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