Substance

ID:739962

Names and Identifiers
Synonyms
Copper(I) bromide溴化亚铜(I)
IUPAC name
λ1-copper(1+) ion bromide
IUPAC Traditional name
λ1-copper(1+) ion bromide
Registration numbers
CAS Number
Merck Index
EC Number
MDL Number
Properties
Physical Property
Density
4.98
Solubility
Slightly soluble in cold water. Decomposes in hot water. Soluble in HBr, HCl, NH4OH
Boiling Point
1345°C
Apperance
Powder
Melting Point
492°C
Safety Information
GHS Hazard statements
H315-H319-H335
Safety Statements
26-37
GHS Precautionary statements
P261-P305+P351+P338-P302+P352-P321-P405-P501A
Storage Warning
Air Sensitive
European Hazard Symbols
Irritant Irritant (Xi)
Risk Statements
36/37/38
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
TSCA Listed
Product Information
Purity
98%
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• Catalyst for 1,4-addition of Grignard reagents to enones: J. Org. Chem., 27, 707 (1962); Org. Synth. Coll., 8, 522 (1993).
• Reaction of Grignard reagents with aromatic nitriles is potentially a useful route to ketones via the imine. However, in the absence of a catalyst, reaction is generally very slow and gives indifferent yields. In the presence of CuBr, tert-butylmagnesium chloride reacts readily with benzonitrile to give tert-butyl phenyl ketone in 94% yield: J. Org. Chem., 52, 3901 (1987).
• Precursor of organocopper reagents. For reviews, see: Org. React., 22, 253 (1975); 41, 135 (1992); Synthesis, 63 (1972); Tetrahedron, 45, 349 (1989).