Date published: 2026-5-9

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2-Formylphenoxyacetic acid (CAS 6280-80-4)

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CAS Number:
6280-80-4
Molecular Weight:
180.16
Molecular Formula:
C9H8O4
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-Formylphenoxyacetic acid is an organic compound classified as a phenoxyacetic acid. It holds significant importance as an intermediate compound in the synthesis of various compounds. Several synthetic pathways exist for the production of 2-Formylphenoxyacetic acid, and its applications in scientific research are diverse. Additionally, 2-Formylphenoxyacetic acid finds utility in the creation of polymers such as polyphenols, as well as in the synthesis of polyamides, polyesters, dyes, and optical materials. As an intermediate compound, 2-Formylphenoxyacetic acid assumes a catalytic role in various reactions, leading to the formation of desired products. Although the precise mechanism of action remains incompletely understood, it is believed to participate in the establishment of a covalent bond between the reactants.


2-Formylphenoxyacetic acid (CAS 6280-80-4) References

  1. A self-replicating ligase ribozyme.  |  Paul, N. and Joyce, GF. 2002. Proc Natl Acad Sci U S A. 99: 12733-40. PMID: 12239349
  2. Synthesis, characterization and antibacterial activity of azomethine derivatives derived from 2-formylphenoxyacetic acid.  |  Iqbal, A., et al. 2007. Molecules. 12: 245-54. PMID: 17846575
  3. Synthesis and spectroscopic studies of new Schiff bases.  |  Siddiqui, HL., et al. 2006. Molecules. 11: 206-11. PMID: 17962791
  4. Design, synthesis and DNA binding activities of late first row transition metal(II) complexes of bi- functional tri - and tetratopic imines.  |  Netalkar, PP., et al. 2012. Spectrochim Acta A Mol Biomol Spectrosc. 97: 762-70. PMID: 22902573
  5. In situ Bronsted-Lowry acid catalyzed syntheses, characterization, single crystal XRD, electronic spectral-, DPPH radical scavenging-, and DNA protection studies of aryl-3,3'-bis(indolyl)methanes.  |  Suresh Kumar, GS., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 123: 249-56. PMID: 24398468
  6. Titania-promoted carboxylic acid alkylations of alkenes and cascade addition-cyclizations.  |  Manley, DW., et al. 2014. J Org Chem. 79: 1386-98. PMID: 24437519
  7. Molecular structure investigation of organic cocrystals of 1,10-phenanthroline-5,6-dione with aryloxyacetic acid: a combined experimental and theoretical study.  |  Suresh Kumar, GS., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 132: 465-76. PMID: 24887507
  8. Synthesis and antibacterial activity of Schiff bases and amines derived from alkyl 2-(2-formyl-4-nitrophenoxy)alkanoates.  |  Goszczyńska, A., et al. 2015. Med Chem Res. 24: 3561-3577. PMID: 26213456
  9. Metabolism of 4-chloro-2-methylphenoxyacetate by a soil pseudomonad. Preliminary evidence for the metabolic pathway.  |  Gaunt, JK. and Evans, WC. 1971. Biochem J. 122: 519-26. PMID: 5123885
  10. Effects of antibiotics on platelet functions in human plasma in vitro and dog plasma in vivo.  |  Genua, MI., et al. 1980. J Pharm Sci. 69: 1282-4. PMID: 7452456
  11. Binding of toxic metabolites of isoniazid by aconiazide.  |  Held, HR. and Landi, S. 1980. J Pharm Sci. 69: 1284-7. PMID: 7452457
  12. Pharmacokinetic evaluation of aconiazide, a potentially less toxic isoniazid prodrug.  |  Peloquin, CA., et al. 1994. Pharmacotherapy. 14: 415-23. PMID: 7937278
  13. Molecular cloning, expression and catalytic activity of a human AKR7 member of the aldo-keto reductase superfamily: evidence that the major 2-carboxybenzaldehyde reductase from human liver is a homologue of rat aflatoxin B1-aldehyde reductase.  |  Ireland, LS., et al. 1998. Biochem J. 332 (Pt 1): 21-34. PMID: 9576847

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Formylphenoxyacetic acid, 25 g

sc-230358
25 g
$79.00