2-Propenoic acid, 3-(2-furanyl)-, (2E)-, commonly known as furfuryl acrylate, is an organic compound characterized by its acrylate functional group and a furan ring. This compound features a double bond between the first and second carbon atoms of the propenoic acid moiety, which contributes to its reactivity, particularly in polymerization processes. The presence of the furan ring imparts unique properties, such as increased stability and potential for various chemical reactions, including electrophilic substitutions. Furfuryl acrylate is typically a colorless to pale yellow liquid with a characteristic odor, and it is soluble in organic solvents. It is utilized in the synthesis of polymers and resins, often in applications requiring UV-curable coatings and adhesives. Additionally, due to its unsaturated nature, it can participate in various chemical reactions, making it a valuable intermediate in organic synthesis. Safety considerations include handling it in well-ventilated areas and using appropriate personal protective equipment, as it may cause skin and eye irritation.

2-Propenoic acid,3-(2-furanyl)-, (2E)-

15690-24-1: 2-Furanacrylicacid, (E)- (8CI), 2-Propenoic acid, 3-(2-furanyl)-, (E)-, (2E)-3-(2-Furanyl)-2-propenoic acid, (2E)-3-(2-Furyl)-2-propenoic acid, (E)-3-(2-Furyl)acrylic acid, (E)-3-(2-Furyl)propenoic acid, (E)-3-(Furan-2-yl)-2-propenoic acid, (E)-3-(Furan-2-yl)acrylic acid, Nsc 74521, trans-2-Furanacrylic acid, trans-3-(2-Furanyl)-2-propenoic acid, trans-b-2-Furylacrylic acid

3-(2-Furanyl)-2-Propenoic Acid

2-Propenoic acid, 3-(2-furanyl)-, (2E)-

(E)-3-(Furan-2-yl)acrylic acid is an inhibitor of lipoprotein lipase, a key enzyme involved in the hydrolysis of triglycerides. It has been shown to inhibit the activity of lipoprotein lipase and reduce blood lipid levels in animal models. (E)-3-(Furan-2-yl)acrylic acid has been used as a lead compound for the development of drugs for treatment of autoimmune diseases such as rheumatoid arthritis. The reaction mechanism is proposed to involve the formation of p-hydroxybenzoic acid and its subsequent reaction with malonic acid to form methyl ethyl malonic ester. This ester then reacts with chloride ions to form hippuric acid, which can be detected by gas chromatography at low concentrations.

CAS 15690-24-1: 2-Propenoic acid,3-(2-furanyl)-, (2E)-

3-(2-Furanyl)-2-Propenoic Acid

Ref: 54-OR1010639

2-Propenoic acid, 3-(2-furanyl)-, (2E)-

Ref: IN-DA001P2H

(E)-3-(Furan-2-yl)acrylic acid

Ref: 3D-FF155945

(E)-3-(2-FURYL)PROP-2-ENOIC ACID

Ref: 10-F834910