1-(2-Bromoethyl)-2,3-dihydro-1H-indole hydrobromide is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a bromoethyl substituent, which introduces a bromine atom and an ethyl group, enhancing its reactivity and potential for further chemical transformations. The hydrobromide form indicates that the compound is a salt formed with hydrobromic acid, which typically enhances its solubility in polar solvents. This substance may exhibit biological activity due to the presence of the indole moiety, which is common in many natural products and pharmaceuticals. Its properties, such as melting point, solubility, and stability, can be influenced by the presence of the bromine atom and the hydrobromide salt formation. As with many halogenated compounds, it may also exhibit unique reactivity patterns in organic synthesis, making it of interest in medicinal chemistry and material science. Safety precautions should be taken when handling this compound due to the presence of bromine, which can be hazardous.

1-(2-bromoethyl)-2,3-dihydro-1H-indole hydrobromide

1803586-01-7: 1-(2-Bromoethyl)-2,3-dihydro-1H-indole hydrobromide is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a bromoethyl substituent, which introduces a bromine atom and an ethyl group, enhancing its reactivity and potential for further chemical transformations. The hydrobromide form indicates that the compound is a salt formed with hydrobromic acid, which typically enhances its solubility in polar solvents. This substance may exhibit biological activity due to the presence of the indole moiety, which is common in many natural products and pharmaceuticals. Its properties, such as melting point, solubility, and stability, can be influenced by the presence of the bromine atom and the hydrobromide salt formation. As with many halogenated compounds, it may also exhibit unique reactivity patterns in organic synthesis, making it of interest in medicinal chemistry and material science. Safety precautions should be taken when handling this compound due to the presence of bromine, which can be hazardous.

CAS 1803586-01-7

1-(2-bromoethyl)-2,3-dihydro-1H-indole hydrobromide

1-(2-Bromoethyl)-2,3-dihydro-1H-indole hydrobromide

Ref: 3D-DXC58601