The chemical substance with the name "(3aR,4S,6E,10Z,11aR)-3a,4,5,8,9,11a-Hexahydro-4-hydroxy-10-(hydroxymethyl)-6-methyl-3-methylenecyclodeca[b]furan-2(3H)-one" and CAS number "26931-94-2" is a complex organic compound characterized by its unique bicyclic structure, which includes multiple stereocenters contributing to its specific three-dimensional configuration. This compound features a hexahydro furan ring, indicating it is a saturated derivative of furan, and contains hydroxyl groups that suggest potential for hydrogen bonding, influencing its solubility and reactivity. The presence of a methylene group and a methyl group indicates branching in its carbon skeleton, which can affect its physical properties such as boiling point and melting point. Additionally, the stereochemistry denoted by the R and S configurations implies that the compound may exhibit chiral properties, which can be significant in biological interactions and pharmacological activity. Overall, this compound's structural complexity and functional groups suggest it may have interesting applications in medicinal chemistry or as a natural product derivative.

(3aR,4S,6E,10Z,11aR)-3a,4,5,8,9,11a-Hexahydro-4-hydroxy-10-(hydroxymethyl)-6-methyl-3-methylenecyclodeca[b]furan-2(3H)-one

26931-94-2: The chemical substance with the name "(3aR,4S,6E,10Z,11aR)-3a,4,5,8,9,11a-Hexahydro-4-hydroxy-10-(hydroxymethyl)-6-methyl-3-methylenecyclodeca[b]furan-2(3H)-one" and CAS number "26931-94-2" is a complex organic compound characterized by its unique bicyclic structure, which includes multiple stereocenters contributing to its specific three-dimensional configuration. This compound features a hexahydro furan ring, indicating it is a saturated derivative of furan, and contains hydroxyl groups that suggest potential for hydrogen bonding, influencing its solubility and reactivity. The presence of a methylene group and a methyl group indicates branching in its carbon skeleton, which can affect its physical properties such as boiling point and melting point. Additionally, the stereochemistry denoted by the R and S configurations implies that the compound may exhibit chiral properties, which can be significant in biological interactions and pharmacological activity. Overall, this compound's structural complexity and functional groups suggest it may have interesting applications in medicinal chemistry or as a natural product derivative.

<p>Salonitenolide is a germacranolide isolated from from Aegialophila pumila Jus. Boiss.</p>

CAS 26931-94-2

(3aR,4S,6E,10Z,11aR)-3a,4,5,8,9,11a-Hexahydro-4-hydroxy-10-(hydroxymethyl)-6-methyl-3-methylenecyclodeca[b]furan-2(3H)-one

Salonitenolide

Ref: TM-T34497