CAS 51086-08-9
:5-(prop-2-en-1-yloxy)-1H-indole
Description:
5-(Prop-2-en-1-yloxy)-1H-indole, with the CAS number 51086-08-9, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a prop-2-en-1-yloxy group attached to the 5-position of the indole ring, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of the alkenyl ether group enhances its ability to participate in various chemical reactions, such as nucleophilic substitutions and polymerizations. The indole moiety is known for its biological significance, often serving as a core structure in many natural products and pharmaceuticals. This compound may exhibit interesting properties, including fluorescence and potential biological activity, making it a subject of interest in research fields such as drug development and materials science. Its solubility and stability can vary depending on the solvent and environmental conditions, which are important factors to consider in practical applications.
Formula:C11H11NO
InChI:InChI=1/C11H11NO/c1-2-7-13-10-3-4-11-9(8-10)5-6-12-11/h2-6,8,12H,1,7H2
SMILES:C=CCOc1ccc2c(cc[nH]2)c1
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
5-(Prop-2-en-1-yloxy)-1H-indole
CAS:<p>5-(Prop-2-en-1-yloxy)-1H-indole is a synthetic compound that acts as a dopaminergic agonist. It has been shown to induce thermolysis in the presence of organic solvents, such as ether and benzene. 5-(Prop-2-en-1-yloxy)-1H-indole has been used in the synthesis of ellipticines, which are examples of dibenzofuran derivatives. This compound has also been used in multistep synthesis reactions, including filtration and recrystallization.</p>Formula:C11H11NOPurity:Min. 95%Molecular weight:173.21 g/mol
