| Company Name: |
VladaChem GmbH |
| Tel: |
+49-7246-3082843 +86-18411632868 |
| Email: |
info@vladachem.de |
| Company Name: |
Accela ChemBio Inc. |
| Tel: |
+1-858-6993322 +86-18019713315 |
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info@accelachem.com |
Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- manufacturers
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| | Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- Basic information |
| | Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- Chemical Properties |
| 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) | | pka | 9.99±0.26(Predicted) | | form | Solid | | color | White to off-white |
| | Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- Usage And Synthesis |
| 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 |
| | Phenol, 4-[(1E)-3-hydroxy-1-propenyl]- Preparation Products And Raw materials |
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