Copper(I) bromide
Product Information
Molecular Formula
CuBr
Molecular Weight
143.45
Description
Some applications of copper bromide reported are as a :• 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.
Synonyms
COPPER BROMIDE; COPPER(+1)BROMIDE; COPPER(I) BROMIDE; CUPROUS BROMIDE; copperbromide(cubr); coppermonobromide; Copperbromideoffwhitepowder; Cupper(Ⅰ) bromide
IUPAC Name
bromocopper
SMILES
[Cu]Br
InChI
InChI=1S/BrH.Cu/h1H/q+1/p-1
InChI Key
NKNDPYCGAZPOFS-UHFFFAOYSA-M
Boiling Point
1345°C
Melting Point
504°C
Flash Point
Not applicable
Purity
95%
Density
4.71
Solubility
Slightly sol in cold water
Appearance
White powder or crystal. Turns green to dark blue on exposure to sunlight. Sinks and mixes slowly with water.
Application
Used as a polymerization catalyst.
Storage
Store in a cool, dry place. Store in a tightly closed container.
Refractive Index
2.09
Stability
Stable, but may be air or light sensitive. Incompatible with alkali metals, strong oxidizing agents.
LogP
0.84310
Vapor Pressure
1 MM HG at 572 °C
Decomposition
WHEN STRONGLY HEATED, THEY EMIT HIGHLY TOXIC FUMES OF /HYDROGEN BROMIDE. /BROMIDES/
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
0
Exact Mass
141.84793 g/mol
Monoisotopic Mass
141.84793 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
2
Formal Charge
0
Complexity
2
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114163428-A | Preparation method of topramezone | 2022-02-11 |
| CN-114085667-A | Copper-based quantum dot/nanocrystal composite material and preparation method and application thereof | 2022-01-19 |
| CN-114014913-A | Purification method of triptorelin acetate | 2022-01-10 |
| CN-113999262-A | Preparation method of di (1-adamantyl) cycloalkylphosphine ligand | 2021-12-31 |
| CN-114134707-A | Preparation process method of antibacterial yarn | 2021-12-29 |
| CN-114149600-A | Preparation method and application of temperature-responsive hydrogel | 2021-12-27 |
| CN-114163377-A | Preparation method of N-Boc-5-bromoisoindoline | 2021-12-24 |
| CN-114163452-A | Preparation method of 1, 3-oxazine-1, 3-oxazole derivative | 2021-12-24 |
| CN-114059560-A | Inclined pile construction method | 2021-12-22 |
| CN-113956209-A | Preparation method of NH-1,2, 3-triazole compound | 2021-12-21 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 4615 | 1975-12-01 | [Blood acid-base changes produced by variations of water oxygenation in the crab Carcinus maenas (author's transl)] | Journal de physiologie |