CAS 26187-80-4
:2,6-Octadienoic acid,8-hydroxy-2,6-dimethyl-, (2E,6E)-
Description:
2,6-Octadienoic acid, 8-hydroxy-2,6-dimethyl-, (2E,6E)-, commonly known as a derivative of octadienoic acid, is an organic compound characterized by its unsaturated fatty acid structure. It features a long carbon chain with two double bonds located at the 2nd and 6th positions, which contributes to its reactivity and potential applications in various chemical processes. The presence of a hydroxyl group at the 8th position enhances its solubility in polar solvents and may influence its biological activity. This compound is typically found in certain natural products and can be synthesized through various organic reactions. Its structural features suggest potential uses in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Additionally, the specific stereochemistry indicated by the (2E,6E) notation implies that the double bonds have a trans configuration, which can affect the compound's physical properties, such as melting and boiling points, as well as its interaction with biological systems. Overall, 2,6-Octadienoic acid, 8-hydroxy-2,6-dimethyl- is a compound of interest in both synthetic and natural product chemistry.
Formula:C10H16O3
Synonyms:- 2,6-Octadienoicacid, 8-hydroxy-2,6-dimethyl-, (E,E)- (8CI)
- Foliamenthic acid
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Found 4 products.
2,6-Octadienoic acid, 8-hydroxy-2,6-dimethyl-, (2E,6E)-
CAS:Formula:C10H16O3Purity:93.0%Molecular weight:184.2322Foliamenthoic acid
CAS:Foliamenthoic acid shows α-glucosidase inhibition.Formula:C10H16O3Purity:98%Color and Shape:SolidMolecular weight:184.23Foliamenthoic acid
CAS:<p>Foliamenthoic acid is a synthetic compound that falls under the category of organic acids. It is primarily derived through complex chemical synthesis methods involving the manipulation of carbon chains and functional groups to achieve a precise molecular structure. The mode of action of foliamenthoic acid involves its interaction with specific biological pathways, often targeting enzymes or receptors to induce or inhibit particular biochemical reactions. This interaction is highly specific, allowing for targeted applications across various fields of research.</p>Formula:C10H16O3Purity:Min. 95%Molecular weight:184.23 g/mol



