trans-Anethole

CAS: 4180-23-8

Ref. 3D-FA74379

Produktinformation

• Name: trans-Anethole
• Synonyme: 1-Methoxy-4-[(1E)-1-propenyl]benzenetrans-1-p-Anisylpropene, (E)-1-(4-Methoxyphenyl)propene, (E)-1-Methoxy-4-(prop-1-en-1-yl)benzene, (E)-1-p-Methoxyphenylpropene, (E)-Anethol, (E)-Anethole, (E)-anetol, 1-Methoxy-4-(1E)-1-propen-1-ylbenzene, 1-Methoxy-4-[(1E)-1-propenyl]benzene, Anethole, Anethole, trans-, Anisole, p-propenyl-, (E)-, Benzene, 1-methoxy-4-(1-propenyl)-, (E)-, Benzene, 1-methoxy-4-(1E)-1-propen-1-yl-, Benzene, 1-methoxy-4-(1E)-1-propenyl-, Benzene, 1-methoxy-4-(E)-1-propenyl-, Nsc 209529, Synthetic Anethole, Tran-Anethole, trans-1-(4-Methoxyphenyl)-1-propene, trans-1-(p-Methoxyphenyl)-1-propene, trans-1-(p-Methoxyphenyl)propene, trans-1-p-Anisylpropene, trans-4-(1-Propenyl)anisole, trans-Anethol, trans-p-Anethole, trans-p-Methoxy-β-methylstyrene

Beschreibung

Trans-Anethole is a natural phenolic compound that is used in the synthesis of eugenol and vanillin. It can be extracted from plants such as anise, star anise, fennel, and dill. Trans-anethole has been shown to inhibit the activity of enzymes such as p-hydroxybenzoic acid oxidase, which are involved in the metabolism of xenobiotics in human cells. Studies have shown that trans-anethole has a physiological effect on the immune system by activating toll-like receptors (TLR) through which it induces cellular responses against pathogens. Trans-Anethole also has toxicological properties that have been studied using a model system and experimental models.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 148.2 g/mol
• Formel: C₁₀H₁₂O
• Reinheit: Min. 98%
• Farbe/Form: Colorless Clear Liquid
• InChl: InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3-8H,1-2H3/b4-3+
• InChI Key: InChIKey=RUVINXPYWBROJD-ONEGZZNKSA-N
• SMILES: C/C=C/c1ccc(OC)cc1