D-2-fluoro mandelic acid is a chiral compound that belongs to the class of mandelic acids, which are aromatic alpha-hydroxy acids. It features a fluorine atom substituted at the second carbon of the mandelic acid structure, which contributes to its unique chemical properties. This compound typically appears as a white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydroxyl group. D-2-fluoro mandelic acid exhibits characteristics typical of carboxylic acids, including the ability to donate protons (H+) in solution, which can influence its reactivity and interactions with other chemical species. Its chirality allows for potential applications in pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. Additionally, the presence of the fluorine atom can enhance the compound's biological activity and lipophilicity, making it of interest in medicinal chemistry. As with many fluorinated compounds, it may also exhibit unique metabolic pathways and biological interactions, warranting further investigation in drug development contexts.

D-2-fluoro mandelic acid

32222-48-3: D-2-fluoro mandelic acid is a chiral compound that belongs to the class of mandelic acids, which are aromatic alpha-hydroxy acids. It features a fluorine atom substituted at the second carbon of the mandelic acid structure, which contributes to its unique chemical properties. This compound typically appears as a white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydroxyl group. D-2-fluoro mandelic acid exhibits characteristics typical of carboxylic acids, including the ability to donate protons (H+) in solution, which can influence its reactivity and interactions with other chemical species. Its chirality allows for potential applications in pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. Additionally, the presence of the fluorine atom can enhance the compound's biological activity and lipophilicity, making it of interest in medicinal chemistry. As with many fluorinated compounds, it may also exhibit unique metabolic pathways and biological interactions, warranting further investigation in drug development contexts.

CAS 32222-48-3

D-2-fluoro mandelic acid

(R)-2-Fluoromandelic acid

Ref: IN-DA00BXD4

(R)-2-Fluoromandelic acid

Ref: 54-PC900788

(R)-2-(2-Fluorophenyl)-2-hydroxyacetic acid

Ref: 10-F221526