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Merck
CN

292583

powder, +45 μm particle size (2% max), 99%

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关于此项目

经验公式(希尔记法):
Cu
化学文摘社编号:
分子量:
63.55
UNSPSC Code:
11101604
PubChem Substance ID:
EC Number:
231-159-6
MDL number:
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assay

99%

form

powder

reaction suitability

reagent type: catalyst
core: copper

resistivity

1.673 μΩ-cm, 20°C

particle size

+45 μm (2% max)

bp

2567 °C (lit.)

mp

1083.4 °C (lit.)

density

8.94 g/mL at 25 °C (lit.)

SMILES string

[Cu]

InChI

1S/Cu

InChI key

RYGMFSIKBFXOCR-UHFFFAOYSA-N

Application

用于有机合成
Catalyst for the cyclization and coupling reactions; e.g. Ullmann coupling reactions, preparation of cyclopropanes, decomposition of diazoketones or diazoesters, insertion to C-O bonds, [3 + 2] cycloaddition of terminal alkynes and azides, hydrogenation.


存储类别

4.1B - Flammable solid hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

法规信息

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历史批次信息供参考:

分析证书(COA)

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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
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