1H-Indole, 7-bromo-3-methyl- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a bromine atom at the 7-position and a methyl group at the 3-position distinguishes it from other indole derivatives. This compound typically exhibits a pale yellow to brownish appearance and is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The bromine substituent can enhance the compound's reactivity, making it useful in various chemical reactions, including electrophilic substitutions. Additionally, 1H-Indole derivatives are often studied for their roles in biological systems, including their involvement in neurotransmitter functions and as precursors to various natural products. Safety data should be consulted, as halogenated compounds can pose health risks if not handled properly.

1H-Indole, 7-bromo-3-methyl-

86915-22-2: 1H-Indole, 7-bromo-3-methyl- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a bromine atom at the 7-position and a methyl group at the 3-position distinguishes it from other indole derivatives. This compound typically exhibits a pale yellow to brownish appearance and is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The bromine substituent can enhance the compound's reactivity, making it useful in various chemical reactions, including electrophilic substitutions. Additionally, 1H-Indole derivatives are often studied for their roles in biological systems, including their involvement in neurotransmitter functions and as precursors to various natural products. Safety data should be consulted, as halogenated compounds can pose health risks if not handled properly.

CAS 86915-22-2

1H-Indole, 7-bromo-3-methyl-

7-bromo-3-methyl-1H-indole

Ref: IN-DA004I5K

7-Bromo-3-methylindole

Ref: FT-CAPOB13700

7-Bromo-3-methyl-1H-indole

Ref: 54-OR952575

7-Bromo-3-methyl-1H-indole

Ref: 10-F238522