N-(9H-fluoren-2-yl)-N-oxido-acetamide

Identification

Molecular formula

C₁₅H₁₁NO₂

CAS number

not assigned

IUPAC name

N-(9H-fluoren-2-yl)-N-oxido-acetamide

State

This compound is a solid at room temperature, typically found as a crystalline powder. It is stable under standard conditions of temperature and pressure.

Melting point (Celsius)

154.00

Melting point (Kelvin)

427.15

Boiling point (Celsius)

340.00

Boiling point (Kelvin)

613.15

General information

Molecular weight

239.26g/mol

Molar mass

239.2590g/mol

Density

1.6205g/cm³

Appearence

N-(9H-fluoren-2-yl)-N-oxido-acetamide typically appears as a white to off-white crystalline powder. This compound is usually found in a solid state at room temperature.

Comment on solubility

Solubility of N-(9H-fluoren-2-yl)-N-oxido-acetamide

N-(9H-fluoren-2-yl)-N-oxido-acetamide exhibits intriguing solubility characteristics, which are influenced by its unique molecular structure. Understanding its solubility can be broken down into several key factors:

Polarity: The presence of the N-oxido group suggests a level of polarity, which typically enhances solubility in polar solvents. However, the fluorenyl moiety may introduce hydrophobic characteristics that can complicate solubility.
Solvent Interactions: N-(9H-fluoren-2-yl)-N-oxido-acetamide is likely to be more soluble in polar organic solvents (e.g., dimethyl sulfoxide, acetonitrile) compared to non-polar solvents (e.g., hexane).
Temperature Influence: Increasing the temperature often increases the solubility of solid compounds, potentially enabling better dissolution in selected solvents.
HX Formulation: This compound may have limited solubility in water, typical for many organic amides, but one might observe increased solubility with the formation of salts or derivatives.

Overall, while N-(9H-fluoren-2-yl)-N-oxido-acetamide's solubility in water may be limited, its behavior in organic solvents can yield interesting results. Understanding the interplay of these factors is crucial for predicting the solubility of this compound in various applications.

Interesting facts

Interesting Facts about N-(9H-fluoren-2-yl)-N-oxido-acetamide

N-(9H-fluoren-2-yl)-N-oxido-acetamide is a fascinating compound with numerous applications and characteristics that intrigue both researchers and students alike. Here are some remarkable points to consider:

Structural Complexity: The compound features a unique fluorenyl moiety, which contributes to its stability and reactivity. The presence of a nitrogen-oxide functional group adds to its chemical versatility.
Applications in Organic Synthesis: This compound is often employed in organic synthesis, where it can act as a useful intermediate. Its reactivity makes it a key player in various chemical reactions.
Role in Medicinal Chemistry: The structure of N-(9H-fluoren-2-yl)-N-oxido-acetamide may lend itself to potential therapeutic applications. Exploring derivatives of this compound can lead to discovering new pharmaceutical agents.
Research Interest: Scientists have shown an increasing interest in related oxido compounds due to their biological activities. Understanding the properties of N-(9H-fluoren-2-yl)-N-oxido-acetamide can pave the way for novel discoveries.
Photophysical Properties: Fluorene derivatives are known for their interesting photophysical properties, such as fluorescence. This attribute could open avenues in the development of functional materials or sensors.

In summary, N-(9H-fluoren-2-yl)-N-oxido-acetamide stands out in the field of chemistry not only for its structural uniqueness but also for its potential contributions to both organic synthesis and medicinal chemistry. As research continues, this compound may unveil even more exciting applications and insights.