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DBF

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Identification
Molecular formula
C25H31NO2
CAS number
301-05-5
IUPAC name
2-(dibutylamino)ethyl 9H-fluorene-9-carboxylate
State
State

At room temperature, it is typically found in the solid state.

Melting point (Celsius)
57.00
Melting point (Kelvin)
330.15
Boiling point (Celsius)
388.00
Boiling point (Kelvin)
661.15
General information
Molecular weight
367.53g/mol
Molar mass
367.5040g/mol
Density
1.0485g/cm3
Appearence

It appears as a solid, typically in the form of a crystalline powder, and is often colorless to pale yellow.

Comment on solubility

Solubility of 2-(dibutylamino)ethyl 9H-fluorene-9-carboxylate

The solubility of 2-(dibutylamino)ethyl 9H-fluorene-9-carboxylate is influenced by various factors, given its complex chemical structure. Understanding its solubility can be quite fascinating:

  • Polarity: This compound contains both hydrophobic (the fluorene moiety) and hydrophilic (the amino and carboxylate functional groups) characteristics, which suggest that its solubility in water may be limited.
  • Solvent Compatibility: It is likely to dissolve better in organic solvents such as ethanol, acetone, and dichloromethane due to the presence of the non-polar fluorene structure.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, allowing for better dissolution in organic media.

While no exact solubility values are widely reported, it is essential to consider the following elements:

  1. Hydrophobic Interactions: These may hinder aqueous solubility but facilitate interactions with organic phase solvents.
  2. Concentration Effects: Higher concentrations might lead to precipitation in polar solvents, indicating a threshold for solubility.

In conclusion, while 2-(dibutylamino)ethyl 9H-fluorene-9-carboxylate's solubility may not be straightforward, its behavior in varying solvents and conditions provides intriguing avenues for exploration in practical applications!

Interesting facts

Interesting Facts about 2-(Dibutylamino)ethyl 9H-Fluorene-9-carboxylate

2-(Dibutylamino)ethyl 9H-fluorene-9-carboxylate is a fascinating compound that exemplifies the intersection of organic chemistry and medicinal applications. Here are some compelling aspects:

  • Fluorene Derivative: This compound is derived from fluorene, a polycyclic aromatic hydrocarbon known for its unique structure, which consists of a benzene ring fused to a cyclopentane ring. The presence of such a framework often imparts interesting electronic properties to the molecule.
  • Biological Relevance: Compounds like this one are significant in the pharmaceutical industry. The dibutylamino group can enhance solubility and potential bioactivity, making it a subject of interest in drug design and development.
  • Versatile Applications: The ability to modify molecular structures allows for tailoring the compound for specific functions—ranging from pharmaceutical uses in drug development to applications in organic materials and dyes.
  • Surface Properties: The carboxylate functional group contributes to the compound's reactivity and interaction with other molecules, enabling it to participate in various chemical reactions, or serve as a precursor for further synthesis.
  • Research & Innovation: The exploration of compounds such as 2-(dibutylamino)ethyl 9H-fluorene-9-carboxylate can lead to the discovery of new materials or therapeutic solutions, highlighting the critical role of organic chemistry in modern science.

Overall, understanding the characteristics and applications of this compound not only broadens our knowledge of chemical diversity but also emphasizes the continual innovation in the field of chemistry.