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About This Item
Linear Formula:
CuCl2 · 2H2O
CAS Number:
Molecular Weight:
170.48
UNSPSC Code:
12352302
PubChem Substance ID:
EC Number:
231-210-2
MDL number:
grade
JIS special grade
vapor density
>1 (vs air)
assay
≥99.0%
form
solid
reaction suitability
reagent type: catalyst
core: copper
availability
available only in Japan
pH
3.0-3.8
mp
100 °C (dec.) (lit.)
SMILES string
Cl[Cu]Cl.[H]O[H].[H]O[H]
InChI
1S/2ClH.Cu.2H2O/h2*1H;;2*1H2/q;;+2;;/p-2
InChI key
MPTQRFCYZCXJFQ-UHFFFAOYSA-L
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signalword
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
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Bin Wu et al.
Carbohydrate research, 351, 68-73 (2012-03-01)
Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl(2). A new sugar ester (3) and two known compounds (4 and 5) were
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.


