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Bistriflimide

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Identification
Molecular formula
C17H20NS2
CAS number
162091-96-5
IUPAC name
3-[bis(2-thienyl)methylene]-1,1-dimethyl-piperidin-1-ium
State
State
At room temperature, the compound is typically a solid, often presented as a fine powder or crystalline form.
Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
324.48g/mol
Molar mass
324.4500g/mol
Density
0.6891g/cm3
Appearence
The compound typically appears as a brown to black powder or crystals. However, the exact appearance can vary depending on its form and purity.
Comment on solubility

Solubility of 3-[bis(2-thienyl)methylene]-1,1-dimethyl-piperidin-1-ium (C17H20NS2)

The solubility of 3-[bis(2-thienyl)methylene]-1,1-dimethyl-piperidin-1-ium is notably influenced by its structural complexity and polarity. This compound contains both thienyl groups and a piperidine backbone, which can have a significant impact on its interactions with solvents. Here are some key points regarding its solubility:

  • Polar vs. Non-Polar Solvents: Due to the presence of sulfur and nitrogen atoms in its structure, the compound may exhibit higher solubility in polar solvents compared to non-polar solvents. The thienyl moieties can provide some degree of polarity which facilitates solvation in aqueous medium.
  • Temperature Dependency: Solubility may also increase with temperature, as is often the case with organic compounds, allowing for better solvation dynamics.
  • Influence of Ionic Strength: As a quaternary ammonium ion, its solubility could be influenced by the ionic strength of the solution, possibly leading to enhanced solubility in saline solutions.

In conclusion, the solubility of 3-[bis(2-thienyl)methylene]-1,1-dimethyl-piperidin-1-ium is subject to various factors including solvent polarity, temperature, and ionic conditions. Understanding these factors is crucial for potential applications and utilizations in chemical processes.

Interesting facts

Interesting Facts about 3-[bis(2-thienyl)methylene]-1,1-dimethyl-piperidin-1-ium

3-[bis(2-thienyl)methylene]-1,1-dimethyl-piperidin-1-ium is a fascinating compound that exemplifies the rich interplay between organic chemistry and functional materials. Here are some intriguing aspects:

  • Unique Structure: This compound features a piperidinium backbone, which is significant in the study of cationic species. The presence of thienyl groups (derived from thiophene) adds aromatic character, contributing to the compound's electronic properties.
  • Potential Applications: Due to its unique electronic configuration, this compound could have applications in areas such as material science and pharmaceuticals. Its properties may allow for novel uses in organic semiconductors or as a potential drug candidate.
  • Electrochemical Activity: The piperidinium moiety enhances the compound’s stability in various electrochemical environments, which makes it an interesting subject for studying interactions in electrolyte solutions.
  • Research Interest: Scientists are particularly interested in compounds like this one due to their ability to form complex structures and their varied reactivity, which can inspire further research into synthetic methodologies and applications.

This compound not only serves as a strong example of the potential complexity in organic molecules but also emphasizes the importance of multidisciplinary approaches in chemical research. As emphasized by many chemists, “Chemistry is the central science” connecting biology, physics, and engineering through intricate organic compounds like this one.