5-Bromo-4-ethylpyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a bromine atom at the 5-position and an ethyl group at the 4-position. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic ethyl group. The presence of the bromine atom introduces notable reactivity, making it a useful intermediate in various organic synthesis reactions, particularly in the development of pharmaceuticals and agrochemicals. The ethyl substituent can influence the compound's electronic properties and steric hindrance, affecting its reactivity and interactions with biological targets. Additionally, 5-bromo-4-ethylpyrimidine can participate in nucleophilic substitution reactions and can serve as a building block for more complex molecular architectures. Its unique structure and properties make it a valuable compound in medicinal chemistry and materials science.

5-bromo-4-ethylpyrimidine

951884-36-9: 5-Bromo-4-ethylpyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a bromine atom at the 5-position and an ethyl group at the 4-position. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic ethyl group. The presence of the bromine atom introduces notable reactivity, making it a useful intermediate in various organic synthesis reactions, particularly in the development of pharmaceuticals and agrochemicals. The ethyl substituent can influence the compound's electronic properties and steric hindrance, affecting its reactivity and interactions with biological targets. Additionally, 5-bromo-4-ethylpyrimidine can participate in nucleophilic substitution reactions and can serve as a building block for more complex molecular architectures. Its unique structure and properties make it a valuable compound in medicinal chemistry and materials science.

CAS 951884-36-9

5-bromo-4-ethylpyrimidine

5-Bromo-4-ethylpyrimidine

Ref: IN-DA0066CH

5-Bromo-4-ethylpyrimidine

Ref: 54-OR11580

5-Bromo-4-ethylpyrimidine

Ref: 10-F318139

5-Bromo-4-ethylpyrimidine

Ref: 3D-BNB88436