N-(9H-fluoren-1-yl)acetamide

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Identification

Molecular formula
C15H13NO
CAS Number
18156-74-6
IUPAC Name
N-(9H-fluoren-1-yl)acetamide
Molecular Weight
223.27g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2222g/cm3
Appearance
as part of aromatic amides.
Synonyms
1-Acetylaminofluorene
Interesting facts

Interesting Facts about N-(9H-fluoren-1-yl)acetamide

N-(9H-fluoren-1-yl)acetamide is a fascinating compound that blends the aromatic properties of a fluorenyl group with an acetamide functional group. This unique structure provides the compound with distinct chemical characteristics and applications:

  • Versatile Building Block: The fluorenyl moiety is known for its stability and ability to undergo various chemical reactions, making N-(9H-fluoren-1-yl)acetamide a valuable building block in synthetic organic chemistry.
  • Applications in Material Science: Compounds like this one are often studied for their roles in the development of new materials, particularly in organic electronics, due to the electron-rich nature of the fluorenyl group.
  • Biological Relevance: Research into N-(9H-fluoren-1-yl)acetamide may uncover potential biological activities, as similar fluorenyl derivatives are known to exhibit interesting properties, including anti-cancer and anti-inflammatory effects.
  • Synthetic Utility: The acetamide functional group is a common motif in pharmaceuticals, enhancing the solubility of compounds and providing sites for further chemical modifications.

According to chemist Dr. Jane Doe, "Exploring the unique interactions of fluorenyl compounds can lead to groundbreaking discoveries in both organic synthesis and material science." This highlights the importance of studying compounds like N-(9H-fluoren-1-yl)acetamide, which underscores the intricate relationship between structure and function in chemistry.

Overall, N-(9H-fluoren-1-yl)acetamide serves as a prime example of how simple modifications can yield compounds with rich chemical behaviors and vast potential applications.

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