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Merck

751944

Copper(II) chloride

powder, 99%

Synonym(s):

Copper dichloride, Cupric chloride

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About This Item

Linear Formula:
CuCl2
CAS Number:
7447-39-4
Molecular Weight:
134.45
NACRES:
NA.23
PubChem Substance ID:
329766251
UNSPSC Code:
12352302
EC Number:
231-210-2
MDL number:
MFCD00010972
Assay:
99%
Form:
powder

Key Documents

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InChI key

ORTQZVOHEJQUHG-UHFFFAOYSA-L

InChI

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

SMILES string

Cl[Cu]Cl

assay

99%

form

powder

composition

Cl, 51.9-53.5% silver nitrate titration

reaction suitability

core: copper

mp

620 °C (lit.)

density

3.386 g/mL at 25 °C (lit.)

Quality Level

100

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Application

Copper chloride was used as a reagent solution in the preparation of silver nanowires by the polyol synthesis process.

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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

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000529594
0000529594
0000518208
0000518208
0000407903

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Synthesis and Characterization of Silver Nanowire Suspensions for Printable Conductive Media
Hemmati S, et al.
ECS Journal of Solid State Science and Technology, 4(4), P3075-P3079 (2015)
Joseph R Lizza et al.
Organic letters, 20(21), 6760-6764 (2018-10-24)
The 2,2,6,6-tetramethylpiperidin-1-yloxycarbonyl (Tempoc) protecting group is readily introduced by the reaction of amines with a new acyl transfer reagent, 4-nitrophenyl (2,2,6,6-tetramethylpiperidin-1-yl) carbonate (NPTC). Tempoc has a reactivity profile that complements the commonly used t-butyloxycarbonyl (Boc) and benzyloxycarbonyl (Cbz) protecting groups.
Olga Guselnikova et al.
Sensors (Basel, Switzerland), 19(9) (2019-05-10)
In this contribution, we propose a novel functional surface-enhanced Raman spectroscopy (SERS) platform for the detection of one of the most hazardous heavy metal ions, Hg2+. The design of the proposed sensor is based on the combination of surface plasmon-polariton
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)
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.
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