Molecular structure of Ferroceneboronic acid, CAS Number: 12152-94-2
Ferroceneboronic acid (CAS 12152-94-2)
Alternate Names:
(Boronocyclopentadienyl)cyclopentadienyl iron
Application:
Ferroceneboronic acid is a redox-acitce electrochemical probe
CAS Number:
12152-94-2
Molecular Weight:
229.85
Molecular Formula:
C10H11BFeO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Ferroceneboronic acid is synthesized through a direct reaction between ferrocenyl Grignard reagents and trimethyl borate, followed by hydrolysis. The boronic acid group in ferroceneboronic acid can act as a Lewis acid catalyst in various organic reactions. The ferrocene moiety can potentially stabilize the transition state of the reaction or modify the electronic properties of the boronic acid, affecting the catalytic activity. Researchers investigate the mechanistic aspects of these reactions and the reusability of the ferroceneboronic acid catalyst. The electrochemical properties of ferroceneboronic acid are significant due to the redox-active ferrocene core. Studies focus on the electrochemical behavior of this compound and its potential applications in sensors or electronic devices.
Ferroceneboronic acid (CAS 12152-94-2) References
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- Electrochemical determination of catechin, protocatechuic acid, and L-lactic acid based on voltammetric response of ferroceneboronic acid. | Shi, W., et al. 2014. J AOAC Int. 97: 1742-5. PMID: 25632453
- A sensitive signal-off electrogenerated chemiluminescence biosensing method for the discrimination of DNA hydroxymethylation based on glycosylation modification and signal quenching from ferroceneboronic acid. | Zhang, Y., et al. 2017. Talanta. 170: 546-551. PMID: 28501209
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- Magnetic bead-based electrochemical and colorimetric assays of circulating tumor cells with boronic acid derivatives as the recognition elements and signal probes. | Xia, N., et al. 2021. Talanta. 221: 121640. PMID: 33076160
- Self-healing mechanism and bioelectrochemical interface properties of core-shell guanosine-borate hydrogels. | Wang, H., et al. 2021. J Colloid Interface Sci. 590: 103-113. PMID: 33524710
- Self-Assembly of Functionalized Lipophilic Guanosines into Cation-Free Stacked Guanine-Quartets. | Campitiello, M., et al. 2021. J Org Chem. 86: 9970-9978. PMID: 34279932
- Redox-dependent cytotoxicity of ferrocene derivatives and ROS-activated prodrugs based on ferrocenyliminoboronates. | Věžník, J., et al. 2021. J Inorg Biochem. 224: 111561. PMID: 34385077
- Synthesis, structure and in vitro antiproliferative effects of alkyne-linked 1,2,4-thiadiazole hybrids including erlotinib- and ferrocene-containing derivatives. | Boulhaoua, M., et al. 2021. RSC Adv. 11: 28685-28697. PMID: 35478544
- Ferrocene donor linked to pyridine/pyridinium acceptor via a systematically enlarged π-linker. | Kulhánek, J., et al. 2021. RSC Adv. 11: 38804-38813. PMID: 35493213
- The combination of highly efficient resonance energy transfer in one nanocomposite and ferrocene-quenching for ultrasensitive electrochemiluminescence bioanalysis. | Wang, Y., et al. 2022. Biosens Bioelectron. 210: 114347. PMID: 35550937
- Optimization of Nanohybrid Biosensors Based on Electro-Crosslinked Tannic Acid Capped Nanoparticles/Enzyme. | Savin, R., et al. 2022. Molecules. 27: PMID: 35630787
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Ferroceneboronic acid, 1 g | sc-500783 | 1 g | $265.00 |