1-(2-Chloroethyl)indoline-2,3-dione, with the CAS number 77218-99-6, is a synthetic organic compound characterized by its indoline structure, which features a fused bicyclic system containing both a benzene and a pyrrole-like ring. This compound contains a chloroethyl substituent, which contributes to its reactivity and potential applications in medicinal chemistry. The presence of the dione functional groups indicates that it has two carbonyl (C=O) groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure allows for potential use in the development of pharmaceuticals, particularly in targeting specific biological pathways. Additionally, the chloroethyl group may enhance its ability to form covalent bonds with biological macromolecules, making it of interest in drug design and development. Safety and handling precautions should be observed due to the presence of chlorine, which can pose health risks.

1-(2-chloroethyl)indoline-2,3-dione

77218-99-6: 1-(2-Chloroethyl)indoline-2,3-dione, with the CAS number 77218-99-6, is a synthetic organic compound characterized by its indoline structure, which features a fused bicyclic system containing both a benzene and a pyrrole-like ring. This compound contains a chloroethyl substituent, which contributes to its reactivity and potential applications in medicinal chemistry. The presence of the dione functional groups indicates that it has two carbonyl (C=O) groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure allows for potential use in the development of pharmaceuticals, particularly in targeting specific biological pathways. Additionally, the chloroethyl group may enhance its ability to form covalent bonds with biological macromolecules, making it of interest in drug design and development. Safety and handling precautions should be observed due to the presence of chlorine, which can pose health risks.

CAS 77218-99-6

1-(2-chloroethyl)indoline-2,3-dione

1-(2-Chloroethyl)-1H-indole-2,3-dione

Ref: 54-OR1003128