CAS:81311-95-7 | Trans-3-Furanacrylic Acid

Introduction of CAS:81311-95-7 | trans-3-Furanacrylic acid

3-(3-Furyl)acrylic acid, also known as 3-Furylacrylic acid, is an organic compound with a molecular formula of C6H5COOH. It is an aromatic carboxylic acid with a pungent odor. It is a colorless solid that is soluble in water and alcohol. 3-Furylacrylic acid is used in a variety of scientific research applications, including biochemical and physiological studies.

Specification of CAS:81311-95-7 | trans-3-Furanacrylic acid

Research Application of CAS:81311-95-7 | trans-3-Furanacrylic acid

Synthesis of Novel Compounds: 3-(5-nitro-2-furyl)-2-(2-furyl)acrylonitrile and its bromine derivatives have shown potential in the synthesis of novel compounds. These compounds are potentially useful in organic synthesis and catalysis (Kato, Kuboyama, & Hirao, 1972).

Antimicrobial Activity: Esters and amides of 3-(5-nitro-2-furyl)acrylic acid demonstrate antimicrobial activity against various microorganisms, including bacteria, yeasts, molds, and algae. Notably, the antimycotic activity decreases with the increasing length of the alkyl chain and the introduction of amino nitrogen (Kellová et al., 2008).

Composite Material Fabrication: Glass fiber reinforced composites have been successfully fabricated from 2,3-epoxypropyl 3-(2-furyl)acrylate and acrylonitrile. These composites exhibit promising mechanical, electrical, and chemical resistance properties (Raval, Patel, & Vyas, 2002).

Pharmaceutical Applications: The Wittig reaction, using mono- and dihalogenofurfurals, produces halogen-substituted furylacrylic acids. These acids have potential applications in the pharmaceutical and cosmetic industries (Nazarova et al., 1973).

Synthesis of Chiral Building Blocks: Asymmetric aminohydroxylation selectively targets furyl and thienyl acrylates, yielding chiral building blocks for polyhydroxy indolizidine alkaloids. This process is significant for the development of new drugs and active pharmaceutical ingredients (Zhang, Xia, & Zhou, 2000).

Optimizing Synthesis and Application: Understanding the thermodynamic properties of derivatives of 3-(3-Furyl)acrylic acid helps in optimizing their synthesis, purification, and application. This knowledge provides insights into the nature and potential applications of these compounds (Dibrivnyi et al., 2019).

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