The chemical substance with the name "(3bS,9bR)-6-hydroxy-9b-methyl-7-(propan-2-yl)-3,3b,4,9b,10,11-hexahydrophenanthro[1,2-c]furan-1,5-dione" and CAS number "79548-61-1" is a complex organic compound characterized by its unique structural features, including a fused polycyclic framework and multiple functional groups. It contains a hydroxyl group, which contributes to its potential reactivity and solubility in polar solvents. The presence of a ketone functional group (as indicated by the dione designation) suggests that it may participate in various chemical reactions, such as nucleophilic additions or reductions. The stereochemistry, denoted by the specific configuration at certain carbon centers, implies that the compound may exhibit distinct biological activities or interactions, making it of interest in medicinal chemistry or pharmacology. Additionally, the branched alkyl group (propan-2-yl) may influence its lipophilicity and overall molecular interactions. Overall, this compound's structural complexity and functional diversity suggest potential applications in various fields, including drug development and organic synthesis.

(3bS,9bR)-6-hydroxy-9b-methyl-7-(propan-2-yl)-3,3b,4,9b,10,11-hexahydrophenanthro[1,2-c]furan-1,5-dione

79548-61-1: The chemical substance with the name "(3bS,9bR)-6-hydroxy-9b-methyl-7-(propan-2-yl)-3,3b,4,9b,10,11-hexahydrophenanthro[1,2-c]furan-1,5-dione" and CAS number "79548-61-1" is a complex organic compound characterized by its unique structural features, including a fused polycyclic framework and multiple functional groups. It contains a hydroxyl group, which contributes to its potential reactivity and solubility in polar solvents. The presence of a ketone functional group (as indicated by the dione designation) suggests that it may participate in various chemical reactions, such as nucleophilic additions or reductions. The stereochemistry, denoted by the specific configuration at certain carbon centers, implies that the compound may exhibit distinct biological activities or interactions, making it of interest in medicinal chemistry or pharmacology. Additionally, the branched alkyl group (propan-2-yl) may influence its lipophilicity and overall molecular interactions. Overall, this compound's structural complexity and functional diversity suggest potential applications in various fields, including drug development and organic synthesis.

CAS 79548-61-1

(3bS,9bR)-6-hydroxy-9b-methyl-7-(propan-2-yl)-3,3b,4,9b,10,11-hexahydrophenanthro[1,2-c]furan-1,5-dione

Triptonolide

Ref: IN-DA00G3LN