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212946

Sigma-Aldrich

Copper(I) chloride

reagent grade, 97%

Sinónimos:

Copper monochloride, Cuprous chloride

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About This Item

Fórmula lineal:
CuCl
Número de CAS:
7758-89-6
Peso molecular:
99.00
EC Number:
231-842-9
MDL number:
MFCD00010971
UNSPSC Code:
12352302
PubChem Substance ID:
329752134
NACRES:
NA.55
assay:
97%
grade:
reagent grade
form:
powder
solubility:
dimethyl sulfide: partially soluble(lit.)
water: insoluble(lit.)

grade

reagent grade

Quality Level

200

vapor pressure

1.3 mmHg ( 546 °C)

assay

97%

form

powder

reaction suitability

reagent type: catalyst
core: copper

pH

5 (20 °C, 50 g/L)

bp

1490 °C (lit.)

mp

430 °C (lit.)

solubility

dimethyl sulfide: partially soluble(lit.)
water: insoluble(lit.)

SMILES string

Cl[Cu]

InChI

1S/ClH.Cu/h1H;/q;+1/p-1

InChI key

OXBLHERUFWYNTN-UHFFFAOYSA-M

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General description

Cu is present in +1 (cuprous) valence state in CuCl. CuCl is a semiconductor having a wide band gap. It is a promising candidate for use in silicon-based optoelectronics since its lattice resembles with silicon. It participates in various reactions with Grignard reagents.

Application

Copper(I) chloride (Cuprous chloride, CuCl) has been used to synthesize 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-ol. CuCl may be used in the stereospecific synthesis of cyclic conjugated dienes. It may be employed as a reactant to investigate the stability of copper chloride complexes in hydrothermal solutions.
Shows unique character as an initiator of radical reactions such as the hydrostannation of α,β-unsaturated ketones.

signalword

Danger

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
MKCP3179
MKCL7839
MKCK6056
MKCJ3197
MKCG0775

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Copper (I) chloride-mediated intramolecular coupling of vinyltrimethylstannane and vinyl halide functions.
Piers E and Wong T.
The Journal of Organic Chemistry, 58(14), 3609-3610 (1993)
Copper (I) Chloride.
Bertz SH, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2007)
Experimental study of copper (I) chloride complexing in hydrothermal solutions at 40 to 300 ?C and saturated water vapor pressure.
Xiao Z, et al.
Geochimica et Cosmochimica Acta, 62(17), 2949-2964 (1998)
Beeraiah Baire et al.
Nature protocols, 8(3), 501-508 (2013-02-16)
The hexadehydro-Diels-Alder (HDDA) cascade enables the synthesis of complex benzenoid products with various substitution patterns through aryne intermediates. The first stage of this cascade involves the generation of a highly reactive ortho-benzyne intermediate by a net [4+2] cycloisomerization of a
N Raman et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 873-883 (2011-05-10)
A new ligand [C28H20N6O8] (L2) has been synthesized by the condensation reaction of 3-hydroxy-4-nitrobenzaldehydenephenylhydrazine (L1) with diethyloxalate. This ligand L2 is allowed to react with bis(ethylenediamine)Cu(II)/Ni(II)/Zn(II) complexes. It affords [(L2)Cu(en)2]Cl2(1)/[(L2)Ni(en)2]Cl2(2)/[(L2)Zn(en)2]Cl2(3) complexes, respectively. These complexes (1-3) have been characterized by the
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