CAS 16909-11-8
:3-(3,5-Dimethoxyphenyl)-2-propenoic acid
Description:
3-(3,5-Dimethoxyphenyl)-2-propenoic acid, also known by its CAS number 16909-11-8, is an organic compound characterized by its propenoic acid structure, which features a double bond between the second and third carbon atoms of the propene chain. The presence of a 3,5-dimethoxyphenyl group indicates that the compound has two methoxy (-OCH3) substituents on the aromatic ring, which can influence its chemical reactivity and solubility. This compound is typically a white to off-white solid and is soluble in organic solvents. It may exhibit biological activity, making it of interest in pharmaceutical and biochemical research. The methoxy groups can enhance the lipophilicity of the molecule, potentially affecting its interaction with biological systems. Additionally, the compound may participate in various chemical reactions, such as esterification or polymerization, due to the presence of the carboxylic acid functional group. Overall, 3-(3,5-Dimethoxyphenyl)-2-propenoic acid is a versatile compound with potential applications in various fields of chemistry and biology.
Formula:C11H12O4
InChI:InChI=1S/C11H12O4/c1-14-9-5-8(3-4-11(12)13)6-10(7-9)15-2/h3-7H,1-2H3,(H,12,13)
InChI key:InChIKey=VLSRUFWCGBMYDJ-UHFFFAOYSA-N
SMILES:C(=CC(O)=O)C1=CC(OC)=CC(OC)=C1
Synonyms:- (2E)-3-(3,5-dimethoxyphenyl)prop-2-enoate
- (2E)-3-(3,5-dimethoxyphenyl)prop-2-enoic acid
- (E)-3-(3,5-dimethoxyphenyl)acrylic acid
- 2-Propenoic acid, 3-(3,5-dimethoxyphenyl)-
- 3-(3,5-Dimethoxyphenyl)-2-propenoic acid
- 3-(3,5-Dimethoxyphenyl)Prop-2-Enoic Acid
- 3-(3,5-Dimethoxyphenyl)acrylic acid
- Cinnamic acid, 3,5-dimethoxy-
- Predominantlytrans Isomer
- 3,5-Dimethoxycinnamic acid
- See more synonyms
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Found 5 products.
2-Propenoic acid, 3-(3,5-dimethoxyphenyl)-
CAS:Formula:C11H12O4Purity:98%Color and Shape:SolidMolecular weight:208.21063,5-Dimethoxycinnamic acid
CAS:<p>3,5-Dimethoxycinnamic acid is a compound that belongs to the class of cinnamic acid derivatives. It is a synthetic substance obtained by demethylation of 3,5-dimethoxybenzoic acid. This substance has been shown to have an antifungal activity in vitro against filamentous fungi and many other microorganisms. The antimicrobial effect can be explained by the presence of functional groups such as hydroxyl and methoxyl on the aromatic ring. Hydroxide solution can be used as an analytical reagent for determining the formation rate of this compound.</p>Formula:C11H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:208.21 g/mol3-(3,5-Dimethoxyphenyl)acrylic acid
CAS:Formula:C11H12O4Purity:95%Color and Shape:SolidMolecular weight:208.2133,5-Dimethoxycinnamic acid, predominantly trans
CAS:<p>3,5-Dimethoxycinnamic acid, predominantly trans is a useful organic compound for research related to life sciences. The catalog number is T67479 and the CAS number is 16909-11-8.</p>Formula:C11H12O4Color and Shape:SolidMolecular weight:208.213




