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fluorenyl ethylaminopropanoate

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Identification
Molecular formula
C23H25NO2
CAS number
117401-84-2
IUPAC name
9H-fluoren-9-yl 3-(diethylamino)propanoate
State
State

At room temperature, this compound is in a solid state, characterized by a crystalline structure.

Melting point (Celsius)
67.00
Melting point (Kelvin)
340.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
353.46g/mol
Molar mass
353.4560g/mol
Density
1.1742g/cm3
Appearence

The compound is typically an off-white to beige crystalline solid. It may appear as fine powder or small crystals depending on its purification form.

Comment on solubility

Solubility of 9H-fluoren-9-yl 3-(diethylamino)propanoate

The solubility of 9H-fluoren-9-yl 3-(diethylamino)propanoate can be influenced by various factors, including its molecular structure and polarity. Generally, this compound exhibits interesting solubility characteristics:

  • Polarity: The presence of both hydrophobic (fluorene group) and hydrophilic (diethylamino group) components suggests that this compound may be soluble in organic solvents but could have limited solubility in water.
  • Common Solvents: Organic solvents such as ethanol, chloroform, and dimethyl sulfoxide (DMSO) are likely to dissolve this compound effectively due to their compatibility with its molecular structure.
  • Temperature Effects: Increasing temperature often enhances solubility; thus, this compound may show better solubility in warm organic solvents.
  • pH Sensitivity: The solubility of compounds containing amine groups can vary with pH, as ionization can occur. An alkaline environment might increase its solubility due to the potential conversion of the amine group into a more soluble amine salt.

Ultimately, experimental measurements would be necessary to determine the precise solubility parameters of 9H-fluoren-9-yl 3-(diethylamino)propanoate under different conditions, as its solubility can significantly impact its applicability in various fields.

Interesting facts

Interesting Facts about 9H-fluoren-9-yl 3-(diethylamino)propanoate

9H-fluoren-9-yl 3-(diethylamino)propanoate is a fascinating compound that serves as a testament to the ingenuity of organic chemistry. Here are some intriguing aspects of this compound:

  • Versatile Building Block: This compound is often utilized in the synthesis of complex molecules due to its unique structural features, particularly the fluorenyl moiety which acts as a robust scaffold for various chemical transformations.
  • Pharmaceutical Applications: The diethylamino group attached to the propanoate chain is known for enhancing the solubility and biological activity of compounds, making this molecule potentially significant in medicinal chemistry.
  • Fluorene Derivatives: As a derivative of fluorene, this compound shares properties with other fluorene-based compounds, such as photophysical characteristics that are valuable in organic light-emitting diodes (OLEDs).
  • Research Interest: Scientists are exploring the potential of this compound in various fields, from drug development to polymer science, highlighting its importance in innovative research.
  • Reaction Versatility: 9H-fluoren-9-yl groups are known to participate in numerous chemical reactions, including coupling reactions, making them important in creating new carbon-carbon bonds in synthetic organic chemistry.

In summary, 9H-fluoren-9-yl 3-(diethylamino)propanoate exemplifies the dynamic possibilities within organic synthesis, and it continues to attract the attention of researchers aiming to expand its applicability in various technological and pharmaceutical realms. As a chemist, one can truly appreciate the significant role such compounds play in the advancement of science.

Synonyms
9H-fluoren-9-yl 3-(diethylamino)propanoate
SCHEMBL8097202