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Furylfurylaminoxadiazole

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Identification
Molecular formula
C12H8N4O5
CAS number
4547-62-8
IUPAC name
5-[1-(2-furyl)-2-(5-nitro-2-furyl)vinyl]-1,3,4-oxadiazol-2-amine
State
State

At room temperature, this compound is typically a solid.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.15
Boiling point (Celsius)
202.00
Boiling point (Kelvin)
475.15
General information
Molecular weight
274.22g/mol
Molar mass
274.2180g/mol
Density
1.5900g/cm3
Appearence

This compound typically appears as a yellow to orange crystalline powder.

Comment on solubility

Solubility of 5-[1-(2-furyl)-2-(5-nitro-2-furyl)vinyl]-1,3,4-oxadiazol-2-amine

The solubility characteristics of the compound 5-[1-(2-furyl)-2-(5-nitro-2-furyl)vinyl]-1,3,4-oxadiazol-2-amine are noteworthy and can be influenced by several factors. Understanding its solubility is crucial for applications in pharmaceuticals and materials science. Here are some key points regarding its solubility:

  • Solvent Interaction: The presence of furan rings and nitro groups suggests varying solubility in polar and non-polar solvents.
  • Polar Solvents: Likely to have some solubility in water and alcohols due to the amino group, which can form hydrogen bonds.
  • Non-Polar Solvents: May display increased solubility in organic solvents such as dichloromethane or ether due to its hydrophobic components.
  • Effect of pH: Solubility may be pH-dependent, with increased solubility at higher pH levels owing to the amine group's protonation.
  • Temperature Influence: Dissolution can be temperature-sensitive; elevated temperatures may enhance solubility in certain solvents.

In conclusion, while definitive solubility data may be limited, the structural features of 5-[1-(2-furyl)-2-(5-nitro-2-furyl)vinyl]-1,3,4-oxadiazol-2-amine suggest a multifaceted behavior in various solvents attributed to its complex composition.

Interesting facts

Interesting Facts about 5-[1-(2-furyl)-2-(5-nitro-2-furyl)vinyl]-1,3,4-oxadiazol-2-amine

This compound is a fascinating member of the oxadiazole family, known for its diverse applications in pharmaceuticals and material sciences. The structural complexity of this compound, with its multiple functional groups, makes it an excellent subject of study for scientists interested in organic synthesis and medicinal chemistry.

Chemical Properties and Significance

  • Oxadiazole Backbone: The oxadiazole ring contributes to a unique combination of electronic properties, enabling the compound to participate in various chemical reactions.
  • Furyl Groups: The presence of furyl groups enhances the compound's potential in designing novel therapeutic agents due to their biological activity, including antimicrobial and anticancer properties.
  • Nitro Substitution: Nitro groups are known for increasing the reactivity of organic compounds. This compound’s nitro-derivatives can serve as key intermediates in synthetic pathways.

Applications and Research Avenues

Research into this compound has unveiled numerous potential applications, particularly in the fields of:

  • Medicinal Chemistry: Its unique structure may lead to compounds that can target specific diseases.
  • Material Science: Oxadiazole compounds have shown promising properties in light-emitting devices and organic photovoltaics.
  • Agricultural Science: Investigations suggest it might possess properties that can help in developing agrochemicals.

In Summary

5-[1-(2-furyl)-2-(5-nitro-2-furyl)vinyl]-1,3,4-oxadiazol-2-amine is not just a chemical compound; it is a roadmap for future discoveries in various scientific domains. Its intriguing structure opens doors to numerous avenues of research, making it a significant player in the search for new and innovative solutions.

Synonyms
DTXSID101318407