4-Bromo-2-chloropyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of bromine and chlorine substituents at the 4 and 2 positions, respectively, introduces significant reactivity and influences its chemical properties. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide, but has limited solubility in water. 4-Bromo-2-chloropyrimidine is often utilized in medicinal chemistry and material science for the synthesis of various pharmaceuticals and agrochemicals due to its ability to participate in nucleophilic substitution reactions. Its reactivity can be attributed to the electron-withdrawing effects of the halogen substituents, which enhance electrophilic attack at the nitrogen atoms or other reactive sites on the pyrimidine ring. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

4-Bromo-2-chloropyrimidine

885702-34-1: 4-Bromo-2-chloropyrimidine, Pyrimidine, 4-bromo-2-chloro-

4-Bromo-2-chloropyrimidine is an alkaloid that belongs to the group of phosphorus compounds. It has been shown to be a scalable, efficient, and green synthetic route to hyrtinadine. 4-Bromo-2-chloropyrimidine can be prepared by coupling with alkyne in presence of catalysts such as palladium or reductive conditions such as NaBH

CAS 885702-34-1: 4-Bromo-2-chloropyrimidine

4-Bromo-2-chloropyrimidine

Ref: 10-F225578

4-Bromo-2-chloropyrimidine

Ref: 54-OR52309

4-Bromo-2-chloropyrimidine

Ref: FT-B12149

4-Bromo-2-chloropyrimidine

Ref: IN-DA0038DK

4-bromo-2-chloropyrimidine

Ref: 3D-KKB70234