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Merck

221775

Copper(II) bromide

99%, solid

Synonym(s):

brominating agent, Cupric bromide

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About This Item

Linear Formula:
CuBr2
CAS Number:
7789-45-9
Molecular Weight:
223.35
UNSPSC Code:
12161600
eCl@ss:
38150112
PubChem Substance ID:
24853260
NACRES:
NA.22
EC Number:
232-167-2
MDL number:
MFCD00010970

Key Documents

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Product Name

Copper(II) bromide, 99%

Quality Level

200

assay

99%

form

solid

reaction suitability

core: copper, reagent type: catalyst

mp

498 °C (lit.)

density

4.77 g/mL at 25 °C (lit.)

SMILES string

Br[Cu]Br

InChI

1S/2BrH.Cu/h2*1H;/q;;+2/p-2

InChI key

QTMDXZNDVAMKGV-UHFFFAOYSA-L

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General description

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.

Application

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.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Deleterious substance

pdsc

Class I Designated Chemical Substances

prtr

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

221775-BULK: + 221775-5G:4548173118161 + 221775-500G:4548173118154 + 221775-100G:4548173118147 + 221775-VAR:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
MKAA3710
MKAA0271
S69011
68197LJ
06609JJ

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Jian Wang et al.
Macromolecular rapid communications, 40(2), e1800332-e1800332 (2018-06-28)
Polymerization-induced self-assembly (PISA) and in situ crosslinking of the formed nanoparticles are successfully realized by activators regenerated by electron-transfer atom transfer radical polymerization (ARGET ATRP) of glycidyl methacrylate (GMA) or a mixture of GMA/benzyl methacrylate (BnMA) monomers in ethanol. Poly(oligo(ethylene
Synthesis, 1535-1535 (2007)
Denissova I and Barriault L
Handbook of Reagents for Organic Synthesis null
Lu-Ying Han et al.
Pharmaceutics, 11(2) (2019-01-30)
Icariin (ICA) is a major flavonoid that contains the active compound Epimedii Folium. However, ICA's pharmacokinetic characteristics remain unsatisfactory due to its low bioavailability, and hence limited drugability. In order to improve its pharmacokinetics and achieve prolonged blood circulation time
Yu Wang
Polymers, 11(8) (2019-07-31)
Atom transfer radical polymerization (ATRP) of methyl acrylate (MA) was carried out by continuous feeding of Cu(I) activators. Typically, the solvent, the monomer, the initiator, and the CuBr2/Me6TREN deactivator are placed in a Schlenk flask (Me6TREN: tris[2-(dimethylamino)ethyl]amine), while the CuBr/Me6TREN
View All Related Papers

Protocols

ARGET ATRP: Procedure for PMMA Polymer Brush Growth

ARGET ATRP procedure facilitates PMMA polymer brush growth with surface cleaning and initiator monolayer deposition.

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