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Sigma-Aldrich

Copper(I) iodide

99.999% trace metals basis

Sinónimos:

Cuprous iodide

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About This Item

Fórmula empírica (notación de Hill):
CuI
Número de CAS:
7681-65-4
Peso molecular:
190.45
EC Number:
231-674-6
MDL number:
MFCD00010978
UNSPSC Code:
12352302
eCl@ss:
38150105
PubChem Substance ID:
24852902
NACRES:
NA.23

vapor pressure

10 mmHg ( 656 °C)

assay

99.999% trace metals basis

form

powder and chunks

impurities

≤15.0 ppm Trace Metal Analysis

bp

1290 °C/1 atm (decomp)(lit.)

mp

605 °C (lit.)

solubility

dilute aqueous acid: insoluble(lit.)

density

5.62 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

[Cu+].[I-]

InChI

1S/Cu.HI/h;1H/q+1;/p-1

InChI key

LSXDOTMGLUJQCM-UHFFFAOYSA-M

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Application

Copper(I) iodide can be used as a catalyst for:
  • For arylation of pyrazole and derivatives by coupling arenediazonium species under mild and ligand-free conditions.
  • Selective cross-coupling of dibromo alkenes and heteronucleophiles which leads to numerous building blocks such as 1-bromoenamides, ynamides, ketene N, N-acetals, 1-bromoenol ethers, ynol ethers, ketene O, O-acetals, and vinyl phosphonates.
  • Stereospecific and the regioselective reaction of silacyclopropanes with carbonyl compounds.
It can also be used as a starting material in the preparation of diphenylphosphinepyridine-derivatives (PyrPHOS)-copper iodide complexes which are suitable for use in OLEDs.

Features and Benefits

  • Low toxicity
  • Mild reaction condition
  • High purity ensures reproducibility and avoids cocatalysis by contaminants.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT RE 1 Oral

target_organs

Thyroid

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Synlett, 1917-1917 (2007)
Synlett, 1836-1836 (2007)
Zhuangzhuang Ma et al.
Advanced materials (Deerfield Beach, Fla.), 33(2), e2001367-e2001367 (2020-11-24)
White light-emitting diodes (WLEDs) are promising next-generation solid-state light sources. However, the commercialization route for WLED production suffers from challenges in terms of insufficient color-rendering index (CRI), color instability, and incorporation of rare-earth elements. Herein, a new two-component strategy is
Roberta Berrino et al.
The Journal of organic chemistry, 77(5), 2537-2542 (2012-01-31)
Free NH 3,3-diarylacrylamides are cyclized to substituted 2-quinolones in the presence of CuI, PPh(3), and KO-t-Bu in o-xylene at 100 °C. The reaction proceeds through a C-H functionalization/C-N bond formation process. With unsymmetrical 3,3-diarylacrylamides, high selectivity is observed using substrates
Rodolfo Tello-Aburto et al.
Organic letters, 14(8), 2150-2153 (2012-04-06)
The first asymmetric total synthesis and determination of the absolute configuration for the neuroactive marine macrolide palmyrolide A is described. The highlight of the synthesis is macrocyclization via trans-enamide formation catalyzed by copper(I) iodide and cesium carbonate. Comparison with the
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