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Atomfair Magnesium bromide 4-(trifluoromethoxy)benzen-1-ide (1/1/1) C7H4BrF3MgO

Description Magnesium bromide 4-(trifluoromethoxy)benzen-1-ide (1/1/1) (CAS No. 169222-42-8) is a highly specialized organomagnesium compound with the molecular formula C7H4BrF3MgO . This reagent is meticulously synthesized for advanced synthetic applications, particularly in Grignard reactions and as a precursor in the formation of carbon-carbon bonds. Its unique trifluoromethoxybenzene moiety enhances reactivity and selectivity in cross-coupling reactions, making it invaluable for pharmaceutical and materials science research. Supplied as a high-purity solid with strict quality control, this compound is ideal for researchers requiring precision in organometallic chemistry. Store under inert conditions to maintain stability and reactivity.

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Description

Description

Magnesium bromide 4-(trifluoromethoxy)benzen-1-ide (1/1/1) (CAS No. 169222-42-8) is a highly specialized organomagnesium compound with the molecular formula C7H4BrF3MgO. This reagent is meticulously synthesized for advanced synthetic applications, particularly in Grignard reactions and as a precursor in the formation of carbon-carbon bonds. Its unique trifluoromethoxybenzene moiety enhances reactivity and selectivity in cross-coupling reactions, making it invaluable for pharmaceutical and materials science research. Supplied as a high-purity solid with strict quality control, this compound is ideal for researchers requiring precision in organometallic chemistry. Store under inert conditions to maintain stability and reactivity.

  • CAS No: 169222-42-8
  • Molecular Formula: C7H4BrF3MgO
  • Molecular Weight: 265.31
  • Exact Mass: 263.92480
  • Monoisotopic Mass: 263.92480
  • IUPAC Name: magnesium;trifluoromethoxybenzene;bromide
  • SMILES: C1=CC(=CC=[C-]1)OC(F)(F)F.[Mg+2].[Br-]
  • Synonyms: 169222-42-8, DTXSID70542402, Magnesium bromide 4-(trifluoromethoxy)benzen-1-ide (1/1/1), DTXCID30493188, Magnesium, bromo[4-(trifluoromethoxy)phenyl]-

Application

This compound is primarily used as a Grignard reagent in organic synthesis, enabling the formation of carbon-carbon bonds in complex molecule construction. It is particularly useful in the preparation of trifluoromethoxy-substituted aromatic compounds, which are prevalent in agrochemical and pharmaceutical intermediates. Researchers also employ it in catalytic systems and as a precursor for advanced material development.

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