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05-5895

Sigma-Aldrich

Copper(II) chloride

SAJ first grade, ≥98.0%

Synonym(s):

Cupric chloride

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About This Item

Linear Formula:
CuCl2
CAS Number:
7447-39-4
Molecular Weight:
134.45
MDL number:
MFCD00010972
UNSPSC Code:
12352302
PubChem Substance ID:
329748107

grade

SAJ first grade

Assay

≥98.0%

form

solid

reaction suitability

reagent type: catalyst
core: copper

availability

available only in Japan

mp

620 °C (lit.)

density

3.386 g/mL at 25 °C (lit.)

storage temp.

15-25°C

SMILES string

Cl[Cu]Cl

InChI

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

InChI key

ORTQZVOHEJQUHG-UHFFFAOYSA-L

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Signal Word

Danger

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Certificates of Analysis (COA)

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Kenji Funaki et al.
Organic letters, 14(24), 6186-6189 (2012-12-12)
Direct arylation of thiophenes and benzothiophenes with aryltrimethylsilanes was effectively catalyzed by PdCl(2)(MeCN)(2) in the presence of CuCl(2) as an oxidant. The reaction preferentially occurred at the β-position of both thiophenes and benzothiophenes.
Mónica João Barros Amorim et al.
Environmental pollution (Barking, Essex : 1987), 164, 164-168 (2012-03-01)
Environmental effects of copper nanoparticles are little studied in terrestrial ecosystems. In the present article, the toxicity of copper nanoparticles (Cu-NP) on the enchytraeid Enchytraeus albidus is compared to the toxicity of a copper-salt (CuCl(2)). The effect parameters studied were
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
Iron(II)-catalyzed trifluoromethylation of potassium vinyltrifluoroborates.
Andrew T Parsons et al.
Angewandte Chemie (International ed. in English), 51(12), 2947-2950 (2012-02-14)
Francesca Cima et al.
Chemosphere, 89(1), 19-29 (2012-05-01)
After the widespread ban of TBT, due to its severe impact on coastal biocoenoses, mainly related to its immunosuppressive effects on both invertebrates and vertebrates, alternative biocides such as Cu(I) salts and the triazine Irgarol 1051, the latter previously used
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