Methyl 5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridine-3-carboxylate is a chemical compound characterized by its complex structure, which includes a pyrrolo[2,3-b]pyridine core, a methyl ester functional group, and a sulfonyl group attached to a p-tolyl moiety. This compound typically exhibits properties associated with heterocyclic compounds, such as potential biological activity and solubility in organic solvents. The presence of the chloro substituent may influence its reactivity and interaction with biological targets. The sulfonyl group can enhance the compound's polarity and solubility, potentially affecting its pharmacokinetic properties. Methyl esters are often used in medicinal chemistry for their ability to participate in various chemical reactions, including hydrolysis and transesterification. Overall, this compound may be of interest in pharmaceutical research, particularly in the development of new therapeutic agents, due to its unique structural features and potential biological activities. However, specific characteristics such as melting point, boiling point, and spectral data would require experimental determination or literature reference for precise values.

methyl 5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridine-3-carboxylate

952182-24-0: Methyl 5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridine-3-carboxylate is a chemical compound characterized by its complex structure, which includes a pyrrolo[2,3-b]pyridine core, a methyl ester functional group, and a sulfonyl group attached to a p-tolyl moiety. This compound typically exhibits properties associated with heterocyclic compounds, such as potential biological activity and solubility in organic solvents. The presence of the chloro substituent may influence its reactivity and interaction with biological targets. The sulfonyl group can enhance the compound's polarity and solubility, potentially affecting its pharmacokinetic properties. Methyl esters are often used in medicinal chemistry for their ability to participate in various chemical reactions, including hydrolysis and transesterification. Overall, this compound may be of interest in pharmaceutical research, particularly in the development of new therapeutic agents, due to its unique structural features and potential biological activities. However, specific characteristics such as melting point, boiling point, and spectral data would require experimental determination or literature reference for precise values.

Methyl 5-chloro-1-(toluene-4-sulphonyl)-7-azaindole-3-carboxylate

CAS 952182-24-0

methyl 5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridine-3-carboxylate

Methyl 5-chloro-1-(toluene-4-sulphonyl)-7-azaindole-3-carboxylate

Ref: 54-OR41117