The chemical substance with the name "9aH,10aH-2,3a,6a-[1]Propanyl[3]ylidene-4H-difuro[2,3-b:3',2'-g]oxocin-3-carboxylic acid, 8-(3-furanyl)hexahydro-6-methyl-, methyl ester, (2R,3R,3aS,6R,6aR,8S,9aR,10aS,11R)-rel-(-)-" and CAS number 142409-09-4 is a complex organic compound characterized by its intricate fused ring structure, which includes multiple furan and oxocin moieties. This compound features stereocenters, indicating chirality, which contributes to its potential biological activity and specificity in interactions. The presence of a carboxylic acid functional group suggests it may exhibit acidic properties, while the methyl ester indicates potential for reactivity and solubility in organic solvents. Its structural complexity may confer unique pharmacological properties, making it of interest in medicinal chemistry. The specific stereochemistry may influence its binding affinity and efficacy in biological systems, highlighting the importance of chirality in drug design. Overall, this compound exemplifies the diversity of organic molecules and their potential applications in various fields, including pharmaceuticals and materials science.

9aH,10aH-2,3a,6a-[1]Propanyl[3]ylidene-4H-difuro[2,3-b:3',2'-g]oxocin-3-carboxylicacid, 8-(3-furanyl)hexahydro-6-methyl-, methyl ester,(2R,3R,3aS,6R,6aR,8S,9aR,10aS,11R)-rel-(-)-

142409-09-4: The chemical substance with the name "9aH,10aH-2,3a,6a-[1]Propanyl[3]ylidene-4H-difuro[2,3-b:3',2'-g]oxocin-3-carboxylic acid, 8-(3-furanyl)hexahydro-6-methyl-, methyl ester, (2R,3R,3aS,6R,6aR,8S,9aR,10aS,11R)-rel-(-)-" and CAS number 142409-09-4 is a complex organic compound characterized by its intricate fused ring structure, which includes multiple furan and oxocin moieties. This compound features stereocenters, indicating chirality, which contributes to its potential biological activity and specificity in interactions. The presence of a carboxylic acid functional group suggests it may exhibit acidic properties, while the methyl ester indicates potential for reactivity and solubility in organic solvents. Its structural complexity may confer unique pharmacological properties, making it of interest in medicinal chemistry. The specific stereochemistry may influence its binding affinity and efficacy in biological systems, highlighting the importance of chirality in drug design. Overall, this compound exemplifies the diversity of organic molecules and their potential applications in various fields, including pharmaceuticals and materials science.

<p>Crovatin is extracted from Croton laevigatus Vahl.</p>

CAS 142409-09-4

9aH,10aH-2,3a,6a-[1]Propanyl[3]ylidene-4H-difuro[2,3-b:3',2'-g]oxocin-3-carboxylicacid, 8-(3-furanyl)hexahydro-6-methyl-, methyl ester,(2R,3R,3aS,6R,6aR,8S,9aR,10aS,11R)-rel-(-)-

Crovatin

Ref: TM-T22695

Crovatin

Ref: BP-BP0409