2-[(4-Fluorophenyl)amino]-1,3-thiazol-4(5H)-one, with the CAS number 21262-73-7, is a chemical compound characterized by its thiazole ring structure, which is a five-membered heterocyclic ring containing sulfur and nitrogen. This compound features an amino group attached to a phenyl ring that is further substituted with a fluorine atom, contributing to its unique chemical properties. The presence of the thiazole moiety often imparts biological activity, making such compounds of interest in medicinal chemistry. Typically, compounds like this may exhibit properties such as antimicrobial, antifungal, or anti-inflammatory activities, although specific biological effects would depend on further empirical studies. The molecular structure suggests potential for hydrogen bonding and interactions with biological targets, which can influence its solubility and reactivity. Additionally, the fluorine substitution can enhance lipophilicity and metabolic stability, making it a valuable candidate for drug development. Overall, this compound exemplifies the intersection of organic chemistry and pharmacology, highlighting the importance of structural modifications in the design of bioactive molecules.

2-[(4-fluorophenyl)amino]-1,3-thiazol-4(5H)-one

21262-73-7: 2-[(4-Fluorophenyl)amino]-1,3-thiazol-4(5H)-one, with the CAS number 21262-73-7, is a chemical compound characterized by its thiazole ring structure, which is a five-membered heterocyclic ring containing sulfur and nitrogen. This compound features an amino group attached to a phenyl ring that is further substituted with a fluorine atom, contributing to its unique chemical properties. The presence of the thiazole moiety often imparts biological activity, making such compounds of interest in medicinal chemistry. Typically, compounds like this may exhibit properties such as antimicrobial, antifungal, or anti-inflammatory activities, although specific biological effects would depend on further empirical studies. The molecular structure suggests potential for hydrogen bonding and interactions with biological targets, which can influence its solubility and reactivity. Additionally, the fluorine substitution can enhance lipophilicity and metabolic stability, making it a valuable candidate for drug development. Overall, this compound exemplifies the intersection of organic chemistry and pharmacology, highlighting the importance of structural modifications in the design of bioactive molecules.

CAS 21262-73-7

2-[(4-fluorophenyl)amino]-1,3-thiazol-4(5H)-one

2-[(4-fluorophenyl)amino]-1,3-thiazol-4(5H)-one

Ref: 10-F349222