Furo[3,2-c]pyridine-2-carboxylic acid, 7-bromo-3-hydroxy-, ethyl ester is a chemical compound characterized by its complex heterocyclic structure, which includes a fused furan and pyridine ring system. The presence of a carboxylic acid moiety indicates potential acidity, while the ethyl ester group suggests it can participate in esterification reactions. The bromine substituent at the 7-position introduces notable reactivity and can influence the compound's biological activity and solubility. The hydroxyl group at the 3-position contributes to the compound's polarity and may enhance its interaction with biological targets. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its unique structural features allow for potential applications in drug development, particularly in the synthesis of novel therapeutic agents. As with many heterocycles, the compound's reactivity can be modulated through substitution patterns, making it a versatile scaffold for further chemical modifications.

FURO[3,2-C]PYRIDINE-2-CARBOXYLIC ACID, 7-BROMO-3-HYDROXY-, ETHYL ESTER

1009333-80-5: Furo[3,2-c]pyridine-2-carboxylic acid, 7-bromo-3-hydroxy-, ethyl ester is a chemical compound characterized by its complex heterocyclic structure, which includes a fused furan and pyridine ring system. The presence of a carboxylic acid moiety indicates potential acidity, while the ethyl ester group suggests it can participate in esterification reactions. The bromine substituent at the 7-position introduces notable reactivity and can influence the compound's biological activity and solubility. The hydroxyl group at the 3-position contributes to the compound's polarity and may enhance its interaction with biological targets. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its unique structural features allow for potential applications in drug development, particularly in the synthesis of novel therapeutic agents. As with many heterocycles, the compound's reactivity can be modulated through substitution patterns, making it a versatile scaffold for further chemical modifications.

CAS 1009333-80-5

FURO[3,2-C]PYRIDINE-2-CARBOXYLIC ACID, 7-BROMO-3-HYDROXY-, ETHYL ESTER