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Nitrofurazone

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Identification
Molecular formula
C8H6N2O5
CAS number
59-87-0
IUPAC name
2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid
State
State

At room temperature, Nitrofurazone typically exists as a solid in the form of a yellow powder. It is stable under normal conditions and is used frequently in various pharmaceutical applications.

Melting point (Celsius)
236.00
Melting point (Kelvin)
509.00
Boiling point (Celsius)
336.00
Boiling point (Kelvin)
609.00
General information
Molecular weight
225.15g/mol
Molar mass
225.1560g/mol
Density
1.5494g/cm3
Appearence

Nitrofurazone appears as a yellow, crystalline powder. It is known for its bright yellow color and is often available in a finely divided form for medical or laboratory applications.

Comment on solubility

Solubility of 2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid

The solubility characteristics of 2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid can be intriguing, given its unique structural features. Understanding the solubility of this compound is essential for its applications in various fields, particularly in pharmaceuticals and organic synthesis.

Key Factors Affecting Solubility

Several factors influence the solubility of this compound, including:

  • Polarity: The presence of both furyl and nitro groups typically enhances polarity, which may improve solubility in polar solvents.
  • Hydrogen Bonding: The carboxylic acid functional group is likely capable of forming hydrogen bonds, enhancing solubility in water.
  • Solvent Effects: It is expected to demonstrate varying solubility in different solvents, possibly being more soluble in organic solvents like ethanol or dimethyl sulfoxide (DMSO).

Expected Solubility Behavior

In general, compounds with multiple functional groups such as 2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid tend to exhibit:

  • Good solubility in organic solvents, making them useful for chemical reactions and formulations.
  • Moderate solubility in water, particularly if the conditions promote hydrogen bonding.
  • Concentration-dependent behavior, where solubility might significantly change with varying concentrations and temperatures.

To summarize, the solubility of 2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid is multifaceted, primarily influenced by its structural properties, polarity, and the nature of the solvent. Understanding these aspects is crucial for effective application and formulation.

Interesting facts

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

2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid is a notable compound in the realm of organic chemistry, particularly due to its unique structure and potential applications. Here are some engaging insights about this fascinating molecule:

  • Structural Distinction: This compound features two furan rings, which are five-membered aromatic systems containing oxygen. The presence of both a nitro group and a double bond in the prop-2-enoic acid backbone adds layers of complexity to its chemical reactivity.
  • Pharmaceutical Relevance: Compounds similar to 2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid have been studied for their potential anticancer properties. The nitro group can be converted into reactive species that may interact with cellular targets, prompting research into its medicinal chemistry prospects.
  • Material Science Applications: The unique electronic properties of furan-based compounds have led researchers to explore their use in organic electronics, such as organic light-emitting diodes (OLEDs) and organic solar cells. Their ability to act as electron donors or acceptors in conductive pathways is a subject of ongoing investigation.
  • Environmental Impact: The nitro-containing compounds can sometimes exhibit toxicity, raising metabolic and environmental concerns. This leads to studies on biodegradation and the environmental fate of such compounds, which is crucial for sustainable chemistry.
  • Synthesis and Characterization: The synthesis of furan derivatives like this compound often involves intricate organic reactions such as cross-coupling and functionalization. Techniques like nuclear magnetic resonance (NMR) and mass spectrometry are pivotal in characterizing the structure and confirming the identity of the synthesized compounds.

In conclusion, 2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enoic acid represents a meaningful intersection of chemistry, biology, and materials science. As research continues, the potential of this and related compounds may unveil new technologies and medical therapies. Truly, the realms of possibility are as vast as the chemical structures themselves!