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Ketoheptenedioic acid

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Identification
Molecular formula
C7H8O5
CAS number
2794-15-6
IUPAC name
2-oxohept-3-enedioic acid
State
State

At room temperature, Ketoheptenedioic acid is typically a solid. It is stable under normal conditions, but care should be taken as it can degrade if exposed to high temperatures or reacting substances.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.00
Boiling point (Celsius)
415.00
Boiling point (Kelvin)
688.00
General information
Molecular weight
172.15g/mol
Molar mass
172.1470g/mol
Density
1.4000g/cm3
Appearence

Ketoheptenedioic acid appears as a crystalline solid or powder. It may have a pale yellow color, depending on its purity and form. The crystals are sometimes described as slightly glossy or transparent, with a tendency to clump together due to their fine particle size.

Comment on solubility

Solubility of 2-oxohept-3-enedioic acid

2-oxohept-3-enedioic acid, with the chemical formula C7H8O5, exhibits intriguing solubility characteristics that are worth noting.

The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of carboxylic acid functional groups makes 2-oxohept-3-enedioic acid relatively polar. This increases its solubility in polar solvents, especially water.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds enhances its interaction with solvent molecules, contributing to its solubility.
  • Temperature: Solubility can further be affected by temperature, where higher temperatures usually increase the solubility of many organic compounds, including this acid.
  • pH Levels: The solubility of 2-oxohept-3-enedioic acid may also vary with changes in pH, as deprotonation can enhance its solubility in aqueous environments.

In summary, while the specific solubility values may vary, it's generally observed that 2-oxohept-3-enedioic acid is quite soluble in polar solvents such as water, emphasizing the influence of its functional groups and external conditions on its solubility profile.

Interesting facts

Interesting Facts about 2-Oxohept-3-enedioic Acid

2-Oxohept-3-enedioic acid, often referred to in scientific literature as 2-oxoheptenedioic acid, is a fascinating compound that shines in both synthetic chemistry and biochemistry. Here are some engaging insights about this unique acid:

  • Structural Composition: This compound features two carboxylic acid groups and a ketone functional group, setting the stage for its reactivity and potential applications in organic synthesis.
  • Biological Significance: Compounds analogous to 2-oxohept-3-enedioic acid play crucial roles in metabolic pathways, particularly in the synthesis of amino acids and fatty acids.
  • Synthetic Applications: Chemists often utilize this compound as a precursor in the creation of various derivatives, making it a valuable building block in organic synthesis.
  • Research Potential: Due to its unique structure, there is ongoing research into its potential pharmacological properties, which could lead to the development of new therapeutic agents.
  • Catalytic Transformations: The presence of multiple functional groups in 2-oxohept-3-enedioic acid makes it an interesting target for catalytic transformations, potentially leading to more complex molecules.

In the words of chemist Richard Feynman, “What I cannot create, I do not understand.” This perfectly encapsulates the essential nature of compounds like 2-oxohept-3-enedioic acid; understanding its synthesis and function is crucial for advancing in the field of chemistry.

This compound truly exemplifies how the complexities of molecular structures can lead to significant implications in both synthetic and biological chemistry, making it a topic of great interest for scientists and students alike!

Synonyms
2-oxohept-3-enedioic acid
2-oxo-hept-3-ene-1,7-dioic acid
Q27120923