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1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine

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Identification
Molecular formula
C13H10N2O2
CAS number
13140-68-6
IUPAC name
1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine
State
State

At room temperature, the compound exists as a solid crystalline material.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
258.00
Boiling point (Kelvin)
531.15
General information
Molecular weight
210.23g/mol
Molar mass
211.2200g/mol
Density
1.1050g/cm3
Appearence

1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine is a beige to a light brown crystalline solid. It possesses a slight characteristic odor typical of aromatic heterocyclic compounds.

Comment on solubility

Solubility of 1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine

The solubility of 1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine can be described as relatively complex due to its unique structural components. This compound contains multiple aromatic rings, particularly the furan moieties, which can impact its solubility in different solvents.

Key Insights on Solubility:

  • Polar Solvents: The presence of amino groups generally enhances solubility in polar solvents such as water and alcohols. However, the hydrophobic furan rings may counteract this.
  • Non-Polar Solvents: In non-polar solvents (e.g., hexane, toluene), solubility may be increased because of the hydrophobic character of the furan structures.
  • Temperature Dependence: Solubility often increases with temperature, making higher temperatures potentially favorable for increasing the dissolution of this compound.
  • pH Levels: The solubility can also be significantly influenced by pH levels due to ionization of the amine group, which may enhance solubility in acidic or basic conditions.

In summary, while 1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine exhibits variable solubility, its dissolution characteristics depend on several factors, including the solvent polarity, temperature, and pH. This illustrates the fascinating interplay of chemical structure and solubility behavior.

Interesting facts

Interesting Facts about 1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine

This fascinating compound belongs to a class of organic molecules known as amino derivatives. The presence of furyl groups—derived from furan—gives this compound unique properties and potential applications. Here are some noteworthy points:

  • Structural Complexity: The compound exhibits a sophisticated structure that includes multiple furyl components, allowing for interesting interactions and reactivity. The combination of furyl and amino groups can lead to diverse chemical behavior.
  • Potential Biological Activity: Compounds containing furan rings are often explored for their biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. This makes such derivatives a focus of pharmaceutical research.
  • Synthetic Applications: The intricate structure of this compound makes it a candidate for various synthetic applications. In organic chemistry, it could potentially serve as a building block in the synthesis of complex molecules.
  • Functional Group Diversity: This compound showcases a variety of functional groups, which can be manipulated for targeting specific properties or reactivities in future research.

As exemplified by 1-(2-furyl)-N-[2-furyl-(2-furylmethyleneamino)methyl]methanimine, the chemistry behind amino derivatives and furan-based compounds presents both challenges and opportunities for scientists. The potential to create novel materials and drugs from such molecules reflects the ever-evolving field of organic chemistry, where innovation is at the forefront of discovery.

Synonyms
CBDivE_001121
DTXSID00871696
CYGDSXFTXXFMNI-OTYYAQKOSA-N
HMS2360E04
NS00042938
Q15634166
(E,E)-N,N'-[(Furan-2-yl)methylene]bis[1-(furan-2-yl)methanimine]
(Z)-{furan-2-yl[(E)-(furan-2-ylmethylidene)amino]methyl}(furan-2-ylmethylidene)amine