2,3-Difluoromandelic acid is an aromatic carboxylic acid characterized by the presence of two fluorine atoms at the 2 and 3 positions of the mandelic acid structure. This compound features a phenyl group attached to a carbon bearing both a hydroxyl (-OH) and a carboxylic acid (-COOH) functional group, contributing to its acidic properties. The introduction of fluorine atoms enhances the compound's reactivity and can influence its solubility and biological activity. Typically, such fluorinated compounds exhibit unique properties, including increased lipophilicity and altered metabolic pathways. 2,3-Difluoromandelic acid may be utilized in various chemical syntheses and research applications, particularly in medicinal chemistry, where fluorinated compounds are often explored for their potential therapeutic effects. The compound's molecular structure and functional groups suggest it may participate in hydrogen bonding and other intermolecular interactions, which can affect its physical properties, such as melting point and solubility in different solvents. Overall, 2,3-difluoromandelic acid represents a valuable compound in the study of fluorinated organic molecules.

2,3-difluoromandelic acid

207974-19-4: 2,3-Difluoromandelic acid is an aromatic carboxylic acid characterized by the presence of two fluorine atoms at the 2 and 3 positions of the mandelic acid structure. This compound features a phenyl group attached to a carbon bearing both a hydroxyl (-OH) and a carboxylic acid (-COOH) functional group, contributing to its acidic properties. The introduction of fluorine atoms enhances the compound's reactivity and can influence its solubility and biological activity. Typically, such fluorinated compounds exhibit unique properties, including increased lipophilicity and altered metabolic pathways. 2,3-Difluoromandelic acid may be utilized in various chemical syntheses and research applications, particularly in medicinal chemistry, where fluorinated compounds are often explored for their potential therapeutic effects. The compound's molecular structure and functional groups suggest it may participate in hydrogen bonding and other intermolecular interactions, which can affect its physical properties, such as melting point and solubility in different solvents. Overall, 2,3-difluoromandelic acid represents a valuable compound in the study of fluorinated organic molecules.

CAS 207974-19-4

2,3-difluoromandelic acid

2-(2,3-Difluorophenyl)-2-hydroxyacetic acid

Ref: IN-DA002JEC

2,3-Difluoromandelic acid

Ref: 54-PC4111

2,3-Difluoromandelic acid

Ref: 10-F004821