2,3-Difluoro-4-iodobenzoic acid is an aromatic carboxylic acid characterized by the presence of both fluorine and iodine substituents on the benzene ring. The compound features two fluorine atoms located at the 2 and 3 positions and an iodine atom at the 4 position relative to the carboxylic acid group. This substitution pattern influences its chemical reactivity and physical properties, such as solubility and boiling point. The presence of electronegative halogens like fluorine and iodine can enhance the acidity of the carboxylic acid group, making it more reactive in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may exhibit unique properties in terms of polarity and intermolecular interactions due to the halogen substituents. It is important in synthetic organic chemistry and may serve as an intermediate in the synthesis of pharmaceuticals or agrochemicals. Safety and handling precautions should be observed, as with all halogenated compounds, due to potential toxicity and environmental impact.

2,3-Difluoro-4-iodobenzoic acid

501433-05-2: 2,3-Difluoro-4-iodobenzoic acid, Benzoic acid, 2,3-difluoro-4-iodo-

2,3-Difluoro-4-iodobenzoic acid is an organic compound that can be prepared by the reaction of isopropylmagnesium chloride with alkyllithium. It is a strong base and can be used as a reagent to prepare 2,6-difluorobenzoic acid. The compound has been used in the synthesis of fluoroarenes.

CAS 501433-05-2: 2,3-Difluoro-4-iodobenzoic acid

2,3-difluoro-4-iodobenzoic Acid

Ref: 3D-FD106147

4-IODO-2,3-DIFLUOROBENZOIC ACID

Ref: IN-DA00D8EX

2,3-Difluoro-4-iodobenzoic acid

Ref: 54-PC500469