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203149

Sigma-Aldrich

Copper(II) chloride

99.999% trace metals basis

Sinônimo(s):

Cupric chloride

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About This Item

Fórmula linear:
CuCl2
Número CAS:
7447-39-4
Peso molecular:
134.45
Número CE:
231-210-2
Número MDL:
MFCD00010972
Código UNSPSC:
12352302
eCl@ss:
38150111
ID de substância PubChem:
24852150
NACRES:
NA.23

Ensaio

99.999% trace metals basis

forma

powder

adequação da reação

reagent type: catalyst
core: copper

Impurezas

≤15.0 ppm Trace Metal Analysis

pf

620 °C (lit.)

densidade

3.386 g/mL at 25 °C (lit.)

aplicação(ões)

battery manufacturing

cadeia de caracteres SMILES

Cl[Cu]Cl

InChI

1S/2ClH.Cu/h2*1H;/q;;+2/p-2

chave InChI

ORTQZVOHEJQUHG-UHFFFAOYSA-L

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Descrição geral

Copper chloride is a white solid. It is insoluble in water. Copper(II) chloride may be prepared by dissolving excess of copper (II) oxide or copper(II) carbonate in dilute hydrochloric acid.

Aplicação

Noble-Metal Nanostructures with Controlled Morphologies
Adding CuCl2 to AgNO3 with EG1mYAbe is used to produce uniform Ag nanowires. Copper chloride may be used as a catalyst in organic chlorination reactions. Used with palladium in a catalytic synthesis of 3-haloindoles via an annulation process.

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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Chemistry (Weinheim An Der Bergstrasse, Germany) null
Noble-Metal Nanostructures with Controlled Morphologies
Jiang M, et al.
Material Matters, 4(1) null
Synthesis, 1841-1841 (2007)
Handbook of Copper Compounds and Applications null
Landon John G Edgar et al.
Organic letters, 14(16), 4226-4229 (2012-08-01)
Glycosyl 1-phosphates enriched in the α-anomer are obtained without the use of protecting groups in two steps starting from the free hemiacetal. Condensation of free hemiacetals with toluenesulfonylhydrazide yields a range of glycosylsulfonohydrazide donors which can be oxidized using cupric
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