CAS 105900-46-7: 4,13-Dioxabicyclo[8.2.1]tridecan-5-one,7-[(2,6-dideoxy-3-C-methyl-3-O-methyl-a-L-ribo-hexopyranosyl)oxy]-3-[(1R,2R)-1,2-dihydroxy-1-methylbutyl]-1-hydroxy-2,6,8,10,12-pentamethyl-9-[[3,4,6-trideoxy-3-(dimethylamino)-b-D-xylo-hexopyranosyl]oxy]-,(1S,2R,3R,
CAS 105900-46-7: 4,13-Dioxabicyclo[8.2.1]tridecan-5-one,7-[(2,6-dideoxy-3-C-methyl-3-O-methyl-a-L-ribo-hexopyranosyl)oxy]-3-[(1R,2R)-1,2-dihydroxy-1-methylbutyl]-1-hydroxy-2,6,8,10,12-pentamethyl-9-[[3,4,6-trideoxy-3-(dimethylamino)-b-D-xylo-hexopyranosyl]oxy]-,(1S,2R,3R,
Description:4,13-Dioxabicyclo[8.2.1]tridecan-5-one, with the CAS number 105900-46-7, is a complex organic compound characterized by its bicyclic structure and multiple functional groups. This substance features a dioxabicyclo framework, which contributes to its unique chemical properties, including potential reactivity and stability. The presence of hydroxyl groups indicates that it may exhibit hydrogen bonding capabilities, influencing its solubility and interaction with other molecules. Additionally, the compound contains sugar moieties, specifically dideoxy and C-methylated hexopyranosyl units, which may enhance its biological activity and potential as a glycoside. The presence of a dimethylamino group suggests possible basicity, which could affect its behavior in various chemical environments. Overall, this compound's intricate structure and functional diversity may render it of interest in medicinal chemistry and biochemistry, particularly in the development of therapeutics or as a biochemical probe. Its specific characteristics, such as melting point, solubility, and reactivity, would require empirical investigation for detailed understanding.
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