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2-oxalobenzoic acid

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Identification
Molecular formula
C8H6O5
CAS number
612-69-7
IUPAC name
2-oxalobenzoic acid
State
State

At room temperature, 2-oxalobenzoic acid is typically found in a solid state as a white crystalline powder.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
166.13g/mol
Molar mass
166.1300g/mol
Density
1.2700g/cm3
Appearence

2-Oxalobenzoic acid appears as a white crystalline solid. Its structure comprises a benzoic acid core substituted with an additional oxalo group which conveys its distinctive crystalline solid appearance.

Comment on solubility

Solubility of 2-oxalobenzoic acid

2-oxalobenzoic acid, with the chemical formula C9H6O4, exhibits interesting solubility characteristics that warrant discussion.


This compound is known to be:

  • Soluble in organic solvents: It readily dissolves in common organic solvents like ethanol and acetone, which indicates its compatibility with non-polar environments.
  • Less soluble in water: The solubility in water is limited due to its aromatic structure and the presence of carboxylic acid groups that can influence interactions with polar solvents.

As with many organic acids, the solubility can be influenced by factors such as:

  • Temperature: Increased temperatures typically enhance solubility in organic solvents.
  • pH levels: Changes in pH can affect the ionization of the compound, which may improve its solubility in aqueous solutions.

In the context of applications, the solubility of 2-oxalobenzoic acid in various solvents makes it particularly useful for:

  • Chemical syntheses
  • Analytical applications

In summary, the solubility profile of 2-oxalobenzoic acid demonstrates significant variability based on environmental conditions, making it a versatile compound for various scientific explorations.

Interesting facts

Interesting Facts about 2-Oxalobenzoic Acid

2-Oxalobenzoic acid is a fascinating compound that embodies a blend of organic and medicinal chemistry. Here are some key points that highlight its significance:

  • Chemical Structure: This compound features a benzene ring substituted with both oxalic acid and carboxylic acid functionalities, providing a unique platform for various chemical reactions and interactions.
  • Reactivity: 2-Oxalobenzoic acid is known for its ability to engage in decarboxylation reactions, meaning it can lose a carbon dioxide molecule under certain conditions, often leading to the formation of more complex compounds.
  • Biochemical Importance: It can act as a substrate in enzyme-catalyzed reactions within biochemical pathways, making it a subject of interest in studies related to enzymatic activity and metabolic processes.
  • Synthetic Utility: This compound plays a pivotal role in synthesizing different organic compounds, including various pharmaceuticals and agrochemicals, showcasing its versatility in the laboratory.
  • Research Applications: Due to its unique properties, 2-oxalobenzoic acid is used in research related to cancer therapies and treatment strategies, showcasing its potential in medicinal chemistry.

As researchers delve deeper into the chemical nature of 2-oxalobenzoic acid, they uncover new possibilities for its applications and contributions to science.

In the words of a prominent chemist: "The exploration of organic compounds can lead us to unexpected avenues in both theoretical knowledge and practical applications."

Hence, 2-oxalobenzoic acid not only enriches the field of organic chemistry but also serves as a stepping stone for advancements in medicinal discoveries.

Synonyms
528-46-1
PHTHALONIC ACID
2-Carboxy-alpha-oxobenzeneacetic acid
DTXSID10200776
DTXCID40123267
2-(carboxycarbonyl)benzoic acid
2-oxalobenzoic acid
2-Oxalyl-benzoic acid
MFCD00090830
CHEMBL300586
2-oxalo-benzoic acid
Phthalonsaure
SCHEMBL240838
2-(carboxycarbonyl)benzoicacid
BDBM50102181
STK505512
AKOS000321457
SY276744
WS-01222
CS-0322976
NS00067095
D85948