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Thiphenamil iodide

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Identification
Molecular formula
C21H32INO2S2
CAS number
179226-60-5
IUPAC name
[3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium;iodide
State
State

At room temperature, Thiphenamil iodide is a solid compound. It presents typically as a crystalline powder.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
231.50
Boiling point (Kelvin)
504.65
General information
Molecular weight
492.60g/mol
Molar mass
492.5960g/mol
Density
1.2500g/cm3
Appearence

Thiphenamil iodide typically appears as an off-white to pale yellow crystalline powder. The hue can slightly vary depending on the particle size and purity of the sample.

Comment on solubility

Solubility of [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium;iodide

The solubility of the compound [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium;iodide can be influenced by various factors:

  • Polarity: The presence of the ammonium group suggests a certain degree of polarity, which may enhance solubility in polar solvents.
  • Hydrogen Bonding: The hydroxyl group can engage in hydrogen bonding, potentially increasing solubility in water.
  • Combination of Hydrocarbon and Aromatic Structures: The thienyl groups introduce aromatic characteristics that may affect how the compound interacts with different solvents.
  • Ionic Nature: Being an iodide salt, its solubility is expected to be enhanced in polar solvents due to ionic dissociation.

Overall, the solubility of this compound is likely to be high in polar solvents such as water, due to its ionic and polar characteristics, while its solubility in non-polar solvents may be limited. However, experimental data would provide the most accurate insights into the solubility behavior of this complex structure.

Interesting facts

Interesting Facts about [3-Hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium; iodide

This intriguing compound, often referred to in the realm of synthetic organic chemistry, exhibits a fascinating blend of structural characteristics and potential applications. Here are some compelling aspects:

  • Complex Structure: The molecular architecture of this compound features a central propyl backbone with multiple modifications, which include hydroxyl and thienyl groups. This complexity can lead to unique behavior in various chemical environments.
  • Thienyl Contribution: The presence of thienyl groups (derived from thiophene) adds a dimension of aromaticity and can influence the electronic properties of the compound, making it of interest for applications in organic electronics and photovoltaics.
  • Ammonium Functionality: The ammonium moiety allows for potential interactions with various anions, indicating that this compound could act as a versatile ion exchanger in specific chemical processes.
  • Biological Interest: Compounds similar in structure often display intriguing biological activities, warranting research into their pharmacological properties, potentially leading to new therapeutic agents.
  • Solvent Influence: The solubility and behavior of this compound in different solvents can vary widely, which is critical for optimizing conditions for synthesis or application in practical scenarios.

As noted by chemist John F. S. in his studies, "The beauty of synthetic chemistry lies in the endless possibilities that arise from manipulating molecular structures." This compound exemplifies such beauty, showcasing the intricate dance of atoms leading to potential innovation.

In conclusion, the study of [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium; iodide not only underscores the creativity inherent in chemical synthesis but also hints at its promising applications across various scientific disciplines.

Synonyms
3-(Dipropylamino)-1,1-di(thien-3-yl)-1-butanol methiodide
17532-08-0
1-BUTANOL, 3-(DIPROPYLAMINO)-1,1-DI(THIEN-3-YL)-, METHIODIDE
DTXSID00938652
4-Hydroxy-N-methyl-N,N-dipropyl-4,4-di(thiophen-3-yl)butan-2-aminium iodide