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CAS 38637-88-6

:

1,4-Naphthalenedione, 5-hydroxy-2-[(2R,3R)-tetrahydro-3-hydroxy-5-oxo-2-furanyl]-

Description:
1,4-Naphthalenedione, 5-hydroxy-2-[(2R,3R)-tetrahydro-3-hydroxy-5-oxo-2-furanyl]- is a complex organic compound characterized by its naphthalene backbone, which is a fused bicyclic aromatic hydrocarbon. The presence of the 1,4-naphthoquinone structure imparts significant reactivity, particularly in redox reactions, due to the electron-deficient nature of the quinone moiety. The compound features a hydroxyl group, which enhances its solubility in polar solvents and may contribute to its biological activity. The tetrahydrofuran ring indicates the presence of a cyclic ether, which can influence the compound's stereochemistry and reactivity. This compound may exhibit various biological properties, including potential antioxidant activity, owing to the presence of both the hydroxyl and carbonyl functionalities. Its specific stereochemistry, denoted by the (2R,3R) configuration, suggests that it may interact with biological systems in a stereospecific manner. Overall, this compound's unique structural features make it of interest in medicinal chemistry and organic synthesis.
Formula:C14H10O6
Synonyms:
  • 1,4-Naphthalenedione,5-hydroxy-2-(tetrahydro-3-hydroxy-5-oxo-2-furanyl)-, (2R-cis)-
  • 1,4-Naphthalenedione, 5-hydroxy-2-[(2R,3R)-tetrahydro-3-hydroxy-5-oxo-2-furanyl]-
  • Juglomycin A
  • Juglomycin A
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  • Juglomycin A

    CAS:
    <p>Juglomycin A exhibits broad-spectrum antibacterial and anti-mycobacterial activity and can inhibit Ehrlich ascites carcinoma in mice.</p>
    Formula:C14H10O6
    Color and Shape:Solid
    Molecular weight:274.226