The chemical substance with the name "(4aR,7S,7aS)-7-methyl-1-{[(2S,3R,4R,5S,6R)-3,4,5,6-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl (2E)-3-phenylprop-2-enoate" and CAS number 70206-27-8 is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a hexahydrocyclopenta[c]pyran core, which is a bicyclic structure, and is substituted with a phenylprop-2-enoate moiety, indicating the presence of an ester functional group derived from a phenylpropanoic acid. The compound also contains several hydroxyl groups, contributing to its potential solubility in polar solvents and reactivity in various chemical reactions. Its stereochemical configuration, denoted by the specific R and S designations, suggests that it may exhibit unique biological activities or interactions, making it of interest in fields such as medicinal chemistry or natural product synthesis. Overall, this compound's structural complexity and functional diversity may lead to varied applications in pharmaceuticals or biochemistry.

(4aR,7S,7aS)-7-methyl-1-{[(2S,3R,4R,5S,6R)-3,4,5,6-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl (2E)-3-phenylprop-2-enoate (non-preferred name)

70206-27-8: The chemical substance with the name "(4aR,7S,7aS)-7-methyl-1-{[(2S,3R,4R,5S,6R)-3,4,5,6-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl (2E)-3-phenylprop-2-enoate" and CAS number 70206-27-8 is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a hexahydrocyclopenta[c]pyran core, which is a bicyclic structure, and is substituted with a phenylprop-2-enoate moiety, indicating the presence of an ester functional group derived from a phenylpropanoic acid. The compound also contains several hydroxyl groups, contributing to its potential solubility in polar solvents and reactivity in various chemical reactions. Its stereochemical configuration, denoted by the specific R and S designations, suggests that it may exhibit unique biological activities or interactions, making it of interest in fields such as medicinal chemistry or natural product synthesis. Overall, this compound's structural complexity and functional diversity may lead to varied applications in pharmaceuticals or biochemistry.

<p>Laterioside is a bioactive chemical.</p>

CAS 70206-27-8

(4aR,7S,7aS)-7-methyl-1-{[(2S,3R,4R,5S,6R)-3,4,5,6-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl (2E)-3-phenylprop-2-enoate (non-preferred name)

Laterioside

Ref: TM-T32583