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Merck

205540

Copper(I) iodide

98%

Synonym(s):

Cuprous iodide

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About This Item

Empirical Formula (Hill Notation):
CuI
CAS Number:
7681-65-4
Molecular Weight:
190.45
PubChem Substance ID:
329752013
eCl@ss:
38150105
UNSPSC Code:
12352302
NACRES:
NA.21
EC Number:
231-674-6
MDL number:
MFCD00010978
Assay:
98%
Form:
powder

Key Documents

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Product Name

Copper(I) iodide, 98%

InChI key

LSXDOTMGLUJQCM-UHFFFAOYSA-M

InChI

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

SMILES string

[Cu+].[I-]

vapor pressure

10 mmHg ( 656 °C)

assay

98%

form

powder

reaction suitability

reaction type: click chemistry
reagent type: catalyst
core: copper

mp

605 °C (lit.)

density

5.62 g/mL at 25 °C (lit.)

Quality Level

200

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Application

Optimal catalyst for stereospecific and regioselective reaction of silacyclopropanes with carbonyl compounds.

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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

flash_point_f

Not applicable

flash_point_c

Not applicable

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

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Certificates of Analysis (COA)

Lot/Batch Number
0000496936
0000496936
0000458607
0000458607
0000418599

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Simon P H Mee et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(11), 3294-3308 (2005-03-24)
The combination of copper(I) iodide and cesium fluoride significantly enhances the Stille reaction. After extensive optimisation, a variety of electronically unfavourable and sterically hindered substrates were coupled in very high yields under mild conditions.
Alkynyl sulfides and selenides from alkynyl bromides and diorganoyl chalcogenides promoted by copper (I) iodide.
Braga AL, et al.
Tetrahedron Letters, 34(3), 393-394 (1993)
The high-temperature structural behaviour of copper (I) iodide.
Keen DA and Hull S.
Journal of Physics. Condensed Matter : An Institute of Physics Journal, 7(29), 5793-5793 (1995)
Min Jiang et al.
Organic letters, 14(6), 1420-1423 (2012-03-08)
A domino synthesis of 5,12-dihydroindolo[2,1-b]quinazoline derivatives via copper-catalyzed Ullmann-type intermolecular C-C and intramolecular C-N couplings is reported. Good yields of various 5,12-dihydroindolo[2,1-b]quinazoline derivatives were obtained. Reaction scopes, limitations, and the reaction mechanism are discussed.
Mingwen Zhu et al.
The Journal of organic chemistry, 77(20), 9102-9109 (2012-09-26)
A simple and convenient CuI/2-pyridonate catalytic system for the oxidative amidation of aldehydes with secondary amines has been developed. With this system, a variety of useful arylamides have been synthesized in moderate to good yields in the presence of small
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