5-Bromo-2-pyrimidinecarboxaldehyde is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of a bromine atom at the 5-position and an aldehyde functional group at the 2-position contributes to its reactivity and potential applications in organic synthesis. This compound is typically a pale yellow to light brown solid, and it is soluble in polar organic solvents. Its reactivity is influenced by the electron-withdrawing nature of the aldehyde group, making it a useful intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound can participate in nucleophilic addition reactions due to the electrophilic carbonyl carbon, and it may also undergo substitution reactions at the bromine site. Overall, 5-Bromo-2-pyrimidinecarboxaldehyde is valued in synthetic chemistry for its versatility and the functional groups that allow for further chemical transformations.

5-Bromo-2-pyrimidinecarboxaldehyde

944902-05-0: 2-Pyrimidinecarboxaldehyde, 5-bromo-, 5-Bromo-2-formylpyrimidine, 5-Bromo-2-pyrimidinecarboxaldehyde, 5-Bromopyrimidine-2-Carboxaldehyde

CAS 944902-05-0: 5-Bromo-2-pyrimidinecarboxaldehyde

5-Bromopyrimidine-2-carbaldehyde

Ref: 10-F220169

5-Bromopyrimidine-2-carbaldehyde

Ref: 3D-UMB90205

5-Bromopyrimidine-2-carbaldehyde

Ref: IN-DA0038IR