1-Methoxy[1,3]benzodioxolo[5,6-c]phenanthridin-2-ol, with the CAS number 54354-62-0, is a complex organic compound characterized by its unique structural features, including a phenanthridine core fused with a benzodioxole moiety. This compound typically exhibits properties associated with heterocyclic compounds, such as potential fluorescence and biological activity. The presence of the methoxy group suggests that it may have enhanced solubility in organic solvents and could participate in various chemical reactions, including nucleophilic substitutions. Its hydroxyl group likely contributes to its reactivity and potential for hydrogen bonding, influencing its interactions in biological systems. Compounds of this nature are often studied for their pharmacological properties, including potential anticancer or antimicrobial activities. The intricate structure may also impart specific electronic properties, making it of interest in materials science and organic electronics. Overall, 1-methoxy[1,3]benzodioxolo[5,6-c]phenanthridin-2-ol represents a fascinating subject for further research in both synthetic and medicinal chemistry.

The stem bark of Zanthoxylum decaryi yields this alkaloid which forms orange
needles when purified by recrystallization from MeOH-CHC13. It gives a complex
ultraviolet spectrum in EtOH having absorption maxima at 249, 257, 277, 326
and 382 nm with shoulders at 285 and 335 nm. The structure has been determined
from chemical degradation and spectroscopic examination.

1-methoxy[1,3]benzodioxolo[5,6-c]phenanthridin-2-ol

54354-62-0: 1-Methoxy[1,3]benzodioxolo[5,6-c]phenanthridin-2-ol, with the CAS number 54354-62-0, is a complex organic compound characterized by its unique structural features, including a phenanthridine core fused with a benzodioxole moiety. This compound typically exhibits properties associated with heterocyclic compounds, such as potential fluorescence and biological activity. The presence of the methoxy group suggests that it may have enhanced solubility in organic solvents and could participate in various chemical reactions, including nucleophilic substitutions. Its hydroxyl group likely contributes to its reactivity and potential for hydrogen bonding, influencing its interactions in biological systems. Compounds of this nature are often studied for their pharmacological properties, including potential anticancer or antimicrobial activities. The intricate structure may also impart specific electronic properties, making it of interest in materials science and organic electronics. Overall, 1-methoxy[1,3]benzodioxolo[5,6-c]phenanthridin-2-ol represents a fascinating subject for further research in both synthetic and medicinal chemistry.

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Decarine: strong antibacterial, low human macrophage toxicity. Blocks elastase release, IC50 ≤ 5.53µg/mL.

CAS 54354-62-0

1-methoxy[1,3]benzodioxolo[5,6-c]phenanthridin-2-ol

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Ref: IN-DA00DGYG

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Ref: TM-TN1556

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Ref: BP-SBP01768