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Citramalic acid

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Identification
Molecular formula
C7H8O6
CAS number
10491-56-0
IUPAC name
5-(hydroxymethylene)-2-oxo-hept-3-enedioic acid
State
State

Solid: Citramalic acid is generally solid at room temperature.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
315.80
Boiling point (Kelvin)
588.95
General information
Molecular weight
174.14g/mol
Molar mass
174.1410g/mol
Density
1.9000g/cm3
Appearence

It typically appears as a white crystalline solid.

Comment on solubility

Solubility of 5-(hydroxymethylene)-2-oxo-hept-3-enedioic acid (C7H8O6)

The solubility of 5-(hydroxymethylene)-2-oxo-hept-3-enedioic acid is influenced by several factors, primarily its molecular structure and the presence of functional groups. This compound contains both hydroxyl (-OH) and carboxylic acid (-COOH) functional groups, which can significantly enhance its solubility characteristics. Here are some key points regarding its solubility:

  • Polar Nature: The presence of multiple polar functional groups allows for strong interactions with water molecules.
  • Hydrogen Bonding: The -OH and -COOH groups can engage in hydrogen bonding, which often leads to increased solubility in polar solvents such as water.
  • Solvent Compatibility: This compound may exhibit variable solubility in organic solvents depending on their polarity. For instance, it is likely to be less soluble in non-polar solvents.
  • Concentration Dependency: Solubility can be affected by concentration; at higher concentrations, solubility might be reduced due to intermolecular interactions.

In summary, 5-(hydroxymethylene)-2-oxo-hept-3-enedioic acid is expected to demonstrate good solubility in polar solvents, primarily due to its polar functional groups that facilitate strong interactions with the solvent, making it a compound of interest in chemical applications requiring solubility.

Interesting facts

Interesting Facts about 5-(Hydroxymethylene)-2-oxo-hept-3-enedioic acid

5-(hydroxymethylene)-2-oxo-hept-3-enedioic acid, also known by its more common name, has several fascinating aspects that make it noteworthy in the field of chemistry:

  • Functionality: This compound is a dicarboxylic acid, a category known for its ability to undergo various reactions typical of carboxylic acids, making it an important building block in organic synthesis.
  • Versatile Intermediary: It serves as a crucial intermediary in the synthesis of a variety of natural products and pharmaceuticals, showcasing the intersection of synthetic organic chemistry and medicinal chemistry.
  • Biological Applications: Research suggests potential applications in metabolic studies, as dicarboxylic acids are often involved in the citric acid cycle and other crucial metabolic pathways.
  • Keto-Enol Tautomerism: The structure allows for tautomerization between the keto and enol forms, which can influence reactivity and stability in synthetic processes.
  • Research Relevance: Ongoing studies explore its role in drug development, particularly its interaction with biological systems, emphasizing the importance of analyzing even lesser-known compounds for new therapeutic avenues.

In essence, 5-(hydroxymethylene)-2-oxo-hept-3-enedioic acid exemplifies the rich complexity of organic compounds, underlining the creativity and adaptability required in chemical research. As noted by chemists, “Understanding the properties and behaviors of compounds like these paves the way for innovations in both chemistry and medicine.”

In summary, the exploration of this compound not only reveals its intrinsic chemical properties but also highlights its potential impact on future scientific advancements.

Synonyms
2461-62-3
5-(hydroxymethylidene)-2-oxohept-3-enedioic acid
2-Hydroxy-5-formyl-2,4-heptadienedioic acid
DTXSID801252143
Q27102233