Date published: 2026-4-5

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2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid (CAS 652-34-6)

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Application:
2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid is a ligand synthesis reagent
CAS Number:
652-34-6
Purity:
≥96%
Molecular Weight:
210.08
Molecular Formula:
C7H2F4O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid is in materials science, particularly for its role in synthesizing advanced polymers and coatings with enhanced chemical resistance. Due to its fluorinated structure, 2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid hydrate contributes to the study of hydrophobic surfaces, which are useful in creating anti-corrosive and self-cleaning materials. In the field of organic chemistry, 2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid is used to investigate the mechanisms of aromatic substitution reactions, aiding in the understanding of electrophilic and nucleophilic processes on fluorinated aromatic rings. 2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid hydrate is explored in environmental chemistry for its potential in developing more stable and effective herbicides that are less prone to degradation by environmental factors.


2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid (CAS 652-34-6) References

  1. TEAC antioxidant activity of 4-hydroxybenzoates.  |  Tyrakowska, B., et al. 1999. Free Radic Biol Med. 27: 1427-36. PMID: 10641737
  2. Synthesis of certain 2'-deoxyuridine derivatives containing substituted phenoxy groups attached to C-5'; evaluation as potential dUTP analogues.  |  Marriott, JH., et al. 2001. Nucleosides Nucleotides Nucleic Acids. 20: 1691-704. PMID: 11580195
  3. Parallel synthesis and dopamine D3/D2 receptor screening of novel {4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl}carboxamides.  |  Heidler, P., et al. 2005. Bioorg Med Chem. 13: 2009-14. PMID: 15727854
  4. Synthesis and antiplasmodial activity of new N-[3-(4-{3-[(7-chloroquinolin-4-yl)amino]propyl}piperazin-1-yl)propyl]carboxamides.  |  Freitag, M., et al. 2007. Bioorg Med Chem. 15: 2782-8. PMID: 17280835
  5. Synthesis of a series of N6-substituted adenosines with activity against trypanosomatid parasites.  |  Link, A., et al. 2009. Eur J Med Chem. 44: 3665-71. PMID: 19285758
  6. Recent developments in the design and synthesis of hybrid molecules based on aminoquinoline ring and their antiplasmodial evaluation.  |  Kouznetsov, VV. and Gómez-Barrio, A. 2009. Eur J Med Chem. 44: 3091-113. PMID: 19361896
  7. Improved quenched fluorescent probe for imaging of cysteine cathepsin activity.  |  Verdoes, M., et al. 2013. J Am Chem Soc. 135: 14726-30. PMID: 23971698
  8. Live Cell Imaging and Profiling of Cysteine Cathepsin Activity Using a Quenched Activity-Based Probe.  |  Edgington-Mitchell, LE., et al. 2017. Methods Mol Biol. 1491: 145-159. PMID: 27778287
  9. Manipulating Light-Induced Dynamic Macro-Movement and Static Photonic Properties within 1D Isostructural Hydrogen-Bonded Molecular Cocrystals.  |  Li, S., et al. 2020. Angew Chem Int Ed Engl. 59: 22623-22630. PMID: 32875702
  10. Mechanical Motion in Crystals Triggered by Solid State Photochemical [2+2] Cycloaddition Reaction.  |  Khan, S., et al. 2021. Chem Asian J. 16: 2806-2816. PMID: 34355513

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,3,5,6-Tetrafluoro-4-hydroxybenzoic acid, 5 g

sc-225637
5 g
$148.00