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Cupric acetate monohydrate

Base Information Edit
  • Chemical Name:Cupric acetate monohydrate
  • CAS No.:6046-93-1
  • Molecular Formula:Cu(C2H4O2)2.H2O
  • Molecular Weight:199.651
  • Hs Code.:29152900
  • Mol file:6046-93-1.mol
Cupric acetate monohydrate

Synonyms:Copper(2+) acetate monohydrate;Copper(II) acetatemonohydrate;copper(2+) acetate hydrate (1:2:1);acetic acid, copper(2+) salt, hydrate (2:1:1);

Suppliers and Price of Cupric acetate monohydrate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TCI Chemical
  • Copper(II) Acetate Monohydrate >95.0%(T)
  • 500g
  • $ 62.00
  • TCI Chemical
  • Copper(II) Acetate Monohydrate >95.0%(T)
  • 25g
  • $ 26.00
  • Strem Chemicals
  • Copper(II) acetate monohydrate, 98+% (ACS)
  • 50g
  • $ 18.00
  • Strem Chemicals
  • Copper(II) acetate monohydrate, 98+% (ACS)
  • 1kg
  • $ 220.00
  • Strem Chemicals
  • Copper(II) acetate monohydrate, 98+% (ACS)
  • 250g
  • $ 73.00
  • Sigma-Aldrich
  • Copper(II) acetate monohydrate puriss. p.a., ≥99.0% (RT)
  • 100g
  • $ 72.80
  • Sigma-Aldrich
  • Copper(II) acetate monohydrate for analysis EMSURE ACS
  • 1027110250
  • $ 170.00
  • Sigma-Aldrich
  • Copper(II) acetate monohydrate for analysis EMSURE? ACS
  • 250 g
  • $ 162.80
  • Sigma-Aldrich
  • Copper(II) acetate monohydrate ACS reagent, ≥98%
  • 500g
  • $ 206.00
  • Sigma-Aldrich
  • Copper(II) acetate monohydrate 99.99% trace metals basis
  • 10g
  • $ 171.00
Total 114 raw suppliers
Chemical Property of Cupric acetate monohydrate Edit
Chemical Property:
  • Appearance/Colour:Dark green small crystal with odour of acetic acid 
  • Melting Point:115 °C 
  • Boiling Point:117.1 °C at 760 mmHg 
  • Flash Point:40 °C 
  • PSA:89.49000 
  • Density:1.882 
  • LogP:-2.55440 
  • Storage Temp.:Store at +5°C to +30°C. 
  • Solubility.:72g/l 
  • Water Solubility.:72 g/L (20 ºC) 
Purity/Quality:

99.9% *data from raw suppliers

Copper(II) Acetate Monohydrate >95.0%(T) *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn; DangerousN; IrritantXi 
  • Hazard Codes:Xn,N,Xi,C 
  • Statements: 22-36/37/38-50/53-34 
  • Safety Statements: 36/37/39-60-61-36-26-45 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Uses Copper(II) acetate is used as a pigment for ceramics; in the manufacture of Paris green; in textile dyeing; as a fungicide; and as a catalyst.Copper(II) acetate monohydrate is used in DNA extraction in biochemical applications. It is also used as a catalyst or oxidizing agent in organic syntheses.Catalyst for activation of alcohols as greener alkylating reagents.Copper-Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading. Cupric acetate monohydrate can be used in preparation of Fehling's reagent for sugars Copper(II) acetate monohydrate is used in formation of Cu chelates of ?-dicarbonyl compounds as a means of purification and in the eglinton (modified glaser) coupling of terminal alkynes. It is also used as a catalyst for the michael reaction giving increased yields and absence of side-reactions. It Promotes ullmann-type C-O and C-N coupling reactions of arylboronic acids with phenols, amines and various other nitrogen derivatives. It is also used in biochemical applications such as DNA extraction. Catalyst for activation of alcohols as greener alkylating reagentsCopper-Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading
Technology Process of Cupric acetate monohydrate

There total 37 articles about Cupric acetate monohydrate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In dichloromethane; solvent-removed, crystd. (CH2Cl2/Et2O); Kinetics;
DOI:10.1021/ja075575b
Guidance literature:
In dichloromethane; solvent-removed, crystd. (CH2Cl2/Et2O); Kinetics;
DOI:10.1021/ja075575b
Guidance literature:
In dichloromethane; solvent-removed, crystd. (CH2Cl2/Et2O); Kinetics;
DOI:10.1021/ja075575b
Refernces Edit

Synthesis of [(arylselanyl)alkyl]-1,2,3-triazoles by copper-catalyzed 1,3-dipolar cycloaddition of (arylselanyl)alkynes with benzyl azides

10.1055/s-0031-1291135

The study focuses on the copper-catalyzed 1,3-dipolar cycloaddition of (arylselanyl)alkynes with benzyl azides, producing a series of novel [(arylselanyl)alkyl]-1,2,3-triazoles. This reaction, known as click chemistry, was performed under mild conditions using copper(II) acetate monohydrate and sodium ascorbate as catalysts. Various substituted benzyl azides, both electron-withdrawing and electron-donating, were reacted with different (arylselanyl)alkynes, yielding high amounts of selenium-containing triazoles. The synthesized compounds show potential for biological applications, expanding the utility of selenium-containing heterocycles in organic chemistry.

Synthesis of Mesoionic Isoquinolines by Rhodium(III)-Catalyzed C-H Activation

10.1002/chem.201504245

The research focuses on the synthesis of mesoionic isoquinoline derivatives, which are significant intermediates for constructing biologically active compounds. The study aims to develop an efficient method for their synthesis through RhIII (rhodium(III)-catalyzed) C-H activation and annulation with alkynes, using oxygen as an internal anion source. The researchers concluded that this approach is simple, efficient, and has a broad substrate scope, leading to the preparation of unique mesoionic isoquinoline salts for the first time. The chemicals used in the process include hydroxyl-substituted benzaldimines as substrates, alkynes, [{Cp*RhCl2}2] as the catalyst, Cu(OAc)2·H2O as an additive, TsOH (p-toluenesulfonic acid) as an acid, and various solvents such as ethanol, methanol, and dichloromethane for the reaction and purification steps. The study also explored the effects of different substituents on the benzaldimines and alkynes, demonstrating the versatility of the method. The researchers are further investigating the catalytic mechanism and potential applications of this coupling reaction in the synthesis of complex molecules and the synthetic utility of the mesoionic isoquinoline derivatives.

Copper(II) and nickel(II) complexes of a tetradentate ligand containing an N,N'-bis(salicylidene)dodecane-1, 10-diamine core

10.1080/15421400802714098

The study focuses on the synthesis and characterization of Copper(II) and Nickel(II) complexes of a tetradentate Schiff base ligand containing an N,N′-Bis(Salicylidene)Dodecane-1,10-Diamine core. The research investigates the self-assembly and liquid-crystalline properties of these complexes using variable temperature powder X-ray diffraction. The study explores the relationship between the molecular shape and the mesogenic performances, and discusses the potential applications of these molecular materials in the field of magnetic molecule-based devices. The results show that the complexes exhibit thermotropic liquid crystalline behavior, and the influence of the metal center on the mesomorphic properties is also discussed. The study contributes to the development of new functional liquid crystals for use in molecule-based magnetic devices.

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