3,3'-Sulfanediylbis(2-hydroxy-4H-chromen-4-one), also known by its CAS number 1821-13-2, is a synthetic organic compound characterized by its chromone structure, which features two hydroxy groups and a sulfanediyl linkage. This compound exhibits properties typical of flavonoids, including antioxidant activity, which is attributed to the presence of the chromone moiety. The sulfanediyl group enhances its solubility and may influence its biological activity. It is often studied for its potential applications in pharmaceuticals and as a bioactive compound due to its ability to interact with various biological targets. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its solubility can vary depending on the solvent used, and it may undergo various chemical reactions, including oxidation and conjugation, which are common for compounds containing hydroxyl groups. Overall, 3,3'-sulfanediylbis(2-hydroxy-4H-chromen-4-one) represents a class of compounds with significant interest in medicinal chemistry and natural product research.

3,3'-sulfanediylbis(2-hydroxy-4H-chromen-4-one)

1821-13-2: 3,3'-Sulfanediylbis(2-hydroxy-4H-chromen-4-one), also known by its CAS number 1821-13-2, is a synthetic organic compound characterized by its chromone structure, which features two hydroxy groups and a sulfanediyl linkage. This compound exhibits properties typical of flavonoids, including antioxidant activity, which is attributed to the presence of the chromone moiety. The sulfanediyl group enhances its solubility and may influence its biological activity. It is often studied for its potential applications in pharmaceuticals and as a bioactive compound due to its ability to interact with various biological targets. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its solubility can vary depending on the solvent used, and it may undergo various chemical reactions, including oxidation and conjugation, which are common for compounds containing hydroxyl groups. Overall, 3,3'-sulfanediylbis(2-hydroxy-4H-chromen-4-one) represents a class of compounds with significant interest in medicinal chemistry and natural product research.

2H-1-Benzopyran-2-one, 3,3'-thiobis[4-hydroxy-

<p>A-1062, a resolvase-binding inhibitor, inhibits resolvase binding to the res site.</p>

CAS 1821-13-2

3,3'-sulfanediylbis(2-hydroxy-4H-chromen-4-one)

2H-1-Benzopyran-2-one, 3,3'-thiobis[4-hydroxy-

Ref: IN-DA0023DC

A-1062

Ref: TM-T26462