5-Chloro-3-cyano-1H-pyrrolo[2,3-c]pyridine is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both pyrrole and pyridine rings. The presence of a chlorine atom at the 5-position and a cyano group at the 3-position contributes to its chemical reactivity and potential applications in medicinal chemistry and material science. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure allows for various functionalization possibilities, making it of interest in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The cyano group can participate in nucleophilic reactions, while the chlorine atom can serve as a leaving group in substitution reactions. Additionally, the compound's unique electronic properties may influence its behavior in biological systems, making it a candidate for further research in drug discovery and development. Safety and handling precautions should be observed, as with many halogenated and cyano-containing compounds, due to potential toxicity.

5-CHLORO-3-CYANO-1H-PYRROLO[2,3-C]PYRIDINE

1272758-19-6: 5-Chloro-3-cyano-1H-pyrrolo[2,3-c]pyridine is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both pyrrole and pyridine rings. The presence of a chlorine atom at the 5-position and a cyano group at the 3-position contributes to its chemical reactivity and potential applications in medicinal chemistry and material science. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure allows for various functionalization possibilities, making it of interest in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The cyano group can participate in nucleophilic reactions, while the chlorine atom can serve as a leaving group in substitution reactions. Additionally, the compound's unique electronic properties may influence its behavior in biological systems, making it a candidate for further research in drug discovery and development. Safety and handling precautions should be observed, as with many halogenated and cyano-containing compounds, due to potential toxicity.

CAS 1272758-19-6

5-CHLORO-3-CYANO-1H-PYRROLO[2,3-C]PYRIDINE

5-chloro-1H-pyrrolo[2,3-c]pyridine-3-carbonitrile

Ref: IN-DA01X9WV

5-Chloro-1H-pyrrolo[2,3-c]pyridine-3-carbonitrile

Ref: 10-F762908