2-Ethenyl-5-methylfuran, with the CAS number 10504-13-9, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. This compound features a vinyl group (ethenyl) at the 2-position and a methyl group at the 5-position of the furan ring, contributing to its unique reactivity and properties. It is typically a colorless to pale yellow liquid with a distinctive odor. The presence of the double bond in the ethenyl group makes it reactive, particularly in addition reactions, and it can participate in polymerization processes. 2-Ethenyl-5-methylfuran is of interest in organic synthesis and may serve as an intermediate in the production of various chemical compounds. Its solubility in organic solvents and relatively low boiling point make it suitable for various applications in the chemical industry. However, like many unsaturated compounds, it may pose certain health and safety risks, necessitating careful handling and storage.

2-ethenyl-5-methyl-furan

10504-13-9: Furan, 2-methyl-5-vinyl-, 2-Methyl-5-vinylfuran

2-Ethenyl-5-methylfuran is a monomer that belongs to the group of styrene. It has been shown to polymerize with cationic polymerization, and it can be used as a marker for carbohydrate. 2-Ethenyl-5-methylfuran is also able to copolymerize with many other monomers, including acrylonitrile and acrylic acid. The reactions of 2-ethenyl-5-methylfuran are similar to those of coumarin derivatives and trifluoroacetic acid. 2-Ethenyl-5-methylfuran can be used in chemical reactions, such as model systems.

CAS 10504-13-9: 2-ethenyl-5-methyl-furan

2-Ethenyl-5-methylfuran

Ref: 3D-FE171593