2-Phenylnaphthalene-1,4-dione, with the CAS number 2348-77-8, is an organic compound characterized by its structure, which features a naphthalene backbone substituted with a phenyl group and two carbonyl (ketone) functional groups at the 1 and 4 positions. This compound typically appears as a solid at room temperature and is known for its yellow to orange coloration. It is relatively insoluble in water but soluble in organic solvents such as ethanol and acetone. The presence of the carbonyl groups contributes to its reactivity, allowing it to participate in various chemical reactions, including nucleophilic additions and reductions. 2-Phenylnaphthalene-1,4-dione is of interest in organic synthesis and materials science due to its potential applications in dyes, pigments, and as a precursor for more complex organic molecules. Additionally, it may exhibit biological activity, making it a subject of study in medicinal chemistry. Proper handling and safety precautions should be observed, as with many organic compounds, due to potential toxicity and environmental impact.

2-phenylnaphthalene-1,4-dione

2348-77-8: 2-Phenylnaphthalene-1,4-dione, with the CAS number 2348-77-8, is an organic compound characterized by its structure, which features a naphthalene backbone substituted with a phenyl group and two carbonyl (ketone) functional groups at the 1 and 4 positions. This compound typically appears as a solid at room temperature and is known for its yellow to orange coloration. It is relatively insoluble in water but soluble in organic solvents such as ethanol and acetone. The presence of the carbonyl groups contributes to its reactivity, allowing it to participate in various chemical reactions, including nucleophilic additions and reductions. 2-Phenylnaphthalene-1,4-dione is of interest in organic synthesis and materials science due to its potential applications in dyes, pigments, and as a precursor for more complex organic molecules. Additionally, it may exhibit biological activity, making it a subject of study in medicinal chemistry. Proper handling and safety precautions should be observed, as with many organic compounds, due to potential toxicity and environmental impact.

1,4-Naphthalenedione, 2-phenyl-

<p>Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.</p>

CAS 2348-77-8

2-phenylnaphthalene-1,4-dione

1,4-Naphthalenedione, 2-phenyl-

Ref: IN-DA002NDN

Anti-infective agent 1

Ref: TM-T60315