6-Chloro-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde is a heterocyclic organic compound characterized by its pyrazolo-pyridine structure, which incorporates both a pyrazole and a pyridine ring. The presence of a chloro group at the 6-position and a methyl group at the 3-position contributes to its unique reactivity and potential biological activity. The aldehyde functional group at the 5-position is significant for its reactivity, allowing for various chemical transformations, including condensation reactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential interactions with biological targets, which could be explored in drug development. Additionally, the compound's solubility and stability can be influenced by the substituents on the rings, affecting its application in various chemical and pharmaceutical contexts. As with many heterocycles, the compound's properties can be further studied through techniques such as spectroscopy and crystallography to elucidate its behavior in different environments.

6-chloro-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde

81933-75-7: 6-Chloro-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde is a heterocyclic organic compound characterized by its pyrazolo-pyridine structure, which incorporates both a pyrazole and a pyridine ring. The presence of a chloro group at the 6-position and a methyl group at the 3-position contributes to its unique reactivity and potential biological activity. The aldehyde functional group at the 5-position is significant for its reactivity, allowing for various chemical transformations, including condensation reactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential interactions with biological targets, which could be explored in drug development. Additionally, the compound's solubility and stability can be influenced by the substituents on the rings, affecting its application in various chemical and pharmaceutical contexts. As with many heterocycles, the compound's properties can be further studied through techniques such as spectroscopy and crystallography to elucidate its behavior in different environments.

CAS 81933-75-7

6-chloro-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde

6-Chloro-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde

Ref: IN-DA008L5A

6-Chloro-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde

Ref: 3D-GDA93375