349216
Copper
wire, diam. 1.0 mm, ≥99.9%
Synonyme(s) :
Cu
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About This Item
Formule empirique (notation de Hill):
Cu
Numéro CAS:
Poids moléculaire :
63.55
Numéro MDL:
Code UNSPSC :
12141711
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
≥99.9%
Forme
wire
Pertinence de la réaction
core: copper
reagent type: catalyst
Résistivité
1.673 μΩ-cm, 20°C
Diamètre
1.0 mm
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
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).
Quantité
70 g = 10 m; 350 g = 50 m
Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
nwg
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Les clients ont également consulté
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
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
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.
Seiko Ishida et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(48), 19507-19512 (2013-11-13)
Copper is an essential trace element, the imbalances of which are associated with various pathological conditions, including cancer, albeit via largely undefined molecular and cellular mechanisms. Here we provide evidence that levels of bioavailable copper modulate tumor growth. Chronic exposure
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