4-(3-Bromo-5-methyl-phenyl)-4-oxo-butanoic acid is an organic compound characterized by its unique structure, which includes a butanoic acid backbone with a ketone functional group and a substituted phenyl ring. The presence of a bromine atom and a methyl group on the phenyl ring contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. This compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic aromatic component, while the carboxylic acid group may impart some polar characteristics, allowing for hydrogen bonding interactions. The compound's molecular structure suggests it may participate in various chemical reactions, such as esterification or amidation, making it a versatile intermediate in synthetic chemistry. Additionally, the bromine substituent may enhance its biological activity, potentially influencing its pharmacological properties. As with many organic compounds, safety and handling precautions should be observed, particularly due to the presence of bromine, which can be hazardous.

4-(3-bromo-5-methyl-phenyl)-4-oxo-butanoic acid

898767-43-6: 4-(3-Bromo-5-methyl-phenyl)-4-oxo-butanoic acid is an organic compound characterized by its unique structure, which includes a butanoic acid backbone with a ketone functional group and a substituted phenyl ring. The presence of a bromine atom and a methyl group on the phenyl ring contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. This compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic aromatic component, while the carboxylic acid group may impart some polar characteristics, allowing for hydrogen bonding interactions. The compound's molecular structure suggests it may participate in various chemical reactions, such as esterification or amidation, making it a versatile intermediate in synthetic chemistry. Additionally, the bromine substituent may enhance its biological activity, potentially influencing its pharmacological properties. As with many organic compounds, safety and handling precautions should be observed, particularly due to the presence of bromine, which can be hazardous.

CAS 898767-43-6

4-(3-bromo-5-methyl-phenyl)-4-oxo-butanoic acid

4-(3-Bromo-5-methylphenyl)-4-oxobutyric acid

Ref: 10-F207306