产品名称
铜, turnings, purum p.a., ≥99.0%
InChI key
RYGMFSIKBFXOCR-UHFFFAOYSA-N
InChI
1S/Cu
SMILES string
[Cu]
grade
purum p.a.
assay
≥99.0%
quality
turnings
reaction suitability
core: copper, reagent type: catalyst
resistivity
1.673 μΩ-cm, 20°C
turnings L
~0.5 cm
bp
2567 °C (lit.)
mp
1083.4 °C (lit.)
density
8.94 g/mL at 25 °C (lit.)
cation traces
Al: ≤50 mg/kg, Cd: ≤50 mg/kg, Co: ≤50 mg/kg, Fe: ≤200 mg/kg, Mg: ≤50 mg/kg, Mn: ≤50 mg/kg, Ni: ≤50 mg/kg, Pb: ≤100 mg/kg, Zn: ≤200 mg/kg
Quality Level
General description
Copper turnings are a form of copper metal that has been specifically cut to have a high surface area. This form of copper is particularly useful because it provides a greater contact area for reagents to interact with which can help speed up reactions and increase yields.
Application
Copper turnings are used to synthesize inorganic salts and organometallic complexes and catalysts that can be employed in a variety of synthetic transformations. It is useful in:
- Synthesis of polynitro[60]fullerene.
- Copper-catalyzed azide-alkyne Huisgen cycloaddition (click reaction) to synthesize 5-membered heterocycles.
- Trifluoromethylation of heteroaromatic compounds.
- Preparation of electrolyte for all-copper hybrid flow batteries.
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Synthesis and explosive decomposition of polynitro [60] fullerene.
Cataldo F, et al.
Carbon, 62, 413-421 (2013)
Generation of new fluorophore by Click chemistry: synthesis and properties of β-cyclodextrin substituted by 2-pyridyl triazole.
David O, et al.
Tetrahedron Letters, 48(37), 6527-6530 (2007)
Three-component coupling of alkynes, Baylis?Hillman adducts and sodium azide: A new synthesis of substituted triazoles.
Chandrasekhar S, et al.
Tetrahedron Letters, 47(18), 3059-3063 (2006)
Structural and thermal properties of the alkaline cuprate KCuO2
Giorgio A. Costa, Elena Kaiser
Thermochimica Acta, 591-598 (1995)
Copper catalysis in organic synthesis.
Sherry R C.
Beilstein Journal of Organic Chemistry, 11, 2252?2253-2252?2253 (2015)
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