CAS 880094-83-7

5-Bromo-3,4-dihydroquinolin-2(1H)-one

Description:

5-Bromo-3,4-dihydroquinolin-2(1H)-one is a heterocyclic organic compound characterized by its quinoline structure, which includes a bromine substituent at the 5-position and a carbonyl group at the 2-position. This compound typically exhibits a fused bicyclic system, contributing to its unique chemical properties. It is often studied for its potential biological activities, including antimicrobial and anticancer properties, due to the presence of the quinoline moiety, which is known for its pharmacological significance. The compound is generally soluble in organic solvents, and its reactivity can be influenced by the bromine atom, which can participate in nucleophilic substitution reactions. Additionally, the presence of the carbonyl group can engage in hydrogen bonding and contribute to the compound's overall stability and reactivity. As with many heterocycles, the electronic properties of 5-Bromo-3,4-dihydroquinolin-2(1H)-one can be modulated by substituents, making it a valuable compound in medicinal chemistry and synthetic applications.

Formula: C₉H₈BrNO

Synonyms:

• 2(1H)-Quinolinone, 5-bromo-3,4-dihydro-

5-Bromo-3,4-dihydroquinolin-2(1H)-one

CAS: 880094-83-7

Formula: C₉H₈BrNO

Purity: 97%

Color and Shape: Solid

Molecular weight: 226.0699

Ref: IN-DA004NXQ

5-Bromo-3,4-dihydro-2(1H)-quinolinone

CAS: 880094-83-7

5-Bromo-3,4-dihydro-2(1H)-quinolinone

Purity: 98%

Molecular weight: 226.07g/mol

Ref: 54-OR91786

5-Bromo-3,4-dihydroquinolin-2(1H)-one

CAS: 880094-83-7

Formula: C₉H₈BrNO

Purity: 95%

Color and Shape: Solid, Yellow powder

Molecular weight: 226.073

Ref: 10-F211250