TFNA (Trifluoroacetamide)

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Identification

Molecular formula
C15H9F3N2O3
CAS Number
.
IUPAC Name
2,2,2-trifluoro-N-(7-nitro-9H-fluoren-2-yl)acetamide
Molecular Weight
308.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5120g/cm3
Synonyms
2926-70-7
Interesting facts

Interesting Facts about 2,2,2-Trifluoro-N-(7-nitro-9H-fluoren-2-yl)acetamide

2,2,2-Trifluoro-N-(7-nitro-9H-fluoren-2-yl)acetamide is a compound that presents fascinating characteristics and applications, particularly in the realms of medicinal and synthetic chemistry. Here are some engaging insights into this intriguing compound:

  • Unique Structure: This compound features a trifluoromethyl group, which dramatically affects its chemical properties, often enhancing its ability to interact with biological systems.
  • Medicinal Chemistry: Due to the presence of both the nitro and acetamide functional groups, it shows potential as a lead compound in the development of pharmaceuticals. Compounds with such moieties can be vital in the design of novel drugs.
  • Fluorine's Influence: The trifluoro group is known for modifying a compound's lipophilicity and metabolic stability, making it a focus of research in drug design. As a highlight, fluorinated compounds often exhibit improved pharmacokinetics.
  • Research Applications: The unique properties of 2,2,2-trifluoro-N-(7-nitro-9H-fluoren-2-yl)acetamide also make it a useful tool in the fields of materials science and agrochemicals.
  • Potential Toxicity: As with many nitro compounds, toxicity is an important consideration. Understanding the environmental and biological impact of this compound is crucial, guiding scientists in its safe application.

In conclusion, 2,2,2-trifluoro-N-(7-nitro-9H-fluoren-2-yl)acetamide is not just a compound of theoretical interest but is at the intersection of innovative research avenues. Its unique structure and multifaceted applications continue to inspire scientists and chemists alike.

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