Interesting facts
Exploring N-(5-Fluoro-9H-Fluoren-2-yl)acetamide
N-(5-Fluoro-9H-fluoren-2-yl)acetamide is a fascinating chemical compound that has garnered interest in various fields, particularly in medicinal chemistry and materials science. Below are some intriguing facts that showcase its significance:
- Fluorine's Role: The incorporation of a fluoro group is known to influence the biological activity of compounds. Fluorine can enhance lipophilicity and metabolic stability, making N-(5-fluoro-9H-fluoren-2-yl)acetamide a candidate for pharmaceutical applications in drug design.
- Structural Versatility: As a derivative of fluoren, this compound exhibits a unique aromatic structure that can interact with various biological targets. The planar conformation allows for stacking interactions, which is often important in ligand-receptor binding.
- Applications in Material Science: The remarkable structural properties mean that N-(5-fluoro-9H-fluoren-2-yl)acetamide can also be employed in the synthesis of organic semiconductors and other advanced materials. The stability and versatility of the fluoren group provide avenues for creating innovative materials.
- Potential Anticancer Properties: Research indicates that fluorinated compounds can exhibit anticancer activity. As such, this compound is being studied for its potential effectiveness against certain types of cancer by targeting specific cellular pathways.
- Research Interest: The compound has been the subject of several studies focusing on its chemical reactivity and interaction with various biological systems, illustrating the continuous exploration within various branches of chemistry.
In conclusion, N-(5-fluoro-9H-fluoren-2-yl)acetamide stands as a compound of great interest, representing both the complexity of its chemical structure and the vast array of potential applications in scientific research. As chemists delve deeper into understanding its properties, the contributions of this compound to both medicine and material science may continue to expand.
Synonyms
5-Fluoro-2-faa
5-Fluoro-2-acetylaminofluorene
ACETAMIDE, N-(5-FLUOROFLUOREN-2-YL)-
2823-90-7
N-(5-Fluorofluoren-2-yl)acetamide
Acetamide, N-(5-fluoro-9H-fluoren-2-yl)-
RQU33HD7SA
NSC-46524
NSC 46524
BRN 2811031
N-(5-fluoro-9H-fluoren-2-yl)acetamide
NSC46524
UNII-RQU33HD7SA
CHEMBL85787
DTXSID10182482
WLN: L B656 HHJ CF KMV1
Acetamide,n-(5-fluoro-9h-fluoren-2-yl)-
DS-006287
Solubility of N-(5-fluoro-9H-fluoren-2-yl)acetamide
N-(5-fluoro-9H-fluoren-2-yl)acetamide presents interesting solubility characteristics that can be influenced by several factors. Its solubility can be summarized as follows:
When considering solubility, it is crucial to note that factors such as molecular structure, polarity, and intermolecular interactions all play significant roles. As a rule of thumb, "like dissolves like," meaning that N-(5-fluoro-9H-fluoren-2-yl)acetamide, being predominantly non-polar, will dissolve well in non-polar to slightly polar organic solvents while struggling in polar aqueous environments.
Overall, understanding the solubility of this compound is essential for its applications in various fields, including pharmaceuticals and organic synthesis.