CAS 214701-49-2
:Ethanone, 1-(5-bromo-2-pyridinyl)-
Description:
Ethanone, 1-(5-bromo-2-pyridinyl)-, also known by its CAS number 214701-49-2, is an organic compound characterized by the presence of a pyridine ring substituted with a bromine atom and an ethanone functional group. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and acetone, but may have limited solubility in water due to its hydrophobic characteristics. The bromine substituent can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of the pyridine ring contributes to its aromatic properties, which can affect its stability and interaction with other molecules. This compound may be of interest in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. As with many brominated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.
Formula:C7H6BrNO
Synonyms:- 1-(5-Bromopyridin-2-yl)ethanone
- 2-Acetyl-5-Bromopyridine
- 1-(5-Bromo-Pyridin-2-Yl)-Ethanone
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
2-Acetyl-5-bromopyridine
CAS:Formula:C7H6BrNOPurity:98%Color and Shape:SolidMolecular weight:200.03262-Acetyl-5-bromopyridine
CAS:<p>2-Acetyl-5-bromopyridine</p>Formula:C7H6BrNOPurity:≥95%Color and Shape: pale yellow solidMolecular weight:200.03g/mol1-(5-Bromo-2-pyridyl)ethanone
CAS:Controlled Product<p>Applications 1-(5-Bromo-2-pyridyl)ethanone is a reagent used to synthesize substituted pyridin-3-yl)phenyloxazolidinones as antibacterial agents with reduced activity against monoamine oxidase A.<br>References Reck, F., et al.: J. Med. Chem., 50, 4868 (2007)<br></p>Formula:C7H6BrNOColor and Shape:NeatMolecular weight:200.03



