3-Chlorothieno[2,3-b]pyridine-2-carboxylic acid is a heterocyclic compound characterized by the presence of a thieno[2,3-b]pyridine ring system, which incorporates both sulfur and nitrogen atoms in its structure. This compound features a carboxylic acid functional group, contributing to its acidity and potential reactivity. The chlorine substituent at the 3-position of the thieno ring influences its electronic properties and may affect its biological activity. Generally, compounds of this type can exhibit a range of pharmacological activities, making them of interest in medicinal chemistry. The presence of the thieno and pyridine moieties often enhances the compound's ability to interact with biological targets, such as enzymes or receptors. Additionally, the compound's solubility, stability, and reactivity can be influenced by the functional groups present, making it a subject of study for various applications, including drug development and synthesis of novel materials. As with many heterocycles, the specific characteristics and behavior of this compound can be further elucidated through experimental studies and computational modeling.

3-chlorothieno[2,3-b]pyridine-2-carboxylic acid

937640-24-9: 3-Chlorothieno[2,3-b]pyridine-2-carboxylic acid is a heterocyclic compound characterized by the presence of a thieno[2,3-b]pyridine ring system, which incorporates both sulfur and nitrogen atoms in its structure. This compound features a carboxylic acid functional group, contributing to its acidity and potential reactivity. The chlorine substituent at the 3-position of the thieno ring influences its electronic properties and may affect its biological activity. Generally, compounds of this type can exhibit a range of pharmacological activities, making them of interest in medicinal chemistry. The presence of the thieno and pyridine moieties often enhances the compound's ability to interact with biological targets, such as enzymes or receptors. Additionally, the compound's solubility, stability, and reactivity can be influenced by the functional groups present, making it a subject of study for various applications, including drug development and synthesis of novel materials. As with many heterocycles, the specific characteristics and behavior of this compound can be further elucidated through experimental studies and computational modeling.

CAS 937640-24-9

3-chlorothieno[2,3-b]pyridine-2-carboxylic acid

3-CHLOROTHIENO[2,3-B]PYRIDINE-2-CARBOXYLIC ACID

Ref: IN-DA00364K

3-Chlorothieno[2,3-b]pyridine-2-carboxylic acid

Ref: 10-F321239

3-Chlorothieno[2,3-b]pyridine-2-carboxylic acid

Ref: 3D-MMB64024