3-Amino-5-(4-chlorophenyl)thiophene-2-carboxamide is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a carboxamide group (-C(=O)NH2) that contribute to its reactivity and potential biological activity. The presence of a 4-chlorophenyl substituent enhances its lipophilicity and may influence its interaction with biological targets. The compound's molecular structure suggests it may exhibit properties such as antimicrobial or anticancer activity, making it of interest in pharmaceutical research. Additionally, the thiophene moiety is known for its electronic properties, which can be beneficial in various applications, including organic electronics and materials science. The compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups. Overall, 3-amino-5-(4-chlorophenyl)thiophene-2-carboxamide represents a versatile scaffold for further chemical modifications and potential therapeutic applications.

3-AMINO-5-(4-CHLOROPHENYL)THIOPHENE-2-CARBOXAMIDE

175137-05-0: 3-Amino-5-(4-chlorophenyl)thiophene-2-carboxamide is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a carboxamide group (-C(=O)NH2) that contribute to its reactivity and potential biological activity. The presence of a 4-chlorophenyl substituent enhances its lipophilicity and may influence its interaction with biological targets. The compound's molecular structure suggests it may exhibit properties such as antimicrobial or anticancer activity, making it of interest in pharmaceutical research. Additionally, the thiophene moiety is known for its electronic properties, which can be beneficial in various applications, including organic electronics and materials science. The compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups. Overall, 3-amino-5-(4-chlorophenyl)thiophene-2-carboxamide represents a versatile scaffold for further chemical modifications and potential therapeutic applications.

2-Thiophenecarboxamide, 3-amino-5-(4-chlorophenyl)-

<p>3-Amino-5-(4-chlorophenyl)thiophene-2-carboxamide</p>

CAS 175137-05-0

3-AMINO-5-(4-CHLOROPHENYL)THIOPHENE-2-CARBOXAMIDE

2-Thiophenecarboxamide, 3-amino-5-(4-chlorophenyl)-

Ref: IN-DA0020A2

3-Amino-5-(4-chlorophenyl)thiophene-2-carboxamide

Ref: 54-OR103678

3-Amino-5-(4-chlorophenyl)thiophene-2-carboxamide

Ref: 10-F017006