The chemical substance with the name "(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxododecahydroazuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate" and CAS number "62462-98-0" is a complex organic compound characterized by its unique structural features, including multiple stereocenters and functional groups. It contains a chloromethyl group, which suggests potential reactivity, particularly in nucleophilic substitution reactions. The presence of hydroxyl groups indicates that the compound may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The dodecahydroazuleno structure contributes to its potential biological activity, as compounds with such frameworks are often found in natural products with medicinal properties. Additionally, the presence of an ester functional group (2-methylprop-2-enoate) suggests that it may participate in reactions typical of esters, such as hydrolysis or transesterification. Overall, this compound's intricate structure and functional groups may confer specific chemical properties and biological activities, making it of interest in fields such as medicinal chemistry and organic synthesis.

(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxododecahydroazuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate

62462-98-0: The chemical substance with the name "(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxododecahydroazuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate" and CAS number "62462-98-0" is a complex organic compound characterized by its unique structural features, including multiple stereocenters and functional groups. It contains a chloromethyl group, which suggests potential reactivity, particularly in nucleophilic substitution reactions. The presence of hydroxyl groups indicates that the compound may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The dodecahydroazuleno structure contributes to its potential biological activity, as compounds with such frameworks are often found in natural products with medicinal properties. Additionally, the presence of an ester functional group (2-methylprop-2-enoate) suggests that it may participate in reactions typical of esters, such as hydrolysis or transesterification. Overall, this compound's intricate structure and functional groups may confer specific chemical properties and biological activities, making it of interest in fields such as medicinal chemistry and organic synthesis.

Linichlorin A is used as a p27(Kip1) ubiquitination inhibitor.

CAS 62462-98-0

(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxododecahydroazuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate

Linichlorin A

Ref: TM-T25738