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Atomfair 3,5-Difluoro-2-methoxybenzaldehyde C8H6F2O2

Description 3,5-Difluoro-2-methoxybenzaldehyde (CAS No. 131782-50-8) is a high-purity fluorinated aromatic aldehyde with the molecular formula C8H6F2O2. This compound features a benzaldehyde core substituted with two fluorine atoms at the 3 and 5 positions and a methoxy group at the 2 position, offering unique electronic and steric properties for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and materials science, this reagent is rigorously tested for consistency and purity (typically ??95% by GC or HPLC). Packaged under inert gas to ensure stability, it is available in quantities ranging from milligrams to kilograms to meet both lab-scale and bulk production needs.…

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Description

Description

3,5-Difluoro-2-methoxybenzaldehyde (CAS No. 131782-50-8) is a high-purity fluorinated aromatic aldehyde with the molecular formula C8H6F2O2. This compound features a benzaldehyde core substituted with two fluorine atoms at the 3 and 5 positions and a methoxy group at the 2 position, offering unique electronic and steric properties for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and materials science, this reagent is rigorously tested for consistency and purity (typically ??95% by GC or HPLC). Packaged under inert gas to ensure stability, it is available in quantities ranging from milligrams to kilograms to meet both lab-scale and bulk production needs. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 131782-50-8
  • Molecular Formula: C8H6F2O2
  • Molecular Weight: 172.13
  • Exact Mass: 172.03358575
  • Monoisotopic Mass: 172.03358575
  • IUPAC Name: 3,5-difluoro-2-methoxybenzaldehyde
  • SMILES: COC1=C(C=C(C=C1F)F)C=O
  • Synonyms: 3,5-Difluoro-2-methoxybenzaldehyde, 131782-50-8, Benzaldehyde, 3,5-difluoro-2-methoxy-, 3,5-difluoro-2-methoxy-benzaldehyde, C8H6F2O2

Application

3,5-Difluoro-2-methoxybenzaldehyde serves as a versatile building block in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. Its electron-withdrawing fluorine atoms enhance reactivity in cross-coupling reactions, while the methoxy group directs electrophilic substitutions. Researchers also utilize it to develop liquid crystal materials and fluorescent probes due to its aromatic stability and tunable polarity. This compound is especially valuable in medicinal chemistry for designing kinase inhibitors and CNS-active molecules.

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