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Furfural oxime

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Identification
Molecular formula
C5H5NO2
CAS number
1742-40-1
IUPAC name
furan-2-carbaldehyde oxime
State
State

At room temperature, furfural oxime is typically found as a solid.

Melting point (Celsius)
49.50
Melting point (Kelvin)
322.65
Boiling point (Celsius)
93.00
Boiling point (Kelvin)
366.15
General information
Molecular weight
111.11g/mol
Molar mass
111.1110g/mol
Density
1.1215g/cm3
Appearence

Furfural oxime typically appears as a colorless to pale yellow crystalline solid.

Comment on solubility

Solubility of Furan-2-carbaldehyde oxime

Furan-2-carbaldehyde oxime, with the chemical formula C5H5NO, exhibits interesting solubility characteristics that merit attention.

In terms of solubility:

  • Polarity: The presence of the oxime functional group contributes to the polarity of the compound, promoting solubility in polar solvents.
  • Solvent Compatibility: Furan-2-carbaldehyde oxime is known to be soluble in:
    • Water
    • Alcohols (e.g., ethanol, methanol)
    • Certain organic solvents (e.g., acetone, dimethyl sulfoxide)
  • Temperature Dependence: Solubility can vary with temperature; higher temperatures may increase solubility due to enhanced molecular interactions.
  • Chemical Reactions: This compound may interact with other chemical species in solution, affecting its solubility behavior.

As a general statement, it can be said that the solubility of furan-2-carbaldehyde oxime in various solvents is primarily driven by its functional groups and the solvent's nature. Understanding these solubility properties is crucial for its applications in organic synthesis and other fields.

Interesting facts

Furan-2-carbaldehyde oxime: An Overview

Furan-2-carbaldehyde oxime is an intriguing organic compound that combines the aromatic properties of furan with the reactivity of oxime groups. This compound is not just a simple derivative; it exhibits fascinating attributes that make it notable in various fields of chemistry.

Key Characteristics

  • Structure: The presence of the furan ring contributes to its unique reactivity and stability, making it an essential building block in synthetic organic chemistry.
  • Applications: Furan-2-carbaldehyde oxime finds its use in the synthesis of various pharmaceuticals, agrochemicals, and in the preparation of complex organic structures.
  • Reactivity: The oxime functional group present in the compound is known for its ability to undergo condensation reactions, making it a valuable reactive intermediate.

Importance in Research

The significance of furan-2-carbaldehyde oxime extends beyond its chemical structure. It plays a crucial role in:

  • Coordination Chemistry: It can act as a ligand in the formation of metal complexes, which are important in catalysis and material science.
  • Biological Studies: Some derivatives of furan-2-carbaldehyde oxime have been investigated for potential biological activity, making it valuable for medicinal chemistry.
  • Green Chemistry: Its synthesis can often be aligned with environmentally favorable practices, enhancing its appeal in sustainability-focused research.

In summary, furan-2-carbaldehyde oxime is not merely an organic compound but a versatile component that underscores the interconnectedness of chemistry and various scientific disciplines. The compound exemplifies how simple structures can lead to complex functionalities, driving innovation in research and application.

Synonyms
N-(furan-2-ylmethylidene)hydroxylamine
2-FURALDEHYDEOXIME
furan-2-carbaldehyde oxime
Furfuraldoxime
Furfuraldoxim
furyl nitrone
2-furancarbaldehyde oxime
SCHEMBL1444944
SCHEMBL11305740
UYTMLDBQFLIQJA-UHFFFAOYSA-N
BAA45058
AKOS030239767
DB-041045
DB-293078
G77396