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212865

Sigma-Aldrich

Copper(I) bromide

98%

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Synonym(s):
Cuprous bromide
Linear Formula:
CuBr
CAS Number:
7787-70-4
Molecular Weight:
143.45
EC Number:
232-131-6
MDL number:
MFCD00010969
UNSPSC Code:
12352300
PubChem Substance ID:
329752131
NACRES:
NA.21

Quality Level

100

Assay

98%

form

solid

reaction suitability

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

mp

504 °C (lit.)

density

4.71 g/mL at 25 °C (lit.)

SMILES string

[Cu]Br

InChI

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

InChI key

NKNDPYCGAZPOFS-UHFFFAOYSA-M

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Application

Copper(I) bromide (CuBr) may be used in the synthesis of the following:
  • enantioenriched, functionalized and protected propargylamines
  • polyvinylchloride bearing benzoxazine side groups
  • polybutadiene having benzoxazine side-groups (PB-benzoxazine)
  • mononuclear complexes [Cu(L)(PPh3)2Br]
  • Copper(I) bromide along with N-(n-octyl)-2-pyridylmethanimine participates in the living-radical polymerization of methyl methacrylate.

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Copper (I) bromide/N-(n-octyl)-2-pyridylmethanimine-mediated living-radical polymerization of methyl methacrylate using carbosilane dendritic initiators.
Hovestad NJ, et al.
Macromolecules, 33(11), 4048-4052 (2000)
Enantioselective synthesis of propargylamines by copper-catalyzed addition of alkynes to enamines.
Christopher Koradin et al.
Angewandte Chemie (International ed. in English), 41(14), 2535-2538 (2002-08-31)
Copper (I) bromide complexes with heterocyclic thiones and triphenylphosphine as ligands. The X-ray crystal structure of copper (I) pyrimidine-2-thione bis (triphenylphosphine) bromide [Cu (PPh 3) 2 (PymtH) Br].
Lecomte C, et al.
Polyhedron, 8(8), 1103-1109 (1989)
Thermally curable polyvinylchloride via click chemistry.
Kiskan B, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(11), 3512-3518 (2008)
B Podobnik et al.
Bioconjugate chemistry, 26(3), 452-459 (2015-01-30)
The covalent attachment of poly(ethylene glycol) (PEG) to therapeutic proteins is a commonly used approach for extending in vivo half-lives. A potential limitation of this PEGylation strategy is the adverse effect of PEG on conjugate viscosity. Interferon-alpha (IFN) was conjugated
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