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Merck

735906

Sigma-Aldrich

Kupfer(I)-bromid

AnhydroBeads, -10 mesh, 99.99% trace metals basis

Synonym(e):

Cuprous bromide

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About This Item

Lineare Formel:
CuBr
CAS-Nummer:
Molekulargewicht:
143.45
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352302
PubChem Substanz-ID:
NACRES:
NA.23

Produktlinie

AnhydroBeads

Assay

99.99% trace metals basis

Form

beads

Verunreinigungen

≤150.0 ppm Trace Metal Analysis

Partikelgröße

-10 mesh

mp (Schmelzpunkt)

504 °C (lit.)

Dichte

4.71 g/mL at 25 °C (lit.)

Anwendung(en)

battery manufacturing

SMILES String

[Cu]Br

InChI

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

InChIKey

NKNDPYCGAZPOFS-UHFFFAOYSA-M

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Allgemeine Beschreibung

Cuprous bromide may be prepared by the reduction of cupric bromide or CuSO4-NaBr. In the molten state, it is grayish brown /greenish brown in color.

Anwendung

Some reported applications of copper bromide are:
  • catalyst in cross coupling reactions.
  • co-catalyst in Sonogashira coupling.
  • Lewis acid in enantioselective addition of alkynes.
  • reducing agent, when complexed by three molecules of pyridine initiators for the controlled polymerization of styrene, methyl acrylate and methyl methacrylate.

Reductive homocoupling of α-bromo- α- chlorocarboxylates to dimethyl α, α′ dichlorosuccinate derivatives in presence of CuBr/LiOCH3 in methanol has been reported.

Rechtliche Hinweise

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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A designed ligand-accelerated Cu(I)-catalyzed cycloaddition (CuAAC) reaction was monitored for the first time by real time infrared analysis technique based on ATR-FTIR principles. Principal components analysis (PCA) and two-dimensional correlation spectroscopy (2Dcos) results showed that the consumption of alkyne and
Denissova I and Barriault L et al.
Handbook of Reagents for Organic Synthesis null
Study on atom transfer radical polymerization initiated by p-nitrophenyl initiator and synthesis of amino end-functionalized polymers thereof
Qu, T.; Cai, W.; Fu, Z.; Shi, Y.
Macromolecular Research, 18(7), 623-629 (2010)
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