3-(4-Isopropylbenzylidene)indolin-2-one, identified by its CAS number 186611-55-2, is an organic compound characterized by its indolinone core structure, which is a bicyclic compound featuring both a benzene and a pyrrole-like ring. This compound typically exhibits a yellow to orange coloration and is known for its potential applications in various fields, including pharmaceuticals and organic materials. The presence of the isopropyl group and the benzylidene moiety contributes to its unique chemical properties, such as enhanced lipophilicity and potential biological activity. It may exhibit fluorescence, making it useful in certain imaging applications. Additionally, the compound's structure suggests potential reactivity in various chemical reactions, including electrophilic substitutions and condensation reactions. As with many organic compounds, its solubility, stability, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 3-(4-isopropylbenzylidene)indolin-2-one represents a versatile structure with implications in both synthetic chemistry and material science.

3-(4-ISOPROPYLBENZYLIDENYL)INDOLIN-2-ONE

186611-55-2: 3-(4-Isopropylbenzylidene)indolin-2-one, identified by its CAS number 186611-55-2, is an organic compound characterized by its indolinone core structure, which is a bicyclic compound featuring both a benzene and a pyrrole-like ring. This compound typically exhibits a yellow to orange coloration and is known for its potential applications in various fields, including pharmaceuticals and organic materials. The presence of the isopropyl group and the benzylidene moiety contributes to its unique chemical properties, such as enhanced lipophilicity and potential biological activity. It may exhibit fluorescence, making it useful in certain imaging applications. Additionally, the compound's structure suggests potential reactivity in various chemical reactions, including electrophilic substitutions and condensation reactions. As with many organic compounds, its solubility, stability, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 3-(4-isopropylbenzylidene)indolin-2-one represents a versatile structure with implications in both synthetic chemistry and material science.

CAS 186611-55-2

3-(4-ISOPROPYLBENZYLIDENYL)INDOLIN-2-ONE

3-(4-Isopropylbenzylidenyl)indolin-2-one

Ref: IN-DA00AOSR

SU 4313

Ref: 54-BUP02335

SU 4313

Ref: TM-T3568