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Isopropyl levamisole oxalate

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Identification
Molecular formula
C13H17NO2
CAS number
6152-87-2
IUPAC name
2,3-dihydrobenzofuran-2-ylmethyl(isopropyl)ammonium;4-hydroxy-4-oxo-but-2-enoate
State
State
At room temperature, isopropyl levamisole oxalate is in a solid state. It is not readily soluble in water, often requiring organic solvents for dissolution.
Melting point (Celsius)
217.00
Melting point (Kelvin)
490.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
248.32g/mol
Molar mass
248.3210g/mol
Density
1.2100g/cm3
Appearence

Isopropyl levamisole oxalate typically appears as a white or off-white crystalline powder. It may also be present in fine crystalline form, making it look somewhat translucent. The powder is usually fine, contributing to its slightly burning taste.

Comment on solubility

Solubility of 2,3-dihydrobenzofuran-2-ylmethyl(isopropyl)ammonium; 4-hydroxy-4-oxo-but-2-enoate

The solubility of the compound 2,3-dihydrobenzofuran-2-ylmethyl(isopropyl)ammonium; 4-hydroxy-4-oxo-but-2-enoate can be influenced by several molecular characteristics. Notably, this compound features both hydrophobic furan and benzene rings and a more hydrophilic ammonium and carboxylate group.

To understand its solubility behavior, consider the following aspects:

  • Polar vs. Non-Polar Regions: The presence of the isopropyl group can increase hydrophobicity, while the ammonium and carboxylate impart some degree of hydrophilicity.
  • Solubility in Water: This compound may exhibit limited solubility in water due to the predominance of non-polar structures, but the charged ammonium group enhances potential interactions with water molecules.
  • Solubility in Organic Solvents: It is likely to be more soluble in organic solvents (e.g., ethanol, acetone) that can effectively interact with its hydrophobic regions.

In practical terms, the solubility is likely to be moderate, striking a balance between its polar and non-polar characteristics. Therefore, it may partially dissolve in aqueous solutions but achieve greater solubility in various organic solvents.

In summary:
-   May have limited water solubility
-   Greater solubility in organic solvents
-   Overall solubility affected by molecular structure

Interesting facts

Interesting Facts about 2,3-Dihydrobenzofuran-2-ylmethyl(isopropyl)ammonium; 4-Hydroxy-4-oxo-but-2-enoate

This intricate compound showcases the fascinating interplay of structure and function in organic chemistry. Its dual nature, with components that reflect both nitrogenous and aromatic characteristics, positions it as a notable subject of study.

Key Features:

  • Aromaticity: The 2,3-dihydrobenzofuran segment contains a benzene ring fused to a furan, contributing to its stability and electron-rich characteristics.
  • Biological Activity: Compounds of this nature are often explored for their potential biological activities, including anti-inflammatory and anti-cancer properties.
  • Versatile Applications: The presence of both an ammonium and a carboxylate structure may lend itself to:
    • Pharmaceuticals
    • Agricultural chemicals
    • Material sciences

Unique Structural Characteristics:

The compound's configuration supports an intriguing molecular arrangement that enables various interactions. For instance:

  • The isopropylammonium group can act as a proton donor, engaging in hydrogen bonding.
  • Functional groups like the hydroxy- and keto- can participate in a myriad of chemical reactions, including nucleophilic attacks and condensation reactions.

As scientists continue to unravel the complexities of compounds like this one, they often echo the words of fellow researchers: "Every compound holds a story waiting to be discovered." With applications ranging from medicinal chemistry to advanced materials, this compound is a testament to the beauty and utility of synthetic organic chemistry.