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关于此项目
线性分子式:
CuCl2 · 2H2O
化学文摘社编号:
分子量:
170.48
UNSPSC Code:
12352302
PubChem Substance ID:
EC Number:
231-210-2
MDL number:
InChI key
MPTQRFCYZCXJFQ-UHFFFAOYSA-L
InChI
1S/2ClH.Cu.2H2O/h2*1H;;2*1H2/q;;+2;;/p-2
SMILES string
Cl[Cu]Cl.[H]O[H].[H]O[H]
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.)
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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
存储类别
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
法规信息
新产品
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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
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
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
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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