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Furazolidone

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Identification
Molecular formula
C7H4N2O4
CAS number
67-45-8
IUPAC name
3-(5-nitro-2-furyl)prop-2-enal
State
State

Furazolidone is in a solid state at room temperature, existing as a stable crystalline powder.

Melting point (Celsius)
233.00
Melting point (Kelvin)
506.15
Boiling point (Celsius)
259.00
Boiling point (Kelvin)
532.15
General information
Molecular weight
225.16g/mol
Molar mass
225.1640g/mol
Density
1.4500g/cm3
Appearence

Furazolidone primarily appears as an orange-yellow crystalline powder, which is indicative of many nitrofuran derivatives. The powder is usually bright and quite distinct, making it recognizable in its pure form.

Comment on solubility

Solubility of 3-(5-nitro-2-furyl)prop-2-enal

The solubility of 3-(5-nitro-2-furyl)prop-2-enal can be quite interesting, reflecting its unique structure and functional groups. Solubility often depends on several factors such as the presence of polar or non-polar groups, temperature, and the solvent used.

  • Polar Functional Groups: The presence of the nitro group (–NO2) increases polarity, which tends to enhance solubility in polar solvents such as water.
  • Aromaticity: The furan ring can exhibit some degree of non-polar characteristics, potentially limiting solubility in highly polar solvents.
  • Solvent Interaction: It is likely to be more soluble in organic solvents like ethanol, methanol, and acetone due to the combination of polar and non-polar features.

In summary, while 3-(5-nitro-2-furyl)prop-2-enal may display reasonable solubility in polar solvents, its overall behavior will be significantly influenced by solvent choice. As with many organic compounds, it is essential to understand the specific conditions of solubility to predict its behavior accurately.

As a final note, remember that solubility can vary based on temperature and concentration, meaning evaluations must consider these factors for an accurate assessment.

Interesting facts

Interesting Facts about 3-(5-nitro-2-furyl)prop-2-enal

3-(5-nitro-2-furyl)prop-2-enal is an intriguing organic compound known for its unique structure and versatile applications in various fields. Here are some fascinating insights:

  • Chemical Structure: This compound features a conjugated system, which enhances its reactivity and potential use in organic synthesis.
  • Biological Activity: Compounds that contain furyl rings have been studied for their biological properties, including potential anti-inflammatory and anticancer activities, making them of interest in medicinal chemistry.
  • Versatile Reactivity: The unsaturated aldehyde functionality allows for numerous chemical reactions, such as Michael additions and aldol reactions, showcasing its utility in building complex molecules.
  • Potential Uses in Dyes: The unique chromophore of the furyl group has led to research exploring the compound's use in dyes and pigments, particularly in creating colorants with distinctive shades.
  • Synthetic Routes: Several pathways can be employed to synthesize this compound, providing chemists with valuable options for its production and incorporation into various chemical processes.

This compound serves as an excellent example of how small modifications in structure can lead to significant differences in properties and reactivity, making it a vital topic of study in the realms of organic and medicinal chemistry.

Synonyms
3-(5-nitrofuran-2-yl)prop-2-enal
3-(5-Nitro-2-furyl)-2-propenal
MFCD00009762
SCHEMBL291297
DTXSID50870917
DXWCZMGIIFEEPU-UHFFFAOYSA-N
3-(5-nitro-2-furanyl)-propenal
3-(nitro-2-furanyl)-2-propenal
3-(5-nitro-2-furyl)acrylaldehyde
AKOS030228096
SB60885
SY116526
(2E)-3-(5-nitro-2-furanyl)-2-Propenal
DB-044641
G82849