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Atomfair 2,3,4,5-Tetrafluorobenzoic acid C7H2F4O2
Description 2,3,4,5-Tetrafluorobenzoic Acid (CAS No. 1201-31-6) is a high-purity fluorinated aromatic carboxylic acid with the molecular formula C7H2F4O2. This compound is characterized by its four fluorine substituents on the benzene ring, which impart unique electronic and steric properties, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 2,3,4,5-tetrafluorobenzoic acid , and it is supplied as a white to off-white crystalline powder with a purity of ??98% (HPLC). Suitable for use in cross-coupling reactions, ligand synthesis, and as a building block for advanced materials, this product is rigorously tested for consistency and quality. Store in…
Description
Description
2,3,4,5-Tetrafluorobenzoic Acid (CAS No. 1201-31-6) is a high-purity fluorinated aromatic carboxylic acid with the molecular formula C7H2F4O2. This compound is characterized by its four fluorine substituents on the benzene ring, which impart unique electronic and steric properties, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 2,3,4,5-tetrafluorobenzoic acid, and it is supplied as a white to off-white crystalline powder with a purity of ??98% (HPLC). Suitable for use in cross-coupling reactions, ligand synthesis, and as a building block for advanced materials, this product is rigorously tested for consistency and quality. Store in a cool, dry place, protected from light and moisture.
- CAS No: 1201-31-6
- Molecular Formula: C7H2F4O2
- Molecular Weight: 194.08
- Exact Mass: 193.99909195
- Monoisotopic Mass: 193.99909195
- IUPAC Name: 2,3,4,5-tetrafluorobenzoic acid
- SMILES: C1=C(C(=C(C(=C1F)F)F)F)C(=O)O
- Synonyms: 2,3,4,5-Tetrafluorobenzoic acid, 1201-31-6, Benzoic acid, 2,3,4,5-tetrafluoro-, SFKRXQKJTIYUAG-UHFFFAOYSA-, DTXSID80304992
Application
2,3,4,5-Tetrafluorobenzoic acid is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty materials. Its electron-withdrawing fluorine atoms enhance reactivity in nucleophilic aromatic substitution (SNAr) and metal-catalyzed coupling reactions. Researchers employ it to develop fluorinated liquid crystals, polymers, and ligands for catalysis. In medicinal chemistry, it serves as a scaffold for designing bioactive molecules with improved metabolic stability and lipophilicity.
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