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Atomfair 2-Fluoro-4-methylbenzaldehyde C8H7FO

Description 2-Fluoro-4-methylbenzaldehyde (CAS No. 146137-80-6) is a high-purity aromatic aldehyde derivative with the molecular formula C8H7FO. This compound features a fluorine substituent at the 2-position and a methyl 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 advanced material research, this reagent is supplied as a clear to pale-yellow liquid with ??95% purity (GC). Store under inert conditions at 2-8??C to prevent degradation. Suitable for use in Suzuki couplings, Grignard reactions, and as a building block for fluorinated liquid crystals.

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Description

Description

2-Fluoro-4-methylbenzaldehyde (CAS No. 146137-80-6) is a high-purity aromatic aldehyde derivative with the molecular formula C8H7FO. This compound features a fluorine substituent at the 2-position and a methyl 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 advanced material research, this reagent is supplied as a clear to pale-yellow liquid with ??95% purity (GC). Store under inert conditions at 2-8??C to prevent degradation. Suitable for use in Suzuki couplings, Grignard reactions, and as a building block for fluorinated liquid crystals.

  • CAS No: 146137-80-6
  • Molecular Formula: C8H7FO
  • Molecular Weight: 138.14
  • Exact Mass: 138.048093005
  • Monoisotopic Mass: 138.048093005
  • IUPAC Name: 2-fluoro-4-methylbenzaldehyde
  • SMILES: CC1=CC(=C(C=C1)C=O)F
  • Synonyms: 2-Fluoro-4-methylbenzaldehyde, 146137-80-6, DTXSID80380958, DTXCID60331983, 676-421-4

Application

2-Fluoro-4-methylbenzaldehyde serves as a versatile intermediate in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. Its electron-withdrawing fluorine group enhances reactivity in palladium-catalyzed cross-coupling reactions, making it valuable for constructing complex aromatic systems. Researchers also utilize this compound in the development of liquid crystal materials due to its rigid, polarizable structure.

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