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BIFA

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Identification
Molecular formula
C9H8N2O2
CAS number
16456-21-0
IUPAC name
1-(2-furyl)-N-(2-furylmethyleneamino)methanimine
State
State

At room temperature, BIFA exists in a solid state.

Melting point (Celsius)
86.00
Melting point (Kelvin)
359.15
Boiling point (Celsius)
403.00
Boiling point (Kelvin)
676.15
General information
Molecular weight
160.17g/mol
Molar mass
160.1690g/mol
Density
1.3130g/cm3
Appearence

BIFA, or Bis(furfurylidene)amine, appears as a white to pale yellow crystalline solid.

Comment on solubility

Solubility of 1-(2-furyl)-N-(2-furylmethyleneamino)methanimine

The solubility of 1-(2-furyl)-N-(2-furylmethyleneamino)methanimine, a compound with intriguing structural features, may vary significantly depending on the solvent and environmental conditions. Generally, the solubility of organic compounds can be influenced by factors such as:

  • Polarity of the solvent: Polar solvents tend to dissolve polar compounds, while non-polar solvents are better suited for non-polar compounds.
  • Hydrogen bonding: The capacity for a compound to form hydrogen bonds can significantly enhance its solubility in appropriate solvents.
  • Temperature: Increased temperature often results in higher solubility due to enhanced molecular movements.
  • Structural characteristics: The presence of functional groups such as amino or furan rings can affect the solubility behavior dramatically.

For 1-(2-furyl)-N-(2-furylmethyleneamino)methanimine, one might expect the following:

  • **Moderate solubility in polar solvents** due to potential hydrogen bonding involving the amino group.
  • **Lower solubility in non-polar solvents** due to the presence of polar functionalities.

As stated, "Like dissolves like," making it essential to choose solvents judiciously for optimal solubility outcomes.

Further experimental data is required to ascertain precise solubility values, but understanding these solubility trends can indeed pave the way for practical applications and uses of this fascinating compound.

Interesting facts

Interesting Facts About 1-(2-Furyl)-N-(2-furylmethyleneamino)methanimine

This fascinating compound belongs to a class of substances known as aminomethanines, which are characterized by the presence of an amino group and an imine functional group. The structure of 1-(2-furyl)-N-(2-furylmethyleneamino)methanimine features two furyl groups, which are derived from furan, a five-membered aromatic ring containing oxygen. Here are some interesting aspects of this compound:

  • Biological Activity: Compounds containing furyl groups have garnered attention for their potential pharmaceutical applications, including anti-inflammatory and anti-cancer properties.
  • Research Applications: Due to its unique structure, this compound is often utilized in organic synthesis and may serve as a valuable building block in designing more complex molecules.
  • Photochemical Properties: The furan moiety is known for its excellent photochemical behavior, making this compound a candidate for studies involving light-induced transformations.
  • Reactivity: The presence of both imine and amino functionalities allows for versatile chemical reactions, potentially leading to new derivatives with altered biological properties.

Engagement with this compound is often interdisciplinary, bridging the fields of organic chemistry, medicinal chemistry, and material science. As a scientist or chemistry student, exploring the applications and reactions of 1-(2-furyl)-N-(2-furylmethyleneamino)methanimine can lead to exciting discoveries and innovations in research.

In the words of renowned chemist — "Compounds like these are the unsung heroes of chemical research, paving the way to new therapeutic solutions." This encapsulates the importance of investigating compounds with unique functionalities!

Synonyms
5428-37-5
2-Furancarboxaldehyde, (2-furanylmethylene)hydrazone
SCHEMBL1253529
DTXSID9063873
NS00033024