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5-Oxo-L-proline

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Identification
Molecular formula
C6H9NO3
CAS number
1736-70-9
IUPAC name
2-(5-oxopyrrolidin-2-yl)acetic acid
State
State

At room temperature, 5-Oxo-L-proline is a solid.

Melting point (Celsius)
159.50
Melting point (Kelvin)
432.65
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
129.11g/mol
Molar mass
129.1110g/mol
Density
1.4600g/cm3
Appearence

5-Oxo-L-proline appears as a white crystalline powder.

Comment on solubility

Solubility of 2-(5-oxopyrrolidin-2-yl)acetic acid

The compound 2-(5-oxopyrrolidin-2-yl)acetic acid, with the chemical formula C6H9NO3, exhibits notable solubility characteristics that are important for its application and behavior in various environments.

Key points about its solubility include:

  • Water Solubility: This compound is generally considered to be soluble in water due to the presence of polar functional groups which enhance its ability to interact with water molecules.
  • Solvent Compatibility: In addition to water, it may be soluble in a range of organic solvents, making it versatile for use in different chemical processes.
  • pH Dependency: Its solubility might vary with changes in pH, as modifications in the acidity or basicity of the solution can lead to protonation or deprotonation of certain functional groups, thereby affecting solubility.
  • Temperature Effects: Typically, higher temperatures increase solubility for many compounds, suggesting that careful temperature control could optimize the dissolution of this acid.

To summarize, the solubility of 2-(5-oxopyrrolidin-2-yl)acetic acid is influenced by multiple factors, indicating that a thorough understanding of its solubility profile is crucial for utilizing this compound effectively in various applications.

Interesting facts

Interesting Facts about 2-(5-oxopyrrolidin-2-yl)acetic Acid

2-(5-oxopyrrolidin-2-yl)acetic acid is a fascinating compound with noteworthy applications and characteristics, especially in the field of medicinal chemistry. This compound is particularly interesting due to the following points:

  • Structural Significance: The presence of a pyrrolidine ring, along with a ketone functional group, contributes to its chemical reactivity and versatility in organic synthesis.
  • Medicinal Applications: It may play a role in the development of pharmaceuticals. With its unique structure, it can be utilized in the synthesis of bioactive derivatives.
  • Biological Importance: Compounds similar to this one have been studied for their potential effects on metabolic pathways, particularly relating to amino acid metabolism and neurotransmitter function.
  • Research Potential: The compound serves as a promising scaffold for drug discovery, allowing chemists to design new molecules with enhanced therapeutic properties.

In scientific literature, various analogs of this compound have been reported to exhibit:

  1. Anti-inflammatory properties
  2. Neuroprotective effects
  3. Potential in treating metabolic disorders

Overall, 2-(5-oxopyrrolidin-2-yl)acetic acid stands out for its unique chemical structure that opens avenues for research in pharmacology and organic synthesis. As stated in scientific discourse, "every compound holds secrets in its structure waiting to be unveiled." This compound is no exception.

Synonyms
2-(5-oxopyrrolidin-2-yl)acetic acid
64520-53-2
5-oxo-2-pyrrolidineacetic acid
DTXSID60274785
DTXCID00226243
818-632-8
2-Pyrrolidineacetic acid, 5-oxo-
(5-OXOPYRROLIDIN-2-YL)ACETIC ACID
(5-Oxo-2-pyrrolidinyl)acetic acid
MFCD09040737
(R)-2-(5-Oxopyrrolidin-2-yl)acetic acid
2-Oxo-5-pyrrolidinylessig
CHEMBL358255
SCHEMBL2558286
ALBB-030064
PCA52053
(S)-5-Oxo-2-pyrrolidineacetic acid
2-(5-oxopyrrolidin-2-yl)aceticacid
2-(5-Oxo-2-pyrrolidinyl)acetic Acid
AKOS009132943
AT18838
SB45735
SB46808
BS-13281
SY187734
DB-296267
CS-0208149
EN300-68203
F8887-4128