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O této položce
Lineární vzorec:
Cu(CO2CH3)2
Číslo CAS:
Molekulová hmotnost:
181.63
UNSPSC Code:
12352302
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-553-3
Beilstein/REAXYS Number:
3595638
MDL number:
Assay:
98%
Form:
powder or crystals
Technický servis
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Dovolte nám, abychom vám pomohlivapor density
6.9 (vs air)
Quality Segment
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.
sustainability
Greener Alternative Product
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
General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
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
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
Catalyst for greener amine synthesis by reductive amination with hydrogen gas.
Copper-catalyzed reductive amination of aromatic and aliphatic ketones with anilines using environmental-friendly molecular hydrogen
Copper(II) acetate is used as a catalyst:
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
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Výstražné slovo
Danger
Kódy nebezpečí
Bezpečnostní pokyny
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
Skladovací třída
8B - Non-combustible corrosive hazardous materials
Co se děje?
WGK 3
Bod vzplanutí (°F)
does not flash
Bod vzplanutí (°C)
does not flash
PPE (osobní ochranné prostředky)
dust mask type N95 (US), Eyeshields, Gloves
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