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CAS 383-53-9

:

2-Bromo-1-[4-(trifluoromethyl)phenyl]ethanone

Description:
2-Bromo-1-[4-(trifluoromethyl)phenyl]ethanone, with the CAS number 383-53-9, is an organic compound characterized by its bromine and trifluoromethyl substituents. This compound features a ketone functional group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the bromine atom enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. The trifluoromethyl group is known for imparting unique electronic properties, often increasing the lipophilicity and metabolic stability of the molecule. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structural features suggest potential applications in pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Safety considerations should be taken into account due to the presence of halogenated groups, which can pose environmental and health risks. Proper handling and disposal methods are essential when working with this substance in a laboratory setting.
Formula:C9H6BrF3O
InChI:InChI=1/C4H5ClF2O2/c1-2-9-3(8)4(5,6)7/h2H2,1H3
InChI key:InChIKey=HEMROKPXTCOASZ-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC=C(C(CBr)=O)C=C1
Synonyms:
  • 1-(2-Bromo-1-oxoethyl)-4-trifluoromethylbenzene
  • 2-Bromo-1-[4-(trifluoromethyl)phenyl]ethan-1-one
  • 2-Bromo-1-[4-(trifluoromethyl)phenyl]ethanone
  • 2-Bromo-4'-(trifluoromethyl)acetophenone
  • Acetophenone, 2-bromo-4′-(trifluoromethyl)-
  • Ethanone, 2-bromo-1-[4-(trifluoromethyl)phenyl]-
  • Ethyl Chloro(Difluoro)Acetate
  • NSC 277303
  • p-(Trifluoromethyl)phenacyl bromide
  • α-Bromo-p-(trifluoromethyl)acetophenone
  • See more synonyms
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