CAS 1187933-35-2

5-Bromo-1-methyl-2(1H)-quinolinone

Description:

5-Bromo-1-methyl-2(1H)-quinolinone is a heterocyclic organic compound characterized by its quinolinone structure, which includes a bromine substituent at the 5-position and a methyl group at the 1-position of the quinoline ring. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, but may have limited solubility in water. The presence of the bromine atom enhances its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Its unique structure allows it to participate in biological activities, which may include antimicrobial or anticancer properties, although specific biological data may vary. The compound is often utilized in medicinal chemistry and research applications, particularly in the development of pharmaceuticals. As with many brominated compounds, it is important to handle it with care due to potential toxicity and environmental concerns.

Formula: C₁₀H₈BrNO

InChI: InChI=1S/C10H8BrNO/c1-12-9-4-2-3-8(11)7(9)5-6-10(12)13/h2-6H,1H3

InChI key: InChIKey=PQYPEEUJJRYGPH-UHFFFAOYSA-N

SMILES: CN1C=2C(=C(Br)C=CC2)C=CC1=O

Synonyms:

• 5-Bromo-1-methyl-2(1H)-quinolinone
• 2(1H)-Quinolinone, 5-bromo-1-methyl-

5-BROMO-1-METHYLQUINOLIN-2(1H)-ONE

CAS: 1187933-35-2

Formula: C₁₀H₈BrNO

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 238.084

Ref: 10-F389535