1,8(2H,4bH)-Chrysenedione, with the CAS number 3079028-41-1, is a complex organic compound characterized by its polycyclic structure, which includes multiple fused aromatic rings. This substance features a unique arrangement of hydroxyl groups, contributing to its potential reactivity and solubility in various solvents. The presence of multiple stereocenters indicates that it exists in specific stereoisomeric forms, which can influence its biological activity and interactions with other molecules. The compound's decahydro configuration suggests it is saturated, which may affect its stability and reactivity compared to unsaturated analogs. Additionally, the hydroxymethyl and dimethyl substituents provide further functionalization, potentially enhancing its utility in synthetic applications or as a biological probe. Overall, the structural complexity and functional groups present in this compound suggest it may have interesting properties for research in fields such as medicinal chemistry, materials science, or organic synthesis.

1,8(2H,4bH)-Chrysenedione, 3,4,4a,5,6,10a,10b,11,12,12a-decahydro-2,3,11-trihydroxy-2-(hydroxymethyl)-10a,12a-dimethyl-, (2R,3R,4aS,4bS,10aR,10bS,11S,12aS)-

3079028-41-1: 1,8(2H,4bH)-Chrysenedione, with the CAS number 3079028-41-1, is a complex organic compound characterized by its polycyclic structure, which includes multiple fused aromatic rings. This substance features a unique arrangement of hydroxyl groups, contributing to its potential reactivity and solubility in various solvents. The presence of multiple stereocenters indicates that it exists in specific stereoisomeric forms, which can influence its biological activity and interactions with other molecules. The compound's decahydro configuration suggests it is saturated, which may affect its stability and reactivity compared to unsaturated analogs. Additionally, the hydroxymethyl and dimethyl substituents provide further functionalization, potentially enhancing its utility in synthetic applications or as a biological probe. Overall, the structural complexity and functional groups present in this compound suggest it may have interesting properties for research in fields such as medicinal chemistry, materials science, or organic synthesis.

Adrenal cortical hormones and their derivatives nesoi

17α-Hydroxy13(17)a-homoprednisolone ((2R,3R,4aS,4bS,10aR,10bS,11S,12aS)-2,3,11-trihydroxy-2-(hydroxymethyl)-10a,12a-dimethyl-3,4,4a,5,6,10a,10b,11,12,12a-decahydrochrysene-1,8(2H,4bH)-dione)

CAS 3079028-41-1

1,8(2H,4bH)-Chrysenedione, 3,4,4a,5,6,10a,10b,11,12,12a-decahydro-2,3,11-trihydroxy-2-(hydroxymethyl)-10a,12a-dimethyl-, (2R,3R,4aS,4bS,10aR,10bS,11S,12aS)-

17α-Hydroxy13(17)a-homoprednisolone ((2R,3R,4aS,4bS,10aR,10bS,11S,12aS)-2,3,11-trihydroxy-2-(hydroxymethyl)-10a,12a-dimethyl-3,4,4a,5,6,10a,10b,11,12,12a-decahydrochrysene-1,8(2H,4bH)-dione)

Ref: 45-1A02010