5-Bromo-6-chloro-4(1H)-pyrimidinone is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both bromine and chlorine substituents. This compound features a bromine atom at the 5-position and a chlorine atom at the 6-position of the pyrimidine ring, along with a carbonyl group at the 4-position, contributing to its reactivity and potential biological activity. It is typically a crystalline solid at room temperature and is soluble in polar organic solvents. The presence of halogen atoms often enhances the compound's reactivity, making it useful in various chemical syntheses and applications, particularly in medicinal chemistry and agrochemicals. Its unique structure allows for potential interactions with biological targets, which may lead to pharmacological effects. As with many halogenated compounds, safety precautions should be taken when handling 5-Bromo-6-chloro-4(1H)-pyrimidinone due to its potential toxicity and environmental impact.

5-Bromo-6-chloro-4(1H)-pyrimidinone

89089-19-0: 5-Bromo-6-chloro-4(1H)-pyrimidinone, 4(3H)-Pyrimidinone, 5-bromo-6-chloro-, 4(1H)-Pyrimidinone, 5-bromo-6-chloro-

5-BROMO-6-CHLORO-4(3H)-PYRIMIDINONE

5-Bromo-6-chloropyrimidin-4(1H)-one

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CAS 89089-19-0: 5-Bromo-6-chloro-4(1H)-pyrimidinone

5-BROMO-6-CHLORO-4(3H)-PYRIMIDINONE

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5-BROMO-6-CHLORO-4(3H)-PYRIMIDINONE

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5-Bromo-6-chloropyrimidin-4(1H)-one

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5-Bromo-6-chloro-4(3H)-pyrimidinone

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