N-(8-fluoro-9H-fluoren-2-yl)acetamide

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Identification

Molecular formula
C15H12FNO
CAS Number
1698-67-3
IUPAC Name
N-(8-fluoro-9H-fluoren-2-yl)acetamide
Molecular Weight
227.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3200g/cm3
Synonyms
8-Fluoro-2-faa
Interesting facts

Interesting Facts about N-(8-Fluoro-9H-fluoren-2-yl)acetamide

N-(8-Fluoro-9H-fluoren-2-yl)acetamide is a fascinating compound that belongs to the category of amides, characterized by the presence of the acetamide functional group. Here are some remarkable insights about this intriguing chemical:

  • Fluorine Impact: The presence of the fluorine atom at the 8-position on the fluorenyl ring significantly influences the chemical properties of this compound. Fluorine is known for its electronegativity, which can enhance the compound's stability and reactivity.
  • Pharmaceutical Relevance: Compounds like this are often investigated for their potential in medicinal chemistry, particularly in creating novel drugs, due to their unique structural properties.
  • Synthesis: The synthesis of N-(8-fluoro-9H-fluoren-2-yl)acetamide may involve various organic reactions, making it a subject of interest for synthetic chemists. Techniques such as amide formation via acylation reactions are common in this context.
  • Structure-Activity Relationship (SAR): Understanding the structure-activity relationship is crucial in organic chemistry, and this compound serves as an excellent example to study how modifications (such as fluorination) can impact biological activity.
  • Applications: Beyond medicinal applications, this compound's derivatives may have potential uses in organic electronics and materials science due to the stability imparted by the fluorenyl moiety.

As a chemistry student, appreciating such compounds as N-(8-fluoro-9H-fluoren-2-yl)acetamide opens up a deeper understanding of how molecular modifications can lead to varied functionalities, making it a valuable compound in both research and application.

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