Conditions | Yield |
---|---|
In neat (no solvent) byproducts: Cu-oxide bromide; High Pressure; powdered mixture of the educts, high pressure, primary product;; detected in form of oxide bromide; | |
In neat (no solvent) byproducts: Cu-oxide bromide; High Pressure; powdered mixture of the educts, high pressure, primary product;; detected in form of oxide bromide; |
Conditions | Yield |
---|---|
In neat (no solvent) combustion of Cu with Br2, only small amounts of CuBr2;; | |
In neat (no solvent) combustion of Cu with Br2, only small amounts of CuBr2;; |
Conditions | Yield |
---|---|
In neat (no solvent) treatment of Cu-mirrors with Br2-vapors;; | |
With Cu-sulfide In neat (no solvent) on passing a stream of Br2/CO2 over Cu-sulfide in the heat;; | |
In neat (no solvent) treatment of Cu-mirrors with Br2-vapors;; | |
With Cu-sulfide In neat (no solvent) on passing a stream of Br2/CO2 over Cu-sulfide in the heat;; |
Conditions | Yield |
---|---|
In acetonitrile |
Conditions | Yield |
---|---|
In acetone on addn. of a soln. of Br2 in acetone;; |
Conditions | Yield |
---|---|
In hydrogen bromide dissolving CuO in aq. HBr, evapn. over H2SO4 in the air or in N2-gas of low pressure;; | |
In hydrogen bromide dissolving CuO in aq. HBr, evapn. over H2SO4;; | |
In hydrogen bromide dissolving CuO in aq. HBr, slow evapn.;; |
Conditions | Yield |
---|---|
In water pptn. from aq. soln. of Cu(2+) and alkali bromide by addn. of excess concd. H2SO4;; | |
In water pptn. from aq. soln. of Cu(2+) and alkali bromide by addn. of excess concd. H2SO4;; |
Conditions | Yield |
---|---|
byproducts: SO2; |
Conditions | Yield |
---|---|
In acetonitrile | |
In acetonitrile |
copper(ll) bromide
Conditions | Yield |
---|---|
In solid byproducts: α-picoline; heated up to 400 ° C, heating rate 5 °/min; gaseous phase).; monitored by TG, DTG, DTA;; |
bis(4-methylpyridine) copper(II) dibromide
copper(ll) bromide
Conditions | Yield |
---|---|
In neat (no solvent) sample heating up to 600 K; TG, DTG, DSC; |
bis(2-methylpyridine) copper(II) dibromide
copper(ll) bromide
Conditions | Yield |
---|---|
In neat (no solvent) sample heating up to 600 K; TG, DTG, DSC; |
copper(ll) bromide
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: 3-methylpyridine; sample heating at 5 K/min in air flow up to 600 K; TG, DTG, DSC; |
bis(3-methylpyridine) copper(II) bromide
copper(ll) bromide
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: 3-methylpyridine; sample heating at 5 K/min in air flow up to 600 K; TG, DTG, DSC; |
Conditions | Yield |
---|---|
In methanol Monitored spectrophotometrically (200-400 and 600 to 1200 nm).; |
Conditions | Yield |
---|---|
In neat (no solvent) melts on slightly warming;; | |
In neat (no solvent) melts on slightly warming;; |
copper(ll) bromide
Conditions | Yield |
---|---|
In neat (no solvent) over concd. H2SO4M; | |
In neat (no solvent) over concd. H2SO4M; |
Conditions | Yield |
---|---|
In neat (no solvent) decompn. at ambient temp.;; | |
In neat (no solvent) decompn. at ambient temp.;; |
copper(ll) bromide
Conditions | Yield |
---|---|
In not given heating in water bath; color turns to brown;; ppt. on cooling;; |
Conditions | Yield |
---|---|
In neat (no solvent) decompn. at 250°C,; | |
In neat (no solvent) decompn. at 240-250°C,; | |
In neat (no solvent) decompn. at 250°C,; | |
In neat (no solvent) decompn. at 240-250°C,; |
Conditions | Yield |
---|---|
In dichloromethane byproducts: MeBr; room temp. (N2); not isolated, detected spectroscopically; | A 81% B 100% |
Conditions | Yield |
---|---|
In acetonitrile To a soln. of CuBr2 in CH3CN was added dropwise with stirring a soln. of ligand in warm CH3CN;; ppt. was washed with CH3CN, vac.-dried; elem. anal.;; | 100% |
Conditions | Yield |
---|---|
In methanol soln. of Cu salt and ligand were mixed and stirred for 30 min; ppt. was collected, washed with MeOH, dried in vac.; elem. anal.; | 100% |
N,N'-1,2-ethylenebis(pyridin-2-thione)
copper(ll) bromide
Conditions | Yield |
---|---|
In methanol; nitromethane; dichloromethane elem. anal.; | 100% |
Conditions | Yield |
---|---|
In acetone Reflux; | 100% |
Conditions | Yield |
---|---|
In acetonitrile Cu compd. dissolved in Ar-degassed MeCN, melamine added, suspn. sealed in glass tube, heated with stirring to 100°C for 14 h; filtered, washed with MeCN and Et2O, dried in vac.; elem. anal.; | 99.6% |
Conditions | Yield |
---|---|
In water at 20℃; | 99.5% |
Conditions | Yield |
---|---|
In water molar ratio Cu:bipy:H2O=1:2:167, acid digestion bomb, 170°C, 7 d; washing (water, Me2CO), drying in air; | 99% |
Conditions | Yield |
---|---|
In acetone stoich. amts. (pptn.); collection (filtration), washing (Me2CO), drying (vac.); | 99% |
Conditions | Yield |
---|---|
In ethanol pptn. on addn. Et2O, sepn. (filtration), washing (Et2O); elem. anal.; | 99% |
2,5-dimethyl-N,N'-dicyanoquinone diimine
(E,E)-N,N'-Dicyan-2,5-dimethoxy-1,4-benzochinondiimin
copper(ll) bromide
Conditions | Yield |
---|---|
In acetonitrile Argon atmosphere, keeping a copper wire in a with Ar satd. soln. (2-4 d); washing (CH3CN and pentane), drying (silica gel); elem. anal.; | 99% |
bis-(1,2-diphenylethane-1,2-dione dihydrazone) nickel(II)
salicylaldehyde
copper(ll) bromide
Conditions | Yield |
---|---|
With NaOH In ethanol refluxing (2+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (water, ethanol), drying; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.; | 99% |
2-bromo-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine
2-chloro-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine
copper(ll) bromide
Conditions | Yield |
---|---|
In acetonitrile Argon atmosphere, keeping a copper wire in a with Ar satd. soln. (2-4 d); washing (CH3CN and pentane), drying (silica gel); elem. anal.; | 99% |
Conditions | Yield |
---|---|
With Ce(NH3)2(NO3)4 In methanol refluxing CuBr2, dpds, and Ce(NH3)2(NO3)4 in MeOH for 1 day; elem. anal.; | 99% |
In methanol byproducts: sulfur; react. CuBr2 and dpds in MeOH for several months; elem. anal.; | 70% |
ethanol
pyridine-2-carboxamide thiosemicarbazide
copper(ll) bromide
Conditions | Yield |
---|---|
In ethanol equimol., stirred for 7 d; ppt. filtered, washed (ethanol), dried (vac.); elem. anal., TGA; | 99% |
Conditions | Yield |
---|---|
With Cu In ethanol Electrochem. Process; alternating-current electroreduction of CuBr2 (3 mmol) at copper electrode in the presence of propargylammonium bromide (4 mmol) in ethanol; washing with ethanol, drying; | 99% |
3-Bromopyridine
copper(ll) bromide
trans-[CuBr2(3-bromopyridine)2]
Conditions | Yield |
---|---|
In methanol | 99% |
copper(ll) bromide
Conditions | Yield |
---|---|
In methanol to soln. of phosphonium salt in MeOH soln. of CuBr2 in MeOH was added, stirred for 2 h, left for 24 h; evapd., washed with Et2O, dried in vac., elem. anal.; | 99% |
1,4-bis-(tributylphosphonio)buta-1,3-diene dibromide
copper(ll) bromide
Conditions | Yield |
---|---|
In methanol to soln. of phosphonium salt in MeOH soln. of CuBr2 in MeOH was added, stirred for 6 h, left for 24 h; evapd., washed with Et2O, elem. anal.; | 99% |
(R)-Phenylglycinol
copper(ll) bromide
Conditions | Yield |
---|---|
With triethylamine In methanol soln. of CuBr2 in MeOH added to soln. of (R)-2-phenylglycinol and Et3N in MeOH; ppt. filtered off, washed with MeOH and Et2O, dried in air; elem. anal.; | 99% |
(R)-2-aminopropan-1-ol
copper(ll) bromide
Conditions | Yield |
---|---|
With triethylamine In methanol soln. of CuBr2 in MeOH added to soln. of (R)-2-amino-1-propanol and Et3Nin MeOH; ppt. filtered off, washed with MeOH and Et2O, dried in air; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With triethylamine In methanol soln. of CuBr2 in MeOH added to soln. of 2-amino-ethanol and Et3N in MeOH; ppt. filtered off, washed with MeOH and Et2O, dried in air; elem. anal.; | 99% |
In methanol small glass vial with CuBr2 placed into bigger glass vial with 2-aminoethanol, both vials filled with MeOH, connection for diffusion through solvent established, stored for 2 weeks; crystals isolated; |
Conditions | Yield |
---|---|
With triethylamine In methanol soln. of CuBr2 in MeOH added to soln. of (R)-2-amino-1-butanol and Et3N in MeOH; ppt. filtered off, washed with MeOH and Et2O, dried in air; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With sodium azide In N,N-dimethyl-formamide | 98% |
With NaN3 In N,N-dimethyl-formamide | 98% |
N,N'-dicyano-2-iodo-5-methyl-1,4-benzoquinonediimine
N,N'-dicyano-2-methoxy-5-methyl-1,4-benzoquinonediimine
copper(ll) bromide
Conditions | Yield |
---|---|
In acetonitrile Argon atmosphere, keeping a copper wire in a with Ar satd. soln. (2-4 d); washing (CH3CN and pentane), drying (silica gel); elem. anal.; | 98% |
Conditions | Yield |
---|---|
In ethanol for 12h; Reflux; | 98% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; | 98% |
Conditions | Yield |
---|---|
In ethanol soln. of ligands in EtOH (ice-cooled), addn. of soln. of CuBr2 in EtOH, pptn., stirring (1 h); sepn. (filtration), washing (EtOH, Et2O); elem. anal.; | 97% |
copper(ll) bromide
((C5H4N)2)2CuBr(1+)*PF6(1-)={(C10H8N2)2CuBr}PF6
Conditions | Yield |
---|---|
With 2,2'-bipyridine In water addn. of bpy to a boiling CuBr2 soln. (intensification of the blue color), addn. of NH4PF6 soln., pptn.; filtered, washed (H2O, EtOH); | 97% |
This chemical is called Copper(II) bromide, and its CAS registry number is 7789-45-9. With the molecular formula of Br2Cu, its product category is Inorganics. In addition, this chemical should be sealed in the cool and dry place, away from oxides, alkali metal and water. It's used as catalysts.
Other characteristics of the Copper(II) bromide can be summarised as followings: (1)H-Bond Donor: 0; (2)H-Bond Acceptor: 0; (3)Rotatable Bond Count: 0; (4)Exact Mass: 222.76423; (5)MonoIsotopic Mass: 220.766276; (6)Topological Polar Surface Area: 0; (7)Heavy Atom Count: 3; (8)Formal Charge: 0; (9)Complexity: 2.8; (10)Isotope Atom Count: 0; (11)Undefined Bond StereoCenter Count: 0; (12)Covalently-Bonded Unit Count: 1.
production method of this chemcial: Take the Copper oxide, dissolve it in heat Hydrobromic acid (avoid boiling). Filtration through the glass filters. Placed the filtrate on the sulfuric acid, then getting vacuum concentration. Finally, cure the target product.
When you are using this chemical, please be cautious about it as the following: This chemical is irritating to eyes, respiratory system and skin. It causes burns. You should wear suitable protective clothing to avoid contacting with skin and eyes. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
1.InChI: InChI=1/2BrH.Cu/h2*1H;/q;;+2/p-2/rBr2Cu/c1-3-2
2.Smiles: [Cu](Br)Br
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