N-(2,4-dinitrophenyl)-2-fluoroacetamide

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Identification

Molecular formula
C8H6FN3O5
IUPAC Name
N-(2,4-dinitrophenyl)-2-fluoro-acetamide
Molecular Weight
244.14g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.6300g/cm3
Synonyms
2', 4'-Dinitro-2-fluoroacetanilide
Interesting facts

Interesting Facts about N-(2,4-dinitrophenyl)-2-fluoro-acetamide

N-(2,4-dinitrophenyl)-2-fluoro-acetamide is a fascinating compound with unique properties and applications in the field of chemistry. Here are some compelling aspects that make this compound noteworthy:

  • Prototypical Structure: This compound features a dinitrophenyl group, which is known for its ability to serve as an electron-withdrawing moiety, enhancing the reactivity of the amide nitrogen.
  • Fluorination Impact: The incorporation of a fluorine atom at the 2 position disrupts the electronic landscape of the molecule and can significantly alter its chemical reactivity and biological activity.
  • Applications in Research: N-(2,4-dinitrophenyl)-2-fluoro-acetamide is often utilized as a reagent in organic synthesis. Its ability to form stable adducts makes it an invaluable tool in studying reaction mechanisms.
  • Analytical Chemistry: This compound has roots in analytical chemistry, as it can be utilized in the synthesis of derivatives for various analytical techniques, including chromatography.
  • Toxicological Studies: The dinitrophenyl moiety is known for potential toxicity, prompting research into the safety implications of compounds containing this group, making it an important subject for toxicological assessment.

In summary, N-(2,4-dinitrophenyl)-2-fluoro-acetamide is not just a simple amide; it embodies a rich tapestry of chemical interactions and applications that continue to intrigue scientists and researchers alike. As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." This compound is a testament to the creativity and innovation inherent in the field of chemistry.

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