Tert-butyl 6-methoxyindoline-1-carboxylate is a chemical compound characterized by its indoline structure, which is a bicyclic compound featuring a fused benzene and pyrrole ring. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The methoxy group at the 6-position of the indoline ring contributes to its electronic properties, potentially influencing its reactivity and interaction with biological targets. The carboxylate functionality indicates that the compound can participate in various chemical reactions, such as esterification or amidation. This compound may be of interest in medicinal chemistry due to its potential biological activity, as indoline derivatives are often explored for their pharmacological properties. Additionally, the tert-butyl ester can serve as a protective group in synthetic pathways. Overall, tert-butyl 6-methoxyindoline-1-carboxylate exhibits a combination of structural features that may lend itself to diverse applications in organic synthesis and drug development.

tert-butyl 6-methoxyindoline-1-carboxylate

1394248-15-7: Tert-butyl 6-methoxyindoline-1-carboxylate is a chemical compound characterized by its indoline structure, which is a bicyclic compound featuring a fused benzene and pyrrole ring. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The methoxy group at the 6-position of the indoline ring contributes to its electronic properties, potentially influencing its reactivity and interaction with biological targets. The carboxylate functionality indicates that the compound can participate in various chemical reactions, such as esterification or amidation. This compound may be of interest in medicinal chemistry due to its potential biological activity, as indoline derivatives are often explored for their pharmacological properties. Additionally, the tert-butyl ester can serve as a protective group in synthetic pathways. Overall, tert-butyl 6-methoxyindoline-1-carboxylate exhibits a combination of structural features that may lend itself to diverse applications in organic synthesis and drug development.

tert-Butyl 6-methoxyindoline-1-carboxylate

CAS 1394248-15-7

tert-butyl 6-methoxyindoline-1-carboxylate

tert-Butyl 6-methoxyindoline-1-carboxylate

Ref: 54-OR83433

TERT-BUTYL 6-METHOXYINDOLINE-1-CARBOXYLATE

Ref: 10-F535115