2,3-Difluoro-5-methylbenzoic acid is an aromatic carboxylic acid characterized by the presence of two fluorine atoms and a methyl group on a benzoic acid framework. The fluorine substituents are located at the 2 and 3 positions, while the methyl group is at the 5 position of the benzene ring. This compound exhibits typical properties of benzoic acids, including the ability to form hydrogen bonds due to its carboxylic acid functional group, which contributes to its solubility in polar solvents. The presence of fluorine atoms enhances the compound's acidity compared to non-fluorinated benzoic acids, as fluorine is highly electronegative and can stabilize the carboxylate ion formed upon deprotonation. Additionally, the fluorine substituents can influence the compound's reactivity and interaction with biological systems, making it of interest in medicinal chemistry and material science. Its unique structure may also impart specific physical properties, such as altered melting and boiling points compared to its non-fluorinated counterparts.

2,3-Difluoro-5-methylbenzoic acid

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Benzoic acid, 2,3-difluoro-5-methyl-

2,3-Difluoro-5-methylbenzoic acid is a versatile building block that can be used as a reagent in organic chemistry. It is a useful intermediate for the synthesis of more complex compounds. The compound is also a useful scaffold for the preparation of new chemical entities for research purposes.

CAS 1003709-96-3: 2,3-Difluoro-5-methylbenzoic acid

Benzoic acid, 2,3-difluoro-5-methyl-

Ref: IN-DA0001RU

2,3-Difluoro-5-methylbenzoic acid

Ref: 54-PC56815

2,3-Difluoro-5-methylbenzoic acid

Ref: 10-F037156

2,3-Difluoro-5-methylbenzoic acid

Ref: 3D-FD67030