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Atomfair 3-Bromo-5-fluorobenzaldehyde C7H4BrFO

Description 3-Bromo-5-fluorobenzaldehyde (CAS No. 188813-02-7) is a high-purity aromatic aldehyde compound with the molecular formula C7H4BrFO . This halogenated benzaldehyde derivative features both bromine and fluorine substituents on the benzene ring, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. The compound is supplied as a crystalline solid with ??98% purity (HPLC), ensuring optimal performance in coupling reactions, nucleophilic additions, and as a precursor for heterocyclic synthesis. Ideal for Suzuki-Miyaura cross-coupling, Vilsmeier-Haack formylation, and Grignard reactions. Packaged under inert gas to prevent oxidation and moisture sensitivity. Available in research quantities (100mg to 10g) with optional COA and…

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Description

Description

3-Bromo-5-fluorobenzaldehyde (CAS No. 188813-02-7) is a high-purity aromatic aldehyde compound with the molecular formula C7H4BrFO. This halogenated benzaldehyde derivative features both bromine and fluorine substituents on the benzene ring, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. The compound is supplied as a crystalline solid with ??98% purity (HPLC), ensuring optimal performance in coupling reactions, nucleophilic additions, and as a precursor for heterocyclic synthesis. Ideal for Suzuki-Miyaura cross-coupling, Vilsmeier-Haack formylation, and Grignard reactions. Packaged under inert gas to prevent oxidation and moisture sensitivity. Available in research quantities (100mg to 10g) with optional COA and NMR spectra upon request.

  • CAS No: 188813-02-7
  • Molecular Formula: C7H4BrFO
  • Molecular Weight: 203.01
  • Exact Mass: 201.94296
  • Monoisotopic Mass: 201.94296
  • IUPAC Name: 3-bromo-5-fluorobenzaldehyde
  • SMILES: C1=C(C=C(C=C1F)Br)C=O
  • Synonyms: 3-bromo-5-fluorobenzaldehyde, 188813-02-7, DTXSID70621206, DTXCID80571960, 801-243-2

Application

3-Bromo-5-fluorobenzaldehyde serves as a critical building block in medicinal chemistry for the synthesis of fluorinated drug candidates, particularly kinase inhibitors and CNS-active compounds. Its dual halogen functionality enables regioselective modifications in palladium-catalyzed cross-coupling reactions. Researchers utilize this compound to develop novel PET radiotracers due to the presence of fluorine-19. It also finds application in materials science as a precursor for liquid crystals and OLED intermediates.

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