1-Methyl-1,5,6,7-tetrahydro-4H-indol-4-one, identified by its CAS number 51471-08-0, is a chemical compound that belongs to the indole family, characterized by a bicyclic structure containing a fused benzene and pyrrole ring. This compound features a tetrahydroindole framework, which indicates that it has undergone partial hydrogenation, resulting in a saturated structure. The presence of a methyl group at the nitrogen atom contributes to its unique properties, potentially influencing its reactivity and biological activity. Typically, compounds of this class may exhibit various pharmacological effects, including neuroprotective and antidepressant activities, due to their ability to interact with neurotransmitter systems. The compound is likely to be soluble in organic solvents, and its stability can be influenced by factors such as pH and temperature. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and cyclizations, making it of interest in synthetic organic chemistry and medicinal chemistry research.

1-methyl-1,5,6,7-tetrahydro-4H-indol-4-one

51471-08-0: 1-Methyl-1,5,6,7-tetrahydro-4H-indol-4-one, identified by its CAS number 51471-08-0, is a chemical compound that belongs to the indole family, characterized by a bicyclic structure containing a fused benzene and pyrrole ring. This compound features a tetrahydroindole framework, which indicates that it has undergone partial hydrogenation, resulting in a saturated structure. The presence of a methyl group at the nitrogen atom contributes to its unique properties, potentially influencing its reactivity and biological activity. Typically, compounds of this class may exhibit various pharmacological effects, including neuroprotective and antidepressant activities, due to their ability to interact with neurotransmitter systems. The compound is likely to be soluble in organic solvents, and its stability can be influenced by factors such as pH and temperature. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and cyclizations, making it of interest in synthetic organic chemistry and medicinal chemistry research.

CAS 51471-08-0

1-methyl-1,5,6,7-tetrahydro-4H-indol-4-one

6,7-DIHYDRO-1-METHYL-1H-INDOL-4(5H)-ONE

Ref: IN-DA00DKVM

1-Methyl-6,7-dihydro-1H-indol-4(5H)-one

Ref: 10-F091743