
CAS 20649-40-5
:(E)-p-Coumaryl alcohol
Description:
(E)-p-Coumaryl alcohol, with the CAS number 20649-40-5, is an organic compound that belongs to the class of phenolic compounds. It is characterized by its structure, which features a phenolic ring and an alcohol functional group, specifically a trans configuration at the double bond between the aromatic ring and the aliphatic chain. This compound is typically found in various plant species and is known for its role in the biosynthesis of lignin, a key structural component in plant cell walls. (E)-p-Coumaryl alcohol exhibits antioxidant properties and may contribute to the flavor and aroma profiles of certain plants. It is soluble in organic solvents and has limited solubility in water. The compound is of interest in both natural product chemistry and potential applications in food, cosmetics, and pharmaceuticals due to its bioactive properties. Its reactivity can be influenced by the presence of functional groups, making it a valuable precursor in organic synthesis and material science.
Formula:C9H10O2
InChI:InChI=1S/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+
InChI key:InChIKey=PTNLHDGQWUGONS-OWOJBTEDSA-N
SMILES:C(=C/CO)\C1=CC=C(O)C=C1
Synonyms:- Phenol, 4-[(1E)-3-hydroxy-1-propenyl]-
- trans-p-Coumaryl alcohol
- Phenol, 4-(3-hydroxy-1-propenyl)-, (E)-
- 2-Propen-1-ol, 3-(p-hydroxyphenyl)-, (E)-
- 4-[(1E)-3-Hydroxy-1-propenyl]phenol
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Found 5 products.
(E)-p-Coumaryl alcohol
CAS:(E)-p-Coumaryl alcohol ((E)-p-Hydroxycinnamyl alcohol) is a coumarin metabolite isolated from galangal rhizome extract.Formula:C9H10O2Purity:99.63%Color and Shape:SolidMolecular weight:150.174-[(1E)-3-Hydroxyprop-1-en-1-yl]phenol
CAS:4-[(1E)-3-Hydroxyprop-1-en-1-yl]phenol (4-HP) is a natural compound that belongs to the group of polyphenols. It is one of the main constituents of the plant extract, which is obtained from leaves of the plant Ferula communis. 4-HP has been shown to have antiinflammatory activity by inhibiting prostaglandin synthesis in 3T3-L1 preadipocytes. The synergic effect can be explained by a combination of its antioxidant and antiinflammatory properties. In an analytical method, 4-HP was found to be present in ferulic acid and p-hydroxybenzoic acid. 4-HP also inhibits dna polymerase activity and rna synthesis at low concentration levels. The mechanism of action may be due to the inhibition of bacterial dna gyrase and topoisomerase I, leading to bacterial cell death.Formula:C9H10O2Purity:Min. 95%Molecular weight:150.17 g/mol




