CAS 40433-82-7
:(1S,4aR,8aR)-1,4a-dimethyl-6-methylidene-5-[2-(2-oxo-2,5-dihydrofuran-3-yl)ethyl]decahydronaphthalene-1-carboxylic acid
Description:
The chemical substance known as "(1S,4aR,8aR)-1,4a-dimethyl-6-methylidene-5-[2-(2-oxo-2,5-dihydrofuran-3-yl)ethyl]decahydronaphthalene-1-carboxylic acid" with CAS number 40433-82-7 is a complex organic compound characterized by its multi-ring structure, which includes a decahydronaphthalene framework. This compound features multiple functional groups, including a carboxylic acid and a furan derivative, contributing to its potential reactivity and biological activity. The stereochemistry indicated by the (1S,4aR,8aR) notation suggests specific spatial arrangements of atoms, which can influence the compound's properties, such as solubility, melting point, and interaction with biological targets. The presence of methylidene and dimethyl groups suggests that the compound may exhibit unique steric and electronic properties. Overall, this substance may have applications in fields such as medicinal chemistry or materials science, although specific biological or chemical activities would require further investigation through empirical studies.
Formula:C20H28O4
InChI:InChI=1/C20H28O4/c1-13-5-8-16-19(2,10-4-11-20(16,3)18(22)23)15(13)7-6-14-9-12-24-17(14)21/h9,15-16H,1,4-8,10-12H2,2-3H3,(H,22,23)/t15?,16-,19-,20+/m1/s1
Synonyms:- 1-naphthalenecarboxylic acid, 5-[2-(2,5-dihydro-2-oxo-3-furanyl)ethyl]decahydro-1,4a-dimethyl-6-methylene-, (1S,4aR,8aR)-
- pinusolidic acid
- 1-Naphthalenecarboxylic acid, 5-[2-(2,5-dihydro-2-oxo-3-furanyl)ethyl]decahydro-1,4a-dimethyl-6-methylene-, (1S,4aR,5S,8aR)-
- Conifers acid
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Found 4 products.
Pinusolidic acid
CAS:<p>Pinusolidic acid inhibits PAF binding to rabbit platelets, IC50=2.3x10^-5 M (7.48±2.11 µg/ml).</p>Formula:C20H28O4Purity:98%Color and Shape:SolidMolecular weight:332.43Pinusolidic acid
CAS:<p>Pinusolidic acid is a diterpenoid compound, which is a secondary metabolite isolated from species of the Pinaceae family, particularly from pine trees. Its source lies in the resin produced by these trees, which has evolved as a defense mechanism against various pathogens and herbivores. The mode of action of pinusolidic acid involves disrupting fungal cell membranes and inhibiting their growth, which is facilitated by its lipophilic properties that allow it to integrate into lipid bilayers effectively.</p>Formula:C20H28O4Purity:Min. 95%Molecular weight:332.4 g/mol




