Atomfair 1-(3,5-Dibromo-4-hydroxyphenyl)ethan-1-one C8H6Br2O2

Description 1-(3,5-Dibromo-4-hydroxyphenyl)ethan-1-one (CAS No. 2973-78-6) is a high-purity brominated aromatic ketone with the molecular formula C8H6Br2O2. This compound, also known by its IUPAC name 1-(3,5-dibromo-4-hydroxyphenyl)ethanone, is a valuable intermediate in organic synthesis and pharmaceutical research. The presence of bromine atoms and a hydroxyl group on the phenyl ring makes it a versatile building block for further functionalization. Our product is rigorously tested for purity and consistency, ensuring reliable performance in your laboratory applications. Available in various quantities to suit your research needs, it is supplied with comprehensive analytical data including HPLC, NMR, and MS spectra.

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Description

Description

1-(3,5-Dibromo-4-hydroxyphenyl)ethan-1-one (CAS No. 2973-78-6) is a high-purity brominated aromatic ketone with the molecular formula C8H6Br2O2. This compound, also known by its IUPAC name 1-(3,5-dibromo-4-hydroxyphenyl)ethanone, is a valuable intermediate in organic synthesis and pharmaceutical research. The presence of bromine atoms and a hydroxyl group on the phenyl ring makes it a versatile building block for further functionalization. Our product is rigorously tested for purity and consistency, ensuring reliable performance in your laboratory applications. Available in various quantities to suit your research needs, it is supplied with comprehensive analytical data including HPLC, NMR, and MS spectra.

  • CAS No: 2973-78-6
  • Molecular Formula: C8H6Br2O2
  • Molecular Weight: 293.94
  • Exact Mass: 293.87141
  • Monoisotopic Mass: 291.87345
  • IUPAC Name: 1-(3,5-dibromo-4-hydroxyphenyl)ethanone
  • SMILES: CC(=O)C1=CC(=C(C(=C1)Br)O)Br
  • Synonyms: 1-(3,5-Dibromo-4-hydroxyphenyl)ethan-1-one, EINECS 220-750-4, DTXSID70183071, NSC 41698, DTXCID80105562

Application

1-(3,5-Dibromo-4-hydroxyphenyl)ethan-1-one is commonly used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sites allow for further modifications, making it useful in the development of brominated bioactive compounds. Researchers also employ this compound in the study of halogenated aromatic systems and their properties. Its structural features make it a candidate for investigating enzyme inhibition and receptor binding studies.

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