Date published: 2026-3-30

1-800-457-3801

SCBT Portrait Logo
Seach Input

2,3,4,5,6-Pentafluorocinnamic acid (CAS 719-60-8)

0.0(0)
Write a reviewAsk a question

Alternate Names:
3-(Pentafluorophenyl)acrylic acid; 3-(Pentafluorophenyl)prop-2-enoic acid
CAS Number:
719-60-8
Molecular Weight:
238.11
Molecular Formula:
C9H3F5O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

2,3,4,5,6-Pentafluorocinnamic acid (PFPA) is a versatile fluorinated molecule extensively utilized in scientific applications spanning organic synthesis, analytical chemistry, and biochemistry. Derived from cinnamic acid, an aromatic carboxylic acid, 2,3,4,5,6-Pentafluorocinnamic acid presents as a white, crystalline solid. 2,3,4,5,6-Pentafluorocinnamic acid finds extensive usage in various scientific research applications. In organic synthesis, it serves as a reagent for synthesizing diverse organic compounds. Additionally, it plays a role in analytical chemistry by enabling the detection and quantification of various organic compounds. In the field of biochemistry, 2,3,4,5,6-Pentafluorocinnamic acid acts as a substrate in enzyme assays and as a ligand in protein-ligand binding assays. Regarding its interaction with enzymes, 2,3,4,5,6-Pentafluorocinnamic acid serves as a substrate for a range of enzymes including esterases, amidases, and lipases. Furthermore, it acts as a ligand for proteins such as receptors and enzymes, forming interactions through hydrogen bonding and hydrophobic interactions. The binding of 2,3,4,5,6-Pentafluorocinnamic acid to these proteins and enzymes can influence their activity and function, making it a valuable compound for understanding their mechanisms.


2,3,4,5,6-Pentafluorocinnamic acid (CAS 719-60-8) References

  1. Characterisation of organometallic and coordination compounds by solvent-free matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry.  |  Wyatt, MF., et al. 2008. Analyst. 133: 47-8. PMID: 18087611
  2. Structural modification of the highly potent peptide bradykinin B1 receptor antagonist B9958.  |  Gera, L., et al. 2008. Int Immunopharmacol. 8: 289-92. PMID: 18182242
  3. Mapping the structural requirements of inducers and substrates for decarboxylation of weak acid preservatives by the food spoilage mould Aspergillus niger.  |  Stratford, M., et al. 2012. Int J Food Microbiol. 157: 375-83. PMID: 22726726
  4. Matrix-assisted laser desorption/ionization sample preparation optimization for structural characterization of poly(styrene-co-pentafluorostyrene) copolymers.  |  Tisdale, E., et al. 2014. Anal Chim Acta. 808: 151-62. PMID: 24370101
  5. Glow flow ionization mass spectrometry of small molecules. A comparison of a glow flow ionization source ('GlowFlow') with electrospray ionization and atmospheric pressure chemical ionization.  |  Owen, RN., et al. 2022. Rapid Commun Mass Spectrom. 36: e9327. PMID: 35610187
  6. Synthesis and binding of new polyfluorinated aryl azides to alpha-chymotrypsin. New reagents for photoaffinity labeling.  |  Soundararajan, N., et al. 1993. Bioconjug Chem. 4: 256-61. PMID: 8218481

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,3,4,5,6-Pentafluorocinnamic acid, 10 g

sc-280296
10 g
$459.00