Methyl thieno[3,2-b]pyridine-3-carboxylate is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both a thieno and a pyridine ring. This compound features a carboxylate functional group, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of the methyl ester group enhances its solubility in organic solvents, making it suitable for various chemical reactions. Methyl thieno[3,2-b]pyridine-3-carboxylate is often studied for its biological activity, particularly in the context of drug development, as compounds with similar structures have shown promise in targeting specific biological pathways. Its molecular structure allows for potential interactions with various biological targets, which can be explored in pharmacological studies. Additionally, the compound's stability and reactivity can be influenced by substituents on the rings, making it a versatile building block in synthetic organic chemistry. Overall, methyl thieno[3,2-b]pyridine-3-carboxylate represents an interesting compound for research in both synthetic and medicinal chemistry.

methyl thieno[3,2-b]pyridine-3-carboxylate

952182-41-1: Methyl thieno[3,2-b]pyridine-3-carboxylate is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both a thieno and a pyridine ring. This compound features a carboxylate functional group, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of the methyl ester group enhances its solubility in organic solvents, making it suitable for various chemical reactions. Methyl thieno[3,2-b]pyridine-3-carboxylate is often studied for its biological activity, particularly in the context of drug development, as compounds with similar structures have shown promise in targeting specific biological pathways. Its molecular structure allows for potential interactions with various biological targets, which can be explored in pharmacological studies. Additionally, the compound's stability and reactivity can be influenced by substituents on the rings, making it a versatile building block in synthetic organic chemistry. Overall, methyl thieno[3,2-b]pyridine-3-carboxylate represents an interesting compound for research in both synthetic and medicinal chemistry.

CAS 952182-41-1

methyl thieno[3,2-b]pyridine-3-carboxylate

Methyl thieno[3,2-b]pyridine-3-carboxylate

Ref: 3D-CNB18241