Cinnamic Acids

2,4-Dihydroxycinnamic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Oxygen-heterocyclic compound

Carboxylic acid with additional oxygen functions

Dihydroconiferyl alcohol analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Neochlorogenic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Sinapic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.

4-Methoxycinnamic acid methyl ester is an organic compound that has potential use as a reaction modifier. The C8-C9 alkene, which is a common structural motif in fatty acids and cinnamic acid derivatives, can be efficiently produced through the use of this chemical. This organic acid is also used to modify the reactivity of other molecules by changing their steric or electronic properties. It has been shown to increase the diameter of filamentous fungi and to have a significant effect on the selectivity for reactions involving alkene substrates.

Caftaric acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.

trans-Cinnamic acid (Myricitrine) exerts anti-diabetic activity by improving glucose tolerance in vivo and by stimulating insulin secretion in vitro.

Cinnamyl acetate analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Leontopodic acid B analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

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.

Cynarin analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Leontopodic acid A analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Natural glycoside

Dihydroferulic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.

3-Hydroxycinnamic acid is a natural compound that belongs to the group of caffeic acids. It is found in many plants, including coffee beans and tea leaves. 3-Hydroxycinnamic acid has been shown to inhibit the proliferation of 3T3-L1 preadipocytes and HL-60 cells by inhibiting mitochondrial membrane potential. This compound also inhibits the activity of 4-hydroxyphenylacetic acid (4HPA) hydroxylase, which converts phenylalanine into tyrosine and 4HPA, an intermediate in the synthesis of melanin. 3-Hydroxycinnamic acid can be used as a model system for studying caffeic acids in vitro. Structural analysis has demonstrated that 3-hydroxycinnamic acid contains nitrogen atoms, which may be essential for its anti-inflammatory activities.

The 2-methylcinnamic acid is a derivative of cinnamic acid. It is an organic compound that is a colorless liquid at room temperature. The 2-methylcinnamic acid can be synthesized via the Suzuki coupling reaction between 2-chlorocinnamic acid and 4-hydroxycinnamic acid in the presence of a ruthenium complex, a diphosphine ligand, and an acidic co-solvent. This organic compound has been shown to inhibit prostaglandin synthesis by interacting with the prostanoid receptor, a protein located on the surface of cells that binds to inflammatory agents or hormones. These interactions may also lead to the inhibition of cyclooxygenase (COX) enzymes, which are responsible for prostaglandin synthesis. The 2-methylcinnamic acid can also be converted into flavonoids such as quercetin and apigenin through oxidation reactions.

Carboxylic acid with additional oxygen functions

Oxygen-heterocyclic compound

3-Methoxycinnamic acid is a hydroxycinnamic acid that has been shown to inhibit the migration of polymorphonuclear cells and leukocytes. It also inhibits chemotaxis by blocking the production of intracellular cyclic AMP (cAMP) in these cells. 3-Methoxycinnamic acid has been shown to have an inhibitory effect on the production of cAMP in leukocytes and polymorphonuclear cells, as well as inhibiting chemotaxis. The compound is also known to be a potent antioxidant due to its ability to scavenge reactive oxygen species (ROS).

Phenol alcohol

Natural glycoside

4-Chloro-3-nitrocinnamic acid is a thionyl chloride derivative of cinnamic acid. It is used as an intermediate in the preparation of pharmaceuticals and dyestuffs. 4-Chloro-3-nitrocinnamic acid inhibits the activity of amides, dimethylformamide, alkaline hydrolysis, xylene, carboxyphenyl, cinnamic, refluxing, nitrophenyl and carboxylic acids. 4-Chloro-3-nitrocinnamic acid reacts with chloride to form the corresponding chloride salt. This compound can also react with formamide to form an amide salt. The ester group of 4-chloro-3-nitrocinnamic acid can be cleaved by nitro compounds to produce nitro derivatives.

Ketone phenol

Carboxylic acid with additional oxygen functions

Carboxylic acid with additional oxygen functions