Monepantel | Solubility of Things

Identification

Molecular formula

C₂₈H₃₀N₂O₂

CAS number

887148-69-8

IUPAC name

2-morpholinoimino-1-(4-phenylphenyl)ethanone

State

At room temperature, Monepantel is found in a solid state, specifically as a crystalline solid.

Melting point (Celsius)

108.50

Melting point (Kelvin)

381.65

Boiling point (Celsius)

409.20

Boiling point (Kelvin)

682.35

General information

Molecular weight

474.56g/mol

Molar mass

473.5740g/mol

Density

1.2225g/cm³

Appearence

Monepantel is typically a white to off-white crystalline solid. The compound is stable under recommended storage conditions and is characterized by minimal odor.

Comment on solubility

Solubility of 2-morpholinoimino-1-(4-phenylphenyl)ethanone

The solubility of 2-morpholinoimino-1-(4-phenylphenyl)ethanone can be intriguing to consider, particularly given its chemical structure, which may influence its interactions with solvents.

In general, solubility can vary widely based on several factors, including:

Polarity: The presence of polar and nonpolar groups in the molecule can affect how well it dissolves in different solvents.
Temperature: Increased temperature often enhances solubility for many compounds, allowing them to dissolve more readily.
pH Levels: The solubility of certain compounds can change significantly depending on the acidity or alkalinity of the solution.

For 2-morpholinoimino-1-(4-phenylphenyl)ethanone specifically:

It may be expected to have varied solubility in organic solvents compared to water, due to its complex structure.
Testing in common organic solvents such as ethanol, methanol, or even dichloromethane would provide useful insights into its solubility profile.

Overall, understanding the solubility behavior of this compound is essential for its application in chemical processes, particularly in areas such as synthesis and formulation.

Interesting facts

Interesting Facts about 2-Morpholinoimino-1-(4-phenylphenyl)ethanone

2-Morpholinoimino-1-(4-phenylphenyl)ethanone is a fascinating compound that combines elements of both organic chemistry and medicinal chemistry. Here are some remarkable insights:

Structural Diversity: This compound features a unique structure that includes a morpholino group, which can enhance solubility and biological activity. The presence of the phenyl rings adds aromaticity, which is often associated with increased stability and reactivity.
Biological Relevance: Compounds that share similar structural motifs are often investigated for their potential as pharmaceuticals. They may exhibit interesting interactions with biological macromolecules, offering avenues for drug design and research.
Synthesis Potential: The synthetic pathways to create 2-morpholinoimino-1-(4-phenylphenyl)ethanone can involve various reaction techniques. Chemists often explore methods like condensation reactions and nucleophilic substitutions, allowing for the generation of diverse analogs.
Research Applications: Due to its distinct functional groups, this compound can be a subject of study in material science and organic synthesis, where its derived products could possess unique electronic or optical properties.
In Vitro Activity: Preliminary studies of similar compounds suggest that they could present interesting biological activities, which necessitates in vitro testing to uncover their full potential.

In conclusion, 2-morpholinoimino-1-(4-phenylphenyl)ethanone is not just a chemical entity but an intriguing gateway into the world of organic synthesis and pharmaceutical application. As the scientific community continues to explore its capabilities, it holds promise for innovative discoveries.