5-Bromo-2-fluoro-3-methyl-benzoic acid is an aromatic carboxylic acid characterized by the presence of a bromine atom, a fluorine atom, and a methyl group attached to a benzoic acid framework. The molecular structure features a benzene ring with these substituents positioned at specific locations, which influence its chemical reactivity and physical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functional group. The presence of halogens (bromine and fluorine) can enhance its reactivity, making it useful in various chemical syntheses, including pharmaceuticals and agrochemicals. Additionally, the compound may display unique properties such as altered melting and boiling points compared to its non-halogenated counterparts. Its specific interactions in biological systems or its role in synthetic pathways can be further explored in research contexts, particularly in medicinal chemistry and materials science. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.

5-bromo-2-fluoro-3-methyl-benzoic acid

1427382-02-2: 5-Bromo-2-fluoro-3-methyl-benzoic acid is an aromatic carboxylic acid characterized by the presence of a bromine atom, a fluorine atom, and a methyl group attached to a benzoic acid framework. The molecular structure features a benzene ring with these substituents positioned at specific locations, which influence its chemical reactivity and physical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functional group. The presence of halogens (bromine and fluorine) can enhance its reactivity, making it useful in various chemical syntheses, including pharmaceuticals and agrochemicals. Additionally, the compound may display unique properties such as altered melting and boiling points compared to its non-halogenated counterparts. Its specific interactions in biological systems or its role in synthetic pathways can be further explored in research contexts, particularly in medicinal chemistry and materials science. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.

<p>5-Bromo-2-fluoro-3-methylbenzoic acid</p>

CAS 1427382-02-2

5-bromo-2-fluoro-3-methyl-benzoic acid

5-bromo-2-fluoro-3-methyl-benzoic acid

Ref: IN-DA00HWL4

5-Bromo-2-fluoro-3-methylbenzoic acid

Ref: 54-PC100500

5-BROMO-2-FLUORO-3-METHYLBENZOIC ACID

Ref: 10-F473029