6-Bromo-9H-pyrido[2,3-b]indole is a heterocyclic compound characterized by its fused pyridine and indole structures, which contribute to its unique chemical properties. This compound features a bromine atom at the 6-position of the pyridine ring, influencing its reactivity and potential applications in medicinal chemistry. It is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The presence of both nitrogen atoms in the fused ring system can impart basicity, allowing for interactions with various biological targets. This compound is of interest in research due to its potential pharmacological activities, including antitumor and antimicrobial properties. Its structure allows for various substitution reactions, making it a versatile intermediate in organic synthesis. Additionally, the bromine substituent can facilitate further functionalization, enhancing its utility in developing new therapeutic agents. As with many heterocycles, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature.

6-bromo-9H-pyrido[2,3-b]indole

26066-88-6: 6-Bromo-9H-pyrido[2,3-b]indole is a heterocyclic compound characterized by its fused pyridine and indole structures, which contribute to its unique chemical properties. This compound features a bromine atom at the 6-position of the pyridine ring, influencing its reactivity and potential applications in medicinal chemistry. It is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The presence of both nitrogen atoms in the fused ring system can impart basicity, allowing for interactions with various biological targets. This compound is of interest in research due to its potential pharmacological activities, including antitumor and antimicrobial properties. Its structure allows for various substitution reactions, making it a versatile intermediate in organic synthesis. Additionally, the bromine substituent can facilitate further functionalization, enhancing its utility in developing new therapeutic agents. As with many heterocycles, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature.

CAS 26066-88-6

6-bromo-9H-pyrido[2,3-b]indole

9H-Pyrido[2,3-b]indole, 6-bromo-

Ref: IN-DA002RKA

6-Bromo-9H-pyrido[2,3-b]indole

Ref: 54-OR1004899

6-Bromo-9H-pyrido[2,3-b]indole

Ref: 10-F498698