207780
Copper
powder, <75 μm, 99%
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About This Item
Formule empirique (notation de Hill):
Cu
Numéro CAS:
Poids moléculaire :
63.55
Numéro CE :
Numéro MDL:
Code UNSPSC :
12141711
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Niveau de qualité
Pureté
99%
Forme
powder
Résistivité
1.673 μΩ-cm, 20°C
Taille des particules
<75 μm
Point d'ébullition
2567 °C (lit.)
Pf
1083.4 °C (lit.)
Densité
8.94 g/mL at 25 °C (lit.)
Chaîne SMILES
[Cu]
InChI
1S/Cu
Clé InChI
RYGMFSIKBFXOCR-UHFFFAOYSA-N
Description générale
Copperis a versatile and widely used metal with significant importance in variousfields, particularly in catalysis and material science. In material science,copper is used in various conductive materials due to its excellent electricaland thermal conductivity, ductility, and corrosion resistance. Additionally,copper is also extensively used as a catalyst in various chemical reactions dueto its ability to facilitate electron transfer and promote redox reactions. Itoften acts as a catalyst in various reactions which include reduction, cross-couplingreactions and “click" chemistry (such as copper-catalyzed azide-alkynecycloaddition reactions.
Application
- Photoinduced Copper-Catalyzed Aminoalkylation of Amino-Pendant Olefins.: This study explores the use of copper catalysts in photoinduced aminoalkylation reactions, highlighting the efficiency and potential applications in organic synthesis (Zhang et al., 2023).
- Synthesis of Azoxy Compounds: from Copper Compounds to Mesoporous Silica-Encaged Ultrasmall Copper Catalysts.: This research focuses on the development of copper-based catalysts for the synthesis of azoxy compounds, emphasizing their application in sustainable chemistry (Han et al., 2023).
- Cu-catalyzed enantioselective allylic alkylation with organolithium reagents.: The paper presents a method for enantioselective allylic alkylation using copper catalysts, providing insights into asymmetric synthesis techniques (Hornillos et al., 2017).
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Sol. 1
Code de la classe de stockage
4.1B - Flammable solid hazardous materials
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Les clients ont également consulté
Hiroshi Sato et al.
Science (New York, N.Y.), 343(6167), 167-170 (2013-12-18)
Carbon monoxide (CO) produced in many large-scale industrial oxidation processes is difficult to separate from nitrogen (N2), and afterward, CO is further oxidized to carbon dioxide. Here, we report a soft nanoporous crystalline material that selectively adsorbs CO with adaptable
Seonah Kim et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(1), 149-154 (2013-12-18)
Lytic polysaccharide monooxygenases (LPMOs) exhibit a mononuclear copper-containing active site and use dioxygen and a reducing agent to oxidatively cleave glycosidic linkages in polysaccharides. LPMOs represent a unique paradigm in carbohydrate turnover and exhibit synergy with hydrolytic enzymes in biomass
Stephen G Kaler et al.
The New England journal of medicine, 358(6), 605-614 (2008-02-08)
Menkes disease is a fatal neurodegenerative disorder of infancy caused by diverse mutations in a copper-transport gene, ATP7A. Early treatment with copper injections may prevent death and illness, but presymptomatic detection is hindered by the inadequate sensitivity and specificity of
Daniel L Priebbenow et al.
Organic letters, 15(24), 6155-6157 (2013-11-28)
A method has been developed for the preparation of N-alkynylated sulfoximines involving the copper-catalyzed decarboxylative coupling of sulfoximines with aryl propiolic acids. A range of substituents on both the sulfoximidoyl moiety and the aryl group of the propiolic acid were
Huawen Huang et al.
Organic letters, 15(24), 6254-6257 (2013-11-23)
A rapid and environmentally friendly conversion of pyridine to imidazo[1,2-a]pyridines has been developed via copper-catalyzed aerobic dehydrogenative cyclization with ketone oxime esters.
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