2,3-Dihydrobenzo[g]quinolin-4(1H)-one, with the CAS number 21516-07-4, is a heterocyclic organic compound characterized by its fused ring structure, which includes a quinoline moiety. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential biological activities, including antimicrobial and anticancer properties, making it of interest in medicinal chemistry. The presence of the carbonyl group (C=O) in its structure contributes to its reactivity and potential interactions with biological targets. Solubility can vary depending on the solvent, but it is generally more soluble in organic solvents than in water. The compound's stability is influenced by environmental factors such as light and temperature, and it may undergo various chemical reactions, including oxidation and reduction. Overall, 2,3-dihydrobenzo[g]quinolin-4(1H)-one serves as a valuable scaffold in drug discovery and development, warranting further investigation into its pharmacological properties and applications.

2,3-dihydrobenzo[g]quinolin-4(1H)-one

21516-07-4: Benzo[g]quinolin-4(1H)-one, 2,3-dihydro-

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2,3-Dihydrobenzo(G)quinolin-4(1H)-one

Applications 2,3-dihydrobenzo[g]quinolin-4(1H)-one (cas# 21516-07-4) is a useful research chemical.


CAS 21516-07-4: 2,3-dihydrobenzo[g]quinolin-4(1H)-one

2,3-Dihydrobenzo(G)quinolin-4(1H)-one

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2,3-Dihydrobenzo[g]quinolin-4(1H)-one

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2,3-dihydrobenzo[g]quinolin-4(1H)-one

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