Skip to main content

Nitrofurazone

ADVERTISEMENT
Identification
Molecular formula
C6H6N4O4
CAS number
59-87-0
IUPAC name
N-[(5-nitro-2-furyl)methyleneamino]acetamide
State
State

This compound exists as a solid at room temperature.

Melting point (Celsius)
236.00
Melting point (Kelvin)
509.15
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.15
General information
Molecular weight
198.16g/mol
Molar mass
198.1570g/mol
Density
1.4699g/cm3
Appearence

Nitrofurazone typically appears as a yellow crystalline powder. It is known for its bright, intense yellow color which can be used for identification.

Comment on solubility

Solubility of N-[(5-nitro-2-furyl)methyleneamino]acetamide

The solubility of N-[(5-nitro-2-furyl)methyleneamino]acetamide (C6H6N4O4) is influenced by several factors that are important to consider:

  • Polarity: Given the presence of both furan and nitro groups, the compound exhibits polar characteristics, which may enhance its solubility in polar solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding due to amino and carbonyl functionalities likely contributes to its solubility in water.
  • Solvent Specificity: The compound could be more soluble in organic solvents such as DMSO or ethanol compared to non-polar solvents, which may not interact well with the compound's functional groups.

Generally, solubility can often be assessed through qualitative measures, and in the case of N-[(5-nitro-2-furyl)methyleneamino]acetamide, it is best characterized as:

  • Moderately soluble in water
  • Soluble in organic solvents

Therefore, when working with this compound, it is crucial to consider the choice of solvent depending on the intended application or experiment, as well as potential interactions it may have in various environments. Understanding its solubility can provide insights into its reactivity and behavior in chemical reactions.

Interesting facts

Interesting Facts about N-[(5-nitro-2-furyl)methyleneamino]acetamide

N-[(5-nitro-2-furyl)methyleneamino]acetamide is a fascinating chemical compound that has garnered attention within the fields of medicinal chemistry and organic synthesis. Here are some interesting aspects about this compound:

  • Biological Relevance: Compounds containing nitro groups, such as this one, have been researched for their potential anti-cancer properties. The 5-nitro-2-furyl moiety is particularly known for its role in pharmaceuticals.
  • Versatile Applications: This compound can serve as an important precursor in the synthesis of various bioactive molecules, illustrating how modifying amino acids can lead to diverse functionalities.
  • Synthetic Pathways: The synthesis of N-[(5-nitro-2-furyl)methyleneamino]acetamide often involves methods such as condensation reactions. This showcases the importance of reaction conditions and reagents in obtaining desired compounds.
  • Research Potential: Due to its unique structure, this compound provides a rich area for scientific investigation, allowing researchers to explore its reactivity and interactions with biological systems.
  • Environmental Considerations: As a compound that contains nitro groups, it’s important to consider the environmental impact when synthesizing and using such compounds, as nitro compounds may have specific regulatory measures.

As noted by notable chemists, “The beauty of chemistry lies in the intricate relationships between structure and function.” This compound exemplifies that beauty, merging functional group chemistry with potential medicinal applications.

Continued research into N-[(5-nitro-2-furyl)methyleneamino]acetamide could unlock more of its mysteries and lead to innovative solutions in drug development and chemical synthesis.

Synonyms
DTXSID50859065
n'-[(5-nitrofuran-2-yl)methylidene]acetohydrazide