CAS 1878-29-1
:Ethyl 3,4,5-trimethoxycinnamate
Description:
Ethyl 3,4,5-trimethoxycinnamate, with the CAS number 1878-29-1, is an organic compound belonging to the class of cinnamates, which are esters derived from cinnamic acid. This substance is characterized by its aromatic structure, featuring a cinnamic acid backbone with three methoxy (-OCH3) groups attached to the aromatic ring and an ethyl ester group. Ethyl 3,4,5-trimethoxycinnamate is typically a pale yellow to light brown liquid with a pleasant, sweet aroma, making it of interest in the fragrance and flavor industries. It exhibits solubility in organic solvents, while its solubility in water is limited. The compound is known for its potential antioxidant properties and has been studied for its applications in cosmetics and food preservation. Additionally, it may possess biological activities, including anti-inflammatory and antimicrobial effects, although further research is needed to fully understand its pharmacological potential. As with many organic compounds, proper handling and safety precautions should be observed due to potential toxicity or irritant effects.
Formula:C14H18O5
InChI:InChI=1S/C14H18O5/c1-5-19-13(15)7-6-10-8-11(16-2)14(18-4)12(9-10)17-3/h6-9H,5H2,1-4H3
InChI key:InChIKey=WZFPTWWCXRADLD-UHFFFAOYSA-N
SMILES:O(C)C1=C(OC)C=C(C=CC(OCC)=O)C=C1OC
Synonyms:- 2-Propenoic acid, 3-(3,4,5-trimethoxyphenyl)-, ethyl ester
- Cinnamic acid, 3,4,5-trimethoxy-, ethyl ester
- Ethyl 3,4,5-trimethoxycinnamate
- ethyl (2E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
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Found 3 products.
Ethyl 3-(3,4,5-trimethoxyphenyl)acrylate
CAS:Formula:C14H18O5Purity:%Color and Shape:SolidMolecular weight:266.2897Ethyl 3,4,5-trimethoxycinnamate
CAS:<p>Ethyl 3,4,5-trimethoxycinnamate is a cinnamic acid derivative that has significant cytotoxicity and anticancer activity. It inhibits the growth of Leishmania parasites by inhibiting the production of gamma-aminobutyric acid, which is essential for cell division and survival. Ethyl 3,4,5-trimethoxycinnamate has been shown to inhibit the growth of cancer cells in vitro by binding to DNA at dipole sites and disrupting the integrity of the molecule. This compound also has optical properties that may be due to its ability to absorb light in the blue region of the spectrum. The anti-cancer effects of ethyl 3,4,5-trimethoxycinnamate may be related to its ability to inhibit cell growth.</p>Formula:C14H18O5Purity:Min. 95%Color and Shape:SolidMolecular weight:266.29 g/mol


