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Atomfair 3′,5′-Difluoroacetophenone C8H6F2O
Description 3′,5′-Difluoroacetophenone (CAS No. 123577-99-1) is a high-purity fluorinated aromatic ketone with the molecular formula C8H6F2O and IUPAC name 1-(3,5-difluorophenyl)ethanone . This specialized organic compound is characterized by its two fluorine substituents at the 3 and 5 positions of the acetophenone ring, enhancing its reactivity and utility in advanced synthetic applications. Ideal for pharmaceutical intermediates, material science research, and agrochemical development, our 3′,5′-Difluoroacetophenone is rigorously tested to meet the highest standards of purity and consistency. Available in various quantities, it is supplied with comprehensive analytical data (including GC/MS, HPLC, and1H/13C NMR) to ensure reproducibility in your experiments. Store in a…
Description
Description
3′,5′-Difluoroacetophenone (CAS No. 123577-99-1) is a high-purity fluorinated aromatic ketone with the molecular formula C8H6F2O and IUPAC name 1-(3,5-difluorophenyl)ethanone. This specialized organic compound is characterized by its two fluorine substituents at the 3 and 5 positions of the acetophenone ring, enhancing its reactivity and utility in advanced synthetic applications. Ideal for pharmaceutical intermediates, material science research, and agrochemical development, our 3′,5′-Difluoroacetophenone is rigorously tested to meet the highest standards of purity and consistency. Available in various quantities, it is supplied with comprehensive analytical data (including GC/MS, HPLC, and 1H/13C NMR) to ensure reproducibility in your experiments. Store in a cool, dry place under inert conditions for optimal stability.
- CAS No: 123577-99-1
- Molecular Formula: C8H6F2O
- Molecular Weight: 156.13
- Exact Mass: 156.03867113
- Monoisotopic Mass: 156.03867113
- IUPAC Name: 1-(3,5-difluorophenyl)ethanone
- SMILES: CC(=O)C1=CC(=CC(=C1)F)F
- Synonyms: 3′,5′-Difluoroacetophenone, 123577-99-1, DTXSID90333793, DTXCID00284883, 626-379-8
Application
3′,5′-Difluoroacetophenone serves as a versatile building block in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and bioactive molecules. Its electron-withdrawing fluorine groups make it valuable for cross-coupling reactions and as a precursor for heterocyclic compounds. Researchers also utilize it in material science for designing fluorinated polymers and liquid crystals with tailored properties.
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