CAS 943-89-5
:trans-4-Methoxycinnamic acid
Description:
Trans-4-Methoxycinnamic acid, with the CAS number 943-89-5, is an organic compound characterized by its aromatic structure and the presence of both a methoxy group and a carboxylic acid functional group. It is a derivative of cinnamic acid, where the methoxy group is positioned at the para position relative to the carboxylic acid. This compound typically appears as a white to pale yellow crystalline solid and is known for its moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water. Trans-4-Methoxycinnamic acid exhibits interesting biological activities, including potential antioxidant and anti-inflammatory properties, making it a subject of interest in pharmaceutical and cosmetic applications. Its stability and reactivity can be influenced by environmental factors such as pH and temperature. Additionally, it can undergo various chemical reactions, including esterification and hydrogenation, which are relevant in synthetic organic chemistry. Overall, trans-4-Methoxycinnamic acid is a versatile compound with significant implications in both research and industry.
Formula:C10H10O3
InChI:InChI=1S/C10H10O3/c1-13-9-5-2-8(3-6-9)4-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-4+
InChI key:InChIKey=AFDXODALSZRGIH-QPJJXVBHSA-N
SMILES:C(=C/C(O)=O)\C1=CC=C(OC)C=C1
Synonyms:- (2E)-3-(4-Methoxyphenyl)-2-propenoic acid
- (E)-3-(4-Methoxyphenyl)-2-propenoic acid
- (E)-3-(4-Methoxyphenyl)acrylic acid
- (E)-4-Methoxycinnamic acid
- (E)-p-Methoxycinnamic acid
- 2-Propenoic acid, 3-(4-methoxyphenyl)-, (E)-
- Cinnamic acid, p-methoxy-, (E)-
- trans-2-Propenoic acid, 3-(4-methoxyphenyl)-
- trans-3-(4-Methoxyphenyl)-2-propenoic acid
- trans-4-Methoxycinnamic acid
- trans-p-Methoxycinnamic acid
- See more synonyms
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Found 8 products.
trans-4-Methoxycinnamic Acid
CAS:Formula:C10H10O3Purity:>98.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:178.19trans-4-Methoxycinnamic acid, 98%
CAS:<p>Esters derived from trans-4-methoxycinnamic acid are effective absorbers of UV radiation. The starting material was trans-4-methoxycinnamic acid and 3,5dimethoxybenzoic acid methyl ester in isolated avenanthramide alkaloids synthsis. trans-4-Methoxycinnamic acid was converted into its acid chloride </p>Formula:C10H10O3Purity:98%Color and Shape:Crystals or powder or crystalline powder, White to creamMolecular weight:178.19(2E)-3-(4-methoxyphenyl)prop-2-enoic acid
CAS:Formula:C10H10O3Purity:98%Color and Shape:SolidMolecular weight:178.1846(E)-3-(4-Methoxyphenyl)acrylic acid, 10mM (in DMSO)
CAS:(E)-3-(4-Methoxyphenyl)acrylic acid, 10mM (in DMSO)Purity:≥98%Molecular weight:178.18g/mol(E)-3-(4-Methoxyphenyl)acrylic acid
CAS:(E)-3-(4-Methoxyphenyl)acrylic acid, from Etlingera pavieana, inhibits α-glucosidase, protects liver, boosts cognition, and lowers blood sugar.Formula:C10H10O3Purity:99.99%Color and Shape:SolidMolecular weight:178.184-Methoxycinnamic acid
CAS:<p>4-Methoxycinnamic acid is a compound that is found in plants, such as coffee beans and tea leaves. It has been used to treat wastewater and light-exposed plastics. 4-Methoxycinnamic acid can act as a hydrogen bond donor, which may help break up aggregates of organic contaminants in water. In addition, it has been shown to have genotoxic effects on bacteria when exposed to ultraviolet radiation. 4-Methoxycinnamic acid also has the ability to activate chlorogenic acids from plant material, which are thought to be the major contributor to its protective effect against colon cancer. 4-Methoxycinnamic acid can also inhibit diphenolase activity in certain cells, leading to the accumulation of protocatechuic acid and skin cancer.</p>Formula:C10H10O3Purity:Min. 95%Molecular weight:178.18 g/mol







