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Furoic acid

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Identification
Molecular formula
C6H4O3
CAS number
88-14-2
IUPAC name
3-(2-furyl)prop-2-enoic acid
State
State

At room temperature, furoic acid is typically in a solid state, existing as a crystalline powder.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
235.50
Boiling point (Kelvin)
508.65
General information
Molecular weight
126.11g/mol
Molar mass
126.1110g/mol
Density
1.4090g/cm3
Appearence

Furoic acid is typically encountered as a white crystalline solid with a slight odor reminiscent of furfural. It may have a shiny or dull exterior depending on its purity and the presence of moisture.

Comment on solubility

Solubility of 3-(2-furyl)prop-2-enoic acid

3-(2-furyl)prop-2-enoic acid, a compound with a unique structure, exhibits interesting solubility characteristics. This acid is largely influenced by its functional groups and aromatic nature. Here are some key points regarding its solubility:

  • Solvent Interaction: This compound is expected to be soluble in polar solvents such as water, due to the presence of the carboxylic acid group which can participate in hydrogen bonding.
  • Non-Polar Solubility: Conversely, due to the aromatic furyl ring, it may also exhibit solubility in non-polar organic solvents like ethanol or acetone.
  • pH Influence: The solubility is likely to increase in alkaline conditions, as the carboxylic acid can deprotonate, forming a negatively charged species that enhances its solubility in aqueous solution.

In summary, the solubility of 3-(2-furyl)prop-2-enoic acid is moderate and depends heavily on the nature of the solvent and the pH of the solution. Careful consideration of these factors is essential for optimal application in chemical processes.

Interesting facts

Interesting Facts About 3-(2-furyl)prop-2-enoic Acid

3-(2-furyl)prop-2-enoic acid, often referred to as furanacrylic acid, is a fascinating organic compound that has garnered attention due to its unique structure and properties. Here are some highlights:

  • Chemical Structure: This compound contains a furan ring, which is notable for its aromatic properties and reactivity. The furan ring is a five-membered heterocyclic compound, making it an interesting entity in organic synthesis.
  • Biological Activity: Research in medicinal chemistry has indicated that this compound exhibits significant biological activities, which may lead to potential applications in drug development. Its derivatives have shown promise in antitumor activity and antifungal properties.
  • Versatile Intermediate: As an important building block in organic synthesis, 3-(2-furyl)prop-2-enoic acid can be utilized in the production of various pharmaceuticals and agrochemicals. Its ability to undergo Michael addition reactions makes it a versatile intermediate in the synthesis of more complex molecules.
  • Reaction Pathways: The acidity of the carboxylic acid group enables it to participate in various reactions such as esterifications or amidations, further expanding its utility in organic chemistry.
  • Furan Derivatives: The study of furan and its derivatives, including this compound, has been instrumental in understanding aromatic compounds. These studies provide insight into reactivity patterns that are crucial for designing new materials.

In summary, 3-(2-furyl)prop-2-enoic acid is more than just a chemical compound; it's a compound with rich potential for research and application in various fields. Its combination of a furan ring and a reactive vinyl group makes it a fascinating subject of study for chemists and researchers.

Synonyms
MFCD00003257
3-(2-furanyl)acrylic acid
3-furan-2-yl-acrylic acid
3-(furan-2-yl)-acrylic acid
(E)-3-(2-Furyl)acrylic acid
ZCJLOOJRNPHKAV-UHFFFAOYSA-N
AKOS016038035
SB60967
SY009542
SY056646
DB-021722
Furan-2-acrylic acid;Furfurylideneacetic acid