5-Bromo-4-(2-fluoropropan-2-yl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a bromine atom at the 5-position and a 2-fluoropropan-2-yl group at the 4-position contributes to its unique chemical properties. This compound is likely to exhibit moderate to high lipophilicity due to the presence of the bulky fluoropropyl substituent, which can influence its solubility and reactivity. The bromine atom can participate in nucleophilic substitution reactions, while the fluorine atom may enhance the compound's stability and reactivity in certain chemical environments. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of targeted therapies or as a building block for more complex molecules. Overall, 5-bromo-4-(2-fluoropropan-2-yl)pyrimidine is a versatile compound with significant implications in various chemical and biological contexts.

5-bromo-4-(2-fluoropropan-2-yl)pyrimidine

1823944-93-9: 5-Bromo-4-(2-fluoropropan-2-yl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a bromine atom at the 5-position and a 2-fluoropropan-2-yl group at the 4-position contributes to its unique chemical properties. This compound is likely to exhibit moderate to high lipophilicity due to the presence of the bulky fluoropropyl substituent, which can influence its solubility and reactivity. The bromine atom can participate in nucleophilic substitution reactions, while the fluorine atom may enhance the compound's stability and reactivity in certain chemical environments. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of targeted therapies or as a building block for more complex molecules. Overall, 5-bromo-4-(2-fluoropropan-2-yl)pyrimidine is a versatile compound with significant implications in various chemical and biological contexts.

CAS 1823944-93-9

5-bromo-4-(2-fluoropropan-2-yl)pyrimidine

5-Bromo-4-(2-fluoropropan-2-yl)pyrimidine

Ref: IN-DA01DLU5

5-Bromo-4-(2-fluoropropan-2-yl)pyrimidine

Ref: 54-PC1002368

5-BROMO-4-(2-FLUOROPROPAN-2-YL)PYRIMIDINE

Ref: 10-F513119