Ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate is a chemical compound characterized by its unique structure, which includes a thiophene ring, an amino group, and a furan substituent. This compound typically exhibits properties associated with both heterocyclic compounds and carboxylates, such as moderate solubility in organic solvents and potential reactivity due to the presence of the amino and carboxylate functional groups. The thiophene ring contributes to its aromatic character, which can influence its electronic properties and reactivity. Ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate may also display biological activity, making it of interest in medicinal chemistry and drug development. Its synthesis often involves multi-step organic reactions, and it can serve as a building block for more complex molecules. The compound's specific applications and behavior in various chemical environments can vary, depending on factors such as pH, temperature, and the presence of other reagents. Overall, this compound represents a versatile structure with potential utility in various fields of chemistry.

ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate

256506-99-7: Ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate is a chemical compound characterized by its unique structure, which includes a thiophene ring, an amino group, and a furan substituent. This compound typically exhibits properties associated with both heterocyclic compounds and carboxylates, such as moderate solubility in organic solvents and potential reactivity due to the presence of the amino and carboxylate functional groups. The thiophene ring contributes to its aromatic character, which can influence its electronic properties and reactivity. Ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate may also display biological activity, making it of interest in medicinal chemistry and drug development. Its synthesis often involves multi-step organic reactions, and it can serve as a building block for more complex molecules. The compound's specific applications and behavior in various chemical environments can vary, depending on factors such as pH, temperature, and the presence of other reagents. Overall, this compound represents a versatile structure with potential utility in various fields of chemistry.

3-Thiophenecarboxylic acid, 2-amino-4-(2-furanyl)-, ethyl ester

Ethyl 2-amino-4-(fur-2-yl)thiophene-3-carboxylate

CAS 256506-99-7

ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate

3-Thiophenecarboxylic acid, 2-amino-4-(2-furanyl)-, ethyl ester

Ref: IN-DA00I4WG

Ethyl 2-amino-4-(fur-2-yl)thiophene-3-carboxylate

Ref: 54-OR24477

2-Amino-4-furan-2-yl-thiophene-3-carboxylic acid ethyl ester

Ref: 10-F481546