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Copper(I) acetate (CAS 598-54-9)

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Alternate Names:
Cuprous acetate
Application:
Copper(I) acetate is used in experiments to assemble complexes with various ligands
CAS Number:
598-54-9
Purity:
≥97%
Molecular Weight:
122.59
Molecular Formula:
C2H3CuO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Copper(I) acetate, also known as cuprous acetate, may be used in experiments to assemble complexes with various ligands, thus forming compounds with interesting magnetic properties. Has been used as a mediator for cyclopropylation of azoles, amides and sulfonamides. Copper(I) acetate exhibits the form of a white, crystalline solid that readily dissolves in water. This compound finds widespread employment as a reagent in both organic and inorganic chemistry due to its versatility. Its utility spans numerous domains, encompassing research and industrial applications. Notably, Copper(I) acetate serves as a catalyst, an oxidizing agent, and a reagent for synthesizing diverse compounds. Within scientific research, Copper(I) acetate enjoys frequent usage as a reagent. It exerts its catalytic influence during the organic compound synthesis process, while also playing a pivotal role in the oxidation of alcohols, aldehydes, and ketones. Its functionality extends further to the creation of various compounds, including inorganic salts, pharmaceuticals, and pigments. Furthermore, Copper(I) acetate′s contribution encompasses the synthesis of organometallic compounds, like Cuprous acetate(I) acetylides and Cuprous acetate(I) alkyls. The mechanism underlying the action of cuprous acetate hinges on its capacity to oxidize both organic and inorganic substances. In the context of organic compounds, the oxidation process typically commences through the interaction of Copper(I) acetate with an acid like acetic acid. This interplay generates cupric acetate, subsequently engaging with the organic compound to yield the desired end product. In the realm of inorganic compounds, the initiation of oxidation is instigated by the reaction between Copper(I) acetate and a base, such as sodium hydroxide.


Copper(I) acetate (CAS 598-54-9) References

  1. Synthesis, magnetic behaviour, and X-ray structures of dinuclear copper complexes with multiple bridges. Efficient and selective catalysts for polymerization of 2,6-dimethylphenol.  |  Murugavel, R., et al. 2007. Dalton Trans. 2405-10. PMID: 17844662
  2. The role of p53 in the trafficking of copper-64 to tumor cell nuclei.  |  Eiblmaier, M., et al. 2008. Cancer Biol Ther. 7: 63-9. PMID: 17938576
  3. Copper-mediated N-cyclopropylation of azoles, amides, and sulfonamides by cyclopropylboronic acid.  |  Bénard, S., et al. 2008. J Org Chem. 73: 6441-4. PMID: 18610980
  4. Asymmetric copper(I)-catalyzed Henry reaction with an aminoindanol-derived bisoxazolidine ligand.  |  Spangler, KY. and Wolf, C. 2009. Org Lett. 11: 4724-7. PMID: 19743819
  5. Copper(I) acetate-catalyzed azide-alkyne cycloaddition for highly efficient preparation of 1-(pyridin-2-yl)-1,2,3-triazoles.  |  Zhang, Q., et al. 2012. Org Biomol Chem. 10: 2847-54. PMID: 22388558
  6. Copper-induced N-N bond cleavage results in an octanuclear expanded-core grid-like complex.  |  White, NG., et al. 2012. Chem Commun (Camb). 48: 6229-31. PMID: 22595882
  7. Organo-gallium/indium chalcogenide complexes of copper(I): molecular structures and thermal decomposition to ternary semiconductors.  |  Kluge, O., et al. 2014. Chemistry. 20: 1318-31. PMID: 24338681
  8. Degradation of triphenylborane-pyridine antifouling agent in water by copper ions.  |  Tsuboi, A., et al. 2013. Environ Technol. 34: 2835-40. PMID: 24527648
  9. π-Excess aromatic σ²-P ligands: synthesis and structure of an unprecedented μ²-P-1,3-benzazaphosphole bridged tetranuclear copper(I) acetate complex.  |  Ghalib, M., et al. 2015. Dalton Trans. 44: 1769-74. PMID: 25470656
  10. Tandem Radical Fluoroalkylation-Cyclization: Synthesis of Tetrafluoro Imidazopyridines.  |  Charpentier, J., et al. 2016. Org Lett. 18: 756-9. PMID: 26820164
  11. A new synthetic route to in-chain metallopolymers via copper(i) catalyzed azide-platinum-acetylide iClick.  |  Beto, CC., et al. 2017. Chem Commun (Camb). 53: 9934-9937. PMID: 28829464
  12. Intramolecular Ring-Expansion Reaction (RER) and Intermolecular Coordination of In Situ Generated Cyclic (Amino)(aryl)carbenes (cAArCs).  |  Lorkowski, J., et al. 2019. Chemistry. 25: 11365-11374. PMID: 31276243
  13. Atomic Layer Deposition of Photoconductive Cu2O Thin Films.  |  Iivonen, T., et al. 2019. ACS Omega. 4: 11205-11214. PMID: 31460221

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Copper(I) acetate, 1 g

sc-234411
1 g
$45.00