CAS 32937-55-6
:2',5'-dibromoacetophenone
Description:
2',5'-Dibromoacetophenone is an organic compound characterized by its structure, which features a phenyl ring substituted with two bromine atoms at the 2' and 5' positions and an acetophenone functional group. This compound is typically a solid at room temperature and is known for its pale yellow to off-white appearance. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water due to its hydrophobic nature. The presence of bromine atoms enhances its reactivity, making it useful in various chemical reactions, including electrophilic aromatic substitution and as a potential intermediate in organic synthesis. Additionally, 2',5'-dibromoacetophenone may exhibit biological activity, which can be explored for potential applications in pharmaceuticals or agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health risks, including irritation to the skin and eyes. Proper storage in a cool, dry place away from incompatible substances is recommended to maintain its stability.
Formula:C8H6Br2O
InChI:InChI=1/C8H6Br2O/c1-5(11)7-4-6(9)2-3-8(7)10/h2-4H,1H3
SMILES:CC(=O)c1cc(ccc1Br)Br
Synonyms:- 1-(2,5-Dibromophenyl)Ethanone
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Found 4 products.
2',5'-Dibromoacetophenone
CAS:Formula:C8H6Br2OPurity:97%Color and Shape:SolidMolecular weight:277.94061-(2,5-Dibromophenyl)ethan-1-one
CAS:1-(2,5-Dibromophenyl)ethan-1-onePurity:99%Molecular weight:277.94g/mol1-(2,5-Dibromophenyl)ethanone
CAS:<p>2',5'-Dibromoacetophenone is an imine that has been shown to be a potent inhibitor of NS5A. It is used in the synthesis of elbasvir and other pharmaceuticals. The enantioselective synthesis of 2',5'-dibromoacetophenone is achieved by using a chiral catalyst derived from camphor, which can produce the desired product in large quantities with high purity.</p>Formula:C8H6Br2OPurity:Min. 95%Color and Shape:PowderMolecular weight:277.94 g/mol
