fluorenyl ethylaminopropanoate
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- Molecular formula
- C23H25NO2
- CAS Number
- 117401-84-2
- IUPAC Name
- 9H-fluoren-9-yl 3-(diethylamino)propanoate
- Molecular Weight
- 353.46g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1742g/cm3
- Synonyms
- 9H-fluoren-9-yl 3-(diethylamino)propanoate
Identification
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.