vapor density
6.9 (vs air)
Quality Level
Assay
98%
form
powder or crystals
reaction suitability
reaction type: click chemistry
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
greener alternative category
, Aligned
SMILES string
CC(=O)O[Cu]OC(C)=O
InChI
1S/2C2H4O2.Cu/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
InChI key
OPQARKPSCNTWTJ-UHFFFAOYSA-L
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Related Categories
General description
Copper(II) acetate also known as cupric acetate, can be used as a catalyst in various processes in the field of greener chemistry. It is particularly useful in cross-coupling reactions, where it can promote the formation of carbon-carbon or carbon-heteroatom bonds, without the need for hazardous reagents or solvents
Application
Copper-catalyzed reductive amination of aromatic and aliphatic ketones with anilines using environmental-friendly molecular hydrogen
Copper(II) acetate is used as a catalyst:
- In the N-arylation of α-amino esters with p-tolylboronic acid to synthesize biaryls via cross-coupling reactions
- In the the synthesis of substituted isoxazole derivatives
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8B - Non-combustible, corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
does not flash
Flash Point(C)
does not flash
Personal Protective Equipment
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Articles
Copper metal deposition processes are an essential tool for depositing interconnects used in microelectronic applications, giving group 11 (coinage metals: Copper, Silver, and Gold) an important place in atomic layer deposition (ALD) process development.
Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.
Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.
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