Atomfair 3,5-Dibromobenzaldehyde C7H4Br2O

Description 3,5-Dibromobenzaldehyde (CAS No. 56990-02-4) is a high-purity aromatic aldehyde compound with the molecular formula C7H4Br2O . This white to off-white crystalline solid is a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. With a molecular weight of 263.92 g/mol, it features two bromine substituents at the 3- and 5-positions of the benzaldehyde ring, enhancing its reactivity in cross-coupling reactions such as Suzuki-Miyaura and Ullmann couplings. Our product is rigorously tested for purity (typically ??97% by HPLC) and is supplied in sealed containers under inert gas to ensure stability. Ideal for researchers in…

Description

Description

3,5-Dibromobenzaldehyde (CAS No. 56990-02-4) is a high-purity aromatic aldehyde compound with the molecular formula C7H4Br2O. This white to off-white crystalline solid is a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. With a molecular weight of 263.92 g/mol, it features two bromine substituents at the 3- and 5-positions of the benzaldehyde ring, enhancing its reactivity in cross-coupling reactions such as Suzuki-Miyaura and Ullmann couplings. Our product is rigorously tested for purity (typically ??97% by HPLC) and is supplied in sealed containers under inert gas to ensure stability. Ideal for researchers in medicinal chemistry and material science, it is packaged in amber glass vials or bulk quantities with customizable options.

  • CAS No: 56990-02-4
  • Molecular Formula: C7H4Br2O
  • Molecular Weight: 263.91
  • Exact Mass: 263.86084
  • Monoisotopic Mass: 261.86289
  • IUPAC Name: 3,5-dibromobenzaldehyde
  • SMILES: C1=C(C=C(C=C1Br)Br)C=O
  • Synonyms: 3,5-Dibromobenzaldehyde, 56990-02-4, DTXSID80347485, DTXCID10298557, 611-441-9

Application

3,5-Dibromobenzaldehyde serves as a key building block in the synthesis of brominated pharmaceutical intermediates and liquid crystal materials. It is widely used in palladium-catalyzed cross-coupling reactions to construct complex biaryl structures for drug discovery. The compound also finds applications in the development of organic electronic materials due to its electron-withdrawing bromine groups. Researchers utilize it to prepare ligands for catalysis and as a precursor in the synthesis of antifungal and antibacterial agents.

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