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1-Butanol, 3-(1-methylpyrrolidin-1-yl)-1,1-bis(3-thienyl)-, iodide

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Identification
Molecular formula
C18H23INOS2
CAS number
135482-92-3
IUPAC name
3-(1-methylpyrrolidin-1-ium-1-yl)-1,1-bis(3-thienyl)butan-1-ol;iodide
State
State

At room temperature, this compound exists in a solid state. The presence of the iodide ion suggests it forms an ionic lattice, contributing to its solid state at room temperature.

Melting point (Celsius)
158.50
Melting point (Kelvin)
431.60
Boiling point (Celsius)
273.10
Boiling point (Kelvin)
546.30
General information
Molecular weight
453.37g/mol
Molar mass
453.3680g/mol
Density
1.7088g/cm3
Appearence

This compound typically appears as a crystalline solid. The iodide salt form may give it a slight yellowish or off-white hue. The crystalline nature is consistent with many ionic compounds where intermolecular forces dictate a structured lattice.

Comment on solubility

Solubility of 3-(1-methylpyrrolidin-1-ium-1-yl)-1,1-bis(3-thienyl)butan-1-ol; iodide

The solubility of 3-(1-methylpyrrolidin-1-ium-1-yl)-1,1-bis(3-thienyl)butan-1-ol; iodide can be characterized by several important factors:

  • Ionic Nature: As an iodide salt, its solubility may be influenced by the ionic interactions. Typically, compounds derived from strong acids and bases tend to be more soluble in polar solvents.
  • Polarity: The presence of the pyrrolidin-1-ium cation suggests a positive charge, potentially increasing solubility in polar solvents due to dipole-dipole interactions.
  • Presence of Functional Groups: The alcohol group (butan-1-ol) usually augments solubility in water, making this compound more likely to dissolve in aqueous solutions.
  • Thienyl Substitution: The thienyl groups could contribute to π-π stacking and might affect solubility in organic solvents.

In general, we can expect that this compound will have good solubility in **polar solvents** such as water and alcohols, while it might display variable solubility in **non-polar** solvents, depending on the interactions between the thienyl moieties and the solvent medium.

Overall, understanding the solubility characteristics of this iodide salt is crucial for its applications and behavior in various chemical environments.

Interesting facts

Interesting Facts about 3-(1-methylpyrrolidin-1-ium-1-yl)-1,1-bis(3-thienyl)butan-1-ol; iodide

The compound 3-(1-methylpyrrolidin-1-ium-1-yl)-1,1-bis(3-thienyl)butan-1-ol; iodide is a fascinating example of the intersection of organic chemistry and materials science. Here are some intriguing aspects to consider:

  • Structure and Functionality: This compound features a unique architecture that combines a pyrrolidinium ion with thienyl groups, highlighting the importance of heteroatoms in altering molecular properties.
  • Applications: Compounds similar to this one are often explored for their potential use in organic electronics, such as in the development of organic light-emitting diodes (OLEDs) and solar cells.
  • Research Significance: Due to its intricate structure, this compound serves as a valuable subject for studying charge transfer mechanisms and molecular interactions that are pivotal in various chemical processes.
  • The Role of Iodide: The presence of iodide plays a crucial role in facilitating conductivity and stability, making it essential for applications that require ionic conduction.
  • Biological Interest: Compounds with similar pyrrolidinium motifs are known for their bioactive properties, thus raising questions about their pharmacological potential and underlying mechanisms of action.

In conclusion, 3-(1-methylpyrrolidin-1-ium-1-yl)-1,1-bis(3-thienyl)butan-1-ol; iodide exemplifies the complexity of chemical compound design, where every functional group can contribute to the final utility of the molecule. As we delve deeper into understanding such compounds, we unveil not only their structural elegance but also their potential in real-world applications.

Synonyms
1,1-Di(thien-3-yl)-3-pyrrolidinyl-1-butanol methiodide
17532-09-1
1-BUTANOL, 1,1-DI(THIEN-3-YL)-3-PYRROLIDINO-, METHIODIDE
DTXSID60938653
1-[4-Hydroxy-4,4-di(thiophen-3-yl)butan-2-yl]-1-methylpyrrolidin-1-ium iodide