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Atomfair 2-Fluoro-6-(trifluoromethyl)benzoic acid C8H4F4O2
Description 2-Fluoro-6-(trifluoromethyl)benzoic acid (CAS No. 32890-94-1) is a high-purity fluorinated aromatic carboxylic acid with the molecular formula C8H4F4O2. This compound features a benzoic acid core substituted with a fluorine atom at the 2-position and a trifluoromethyl group at the 6-position, offering unique electronic and steric properties for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this reagent is rigorously tested for consistency (??98% purity by HPLC) and supplied in sealed packaging to ensure stability. Its structural motifs are valuable for designing bioactive molecules, ligands, and fluorinated polymers. Store in a cool, dry place under inert conditions…
Description
Description
2-Fluoro-6-(trifluoromethyl)benzoic acid (CAS No. 32890-94-1) is a high-purity fluorinated aromatic carboxylic acid with the molecular formula C8H4F4O2. This compound features a benzoic acid core substituted with a fluorine atom at the 2-position and a trifluoromethyl group at the 6-position, offering unique electronic and steric properties for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this reagent is rigorously tested for consistency (??98% purity by HPLC) and supplied in sealed packaging to ensure stability. Its structural motifs are valuable for designing bioactive molecules, ligands, and fluorinated polymers. Store in a cool, dry place under inert conditions to maintain integrity.
- CAS No: 32890-94-1
- Molecular Formula: C8H4F4O2
- Molecular Weight: 208.11
- Exact Mass: 208.01474201
- Monoisotopic Mass: 208.01474201
- IUPAC Name: 2-fluoro-6-(trifluoromethyl)benzoic acid
- SMILES: C1=CC(=C(C(=C1)F)C(=O)O)C(F)(F)F
- Synonyms: 2-Fluoro-6-(trifluoromethyl)benzoic acid, 32890-94-1, DTXSID40350793, DTXCID80301860, 626-017-9
Application
2-Fluoro-6-(trifluoromethyl)benzoic acid serves as a versatile building block in medicinal chemistry for the synthesis of fluorinated drug candidates, leveraging its electron-withdrawing groups to modulate pharmacokinetics. It is also employed in agrochemical research to develop herbicides and pesticides with enhanced bioavailability. In materials science, this compound aids in creating fluorinated polymers with improved thermal and chemical resistance.
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