Product Name

  • Name

    Cupric bromide

  • EINECS 232-167-2
  • CAS No. 7789-45-9
  • Article Data59
  • CAS DataBase
  • Density 4.77 g/mL at 25 °C(lit.)
  • Solubility soluble in water
  • Melting Point 498 °C(lit.)
  • Formula Br2Cu
  • Boiling Point 900ºC
  • Molecular Weight 223.354
  • Flash Point 900°C
  • Transport Information UN 3260 8/PG 3
  • Appearance black crystalline powder
  • Safety 26-36/37/39-45-24/25
  • Risk Codes 22-34-36/37/38
  • Molecular Structure Molecular Structure of 7789-45-9 (Cupric bromide)
  • Hazard Symbols CorrosiveC,IrritantXi
  • Synonyms Copperdibromide;Copper(II) bromide;Copper bromide (CuBr2);
  • PSA 0.00000
  • LogP 1.68870

Synthetic route

ammonium bromide

ammonium bromide

copper(II) oxide

copper(II) oxide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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;
bromine
7726-95-6

bromine

A

copper(I) bromide
7787-70-4

copper(I) bromide

B

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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;;
bromine
7726-95-6

bromine

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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;;
bromine
7726-95-6

bromine

copper(I) bromide
7787-70-4

copper(I) bromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In acetonitrile
bromine
7726-95-6

bromine

copper(l) chloride

copper(l) chloride

A

copper(ll) bromide
7789-45-9

copper(ll) bromide

B

copper dichloride

copper dichloride

Conditions
ConditionsYield
In acetone on addn. of a soln. of Br2 in acetone;;
hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

copper(II) oxide

copper(II) oxide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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.;;
copper(II) ion

copper(II) ion

bromide
10097-32-2

bromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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;;
hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

copper(II) sulfate
7758-99-8

copper(II) sulfate

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
byproducts: SO2;
hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

copper dichloride

copper dichloride

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In acetonitrile
In acetonitrile
Cu(α-pic)2Br2

Cu(α-pic)2Br2

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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
14361-69-4, 53991-58-5

bis(4-methylpyridine) copper(II) dibromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In neat (no solvent) sample heating up to 600 K; TG, DTG, DSC;
bis(2-methylpyridine) copper(II) dibromide
13873-38-6, 257890-26-9, 42568-68-3, 6845-04-1

bis(2-methylpyridine) copper(II) dibromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In neat (no solvent) sample heating up to 600 K; TG, DTG, DSC;
tetra(3-methylpyridine) copper(II) bromide

tetra(3-methylpyridine) copper(II) bromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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
42568-70-7, 14361-57-0

bis(3-methylpyridine) copper(II) bromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In neat (no solvent) byproducts: 3-methylpyridine; sample heating at 5 K/min in air flow up to 600 K; TG, DTG, DSC;
copper(II) perchlorate hexahydrate

copper(II) perchlorate hexahydrate

lithium bromide
7550-35-8

lithium bromide

A

copper(II) bromide

copper(II) bromide

B

tribromocuprate

tribromocuprate

C

tetrabromocuprate
14337-09-8

tetrabromocuprate

D

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In methanol Monitored spectrophotometrically (200-400 and 600 to 1200 nm).;
copper(II) bromide*4H2O=Kupfer(II)-bromid*4H2O

copper(II) bromide*4H2O=Kupfer(II)-bromid*4H2O

A

water
7732-18-5

water

B

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In neat (no solvent) melts on slightly warming;;
In neat (no solvent) melts on slightly warming;;
copper(II) bromide*4H2O=Kupfer(II)-bromid*4H2O

copper(II) bromide*4H2O=Kupfer(II)-bromid*4H2O

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In neat (no solvent) over concd. H2SO4M;
In neat (no solvent) over concd. H2SO4M;
hydrogen bromo cuprate(II)

hydrogen bromo cuprate(II)

A

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

B

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In neat (no solvent) decompn. at ambient temp.;;
In neat (no solvent) decompn. at ambient temp.;;
copper(II) monobromoacetate monohydrate

copper(II) monobromoacetate monohydrate

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
In not given heating in water bath; color turns to brown;; ppt. on cooling;;
copper(II) trihydroxide bromide

copper(II) trihydroxide bromide

A

copper(II) oxide

copper(II) oxide

B

copper(ll) bromide
7789-45-9

copper(ll) bromide

Conditions
ConditionsYield
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,;
dicarbonyl(cyclopentadienyl)methyliron(II)

dicarbonyl(cyclopentadienyl)methyliron(II)

copper(ll) bromide
7789-45-9

copper(ll) bromide

A

dicarbonylcyclopentadienylbromoiron(II)

dicarbonylcyclopentadienylbromoiron(II)

B

copper(I) bromide
7787-70-4

copper(I) bromide

Conditions
ConditionsYield
In dichloromethane byproducts: MeBr; room temp. (N2); not isolated, detected spectroscopically;A 81%
B 100%
tetrathiafulvalene
31366-25-3

tetrathiafulvalene

copper(ll) bromide
7789-45-9

copper(ll) bromide

C6H4S4(2+)*CuBr3(2-)
77662-00-1

C6H4S4(2+)*CuBr3(2-)

Conditions
ConditionsYield
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%
water
7732-18-5

water

α,α-di-(4-pyridon-1-yl)-o-xylene

α,α-di-(4-pyridon-1-yl)-o-xylene

copper(ll) bromide
7789-45-9

copper(ll) bromide

[[Cu(II)(N,N'-o-phenylenedimethylenebis(pyridin-4-one))Br2]*0.5H2O]n

[[Cu(II)(N,N'-o-phenylenedimethylenebis(pyridin-4-one))Br2]*0.5H2O]n

Conditions
ConditionsYield
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)
161989-69-1

N,N'-1,2-ethylenebis(pyridin-2-thione)

copper(ll) bromide
7789-45-9

copper(ll) bromide

2Cu(1+)*2Br(1-)*(CH2C5H4(S)N)2=Cu2Br2((CH2C5H4(S)N)2)

2Cu(1+)*2Br(1-)*(CH2C5H4(S)N)2=Cu2Br2((CH2C5H4(S)N)2)

Conditions
ConditionsYield
In methanol; nitromethane; dichloromethane elem. anal.;100%
ethanol
64-17-5

ethanol

10E,13E-11,13-dimethyl-4H-dibenzo[g,n]naphthol[1,8-bc][1,5,9,13]tetraazacyclohexadecine-5,19(12H,20H)-dione

10E,13E-11,13-dimethyl-4H-dibenzo[g,n]naphthol[1,8-bc][1,5,9,13]tetraazacyclohexadecine-5,19(12H,20H)-dione

copper(ll) bromide
7789-45-9

copper(ll) bromide

C29H25BrCuN4O3*0.5C2H6O

C29H25BrCuN4O3*0.5C2H6O

Conditions
ConditionsYield
In acetone Reflux;100%
2,4,6-triamino-s-triazine
108-78-1

2,4,6-triamino-s-triazine

copper(ll) bromide
7789-45-9

copper(ll) bromide

[Cu(II)Br2(melamine)2]*0.5H2O

[Cu(II)Br2(melamine)2]*0.5H2O

Conditions
ConditionsYield
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%
pyrazinamide
98-96-4

pyrazinamide

copper(ll) bromide
7789-45-9

copper(ll) bromide

di-μ2-bromidobis(pyrazinamide)copper(II)

di-μ2-bromidobis(pyrazinamide)copper(II)

Conditions
ConditionsYield
In water at 20℃;99.5%
4,4'-bipyridine
553-26-4

4,4'-bipyridine

copper(ll) bromide
7789-45-9

copper(ll) bromide

(3).infin.[CuBr(4,4'-bipyridine)]
113720-78-8

(3).infin.[CuBr(4,4'-bipyridine)]

Conditions
ConditionsYield
In water molar ratio Cu:bipy:H2O=1:2:167, acid digestion bomb, 170°C, 7 d; washing (water, Me2CO), drying in air;99%
di(pyridin-2-yl)amine
1202-34-2

di(pyridin-2-yl)amine

copper(ll) bromide
7789-45-9

copper(ll) bromide

Cu(2,2'-dipyridylamine)2Br2

Cu(2,2'-dipyridylamine)2Br2

Conditions
ConditionsYield
In acetone stoich. amts. (pptn.); collection (filtration), washing (Me2CO), drying (vac.);99%
copper(II) choride dihydrate

copper(II) choride dihydrate

ethylenediamine
107-15-3

ethylenediamine

copper(ll) bromide
7789-45-9

copper(ll) bromide

CuClBr*2(H2NCH2CH2NH2)*H2O

CuClBr*2(H2NCH2CH2NH2)*H2O

Conditions
ConditionsYield
In ethanol pptn. on addn. Et2O, sepn. (filtration), washing (Et2O); elem. anal.;99%
2,5-dimethyl-N,N'-dicyanoquinone diimine
98507-06-3

2,5-dimethyl-N,N'-dicyanoquinone diimine

(E,E)-N,N'-Dicyan-2,5-dimethoxy-1,4-benzochinondiimin
98507-35-8

(E,E)-N,N'-Dicyan-2,5-dimethoxy-1,4-benzochinondiimin

copper(ll) bromide
7789-45-9

copper(ll) bromide

(N,N'-dicyano-2,5-dimethoxy-1,4-benzoquinonediimine)(N,N'-dicyano-2,5-dimethyl-1,4-benzoquinonediimine)copper

(N,N'-dicyano-2,5-dimethoxy-1,4-benzoquinonediimine)(N,N'-dicyano-2,5-dimethyl-1,4-benzoquinonediimine)copper

Conditions
ConditionsYield
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)
74662-54-7, 263147-04-2

bis-(1,2-diphenylethane-1,2-dione dihydrazone) nickel(II)

salicylaldehyde
90-02-8

salicylaldehyde

copper(ll) bromide
7789-45-9

copper(ll) bromide

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*1.5H2O

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*1.5H2O

Conditions
ConditionsYield
With NaOH In ethanol refluxing (2+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (water, ethanol), drying; elem. anal.;99%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

copper(ll) bromide
7789-45-9

copper(ll) bromide

nickel dibromide

nickel dibromide

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*1.5H2O

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*1.5H2O

Conditions
ConditionsYield
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
111958-86-2

2-bromo-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine

2-chloro-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine
98507-22-3

2-chloro-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine

copper(ll) bromide
7789-45-9

copper(ll) bromide

(2-chloro-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine)(2-bromo-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine)copper

(2-chloro-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine)(2-bromo-N,N'-dicyano-5-methyl-1,4-benzoquinonediimine)copper

Conditions
ConditionsYield
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%
2,2'-dipyridyldisulphide
2127-03-9

2,2'-dipyridyldisulphide

copper(ll) bromide
7789-45-9

copper(ll) bromide

[Cu(μ-Br)(μ-1-(2-pyridyl)pyridinium-2-thiolate)]n

[Cu(μ-Br)(μ-1-(2-pyridyl)pyridinium-2-thiolate)]n

Conditions
ConditionsYield
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
64-17-5

ethanol

pyridine-2-carboxamide thiosemicarbazide
290312-25-3, 676593-94-5

pyridine-2-carboxamide thiosemicarbazide

copper(ll) bromide
7789-45-9

copper(ll) bromide

[dibromo(2-pyridineformamide thiosemicarbazone)copper(II)]-ethanol-water (2/1/1)

[dibromo(2-pyridineformamide thiosemicarbazone)copper(II)]-ethanol-water (2/1/1)

Conditions
ConditionsYield
In ethanol equimol., stirred for 7 d; ppt. filtered, washed (ethanol), dried (vac.); elem. anal., TGA;99%
propargylammonium bromide
89032-97-3

propargylammonium bromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

[HCCCH2NH3]CuBr2
380906-94-5

[HCCCH2NH3]CuBr2

Conditions
ConditionsYield
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
626-55-1

3-Bromopyridine

copper(ll) bromide
7789-45-9

copper(ll) bromide

trans-[CuBr2(3-bromopyridine)2]
22980-94-5, 908368-87-6

trans-[CuBr2(3-bromopyridine)2]

Conditions
ConditionsYield
In methanol99%
buta-1,3-diene-1,4-diylbis(triphenylphosphonium chloride)

buta-1,3-diene-1,4-diylbis(triphenylphosphonium chloride)

copper(ll) bromide
7789-45-9

copper(ll) bromide

1,4-bis-(triphenylphosphino)buta-1,3-dienedichloride dibromocuprate

1,4-bis-(triphenylphosphino)buta-1,3-dienedichloride dibromocuprate

Conditions
ConditionsYield
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
86671-55-8

1,4-bis-(tributylphosphonio)buta-1,3-diene dibromide

copper(ll) bromide
7789-45-9

copper(ll) bromide

1,4-bis-(tributylphosphino)buta-1,3-dienedibormocuprate

1,4-bis-(tributylphosphino)buta-1,3-dienedibormocuprate

Conditions
ConditionsYield
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
56613-80-0

(R)-Phenylglycinol

copper(ll) bromide
7789-45-9

copper(ll) bromide

[Cu3((R)-2-amino-2-phenyl-ethanolate)4(μ-Br)2]

[Cu3((R)-2-amino-2-phenyl-ethanolate)4(μ-Br)2]

Conditions
ConditionsYield
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
35320-23-1

(R)-2-aminopropan-1-ol

copper(ll) bromide
7789-45-9

copper(ll) bromide

[Cu3((R)-2-amino-propan-1-olate)4(μ-Br)2]

[Cu3((R)-2-amino-propan-1-olate)4(μ-Br)2]

Conditions
ConditionsYield
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%
ethanolamine
141-43-5

ethanolamine

copper(ll) bromide
7789-45-9

copper(ll) bromide

[Cu3(2-amino-ethanolate)4(μ-Br)2]

[Cu3(2-amino-ethanolate)4(μ-Br)2]

Conditions
ConditionsYield
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;
(2R)-2-aminobutan-1-ol
5856-63-3

(2R)-2-aminobutan-1-ol

copper(ll) bromide
7789-45-9

copper(ll) bromide

[Cu3((R)-2-amino-butan-1-olate)4(μ-Br)2]

[Cu3((R)-2-amino-butan-1-olate)4(μ-Br)2]

Conditions
ConditionsYield
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%
bromoferrocene
1273-73-0

bromoferrocene

copper(ll) bromide
7789-45-9

copper(ll) bromide

1-azidoferrocene

1-azidoferrocene

Conditions
ConditionsYield
With sodium azide In N,N-dimethyl-formamide98%
With NaN3 In N,N-dimethyl-formamide98%
N,N'-dicyano-2-iodo-5-methyl-1,4-benzoquinonediimine
111958-85-1

N,N'-dicyano-2-iodo-5-methyl-1,4-benzoquinonediimine

N,N'-dicyano-2-methoxy-5-methyl-1,4-benzoquinonediimine
111958-81-7

N,N'-dicyano-2-methoxy-5-methyl-1,4-benzoquinonediimine

copper(ll) bromide
7789-45-9

copper(ll) bromide

Cu(N,N'-dicyano-2-methoxy-5-methyl-1,4-benzoquinonediimine)1.2(N,N'-dicyano-2-iodo-5-methyl-1,4-benzoquinonediimine)0.8

Cu(N,N'-dicyano-2-methoxy-5-methyl-1,4-benzoquinonediimine)1.2(N,N'-dicyano-2-iodo-5-methyl-1,4-benzoquinonediimine)0.8

Conditions
ConditionsYield
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%
C27H19N5O2

C27H19N5O2

water
7732-18-5

water

copper(ll) bromide
7789-45-9

copper(ll) bromide

C27H25BrCuN5O5(1+)*3H2O*Br(1-)

C27H25BrCuN5O5(1+)*3H2O*Br(1-)

Conditions
ConditionsYield
In ethanol for 12h; Reflux;98%
C20H27BrNNiP

C20H27BrNNiP

copper(ll) bromide
7789-45-9

copper(ll) bromide

C20H27Br2NNiP

C20H27Br2NNiP

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h;98%
1-(methyl)-thiourea
598-52-7

1-(methyl)-thiourea

ethylenediamine
107-15-3

ethylenediamine

copper(ll) bromide
7789-45-9

copper(ll) bromide

2CuBr2*3(ethylenediamine)*2(N-methylthiourea)

2CuBr2*3(ethylenediamine)*2(N-methylthiourea)

Conditions
ConditionsYield
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%
ammonium hexafluorophosphate

ammonium hexafluorophosphate

copper(ll) bromide
7789-45-9

copper(ll) bromide

((C5H4N)2)2CuBr(1+)*PF6(1-)={(C10H8N2)2CuBr}PF6
234441-03-3, 130326-01-1

((C5H4N)2)2CuBr(1+)*PF6(1-)={(C10H8N2)2CuBr}PF6

Conditions
ConditionsYield
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%

Cupric bromide Specification

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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