Weight | 206.241 g/mol |
---|---|
Formula | C12H14O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
24393-56-4
ethyl p-methoxycinnamate · ethyl 4-methoxycinnamate
99880-64-5, 24393-56-4, 1929-30-2
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- Inhibition of Ultraviolet Radiation-Induced Skin Tumors in Hairless Mice by Topical Application of the Sunscreen 2-Ethyl Hexyl-P-Methoxycinnamate (Journal of Toxicology-cutaneous and Ocular Toxicology, 1989)
- Ethyl p-methoxycinnamate isolated from a traditional anti-tuberculosis medicinal herb inhibits drug resistant strains of Mycobacterium tuberculosis in vitro (Fitoterapia, 2011)
- Isolation of Ethyl p-methoxycinnamate, the major antifungal principle of Curcumba zedoaria. (1976)
- Supercritical carbon dioxide extraction of ethyl p-methoxycinnamate from Kaempferia galanga L. rhizome and its apoptotic induction in human HepG2 cells. (Natural Product Research, 2010)
- Bioactivity-Guided Isolation of Ethyl-p-methoxycinnamate, an Anti-inflammatory Constituent, from Kaempferia galanga L. Extracts (Molecules, 2012)
- Antiangiogenic effects and mechanisms of trans-ethyl p-methoxycinnamate from Kaempferia galanga L. (Journal of Agricultural and Food Chemistry, 2012)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ethyl p-methoxycinnamate
- ethyl 4-methoxycinnamate
-
SMILESCCOC(=O)C=CC1=CC=C(C=C1)OC
-
InChIKeyDHNGCHLFKUPGPX-UHFFFAOYSA-N
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Most-cited Publications
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Alternate Names
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Synthesis
Reactant
+
Ethanol
(O-acylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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