Cinnamic Acids
Cinnamic acids are a class of phenolic acids that are widely present in plants. They have a basic structure of phenylacrylic acid and are known for their antioxidant and anti-inflammatory properties. Cinnamic acids play a significant role in the biosynthesis of lignin and other plant metabolites. These compounds are valuable in research areas related to plant biology, pharmacology, and synthetic chemistry.
Products of "Cinnamic Acids"
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trans-Cinnamic Acid
CAS:Formula:C9H8O2Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:148.16Trans-2,4-Difluorocinnamic acid
CAS:Purity:98.0%Color and Shape:Solid, White powderMolecular weight:184.14199829101562Syringin
CAS:Syringin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C17H24O9Purity:(HPLC) ≥98%Color and Shape:White To Beige ColouredMolecular weight:372.37(E)-3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylic acid
CAS:Purity:95.0%Molecular weight:274.1199951171875trans-α-Phenylcinnamic Acid
CAS:Formula:C15H12O2Color and Shape:White To Off-White SolidMolecular weight:224.262-Propenoic acid, 3-(3,5-difluorophenyl)-, (2E)-
CAS:Formula:C9H6F2O2Purity:98%Color and Shape:SolidMolecular weight:184.1395Caffeic acid
CAS:Caffeic acid is naturally produced by the metabolism of plants and fungi. Caffeic acid has an antioxidant activity that can be higher than tocopherol in oil-in-water emulsions. Caffeic acid has proven antimicrobial activity against Staphylococcus aureus. In mice, caffeic acid inhibits the enzyme 5-lipoxygenase thus inhibititing the biosynthesis of the inflammatory mediators leukotrienes.Formula:C9H8O4Purity:Min. 98.0 Area-%Molecular weight:180.16 g/mol2-(Trifluoromethyl)cinnamic Acid
CAS:2-(Trifluoromethyl)cinnamic acid (FTFA) is an organic compound that is used as a pesticide. It has been shown to inhibit the growth of amyloid fibrils, which are thought to contribute to Alzheimer's disease. FTFA is immobilized on different supports and then reacted with l-phenylalanine in order to synthesize the final product. The optimal reaction time is 1 hour at pH 9.5 with sodium carbonate. FTFA can be covalently immobilized on surfaces such as glass, polystyrene, and silicon oxide by reacting it with epoxy groups or amino groups.Formula:C10H7F3O2Purity:Min. 95%Molecular weight:216.16 g/mol2-Propenoic acid, 3-(2,6-difluorophenyl)-, (2E)-
CAS:Formula:C9H6F2O2Purity:98%Color and Shape:SolidMolecular weight:184.13952-Propenoic acid, 3-phenyl-, methyl ester
CAS:Formula:C10H10O2Purity:98%Color and Shape:SolidMolecular weight:162.18523-([1,1'-Biphenyl]-4-yl)acrylic acid
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:224.259002685546883-Fluorocinnamic Acid
CAS:Formula:C9H7FO2Purity:>98.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:166.153-(3,4-dichlorophenyl)acrylic acid
CAS:Purity:95Color and Shape:SolidMolecular weight:217.050003051758Caffeic acid
CAS:Caffeic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C9H8O4Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:180.163-(Trifluoromethyl)cinnamic Acid
CAS:Formula:C10H7F3O2Purity:>99.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:216.16
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