N-(9H-fluoren-2-yl)formamide

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Identification

Molecular formula
C14H11NO
CAS Number
null
IUPAC Name
N-(9H-fluoren-2-yl)formamide
Molecular Weight
195.23g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
Synonyms
2-Formylaminofluorene
Interesting facts

Interesting Facts about N-(9H-fluoren-2-yl)formamide

N-(9H-fluoren-2-yl)formamide is a fascinating compound that draws attention not only for its unique structure but also for its applications in various fields. Below are some remarkable aspects of this compound:

  • Chemical Structure: The compound features a fluorenyl group, making it a part of the polycyclic aromatic hydrocarbons. This structure is known for its distinct carbon frameworks that can exhibit interesting electronic properties.
  • Applications in Organic Synthesis: N-(9H-fluoren-2-yl)formamide is utilized as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its versatility makes it a valuable building block in crafting complex organic molecules.
  • Biological Activity: Some derivatives of this compound have shown potential biological activity, which has made them subjects of interest in medicinal chemistry research. The exploration of its derivatives could lead to new therapeutic agents.
  • Fluorescent Properties: Compounds related to fluorenes often exhibit fluorescence, which can be utilized in various applications, including organic light-emitting diodes (OLEDs) and biological imaging techniques.
  • Research Significance: The study of N-(9H-fluoren-2-yl)formamide and its reactions offers insights into reaction mechanisms and can enhance our understanding of fundamental organic chemistry principles.

Understanding compounds like N-(9H-fluoren-2-yl)formamide expands our knowledge and showcases the intricate relationships between chemical structure and function. As stated by famous chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This compound is a testament to the innovative ideas that arise from studying diverse chemical entities.

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