Pyrimidine, 5-bromo-2-ethyl- is a heterocyclic organic compound characterized by a six-membered ring containing two nitrogen atoms at positions 1 and 3, which is typical of pyrimidine derivatives. The presence of a bromine atom at the 5-position and an ethyl group at the 2-position contributes to its unique chemical properties. This compound is likely to exhibit moderate polarity due to the electronegative bromine atom, which can influence its reactivity and solubility in various solvents. Pyrimidine derivatives are often of interest in medicinal chemistry due to their biological activity, including potential applications in pharmaceuticals. The compound may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, owing to the presence of the bromine substituent. Additionally, its structure allows for potential interactions with biological targets, making it a candidate for further research in drug development. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental impact.

Pyrimidine,5-bromo-2-ethyl-

873331-73-8: Pyrimidine, 5-bromo-2-ethyl- is a heterocyclic organic compound characterized by a six-membered ring containing two nitrogen atoms at positions 1 and 3, which is typical of pyrimidine derivatives. The presence of a bromine atom at the 5-position and an ethyl group at the 2-position contributes to its unique chemical properties. This compound is likely to exhibit moderate polarity due to the electronegative bromine atom, which can influence its reactivity and solubility in various solvents. Pyrimidine derivatives are often of interest in medicinal chemistry due to their biological activity, including potential applications in pharmaceuticals. The compound may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, owing to the presence of the bromine substituent. Additionally, its structure allows for potential interactions with biological targets, making it a candidate for further research in drug development. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental impact.

CAS 873331-73-8

Pyrimidine,5-bromo-2-ethyl-

5-broMo-2-ethylpyriMidine

Ref: IN-DA004L1O

5-Bromo-2-ethylpyrimidine

Ref: 54-OR1067970

5-Bromo-2-ethylpyrimidine

Ref: 10-F078232