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Nitrofurazone

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Identification
Molecular formula
C6H4N4O3
CAS number
59-87-0
IUPAC name
5-(5-nitro-2-furyl)-1H-1,2,4-triazole
State
State

At room temperature, Nitrofurazone is in a solid state.

Melting point (Celsius)
237.00
Melting point (Kelvin)
510.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
197.11g/mol
Molar mass
197.1440g/mol
Density
1.6670g/cm3
Appearence

Nitrofurazone appears as a yellow, crystalline powder.

Comment on solubility

Solubility of 5-(5-nitro-2-furyl)-1H-1,2,4-triazole

The solubility of 5-(5-nitro-2-furyl)-1H-1,2,4-triazole in various solvents is a significant consideration in its applications. This compound exhibits the following solubility characteristics:

  • Solvent Polarity: Generally, polar solvents such as water may not dissolve this compound effectively due to its hydrophobic characteristics.
  • Organic Solvents: 5-(5-nitro-2-furyl)-1H-1,2,4-triazole tends to have better solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO).
  • Temperature Dependence: Solubility may increase with temperature, making it crucial to consider thermal conditions during experiments and applications.

In practical applications, the limited solubility in aqueous solutions may necessitate the use of solvent additives or methodologies to enhance its solubility profile. As a compound of interest, understanding its solubility characteristics can lead to more effective utilization in various chemical processes.

Interesting facts

Interesting Facts about 5-(5-nitro-2-furyl)-1H-1,2,4-triazole

5-(5-nitro-2-furyl)-1H-1,2,4-triazole is a fascinating compound widely recognized in the field of medicinal chemistry. This compound belongs to a broader class of triazoles, which are known for their diverse biological and pharmacological activities. Here are some intriguing aspects:

  • Pharmacological Potential: Research has shown that this compound exhibits significant antifungal and antiviral properties, making it an interesting candidate for developing new medications.
  • Synergy with Other Agents: Its unique structural features often allow it to act synergistically with other compounds, enhancing their therapeutic effects.
  • Role in Agriculture: The nitrofuryl group is particularly valuable in agricultural chemistry, where it can aid in producing effective agrochemicals.
  • Scientific Studies: Numerous studies have focused on the synthesis and applications of this compound, employing various methods to explore its reactivity and interactions.

One of the most appealing aspects is the compound’s heterocyclic nature, which contributes to its reactivity and facilitates various chemical transformations. As a chemistry student, you might find it intriguing how triazoles have paved the way for numerous discoveries in drug development and materials science.

In summary, 5-(5-nitro-2-furyl)-1H-1,2,4-triazole highlights the remarkable intersection of chemistry and biology, embodying the potential for innovative solutions in health and agricultural sectors.

Synonyms
5019-55-6
3-(5-Nitro-2-furyl)-4H-1,2,4-triazole
3-(5-Nitro-2-furanyl)-1,2,4-triazole
4H-1,2,4-TRIAZOLE, 3-(5-NITRO-2-FURYL)-
3-(5-NITROFURAN-2-YL)-4H-1,2,4-TRIAZOLE
CCRIS 1203
3-(5-nitro-furan-2-yl)-1H-[1,2,4]triazole
s-Triazole, 3-(5-nitro-2-furyl)-
1H-1,2,4-Triazole, 3-(5-nitro-2-furanyl)-
DTXSID40198233
OHEIGDXIMWTXGW-UHFFFAOYSA-N
AKOS006278708
5-(5-nitro-2-furyl)-1,2,4-triazole
3-(5-Nitro-2-furyl)-1H-1,2,4-triazole #