The chemical substance with the name "(1R,3aS,3bR,5aS,7R,8aS,8bR,10aS)-1,7-diethynyl-10a-methylhexadecahydrodicyclopenta[a,f]naphthalene-1,7-diyl diacetate" and CAS number "70226-89-0" is a complex organic compound characterized by its unique polycyclic structure, which includes multiple fused rings. This compound features ethynyl groups, which are known for their reactivity and ability to participate in various chemical reactions, including polymerization and cross-coupling reactions. The presence of diacetate functional groups suggests that it may exhibit specific solubility properties and reactivity patterns, particularly in organic synthesis. The stereochemistry indicated by the IUPAC name suggests that the compound has multiple chiral centers, which can influence its biological activity and interactions with other molecules. Such compounds are often of interest in medicinal chemistry and materials science due to their potential applications in drug development and as building blocks for more complex molecular architectures. Overall, this substance exemplifies the intricate nature of organic compounds and their diverse functionalities.

Dinordrin I diacetate is an implantation inhibitor and hormone. It may have potential as a female contraceptive, causing uterotrophic activity. There may also be a definite luteolytic effect, i.e. depression of plasma estrogen and progesterone levels.

(1R,3aS,3bR,5aS,7R,8aS,8bR,10aS)-1,7-diethynyl-10a-methylhexadecahydrodicyclopenta[a,f]naphthalene-1,7-diyl diacetate

70226-89-0: The chemical substance with the name "(1R,3aS,3bR,5aS,7R,8aS,8bR,10aS)-1,7-diethynyl-10a-methylhexadecahydrodicyclopenta[a,f]naphthalene-1,7-diyl diacetate" and CAS number "70226-89-0" is a complex organic compound characterized by its unique polycyclic structure, which includes multiple fused rings. This compound features ethynyl groups, which are known for their reactivity and ability to participate in various chemical reactions, including polymerization and cross-coupling reactions. The presence of diacetate functional groups suggests that it may exhibit specific solubility properties and reactivity patterns, particularly in organic synthesis. The stereochemistry indicated by the IUPAC name suggests that the compound has multiple chiral centers, which can influence its biological activity and interactions with other molecules. Such compounds are often of interest in medicinal chemistry and materials science due to their potential applications in drug development and as building blocks for more complex molecular architectures. Overall, this substance exemplifies the intricate nature of organic compounds and their diverse functionalities.

Dinordrin I diacetate is an implantation inhibitor and hormone.

CAS 70226-89-0

(1R,3aS,3bR,5aS,7R,8aS,8bR,10aS)-1,7-diethynyl-10a-methylhexadecahydrodicyclopenta[a,f]naphthalene-1,7-diyl diacetate

Dinordrin I diacetate

Ref: TM-T27181