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
Molecular Weight
207.34g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1500g/cm3
Synonyms
NCIOpen2_005618
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.

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