The chemical substance with the name "(2R,3S,5aR,6R,6aS,6bS,7aR,8aR,8bR,11aS)-2,6,8,8,10,10-hexamethyldodecahydro-3,11b-methanooxireno[3',4']cyclopenta[1',2':3,4]heptaleno[1,2-d][1,3]dioxole-2,6,8a(1H)-triol" and CAS number "28836-76-2" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a dioxole ring, which contributes to its potential reactivity and biological activity. The presence of multiple methyl groups suggests a high degree of branching, which can influence its physical properties such as solubility and volatility. The triol functional groups indicate that the compound has three hydroxyl (-OH) groups, which can participate in hydrogen bonding, affecting its interactions with other molecules. The stereochemical descriptors (R and S) indicate specific configurations at various chiral centers, which can significantly impact the compound's biological activity and pharmacological properties. Overall, this compound's unique structure may confer specific properties that could be of interest in fields such as medicinal chemistry or materials science.

(2R,3S,5aR,6R,6aS,6bS,7aR,8aR,8bR,11aS)-2,6,8,8,10,10-hexamethyldodecahydro-3,11b-methanooxireno[3',4']cyclopenta[1',2':3,4]heptaleno[1,2-d][1,3]dioxole-2,6,8a(1H)-triol

28836-76-2: The chemical substance with the name "(2R,3S,5aR,6R,6aS,6bS,7aR,8aR,8bR,11aS)-2,6,8,8,10,10-hexamethyldodecahydro-3,11b-methanooxireno[3',4']cyclopenta[1',2':3,4]heptaleno[1,2-d][1,3]dioxole-2,6,8a(1H)-triol" and CAS number "28836-76-2" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a dioxole ring, which contributes to its potential reactivity and biological activity. The presence of multiple methyl groups suggests a high degree of branching, which can influence its physical properties such as solubility and volatility. The triol functional groups indicate that the compound has three hydroxyl (-OH) groups, which can participate in hydrogen bonding, affecting its interactions with other molecules. The stereochemical descriptors (R and S) indicate specific configurations at various chiral centers, which can significantly impact the compound's biological activity and pharmacological properties. Overall, this compound's unique structure may confer specific properties that could be of interest in fields such as medicinal chemistry or materials science.

Deacetyllyoniol A acetonide is a biochemical.

CAS 28836-76-2

(2R,3S,5aR,6R,6aS,6bS,7aR,8aR,8bR,11aS)-2,6,8,8,10,10-hexamethyldodecahydro-3,11b-methanooxireno[3',4']cyclopenta[1',2':3,4]heptaleno[1,2-d][1,3]dioxole-2,6,8a(1H)-triol

Deacetyllyoniol A acetonide

Ref: TM-T31245