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Iodide compound (specific name unavailable)

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Identification
Molecular formula
C19H30N2O3I
CAS number
63590-64-9
IUPAC name
2-(2-benzyl-4-ethoxycarbonyl-5-methyl-pyrazol-3-yl)oxyethyl-trimethyl-ammonium;iodide
State
State

At room temperature, this compound exists as a solid. It is typically sensitive to moisture and should be stored in a dry environment to prevent degradation or clumping.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
379.63g/mol
Molar mass
379.6300g/mol
Density
1.3000g/cm3
Appearence

The compound typically presents as a crystalline solid or powder with an off-white to pale yellow color. The iodine component may impart a slight coloration due to the iodide ions present in the compound structure.

Comment on solubility

Solubility of 2-(2-benzyl-4-ethoxycarbonyl-5-methyl-pyrazol-3-yl)oxyethyl-trimethyl-ammonium iodide

The solubility of 2-(2-benzyl-4-ethoxycarbonyl-5-methyl-pyrazol-3-yl)oxyethyl-trimethyl-ammonium iodide can be quite intriguing due to its unique structure. The presence of various functional groups impacts its solubility in different solvents.

  • Solvent Compatibility: This compound is likely to be more soluble in polar solvents such as water or methanol, owing to the ionic nature of the ammonium group and the iodide anion.
  • Hydrophobic Regions: The benzyl and ethoxycarbonyl substituents may create some hydrophobic character, leading to limited solubility in non-polar solvents like hexane.
  • Temperature Influence: As with many ionic compounds, solubility may increase with temperature due to enhanced kinetic energy disrupting intermolecular interactions.
  • Concentration Factors: Increasing the concentration of the compound may lead to saturation, resulting in a dynamic equilibrium where solubility limits are observed.

In summary, the solubility of this compound is governed by a complex interplay of its ionic and hydrophobic characteristics, indicative of the challenges often faced in the dissolution of such organic salts.

Interesting facts

Interesting Facts about 2-(2-benzyl-4-ethoxycarbonyl-5-methyl-pyrazol-3-yl)oxyethyl-trimethyl-ammonium iodide

This intriguing compound, known as 2-(2-benzyl-4-ethoxycarbonyl-5-methyl-pyrazol-3-yl)oxyethyl-trimethyl-ammonium iodide, is a member of a class of substances that merges organic chemistry with medicinal chemistry applications. Here are some noteworthy aspects:

  • Structural Complexity: The compound features a unique combination of a pyrazole ring with ethoxycarbonyl and benzyl functionalities, highlighting its molecular intricacies.
  • Cationic Nature: As a trimethyl-ammonium iodide, it behaves as a cationic surfactant, implying potential applications in enhancing solubility and stability in various formulations.
  • Biological Significance: The presence of the pyrazole moiety is noteworthy due to its occurrence in numerous pharmacologically active compounds, making this structure an interesting candidate for further investigation in drug design.
  • Applications: The compound may find utility in fields such as organic synthesis, materials science, and even as an ionic liquid, enhancing both performance and efficiency in chemical reactions.

In the words of a renowned chemist, “The beauty of chemistry lies in its ability to transform simple elements into complex structures.” This compound serves as a testament to this notion, demonstrating the elegance of molecular design and the potential pathways for innovative research.

Overall, 2-(2-benzyl-4-ethoxycarbonyl-5-methyl-pyrazol-3-yl)oxyethyl-trimethyl-ammonium iodide stands as a fascinating subject for study, inviting chemists to explore its properties and applications further.

Synonyms
Ammonium, (2-((1-benzyl-4-carboxy-3-methylpyrazol-5-yl)oxy)ethyl)trimethyl-, iodide, ethyl ester
19477-45-3
(2-((1-Benzyl-4-carboxy-3-methylpyrazol-5-yl)oxy)ethyl)trimethylammonium iodide ethyl ester
RefChem:318695
DTXSID30941230
2-{[1-Benzyl-4-(ethoxycarbonyl)-3-methyl-1H-pyrazol-5-yl]oxy}-N,N,N-trimethylethan-1-aminium iodide