5-Fluoropyrimidin-4-amine is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a fluorine atom at the 5-position and an amino group (-NH2) at the 4-position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound is often studied for its role as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of antiviral and anticancer agents. It exhibits properties typical of amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility and interaction with biological targets. Additionally, the fluorine substitution can enhance lipophilicity and metabolic stability, making it a valuable scaffold in drug design. As with many nitrogen-containing heterocycles, 5-fluoropyrimidin-4-amine may also exhibit interesting electronic properties, which can be exploited in the development of novel materials or catalysts.

5-fluoropyrimidin-4-amine

811450-26-7: 5-Fluoropyrimidin-4-amine is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a fluorine atom at the 5-position and an amino group (-NH2) at the 4-position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound is often studied for its role as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of antiviral and anticancer agents. It exhibits properties typical of amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility and interaction with biological targets. Additionally, the fluorine substitution can enhance lipophilicity and metabolic stability, making it a valuable scaffold in drug design. As with many nitrogen-containing heterocycles, 5-fluoropyrimidin-4-amine may also exhibit interesting electronic properties, which can be exploited in the development of novel materials or catalysts.

CAS 811450-26-7

5-fluoropyrimidin-4-amine

5-Fluoropyrimidin-4-amine

Ref: IN-DA0036KB

5-Fluoropyrimidin-4-amine

Ref: 54-PC400708

5-Fluoropyrimidin-4-amine

Ref: 10-F208644