Skip to main content

5-Oxo-2-pyrrolidineacetic acid

ADVERTISEMENT
Identification
Molecular formula
C6H6O4
CAS number
23161-01-5
IUPAC name
2-(2-oxo-3H-furan-5-yl)acetic acid
State
State

At room temperature, 5-Oxo-2-pyrrolidineacetic acid is typically in a solid state. It remains stable under standard laboratory conditions, and should be stored in a cool, dry place away from incompatible substances.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.15
Boiling point (Celsius)
407.60
Boiling point (Kelvin)
680.80
General information
Molecular weight
141.13g/mol
Molar mass
141.1310g/mol
Density
1.4230g/cm3
Appearence

5-Oxo-2-pyrrolidineacetic acid typically appears as a white to off-white crystalline solid. It is known for its fine particulate nature and may form clumps due to static. The compound is often handled in powdered form for chemical synthesis and laboratory applications.

Comment on solubility

Solubility of 2-(2-oxo-3H-furan-5-yl)acetic acid (C6H6O4)

The solubility characteristics of 2-(2-oxo-3H-furan-5-yl)acetic acid are quite interesting, reflecting both its structural features and chemical behavior. This compound presents solubility tendencies that are influenced by several factors:

  • Polarity: The presence of carboxylic acid groups contributes to its polar nature, making it fairly soluble in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds enhances its solubility in water, allowing it to readily interact with water molecules.
  • Solvent Interactions: While it is soluble in water, its solubility may vary in organic solvents, where it is generally more soluble in alcohols or ketones compared to non-polar solvents.

In summary, 2-(2-oxo-3H-furan-5-yl)acetic acid showcases a degree of solubility that can be described as:

  1. Soluble in water due to its polar functional groups.
  2. Moderately soluble in alcohols and polar organic solvents.
  3. Low solubility in non-polar solvents.

This compound exemplifies how functional groups like the carboxylic acid moiety significantly impact solubility, underscoring the importance of molecular structure in determining solubility behavior.

Interesting facts

Exploring 2-(2-oxo-3H-furan-5-yl)acetic Acid

2-(2-oxo-3H-furan-5-yl)acetic acid is a fascinating compound that intersects various fields of study, from organic chemistry to medicinal research. Here are some intriguing aspects of this compound:

  • Structural significance: The unique furan ring incorporated in the structure contributes to its reactivity and potential biological activity, making it an interesting subject for synthetic chemists.
  • Versatile applications: This compound can serve as a building block in the synthesis of several therapeutic agents and may have implications in the development of new pharmaceutical compounds.
  • Biological relevance: Compounds featuring furan rings are often studied for their *antioxidant* properties and their roles in various biochemical pathways, showcasing how structural motifs can influence biological activity.
  • Chemical transformation: It can participate in various chemical reactions, including decarboxylation and oxidation, which renders it useful for researchers exploring synthetic methodologies.
  • Historical context: Furan derivatives have a rich research history, often linked to traditional medicine and natural products, and this compound continues that legacy.

As researchers delve into the properties and potential uses of 2-(2-oxo-3H-furan-5-yl)acetic acid, they unlock possibilities that echo through many scientific domains, from *pharmaceutical development* to *organic synthesis*.

Synonyms
5-oxo-4,5-dihydro-2-furylacetic acid
3-Oxoadipate enol-lactone
2-(2-oxo-3H-furan-5-yl)acetic acid
(5-oxo-4,5-dihydrofuran-2-yl)acetic acid
2-oxo-2,3-dihydrofuran-5-acetate
4,5-dihydro-5-oxofuran-2-acetate
5-oxo-4,5-dihydrofuran-2-acetate
C03586
SCHEMBL13176945
CHEBI:18267
4-carboxymethylbut-3-en-4-olide
AKOS006376286
Q27102959