The chemical substance with the name "(3R,4aR,5aS,6aS,7aS,7bS)-2,2-dimethyl-6a-(3-methylbut-3-en-1-yn-1-yl)-6-oxohexahydro-2H,5aH-bisoxireno[e,h]chromen-3-yl acetate" and CAS number "88205-90-7" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a chromene backbone, which is a fused bicyclic structure known for its presence in various natural products and synthetic compounds. The presence of oxirane (epoxide) groups indicates potential reactivity, particularly in nucleophilic addition reactions. The compound also contains an acetate moiety, suggesting it may participate in esterification or hydrolysis reactions. Its structure includes multiple chiral centers, which can influence its biological activity and interactions with other molecules. The presence of a propargylic group (3-methylbut-3-en-1-yn-1-yl) may impart unique reactivity patterns, making it of interest in synthetic organic chemistry and potentially in medicinal chemistry for its pharmacological properties. Overall, this compound exemplifies the complexity and diversity of organic molecules in chemical research.

(3R,4aR,5aS,6aS,7aS,7bS)-2,2-dimethyl-6a-(3-methylbut-3-en-1-yn-1-yl)-6-oxohexahydro-2H,5aH-bisoxireno[e,h]chromen-3-yl acetate

88205-90-7: The chemical substance with the name "(3R,4aR,5aS,6aS,7aS,7bS)-2,2-dimethyl-6a-(3-methylbut-3-en-1-yn-1-yl)-6-oxohexahydro-2H,5aH-bisoxireno[e,h]chromen-3-yl acetate" and CAS number "88205-90-7" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a chromene backbone, which is a fused bicyclic structure known for its presence in various natural products and synthetic compounds. The presence of oxirane (epoxide) groups indicates potential reactivity, particularly in nucleophilic addition reactions. The compound also contains an acetate moiety, suggesting it may participate in esterification or hydrolysis reactions. Its structure includes multiple chiral centers, which can influence its biological activity and interactions with other molecules. The presence of a propargylic group (3-methylbut-3-en-1-yn-1-yl) may impart unique reactivity patterns, making it of interest in synthetic organic chemistry and potentially in medicinal chemistry for its pharmacological properties. Overall, this compound exemplifies the complexity and diversity of organic molecules in chemical research.

CAS 88205-90-7

(3R,4aR,5aS,6aS,7aS,7bS)-2,2-dimethyl-6a-(3-methylbut-3-en-1-yn-1-yl)-6-oxohexahydro-2H,5aH-bisoxireno[e,h]chromen-3-yl acetate

2H,5aH-Bisoxireno[e,h]-1-benzopyran-6(6aH)-one,3-(acetyloxy)tetrahydro-2,2-dimethyl-6a-(3-methyl-3-buten-1-yn-1-yl)-,(3R,4aR,5aS,6aS,7aS,7bS)-

Ref: IN-DA004C3L