5-(2-Fluorophenyl)thiazol-2-amine is an organic compound characterized by the presence of a thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The compound features a fluorophenyl group, indicating the presence of a fluorine atom on a phenyl ring that is attached to the thiazole. This substitution can influence the compound's electronic properties and reactivity. The amine functional group (-NH2) contributes to its potential as a nucleophile, making it reactive in various chemical reactions. The presence of the fluorine atom can enhance lipophilicity and alter the compound's biological activity, making it of interest in medicinal chemistry. Additionally, the thiazole moiety is often associated with various pharmacological activities, including antimicrobial and anti-inflammatory properties. Overall, 5-(2-fluorophenyl)thiazol-2-amine is a compound of interest for research in organic synthesis and drug development, with its unique structural features contributing to its potential applications.

5-(2-fluorophenyl)thiazol-2-amine

1025927-65-4: 5-(2-Fluorophenyl)thiazol-2-amine is an organic compound characterized by the presence of a thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The compound features a fluorophenyl group, indicating the presence of a fluorine atom on a phenyl ring that is attached to the thiazole. This substitution can influence the compound's electronic properties and reactivity. The amine functional group (-NH2) contributes to its potential as a nucleophile, making it reactive in various chemical reactions. The presence of the fluorine atom can enhance lipophilicity and alter the compound's biological activity, making it of interest in medicinal chemistry. Additionally, the thiazole moiety is often associated with various pharmacological activities, including antimicrobial and anti-inflammatory properties. Overall, 5-(2-fluorophenyl)thiazol-2-amine is a compound of interest for research in organic synthesis and drug development, with its unique structural features contributing to its potential applications.

CAS 1025927-65-4

5-(2-fluorophenyl)thiazol-2-amine

2-Amino-5-(2-fluorophenyl)-thiazole

Ref: IN-DA008T2Q

5-(2-Fluorophenyl)-1,3-thiazol-2-amine

Ref: 10-F675908