azepan-1-yl)-1-(2-thienyl)methanimine exhibits unique solubility characteristics that are influenced by its molecular structure and composition. Understanding the solubility of this compound is crucial for its practical applications in various chemical and pharmaceutical processes.

Factors Affecting Solubility

The solubility of N-(azepan-1-yl)-1-(2-thienyl)methanimine can be attributed to several factors:

  • Molecular Structure: The presence of the azepan and thienyl rings can introduce significant steric and electronic interactions that may affect solubility.
  • Polarity: The functional groups present in the compound may demonstrate different polar characteristics, influencing the compound's ability to dissolve in polar or non-polar solvents.
  • Temperature: Generally, an increase in temperature may enhance the solubility of many compounds, potentially influencing this compound as well.

Solubility Insights

While specific solubility data for N-(azepan-1-yl)-1-(2-thienyl)methanimine may not be readily available, one can infer:

  • This compound might have limited solubility in polar solvents due to its complex amine structure.
  • It could show some compatibility with organic solvents like dimethyl sulfoxide (DMSO) or ethanol, which typically solvate organic molecules.

In conclusion, the solubility of N-(azepan-1-yl)-1-(2-thienyl)methanimine is multifaceted, and understanding these dynamics is key to leveraging this compound in various applications. Further experimental determination would provide clarity on its solubility profile in various solvents.

Interesting facts

Interesting Facts about N-(azepan-1-yl)-1-(2-thienyl)methanimine

N-(azepan-1-yl)-1-(2-thienyl)methanimine is a fascinating compound that combines unique structural features and potential applications, particularly in the field of medicinal chemistry.

Structural Insights

  • Azeplan-1-yl Group: The azepan-1-yl moiety introduces a seven-membered nitrogen-containing ring, enhancing the compound's versatility and potential biological activity.
  • Thienyl Substituent: The presence of the thienyl group, derived from thiophene, adds aromatic characteristics, which may contribute to intriguing electronic properties.
  • Amine Functionality: The methanimine functional group is notable for its ability to participate in various chemical reactions, such as nucleophilic addition and cycloaddition.

Potential Applications

The unique structure of N-(azepan-1-yl)-1-(2-thienyl)methanimine opens up avenues for various applications:

  • Pharmaceuticals: Compounds containing azepanes and thiophenes are often evaluated for their biological activities, including anti-inflammatory and anti-cancer properties.
  • Ligand Development: The compound can serve as a versatile ligand in coordination chemistry, enabling the formation of metal complexes with desired catalytic properties.
  • Material Science: Its electronic characteristics may find applications in organic electronics, such as in light-emitting diodes and solar cells.

Research Significance

Scientists are continuously exploring the potential of such compounds in developing new therapies and materials. As one researcher stated, "The interplay between structure and function is what keeps us excited in the realm of chemical science." The investigation of N-(azepan-1-yl)-1-(2-thienyl)methanimine exemplifies the importance of chemical diversity in unlocking new scientific frontiers.

Synonyms
NCIOpen2_005618
DTXSID90937699
N-(Azepan-1-yl)-1-(thiophen-2-yl)methanimine