4-Bromo-5-iodo-2-methylbenzoic acid is an aromatic carboxylic acid characterized by the presence of a benzoic acid core substituted with bromine and iodine atoms, as well as a methyl group. The bromine atom is located at the para position (4-position) and the iodine at the meta position (5-position) relative to the carboxylic acid group, while the methyl group is positioned at the ortho position (2-position). This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure contributes to its potential reactivity, making it useful in various chemical syntheses, particularly in the development of pharmaceuticals and agrochemicals. The presence of halogens can influence the compound's electronic properties, affecting its reactivity and interactions with other molecules. Additionally, the carboxylic acid functional group can participate in hydrogen bonding, which may impact its physical properties and solubility in polar solvents. Overall, 4-bromo-5-iodo-2-methylbenzoic acid is a versatile compound with applications in organic synthesis and medicinal chemistry.

4-BroMo-5-iodo-2-Methyl-benzoic acid

1022983-51-2: 4-Bromo-5-iodo-2-methylbenzoic acid is an aromatic carboxylic acid characterized by the presence of a benzoic acid core substituted with bromine and iodine atoms, as well as a methyl group. The bromine atom is located at the para position (4-position) and the iodine at the meta position (5-position) relative to the carboxylic acid group, while the methyl group is positioned at the ortho position (2-position). This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure contributes to its potential reactivity, making it useful in various chemical syntheses, particularly in the development of pharmaceuticals and agrochemicals. The presence of halogens can influence the compound's electronic properties, affecting its reactivity and interactions with other molecules. Additionally, the carboxylic acid functional group can participate in hydrogen bonding, which may impact its physical properties and solubility in polar solvents. Overall, 4-bromo-5-iodo-2-methylbenzoic acid is a versatile compound with applications in organic synthesis and medicinal chemistry.

CAS 1022983-51-2

4-BroMo-5-iodo-2-Methyl-benzoic acid