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Atomfair 2-Fluoro-4-methoxybenzaldehyde C8H7FO2

Description 2-Fluoro-4-methoxybenzaldehyde (CAS No. 331-64-6) is a high-purity aromatic aldehyde derivative with the molecular formula C8H7FO2. This compound features a fluorine substituent at the 2-position and a methoxy group at the 4-position of the benzaldehyde ring, offering unique reactivity for electrophilic aromatic substitution and nucleophilic addition reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science applications, this reagent is supplied as a crystalline solid with ??98% purity (GC). Store in a cool, dry place under inert atmosphere to ensure stability. Compatible with Grignard reactions, reductive amination, and cross-coupling methodologies.

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Description

Description

2-Fluoro-4-methoxybenzaldehyde (CAS No. 331-64-6) is a high-purity aromatic aldehyde derivative with the molecular formula C8H7FO2. This compound features a fluorine substituent at the 2-position and a methoxy group at the 4-position of the benzaldehyde ring, offering unique reactivity for electrophilic aromatic substitution and nucleophilic addition reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science applications, this reagent is supplied as a crystalline solid with ??98% purity (GC). Store in a cool, dry place under inert atmosphere to ensure stability. Compatible with Grignard reactions, reductive amination, and cross-coupling methodologies.

  • CAS No: 331-64-6
  • Molecular Formula: C8H7FO2
  • Molecular Weight: 154.14
  • Exact Mass: 154.04300762
  • Monoisotopic Mass: 154.04300762
  • IUPAC Name: 2-fluoro-4-methoxybenzaldehyde
  • SMILES: COC1=CC(=C(C=C1)C=O)F
  • Synonyms: 2-Fluoro-4-methoxybenzaldehyde, 331-64-6, UNWQNFJBBWXFBG-UHFFFAOYSA-, DTXSID30370546, DTXCID60321581

Application

2-Fluoro-4-methoxybenzaldehyde serves as a versatile building block in organic synthesis, particularly for constructing fluorinated drug candidates targeting CNS disorders. Its electron-deficient aromatic ring facilitates Suzuki-Miyaura couplings in material science for OLED development. The compound is also employed in asymmetric catalysis studies due to its steric and electronic modulation effects.

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