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Merck
CN

05-5860

Sigma-Aldrich

氯化铜(II) 二水合物

SAJ first grade, ≥97.0%

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别名:
氯化铜 二水合物
线性分子式:
CuCl2 · 2H2O
CAS号:
分子量:
170.48
EC 号:
MDL编号:
UNSPSC代码:
12352300
PubChem化学物质编号:

等级

SAJ first grade

蒸汽密度

>1 (vs air)

检测方案

≥97.0%

形式

solid

反应适用性

reagent type: catalyst
core: copper

存货情况

available only in Japan

pH值(酸碱度)

3.0-3.8

mp

100 °C (dec.) (lit.)

SMILES字符串

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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警示用语:

Danger

危险分类

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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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)
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
Shuxia Zhou et al.
Pharmaceutical research, 30(5), 1311-1327 (2013-02-16)
Metal-catalyzed oxidation (MCO) of proteins is of primary concern in the development of biotherapeutics as it represents a prominent degradation pathway with potential undesired biological and biotherapeutic consequences. We developed a fluorogenic derivatization methodology to study the MCO of IgG1
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
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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