2,3-Dihydroxybenzoic acid
2,3-Dihydroxybenzoic acid is an organic compound with the formula C7H6O4. It is one of the several isomers of dihydroxybenzoic acid. This compound is a type of phenolic acid and is characterized by the presence of two hydroxyl groups attached to the benzene ring.
Structure and properties[edit]
2,3-Dihydroxybenzoic acid consists of a benzene ring with two hydroxyl groups (-OH) and a carboxylic acid group (-COOH) attached. The hydroxyl groups are located at the 2 and 3 positions on the benzene ring, which distinguishes it from other isomers such as 2,5-dihydroxybenzoic acid and 3,4-dihydroxybenzoic acid.
The presence of hydroxyl groups makes this compound a phenol, and the carboxylic acid group contributes to its acidic properties. It is a crystalline solid that is soluble in water and organic solvents.
Biological significance[edit]
2,3-Dihydroxybenzoic acid is involved in various biological processes. It is a known siderophore, which means it can bind and transport iron in biological systems. This property is crucial for microorganisms that require iron for growth and metabolism.
In humans, 2,3-dihydroxybenzoic acid is a metabolite of salicylic acid, which is a major component of aspirin. It is also involved in the shikimate pathway, a biosynthetic route used by bacteria, fungi, and plants to synthesize aromatic compounds.
Applications[edit]
Due to its ability to chelate iron, 2,3-dihydroxybenzoic acid is used in research to study iron metabolism and transport. It is also used in the synthesis of various pharmaceuticals and biochemical compounds.
Synthesis[edit]
2,3-Dihydroxybenzoic acid can be synthesized through the hydroxylation of salicylic acid or by the Kolbe-Schmitt reaction, which involves the carboxylation of phenol derivatives.
Related pages[edit]
Gallery[edit]
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Structural formula of 2,3-Dihydroxybenzoic acid
2,3-Dihydroxybenzoic acid[edit]
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2,3-Dihydroxybenzoic acid structure
