7-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 7-position and a methyl group at the 4-position 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 antitumor 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 interaction with various biological targets. As with many quinoline derivatives, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile building block in organic synthesis.

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

89446-51-5: 7-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 7-position and a methyl group at the 4-position 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 antitumor 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 interaction with various biological targets. As with many quinoline derivatives, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile building block in organic synthesis.

CAS 89446-51-5

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

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

Ref: IN-DA0042WJ

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Ref: 54-OR309468

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Ref: 54-OR310301

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Ref: 10-F790332