Date published: 2026-4-5

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Ferrocenecarboxaldehyde (CAS 12093-10-6)

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Alternate Names:
Cyclopentadienyl(formylcyclopentadienyl)iron
Application:
Ferrocenecarboxaldehyde is used to prepare chiral ferrocene aziridinylmethanols for selective azomethine ylide cycloaddtion
CAS Number:
12093-10-6
Molecular Weight:
214.04
Molecular Formula:
C11H10FeO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ferrocenecarboxaldehyde is a chemical compound that functions as a versatile building block in organic synthesis. Its mode of action involves its ability to undergo various reactions, including condensation, oxidation, and reduction, to form a wide range of complex organic molecules. Ferrocenecarboxaldehyde is known for its reactivity with nucleophiles, allowing for the formation of carbon-carbon and carbon-heteroatom bonds. Ferrocenecarboxaldehyde can participate in cross-coupling reactions, enabling the creation of diverse molecular structures. Its unique molecular structure and reactivity make it the development of novel organic compounds in and development settings.


Ferrocenecarboxaldehyde (CAS 12093-10-6) References

  1. Ferrocenecarboxaldehyde labeled DNA probe for the study on DNA damage and protection.  |  Xu, C., et al. 2000. Fresenius J Anal Chem. 367: 593-5. PMID: 11225838
  2. Determination of structural parameters for ferrocenecarboxaldehyde using Fourier transform microwave spectroscopy.  |  Subramanian, R., et al. 2005. J Chem Phys. 123: 054317. PMID: 16108649
  3. Thermal immobilization of ferrocene derivatives on (111) surface of n-type silicon: parallel between vinylferrocene and ferrocenecarboxaldehyde.  |  Tajimi, N., et al. 2007. Langmuir. 23: 3193-8. PMID: 17274636
  4. Amperometric sensor based on ferrocene-modified multiwalled carbon nanotube nanocomposites as electron mediator for the determination of glucose.  |  Qiu, JD., et al. 2009. Anal Biochem. 385: 264-9. PMID: 19100707
  5. (1R,2R)-N,N'-Bis(ferrocenylmeth-yl)-1,2-diphenyl-ethane-1,2-diamine.  |  Guo, Y., et al. 2010. Acta Crystallogr Sect E Struct Rep Online. 66: m989. PMID: 21588210
  6. Specificity of glucose oxidase from Penicillium funiculosum 46.1 towards some redox mediators.  |  Semashko, T., et al. 2013. Appl Biochem Biotechnol. 171: 1739-49. PMID: 23996117
  7. Effect of some redox mediators on FAD fluorescence of glucose oxidase from Penicillium adametzii LF F-2044.1.  |  Mikhailova, R., et al. 2015. Enzyme Microb Technol. 72: 10-5. PMID: 25837502
  8. One-pot sonochemical synthesis of ferrocenyl derivatives via a three-component reaction in aqueous media.  |  Cappelletti, L., et al. 2015. Ultrason Sonochem. 27: 30-36. PMID: 26186817
  9. Synthesis, characterization and antibacterial behavior of water-soluble carbosilane dendrons containing ferrocene at the focal point.  |  Lozano-Cruz, T., et al. 2015. Dalton Trans. 44: 19294-304. PMID: 26489707
  10. Use of one- and two-mediator systems for developing a BOD biosensor based on the yeast Debaryomyces hansenii.  |  Zaitseva, AS., et al. 2017. Enzyme Microb Technol. 98: 43-51. PMID: 28110663
  11. Nanoconjugates of ferrocene and carbon-encapsulated iron nanoparticles as sensing platforms for voltammetric determination of ceruloplasmin in blood.  |  Sęk, JP., et al. 2018. Biosens Bioelectron. 102: 490-496. PMID: 29195219
  12. Attenuation of hexaconazole induced oxidative stress by folic acid, malic acid and ferrocenecarboxaldehyde in an invertebrate model Bombyx mori.  |  Ashraf, H., et al. 2022. Heliyon. 8: e12577. PMID: 36636222
  13. Acceptor properties of 'carbon nanotubes-redox-active polymer based on bovine serum albumin modified with ferrocenecarboxaldehyde' composite for creating a BOD biosensor with Blastobotrys adeninivorans BKM Y-2677 yeast.  |  Sergeevna, KA., et al. 2023. 3 Biotech. 13: 112. PMID: 36883049

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ferrocenecarboxaldehyde, 5 g

sc-239994
5 g
$63.00