3-Bromo-4-methylquinolin-2(1H)-one is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 3-position and a methyl group at the 4-position of the quinoline ring contributes to its unique chemical properties. This compound typically exhibits a yellow to brown color and is soluble in organic solvents, such as dimethyl sulfoxide (DMSO) and ethanol, but may have limited solubility in water. It is known for its potential biological activities, including antimicrobial and anticancer properties, making it of interest in medicinal chemistry. The compound's reactivity can be influenced by the electron-withdrawing nature of the bromine atom and the electron-donating methyl group, which can affect its interactions with biological targets. As with many heterocycles, it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, depending on the reaction conditions. Safety and handling precautions should be observed due to its potential toxicity and reactivity.

3-bromo-4-methylquinolin-2(1H)-one

37778-22-6: 3-Bromo-4-methylquinolin-2(1H)-one is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 3-position and a methyl group at the 4-position of the quinoline ring contributes to its unique chemical properties. This compound typically exhibits a yellow to brown color and is soluble in organic solvents, such as dimethyl sulfoxide (DMSO) and ethanol, but may have limited solubility in water. It is known for its potential biological activities, including antimicrobial and anticancer properties, making it of interest in medicinal chemistry. The compound's reactivity can be influenced by the electron-withdrawing nature of the bromine atom and the electron-donating methyl group, which can affect its interactions with biological targets. As with many heterocycles, it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, depending on the reaction conditions. Safety and handling precautions should be observed due to its potential toxicity and reactivity.

CAS 37778-22-6

3-bromo-4-methylquinolin-2(1H)-one

3-Bromo-4-methylquinolin-2(1H)-one

Ref: IN-DA0077SG

3-bromo-4-methyl-2-quinolinol

Ref: 10-F311237