3-Amino-2-methyl-N-(1,3-thiazol-2-yl)benzamide is an organic compound characterized by its structural features, which include an amino group, a methyl group, and a thiazole moiety attached to a benzamide framework. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the amino and carbonyl functional groups, while its aromatic nature may contribute to some degree of hydrophobicity. The thiazole ring introduces heteroatoms, which can influence the compound's reactivity and potential biological activity. It may participate in hydrogen bonding due to the amino and carbonyl groups, making it a candidate for various chemical reactions, including nucleophilic substitutions. Additionally, compounds with similar structures often exhibit pharmacological properties, making them of interest in medicinal chemistry. The presence of the thiazole ring may also enhance the compound's ability to interact with biological targets, potentially leading to applications in drug development. Overall, this compound's unique combination of functional groups and structural features contributes to its chemical behavior and potential applications.

3-amino-2-methyl-N-(1,3-thiazol-2-yl)benzamide

402585-79-9: 3-Amino-2-methyl-N-(1,3-thiazol-2-yl)benzamide is an organic compound characterized by its structural features, which include an amino group, a methyl group, and a thiazole moiety attached to a benzamide framework. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the amino and carbonyl functional groups, while its aromatic nature may contribute to some degree of hydrophobicity. The thiazole ring introduces heteroatoms, which can influence the compound's reactivity and potential biological activity. It may participate in hydrogen bonding due to the amino and carbonyl groups, making it a candidate for various chemical reactions, including nucleophilic substitutions. Additionally, compounds with similar structures often exhibit pharmacological properties, making them of interest in medicinal chemistry. The presence of the thiazole ring may also enhance the compound's ability to interact with biological targets, potentially leading to applications in drug development. Overall, this compound's unique combination of functional groups and structural features contributes to its chemical behavior and potential applications.

CAS 402585-79-9

3-amino-2-methyl-N-(1,3-thiazol-2-yl)benzamide

3-amino-2-methyl-N-1,3-thiazol-2-ylbenzamide

Ref: 10-F314788