| Identification | Back Directory | [Name]
Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- | [CAS]
20649-40-5 | [Synonyms]
(E)-p-Hydroxycinnamyl alcohol
(E)-4-(3-Hydroxy-1-propen-1-yl)phenol
Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- | [Molecular Formula]
C9H10O2 | [MOL File]
20649-40-5.mol | [Molecular Weight]
150.17 |
| Chemical Properties | Back Directory | [Melting point ]
114-116 °C(Solv: hexane (110-54-3); ethyl acetate (141-78-6)) | [Boiling point ]
323.5±22.0 °C(Predicted) | [density ]
1.188±0.06 g/cm3(Predicted) | [form ]
Solid | [pka]
9.99±0.26(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
(E)-p-Coumaryl alcohol is a metabolite of coumarin that has significant cytotoxicity. (E)-p-Coumaryl alcohol can be isolated from Alpinia officinarum and Rhodiola rosea and can be used for inflammation research[1]. | [Definition]
ChEBI: Trans-p-coumaryl alcohol is 4-Hydroxycinnamyl alcohol with E-configuration of the propenyl double bond. It is one of the main monolignols. It has a role as a monolignol. It is a phenylpropanoid, a member of phenols and a 4-hydroxycinnamyl alcohol. It is functionally related to an (E)-cinnamyl alcohol. | [References]
[1] Sukhirun N, et.al. Bioefficacy of Alpinia galanga (Zingiberaceae) rhizome extracts, (E)-p-acetoxycinnamyl alcohol, and (E)-p-coumaryl alcohol ethyl ether against Bactrocera dorsalis (Diptera: Tephritidae) and the impact on detoxification enzyme activities. J Econ Entomol. 2011 Oct;104(5):1534-40. DOI:10.1603/ec11080 |
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