2-Bromo-1-(6-bromopyrid-3-yl)ethanone is an organic compound characterized by its brominated structure and ketone functional group. This compound features a bromine atom attached to both the ethyl group and a pyridine ring, which contributes to its unique chemical properties. The presence of the ketone functional group indicates that it can participate in various chemical reactions, such as nucleophilic addition or condensation reactions. The bromine substituents enhance the compound's reactivity, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the pyridine ring can influence the compound's electronic properties and solubility, affecting its behavior in biological systems. The compound's molecular structure suggests potential applications in medicinal chemistry, where brominated derivatives are often explored for their biological activity. As with many brominated compounds, considerations regarding toxicity and environmental impact are essential during handling and application.

2-BROMO-1-(6-BROMOPYRID-3-YL)ETHANONE

136592-20-6: 2-Bromo-1-(6-bromopyrid-3-yl)ethanone is an organic compound characterized by its brominated structure and ketone functional group. This compound features a bromine atom attached to both the ethyl group and a pyridine ring, which contributes to its unique chemical properties. The presence of the ketone functional group indicates that it can participate in various chemical reactions, such as nucleophilic addition or condensation reactions. The bromine substituents enhance the compound's reactivity, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the pyridine ring can influence the compound's electronic properties and solubility, affecting its behavior in biological systems. The compound's molecular structure suggests potential applications in medicinal chemistry, where brominated derivatives are often explored for their biological activity. As with many brominated compounds, considerations regarding toxicity and environmental impact are essential during handling and application.

CAS 136592-20-6

2-BROMO-1-(6-BROMOPYRID-3-YL)ETHANONE

Ethanone, 2-bromo-1-(6-bromo-3-pyridinyl)-

Ref: IN-DA00124J

2-Bromo-1-(6-bromopyridin-3-yl)ethan-1-one

Ref: 54-OR1039071

2-BROMO-1-(6-BROMOPYRIDIN-3-YL)ETHANONE

Ref: 10-F844494