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

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Identification
Molecular formula
C8H6FN3O5
IUPAC name
N-(2,4-dinitrophenyl)-2-fluoro-acetamide
State
State

The compound is in a solid state at room temperature. It is typically found as a crystalline powder given its aromatic structure and the presence of nitro groups.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.00
Boiling point (Celsius)
286.00
Boiling point (Kelvin)
559.00
General information
Molecular weight
244.14g/mol
Molar mass
244.1370g/mol
Density
1.6300g/cm3
Appearence

N-(2,4-dinitrophenyl)-2-fluoroacetamide typically appears as a crystalline solid. The compound has a characteristic yellow color, which is common for many nitro-substituted aromatic compounds. This coloration is due to the nitro groups that are conjugated with the aromatic ring.

Comment on solubility

Solubility of N-(2,4-dinitrophenyl)-2-fluoro-acetamide

N-(2,4-dinitrophenyl)-2-fluoro-acetamide is a compound that exhibits interesting solubility characteristics. Understanding its solubility can provide insights into its behavior in various environments.

Solubility Traits:

  • Polar Nature: Due to the presence of the acetamide functional group, this compound tends to be more soluble in polar solvents like water.
  • Aromatic Interaction: The dinitrophenyl group increases the compound's ability to interact with other compounds, often enhancing solubility in organic solvents.
  • pH Influence: The solubility can also be affected by pH levels, as the ionization of the amide function can occur under certain conditions.

In practice, one may find that:

  • Soluble in: Polar solvents (e.g., water, methanol).
  • Less soluble in: Nonpolar solvents (e.g., hexane, toluene).

As a general rule, compounds with both polar and nonpolar features often demonstrate variable solubility depending on the solvent system employed. It is crucial to consider these factors when working with N-(2,4-dinitrophenyl)-2-fluoro-acetamide to predict its behavior in different chemical scenarios.

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.

Synonyms
2',4'-Dinitro-2-fluoroacetanilide
23554-59-8
ACETANILIDE, 2',4'-DINITRO-2-FLUORO-
BRN 2150209
DTXSID50178142
RefChem:315664
DTXCID80100633