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Furfuryl acrylamide

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Identification
Molecular formula
C8H9NO2
CAS number
3131-53-9
IUPAC name
3-(2-furyl)prop-2-enamide
State
State

Furfuryl acrylamide is typically solid at room temperature. It is characterized by its crystalline form.

Melting point (Celsius)
80.00
Melting point (Kelvin)
353.15
Boiling point (Celsius)
271.30
Boiling point (Kelvin)
544.45
General information
Molecular weight
137.16g/mol
Molar mass
137.1380g/mol
Density
1.1620g/cm3
Appearence

Furfuryl acrylamide appears as white to beige crystals. It may also appear as a powder. The exact appearance can vary depending on the specific conditions of preparation and purity.

Comment on solubility

Solubility of 3-(2-furyl)prop-2-enamide

The solubility of 3-(2-furyl)prop-2-enamide can be influenced by various factors, making it an intriguing compound to study. Generally, this substance exhibits certain properties that dictate its behavior in various solvents.

  • Polarity: The presence of the furan ring contributes to its polarity, allowing it to interact well with polar solvents like water.
  • Solvent Compatibility: It is expected to be more soluble in polar aprotic solvents (like DMSO and DMF) due to its functional groups, while its solubility in non-polar solvents may be limited.
  • Hydrogen Bonding: The amide functional group can form hydrogen bonds, which can enhance solubility in polar environments significantly.

In summary, the solubility of 3-(2-furyl)prop-2-enamide is influenced by its polarity, solvent choice, and its ability to form hydrogen bonds. This makes it versatile in various chemical applications, though the exact solubility can vary considerably with changes in temperature and the specific solvent used.

Interesting facts

Interesting Facts about 3-(2-furyl)prop-2-enamide

3-(2-furyl)prop-2-enamide is a fascinating compound that belongs to the class of amides and is derived from the furyl aromatic system. This compound is not only intriguing in its structure but also has various applications in different fields of science and industry.

Unique Features

  • Heterocyclic Chemistry: The presence of the furan ring in this compound contributes to its unique electronic properties and reactivity, making it a subject of study in heterocyclic chemistry.
  • Potential Biological Activities: Compounds containing furan rings have shown a range of biological activities, including antimicrobial and anticancer properties, making them of interest in medicinal chemistry.
  • Versatile Building Block: Due to its functional groups, 3-(2-furyl)prop-2-enamide can act as a versatile building block for synthesizing more complex molecules in organic synthesis.

Furthermore, its structural features make it an important compound for studying structure-activity relationships in drug design, where minor modifications to the furan or amide groups can lead to significant changes in activity. As scientists explore its reactivity, they often find it serves as a precursor for other valuable chemicals.

Applications of the Compound

The significance of 3-(2-furyl)prop-2-enamide extends to various applications:

  • Synthetic Organic Chemistry: Often utilized in the synthesis of various organic products due to its reactivity.
  • Pharmaceutical Research: Investigated for its potential therapeutic applications, particularly in drug formulation.
  • Material Science: Explored for use in the development of novel materials, highlighting its versatility.

In summary, 3-(2-furyl)prop-2-enamide is a compound worth studying due to its unique structure and promising applications across diverse scientific fields. Whether you're a chemistry student or a seasoned researcher, delving into its properties can lead to exciting discoveries.

Synonyms
3-(furan-2-yl)prop-2-enamide
(2E)-3-(furan-2-yl)prop-2-enamide
SCHEMBL245407
DTXSID401310614