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229628

Sigma-Aldrich

Copper(I) chloride

≥99.995% trace metals basis

Synonym(s):

Copper monochloride, Cuprous chloride

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About This Item

Linear Formula:
CuCl
CAS Number:
Molecular Weight:
99.00
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

1.3 mmHg ( 546 °C)

Assay

≥99.995% trace metals basis

form

powder

reaction suitability

reagent type: catalyst
core: copper

technique(s)

mass spectrometry (MS): suitable

impurities

≤50.0 ppm Trace Rare Earth Analysis

bp

1490 °C (lit.)

mp

430 °C (lit.)

solubility

slightly soluble 0.47 g/L at 20 °C

application(s)

battery manufacturing

SMILES string

Cl[Cu]

InChI

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

InChI key

OXBLHERUFWYNTN-UHFFFAOYSA-M

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General description

The structure of copper(I) chloride is similar to zinc-blende crystal at room temperature; the structure is wurtzite at 407 °C and at higher temperatures it forms copper(I) chloride vapor as per mass spectroscopy.

Application

CuCl may be used as an initiator for hydrostannation of α,α-unsaturated ketones and other similar radical reactions.
Shows unique character as an initiator of radical reactions such as the hydrostannation of α,β-unsaturated ketones.
Shows unique character as an initiator of radical reactions such as the hydrostannation of α,β-unsaturated ketones.

Signal Word

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 Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The Journal of organic chemistry, 73(13), 4903-4906 (2008-06-03)
A catalytic asymmetric Henry reaction has been developed with use of a sulfonyldiamine-CuCl complex as a catalyst. A series of new binaphthyl-containing sulfonyldiamine ligands (2a-h) were readily synthesized in two steps starting from commercially available chiral 1,2-diamines. The (R,R)-diamine-(R)-binaphthyl ligand

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