4-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride is a chemical compound characterized by its unique pyrazolo-pyridine structure, which incorporates both a pyrazole and a pyridine ring. This compound features a chloro substituent at the 4-position and a carbonyl chloride functional group at the 5-position, contributing to its reactivity and potential applications in organic synthesis. The presence of the dimethyl groups at the 1 and 3 positions enhances its lipophilicity and may influence its biological activity. As a carbonyl chloride, it is likely to be reactive towards nucleophiles, making it useful in various chemical transformations, including acylation reactions. The compound's molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Additionally, its unique heterocyclic framework may confer interesting properties, such as fluorescence or specific binding affinities, which could be explored in further research. Safety precautions should be taken when handling this compound due to its reactive nature.

4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride

175201-95-3: 4-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride is a chemical compound characterized by its unique pyrazolo-pyridine structure, which incorporates both a pyrazole and a pyridine ring. This compound features a chloro substituent at the 4-position and a carbonyl chloride functional group at the 5-position, contributing to its reactivity and potential applications in organic synthesis. The presence of the dimethyl groups at the 1 and 3 positions enhances its lipophilicity and may influence its biological activity. As a carbonyl chloride, it is likely to be reactive towards nucleophiles, making it useful in various chemical transformations, including acylation reactions. The compound's molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Additionally, its unique heterocyclic framework may confer interesting properties, such as fluorescence or specific binding affinities, which could be explored in further research. Safety precautions should be taken when handling this compound due to its reactive nature.

4-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride

4-Chloro-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carbonyl chloride

CAS 175201-95-3

4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride

4-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride

Ref: IN-DA0020G1

4-Chloro-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carbonyl chloride

Ref: 54-OR4065