Methyl 3-(piperazin-1-ylsulfonyl)thiophene-2-carboxylate is a chemical compound characterized by its unique structure, which includes a thiophene ring, a carboxylate group, and a piperazine moiety linked through a sulfonyl group. This compound typically exhibits properties such as moderate solubility in polar organic solvents due to the presence of the sulfonyl and carboxylate functional groups, which can engage in hydrogen bonding. The thiophene ring contributes to its aromatic character, potentially influencing its electronic properties and reactivity. Methyl 3-(piperazin-1-ylsulfonyl)thiophene-2-carboxylate may also display biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its molecular structure suggests potential interactions with biological targets, which could be explored in drug discovery. Additionally, the presence of the piperazine ring may enhance its pharmacokinetic properties, such as absorption and distribution. Overall, this compound represents a versatile scaffold for further chemical modifications and applications in various fields, including organic synthesis and medicinal chemistry.

methyl 3-(piperazin-1-ylsulfonyl)thiophene-2-carboxylate

940995-21-1: Methyl 3-(piperazin-1-ylsulfonyl)thiophene-2-carboxylate is a chemical compound characterized by its unique structure, which includes a thiophene ring, a carboxylate group, and a piperazine moiety linked through a sulfonyl group. This compound typically exhibits properties such as moderate solubility in polar organic solvents due to the presence of the sulfonyl and carboxylate functional groups, which can engage in hydrogen bonding. The thiophene ring contributes to its aromatic character, potentially influencing its electronic properties and reactivity. Methyl 3-(piperazin-1-ylsulfonyl)thiophene-2-carboxylate may also display biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its molecular structure suggests potential interactions with biological targets, which could be explored in drug discovery. Additionally, the presence of the piperazine ring may enhance its pharmacokinetic properties, such as absorption and distribution. Overall, this compound represents a versatile scaffold for further chemical modifications and applications in various fields, including organic synthesis and medicinal chemistry.

CAS 940995-21-1

methyl 3-(piperazin-1-ylsulfonyl)thiophene-2-carboxylate