Tetrabutylammonium tetrachlorooxorhenate(V) (CAS 53675-30-2)
CAS Number:
53675-30-2
Molecular Weight:
586.48
Molecular Formula:
C16H36Cl4NORe
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Tetrabutylammonium tetrachlorooxorhenate(V) is an inorganic compound with the chemical formula [N(C4H9)4][ReOCl4]. It is a coordination complex containing the tetrachlorooxorhenate(V) anion and tetrabutylammonium cations. This compound is often used as a catalyst or reagent in various chemical reactions, particularly in organic synthesis.
Tetrabutylammonium tetrachlorooxorhenate(V) (CAS 53675-30-2) References
- Synthesis and characterization of novel rhenium(V) tetradentate N2O2 Schiff base monomer and dimer complexes. | Benny, PD., et al. 2003. Inorg Chem. 42: 6519-27. PMID: 14514329
- Novel rhenium chelate system derived from dimercaptosuccinic acid for the selective labeling of biomolecules. | Heinrich, TK., et al. 2005. Inorg Chem. 44: 9930-7. PMID: 16363864
- Cyclic and acyclic oxorhenium(V)-peptide conjugates as new ligands of the human cyclophilin hCyp-18. | Clavaud, C., et al. 2006. Bioconjug Chem. 17: 807-14. PMID: 16704221
- Combinatorial self-assembly of cyclophilin hCyp-18 ligands through rhenium coordination. | Clavaud, C., et al. 2006. Chembiochem. 7: 1352-5. PMID: 16835860
- Preparation and biological characterization of isomeric 188Re(V) oxocomplexes with tetradentate S4 ligands derived from meso-dimercaptosuccinic acid for labeling of biomolecules. | Seifert, S., et al. 2006. Bioconjug Chem. 17: 1601-6. PMID: 17105241
- Synthesis of a technetium-99m labeled tricyclic ganciclovir analog for non-invasive reporter gene expression imaging. | Zhang, Y., et al. 2007. Bioorg Med Chem Lett. 17: 741-4. PMID: 17110103
- Dynamic combinatorial self-assembly of cyclophilin hCyp-18 ligands through oxorhenium coordination. | Clavaud, C., et al. 2008. Chembiochem. 9: 1823-9. PMID: 18604836
- Oxorhenium-mediated assembly of noncyclic selective integrin antagonists: a combinatorial approach. | Aufort, M., et al. 2011. Chembiochem. 12: 583-92. PMID: 21305682
- Synthesis, in vitro screening and in vivo evaluation of cyclic RGD analogs cyclized through oxorhenium and oxotechnetium coordination. | Aufort, M., et al. 2011. Eur J Med Chem. 46: 1779-88. PMID: 21392860
- Chelate oxorhenium to assemble new integrin antagonists. | Le Gal, J., et al. 2011. J Inorg Biochem. 105: 880-6. PMID: 21510913
- Synthesis and evaluation of a novel (99m)Tc-labeled bioreductive probe for tumor hypoxia imaging. | Kimura, S., et al. 2011. Bioorg Med Chem Lett. 21: 7359-62. PMID: 22078213
- Chemical Conversion of Hardly Ionizable Rhenium Aryl Chlorocomplexes with p-Substituted Anilines. | Štícha, M., et al. 2021. Molecules. 26: PMID: 34198782
- Synthesis and characterization of rhenium complexes of 1, 2, 3-trihydroxybenzene as potential antitumor agents. | Kaliba, D., Sticha, M., & Jelinek, I. (2017). Transition Metal Chemistry,. 42,: 211-218.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Tetrabutylammonium tetrachlorooxorhenate(V), 1 g | sc-237021 | 1 g | $505.00 |