4-(4-Fluorophenyl)-1,3-thiazol-2-amine, with the CAS number 77815-14-6, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. The presence of a fluorophenyl group enhances its chemical properties, potentially influencing its reactivity and biological activity. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to the hydrophobic nature of the fluorophenyl moiety. It is often studied for its potential applications in pharmaceuticals, particularly in the development of compounds with antimicrobial or anticancer properties. The thiazole ring is known for its ability to participate in various chemical reactions, making this compound a valuable intermediate in synthetic chemistry. Additionally, the presence of the amino group can facilitate further functionalization, allowing for the exploration of structure-activity relationships in drug design. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

4-(4-fluorophenyl)-1,3-thiazol-2-amine

77815-14-6: 4-(4-Fluorophenyl)-1,3-thiazol-2-amine, with the CAS number 77815-14-6, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. The presence of a fluorophenyl group enhances its chemical properties, potentially influencing its reactivity and biological activity. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to the hydrophobic nature of the fluorophenyl moiety. It is often studied for its potential applications in pharmaceuticals, particularly in the development of compounds with antimicrobial or anticancer properties. The thiazole ring is known for its ability to participate in various chemical reactions, making this compound a valuable intermediate in synthetic chemistry. Additionally, the presence of the amino group can facilitate further functionalization, allowing for the exploration of structure-activity relationships in drug design. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

CAS 77815-14-6

4-(4-fluorophenyl)-1,3-thiazol-2-amine

4-(4-fluorophenyl)thiazol-2-amine

Ref: IN-DA003GE5

2-Amino-4-(4-fluorophenyl)-1,3-thiazole

Ref: 54-PC5617

4-(4-Fluorophenyl)-1,3-thiazol-2-amine

Ref: 10-F010123