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2-(Butylideneamino)-2H-furan-5-one

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Identification
Molecular formula
C8H9NO2
CAS number
2362-31-2
IUPAC name
2-(butylideneamino)-2H-furan-5-one
State
State

At room temperature, 2-(butylideneamino)-2H-furan-5-one is typically a solid. The compound's stability in its solid form makes it usable for various laboratory applications where solid organic compounds are required.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
165.19g/mol
Molar mass
165.1940g/mol
Density
1.1021g/cm3
Appearence

The compound typically appears as a light yellow crystalline solid. It may exhibit a glossy or shiny surface depending on the size of the crystals and the purity of the sample. The color intensity can vary slightly based on the degree of impurities or degradation.

Comment on solubility

Solubility of 2-(butylideneamino)-2H-furan-5-one

The solubility of 2-(butylideneamino)-2H-furan-5-one can be influenced by various factors, such as temperature, solvent type, and molecular interactions. Here are some key points to consider:

  • Polarity: The presence of polar functional groups may suggest a degree of solubility in polar solvents, like water or alcohols.
  • Hydrogen Bonding: Molecules that can form hydrogen bonds tend to be more soluble in polar solvents, making this compound potentially more soluble.
  • Temperature Effects: Increased temperature usually enhances solubility; thus, solubility can vary significantly with changes in temperature.

However, specific solubility data for this compound is not widely available. As a general guideline, understanding the compound’s structural characteristics can provide insight into its expected solubility behavior:

  • Presence of functional groups: Compounds that contain nitrogen groups, as found in this furan derivative, may show enhanced solubility in polar media.
  • Chain Length: The butylidene portion might impart hydrophobic characteristics, potentially limiting solubility in highly polar solvents.

In conclusion, while the solubility of 2-(butylideneamino)-2H-furan-5-one is expected to demonstrate variability based on solvent interactions and environmental conditions, further experimental studies would provide a clearer picture of its solubility profile.

Interesting facts

Interesting Facts about 2-(butylideneamino)-2H-furan-5-one

2-(butylideneamino)-2H-furan-5-one is a fascinating organic compound that stands out due to its unique structure and properties. Here are some intriguing facts that highlight its significance:

  • Potential Medicinal Applications: This compound is part of a class of molecules that may exhibit pharmacological properties, making it a candidate for pharmaceutical development. Researchers are exploring its potential role in drug design and as an active ingredient in therapeutic formulations.
  • Synthetic Versatility: The synthesis of 2-(butylideneamino)-2H-furan-5-one is of great interest in organic chemistry. It can be synthesized through various methods, which allows chemists to modify its structure and potentially enhance its efficacy.
  • Natural Occurrence: Compounds related to furan and its derivatives can often be found in natural sources, including plants and fungi, where they might play roles in ecological interactions or chemical signaling.
  • Mechanistic Insights: Understanding the reaction mechanisms involving this compound can offer insight into chemical reactivity and stability, which is crucial for both academic study and industrial applications.
  • Analytical Techniques: The compound can be analyzed using advanced methods such as NMR spectroscopy and mass spectrometry. These techniques are essential for characterizing its chemical structure and understanding its behavior in various environments.

In summary, 2-(butylideneamino)-2H-furan-5-one is more than just a chemical entity; it represents a bridge between chemical research and practical applications in medicine and industry. The ongoing exploration of its properties and effects exemplifies the dynamic and evolving field of chemistry.