2-Ethenyl-1H-indole, with the CAS number 53654-35-6, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a vinyl group (ethenyl) attached to the nitrogen-containing indole, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid with a distinct aromatic odor. The presence of the vinyl group makes it susceptible to polymerization and other chemical reactions, which can be exploited in various synthetic pathways. 2-Ethenyl-1H-indole is of interest in fields such as medicinal chemistry and materials science due to its potential biological activity and utility in creating functionalized polymers. Its solubility in organic solvents and relatively low boiling point facilitate its use in various chemical reactions. However, like many indole derivatives, it may exhibit toxicity and should be handled with appropriate safety precautions in laboratory settings.

2-Ethenyl-1H-indole

53654-35-6: 2-Ethenyl-1H-indole, with the CAS number 53654-35-6, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a vinyl group (ethenyl) attached to the nitrogen-containing indole, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid with a distinct aromatic odor. The presence of the vinyl group makes it susceptible to polymerization and other chemical reactions, which can be exploited in various synthetic pathways. 2-Ethenyl-1H-indole is of interest in fields such as medicinal chemistry and materials science due to its potential biological activity and utility in creating functionalized polymers. Its solubility in organic solvents and relatively low boiling point facilitate its use in various chemical reactions. However, like many indole derivatives, it may exhibit toxicity and should be handled with appropriate safety precautions in laboratory settings.

<p>2-Ethenyl-1H-indole is an organic compound that can be synthesized from a Friedel-Crafts reaction of a fatty acid and an alkyl halide. The cycloaddition process of 2-ethenyl-1H-indole to form the bicyclic system was found to proceed through a [4+2] cycloaddition mechanism with the formation of a strained six membered ring between the two carbon atoms at the junction. This product is then converted into biofuels, such as particle or fatty acids, by analytical chemistry. Preparative high performance liquid chromatography (HPLC) has been used to separate glycogen synthase kinase 3 (GSK3) oligosaccharides, which have been shown to be involved in various biological processes.</p>

CAS 53654-35-6

2-Ethenyl-1H-indole

2-Ethenyl-1H-indole

Ref: 3D-DCA65435