2-(diethylhydrazono)-1-(4-biphenyl)ethanone

Identification

Molecular formula

C₁₈H₂₀N₂O

CAS number

818-81-5

IUPAC name

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

State

The compound is typically in a solid state under room temperature conditions. The solid nature of the compound stems from the substantial interactions between its aromatic rings which stabilize its form, alongside the presence of the hydrazono linkage which tends to increase molecular rigidity.

Melting point (Celsius)

85.00

Melting point (Kelvin)

358.15

Boiling point (Celsius)

312.00

Boiling point (Kelvin)

585.15

General information

Molecular weight

280.38g/mol

Molar mass

280.3770g/mol

Density

1.1034g/cm³

Appearence

2-(diethylhydrazono)-1-(4-biphenyl)ethanone appears as a solid material. Its color can vary but is typically a pale yellow or orange hue. This compound is crystalline in nature, with a characteristic structure due to the presence of multiple aromatic rings and a hydrazone group, which may influence its interaction with light and impact its opacity and reflectivity.

Comment on solubility

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

The solubility of 2-(diethylhydrazono)-1-(4-phenylphenyl)ethanone can be influenced by various factors, primarily due to its unique molecular structure. This compound contains both hydrazone and phenyl moieties, which can affect how it interacts with solvents.

Factors Influencing Solubility:

Molecular Structure: The presence of multiple phenyl groups increases the hydrophobic character of the compound, likely resulting in lower solubility in polar solvents like water.
Polar vs. Nonpolar Solvents: Nonpolar solvents such as benzene or toluene might exhibit better solubility for this compound due to enhanced dispersion interactions.
Temperature: As with many compounds, increasing temperature can enhance solubility, particularly in organic solvents.
pH Level: Although this compound is not ionic, the potential for protonation or deprotonation in different pH environments can further influence solubility.

In summary, while specific solubility data may be limited, it is reasonable to deduce that 2-(diethylhydrazono)-1-(4-phenylphenyl)ethanone is more likely to dissolve in nonpolar environments rather than polar, substantiating the classic adage: “like dissolves like.” Thus, experimentation under varying conditions will provide insight into its solubility profile.

Interesting facts

Interesting Facts About 2-(diethylhydrazono)-1-(4-phenylphenyl)ethanone

This fascinating compound, 2-(diethylhydrazono)-1-(4-phenylphenyl)ethanone, is a member of the hydrazone family. Hydrazones are notable for their versatile reactivity and have a wide array of applications in chemistry and materials science. Here are some exciting insights:

Reactive Versatility: Hydrazones can undergo various chemical transformations, including oxidation, reduction, and hydrolysis. This property makes them useful precursors in the synthesis of more complex molecules.
Biological Significance: Some hydrazones exhibit biological activity, making them targets for pharmaceutical research. Their unique structure can result in compounds with potential therapeutic applications.
Color Reactions: Many hydrazones, including this compound, are known for their ability to form colorful complexes with certain metals. These color changes can be utilized in analytical chemistry for qualitative analysis.
Applications in Material Science: This compound can serve as a building block in organic synthesis, leading to diverse applications in material science, such as in the creation of polymers and dyes.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." The study of compounds like 2-(diethylhydrazono)-1-(4-phenylphenyl)ethanone certainly supports this idea, showcasing the endless possibilities that exist within the realm of chemical compounds.

In summary, the intriguing structure and properties of 2-(diethylhydrazono)-1-(4-phenylphenyl)ethanone position it as an essential compound in both academic research and practical applications. Its contribution to chemistry highlights the intertwining nature of scientific exploration and innovation.