The chemical substance with the name "(1R,2S,4aR,8aR)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-en-1-yl)decahydronaphthalen-2-ol" and CAS number "89900-49-2" is a complex organic compound characterized by its specific stereochemistry and structural features. It belongs to the class of terpenoids, which are known for their diverse biological activities and aromatic properties. The presence of multiple methyl groups and a decahydronaphthalene core contributes to its hydrophobic nature, making it less soluble in water but more soluble in organic solvents. The compound features a hydroxyl (-OH) group, indicating it is an alcohol, which can participate in hydrogen bonding, influencing its reactivity and interactions. Its unique structure may confer specific properties such as fragrance or flavor, and it may also exhibit potential applications in pharmaceuticals or as a natural product. The stereochemical configuration suggests that it may have distinct optical activity, which can be important in determining its biological effects. Overall, this compound exemplifies the complexity and diversity found in organic chemistry.

(1R,2S,4aR,8aR)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-en-1-yl)decahydronaphthalen-2-ol

89900-49-2: The chemical substance with the name "(1R,2S,4aR,8aR)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-en-1-yl)decahydronaphthalen-2-ol" and CAS number "89900-49-2" is a complex organic compound characterized by its specific stereochemistry and structural features. It belongs to the class of terpenoids, which are known for their diverse biological activities and aromatic properties. The presence of multiple methyl groups and a decahydronaphthalene core contributes to its hydrophobic nature, making it less soluble in water but more soluble in organic solvents. The compound features a hydroxyl (-OH) group, indicating it is an alcohol, which can participate in hydrogen bonding, influencing its reactivity and interactions. Its unique structure may confer specific properties such as fragrance or flavor, and it may also exhibit potential applications in pharmaceuticals or as a natural product. The stereochemical configuration suggests that it may have distinct optical activity, which can be important in determining its biological effects. Overall, this compound exemplifies the complexity and diversity found in organic chemistry.

<p>Labdane F2 is an antagonist of thromboxane B2 and leukotriene B4 isolated from the Spanish herb Sideritis javalambrensis.</p>

CAS 89900-49-2

(1R,2S,4aR,8aR)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-en-1-yl)decahydronaphthalen-2-ol

Labdane F2

Ref: TM-T25592