4-Oxopiperidine-2,6-dicarboxylic acid

Identification

Molecular formula

C₇H₉NO₅

CAS number

14038-17-8

IUPAC name

4-oxopiperidine-2,6-dicarboxylic acid

State

4-Oxopiperidine-2,6-dicarboxylic acid is typically found in a solid state at room temperature. It can absorb moisture from the air if not stored properly, thus sometimes requiring storage in a dry environment.

Melting point (Celsius)

175.00

Melting point (Kelvin)

448.15

Boiling point (Celsius)

236.00

Boiling point (Kelvin)

509.15

General information

Molecular weight

201.15g/mol

Molar mass

201.1510g/mol

Density

1.8060g/cm³

Appearence

4-Oxopiperidine-2,6-dicarboxylic acid typically appears as a solid substance, often found in the form of a crystalline powder. This compound being a carboxylic acid derivative may sometimes be available in various hydrate forms, potentially influencing its appearance slightly.

Comment on solubility

Solubility of 4-oxopiperidine-2,6-dicarboxylic acid

4-oxopiperidine-2,6-dicarboxylic acid, with the chemical formula C₇H₉NO₅, is a fascinating compound when it comes to solubility characteristics.

This compound exhibits moderate solubility in various solvents, which can be attributed to its polar functional groups. Key considerations regarding its solubility include:

Water: 4-oxopiperidine-2,6-dicarboxylic acid tends to be soluble in water due to the presence of multiple carboxylic acid groups that can form hydrogen bonds with water molecules.
Organic Solvents: It may have varying degrees of solubility in organic solvents, depending on their polarity.
pH Dependence: The solubility can be influenced by the pH of the solution, as the ionization of the carboxylic groups can enhance solubility in alkaline conditions.

Overall, the solubility of this compound provides valuable insights into its reactivity and potential applications in various fields. As one might say, "Understanding solubility is key to mastering chemical behavior!"

Interesting facts

Interesting Facts about 4-Oxopiperidine-2,6-dicarboxylic acid

4-Oxopiperidine-2,6-dicarboxylic acid, often referred to in the scientific community as a versatile compound owing to its unique structure and functional groups, has multiple implications in various fields, particularly in medicinal chemistry and organic synthesis. Here are some compelling aspects:

Structural Significance: This compound features a piperidine ring, which is a saturated six-membered ring that contributes to its stability and reactivity. The presence of two carboxylic acid groups enhances its functionality, allowing it to participate in various chemical reactions.
Biological Relevance: Derivatives of piperidine compounds have shown a range of biological activities. Research indicates that similar compounds can act as potential inhibitors in enzyme systems, making them targets for drug development.
Synthesis and Derivatives: 4-Oxopiperidine-2,6-dicarboxylic acid can be synthesized via different methodologies in organic chemistry. Notably, derivatives of this compound have been explored for their potential as anti-inflammatory and antibacterial agents.
Application in Industry: Beyond medicinal uses, due to its carboxylic acid groups, this compound can be utilized in the synthesis of polymers and other materials, showcasing its versatility in chemical applications.
Interdisciplinary Interest: The compound attracts interest not only from chemists but also from biochemists and material scientists, highlighting its versatile applications across disciplines.

As with many compounds, ongoing research may continue to uncover new and exciting opportunities for 4-oxopiperidine-2,6-dicarboxylic acid in the realms of science and technology. Its multifaceted nature underscores the importance of chemical research in developing innovative solutions to modern challenges.