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This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Synthetic route

hydrogenchloride
7647-01-0

hydrogenchloride

barium(II) perchlorate

barium(II) perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water98.75%
In not given80%
silver perchlorate

silver perchlorate

A

perchloric acid
7601-90-3

perchloric acid

B

silver
7440-22-4

silver

Conditions
ConditionsYield
In acetonitrile byproducts: H2; Electrolysis; electrolysis of AgClO4 in CH3CN, Pt anode, 200 mA, 5V;; cathodic deposition of Ag, current yield 70 %;;A >99
B 97%
In acetonitrile byproducts: H2; Electrolysis; electrolysis of AgClO4 in CH3CN, Pt anode, 200 mA, 5V;; cathodic deposition of Ag, current yield 70 %;;A >99
B 97%
In acetonitrile byproducts: H2; Electrolysis; electrolysis of AgClO4 in CH3CN, Pt anode, 30 mA, 4V;; cathodic deposition of Ag, current yield 94 %;;A >99
B 90%
In acetonitrile byproducts: H2; Electrolysis; electrolysis of AgClO4 in CH3CN, Pt anode, 30 mA, 4V;; cathodic deposition of Ag, current yield 94 %;;A >99
B 90%
hydrogenchloride
7647-01-0

hydrogenchloride

sodium perchlorate

sodium perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In not given concd. HCl is added to NaClO4; filtering; filtrate is heated to 135°C;; acid is free of Cl(1-);;95%
In water part of cyclic process;;
In water byproducts: NaCl; addn. of concd. HCl to NaClO4 under formation of NaCl; concg. soln. under removing of HCl excess;;
In not given byproducts: NaCl; aq. HClO4 is obtained;;
In water part of cyclic process;;
barium(II) perchlorate

barium(II) perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
With hydrogenchloride In hydrogenchloride addition of 20% HCl-solution to solid waterfree Ba(ClO4)2 forms HClO4;;95%
With HCl In hydrogenchloride addition of 20% HCl-solution to solid waterfree Ba(ClO4)2 forms HClO4;;95%
With hydrogenchloride In hydrogenchloride addition of concd. HCl-solution to solid waterfree Ba(ClO4)2 forms HClO4;;90%
With HCl In hydrogenchloride addition of concd. HCl-solution to solid waterfree Ba(ClO4)2 forms HClO4;;90%
fluorosilicic acid

fluorosilicic acid

potassium perchlorate

potassium perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water byproducts: K2SiF6; 30% aq. H2SiF6 is added to a boiling aq. soln. of KClO4; mixt. is boiled for 1 h;; K2SiF6 and KClO4 is filtered off; H2SiF6 and H2SO4 is removed by BaCl2; evapn.; diln.; purity of acid depends on purity of H2SiF6; chem. pure acid is obtained by distn. under reduced pressure;;80%
In water excess of H2SiF6 is removed by BaCl2 or Ba(OH)2; Fe is removed by K4Fe(CN)6; evapn. to remove other impurities; acid contains alkali and K;;
1-benzyl-5,7-dimethyl-4,6-dioxo-4,5,6,7-tetrahydropyrazolo<3,4-d>pyrimidine
106379-46-8

1-benzyl-5,7-dimethyl-4,6-dioxo-4,5,6,7-tetrahydropyrazolo<3,4-d>pyrimidine

A

perchloric acid
7601-90-3

perchloric acid

B

5,7-dimethylpyrazolo<3,4-d>pyrimidine-4,6(5H,7H)-dione
4680-51-7

5,7-dimethylpyrazolo<3,4-d>pyrimidine-4,6(5H,7H)-dione

Conditions
ConditionsYield
With palladium on activated charcoal; ethanol Hydrogenation;
water
7732-18-5

water

fluoren-9-one; perchlorate

fluoren-9-one; perchlorate

A

perchloric acid
7601-90-3

perchloric acid

B

9-fluorenone
486-25-9

9-fluorenone

ethanol
64-17-5

ethanol

triphenylmethyl perchlorate

triphenylmethyl perchlorate

A

perchloric acid
7601-90-3

perchloric acid

B

Triphenylmethylethylether
968-39-8

Triphenylmethylethylether

methanol
67-56-1

methanol

triphenylmethyl perchlorate

triphenylmethyl perchlorate

A

perchloric acid
7601-90-3

perchloric acid

B

methoxytriphenylmethane
596-31-6

methoxytriphenylmethane

chlorine dioxide
10049-04-4, 25052-55-5

chlorine dioxide

water
7732-18-5

water

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water reaction of ClO2 and O3; addn. of water;;
water
7732-18-5

water

chlorine
7782-50-5

chlorine

A

perchloric acid
7601-90-3

perchloric acid

B

chloride
16887-00-6

chloride

Conditions
ConditionsYield
With moisture In water reaction of O3 and Cl2 in presence of moisture; addn. of water;;
water
7732-18-5

water

chlorine
7782-50-5

chlorine

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In neat (no solvent) Irradiation (UV/VIS); at 1800 - 4000 Å; condensation in liquid O2;;
In neat (no solvent) Irradiation (UV/VIS); at 1800 - 4000 Å; condensation in liquid O2;;
hypochloric acid
14989-30-1

hypochloric acid

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water ozonized air is passed through an aq. soln. of HClO;;
sulfuric acid
7664-93-9

sulfuric acid

potassium perchlorate

potassium perchlorate

water
7732-18-5

water

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In not given distg. at a pressure below 100 Torr; steam is added to prevent formation of solid HClO4*H2O;; obtained HClO4 is 88 to 98% in H2O;;
In not given distg. at a pressure below 100 Torr; steam is added to prevent formation of solid HClO4*H2O;; acid contains 20 to 25% H2SO4;;
sodium chlorate

sodium chlorate

water
7732-18-5

water

A

perchloric acid
7601-90-3

perchloric acid

B

sodium hydroxide
1310-73-2

sodium hydroxide

Conditions
ConditionsYield
In water Electrolysis; vacuum distillation under concg. of 2 n HClO4 soln.;;
In water Electrolysis; vacuum distillation under concg. of 2 n HClO4 soln.;;
hydrogenchloride
7647-01-0

hydrogenchloride

water
7732-18-5

water

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water Electrolysis; anodic oxidation;;
In water Electrolysis; anodic oxidation;;
water
7732-18-5

water

chlorine
7782-50-5

chlorine

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water Electrolysis; O2 and H2 are evolved on electrodes; after some time a vol. ratio O2:H2=1:2 has established; oxygen reacts with free chlorine to form perchlorate;;
In water Electrolysis;
In water Electrolysis; O2 and H2 are evolved on electrodes; after some time a vol. ratio O2:H2=1:2 has established; oxygen reacts with free chlorine to form perchlorate;;
dichlorine hexoxide

dichlorine hexoxide

water
7732-18-5

water

A

perchloric acid
7601-90-3

perchloric acid

B

chloric acid
7790-93-4

chloric acid

Conditions
ConditionsYield
In gas common condensing of educts;;
perchloric acid monohydrate
13444-99-0, 501680-61-1

perchloric acid monohydrate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In not given repeated freezing out;;
In neat (no solvent) decompn. at 110°C into anhyd. HClO4 and a less volatile aq. acid;;
In neat (no solvent) decompn. at 110°C into anhyd. HClO4 and a less volatile aq. acid;;
chlorine dioxide
10049-04-4, 25052-55-5

chlorine dioxide

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

perchloric acid
7601-90-3

perchloric acid

C

chloric acid
7790-93-4

chloric acid

Conditions
ConditionsYield
In water Irradiation (UV/VIS); decompn. in sunlight;;
In water Irradiation (UV/VIS); reaction in sunlight;;
In water Irradiation (UV/VIS); reaction in sunlight;;
chlorine dioxide
10049-04-4, 25052-55-5

chlorine dioxide

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In not given Irradiation (UV/VIS); at 20°C;;
In not given Irradiation (UV/VIS);
With PbO2 hydrate In not given
iron(III) perchlorate

iron(III) perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water byproducts: Fe(OH)3, H2O; thermal decompn.;;
dichlorine hexaoxide

dichlorine hexaoxide

hydrogen fluoride
7664-39-3

hydrogen fluoride

A

perchloric acid
7601-90-3

perchloric acid

B

chloryl fluoride
13637-83-7

chloryl fluoride

Conditions
ConditionsYield
Pt apparatus, 6°C, equilibrium reaction;
Pt apparatus, 6°C, equilibrium reaction;
potassium chlorate
3811-04-9

potassium chlorate

sulfuric acid
7664-93-9

sulfuric acid

potassium chloride

potassium chloride

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water heating;;0%
silicon monoxide

silicon monoxide

hydrogen fluoride
7664-39-3

hydrogen fluoride

silver perchlorate

silver perchlorate

A

perchloric acid
7601-90-3

perchloric acid

B

fluorosilicic acid

fluorosilicic acid

C

silver
7440-22-4

silver

Conditions
ConditionsYield
In hydrogen fluoride byproducts: H2O; aq. HF;
sulfuric acid
7664-93-9

sulfuric acid

barium(II) perchlorate

barium(II) perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In not given aq. acid is obtaind; HCl is removed by heating to 135°C;;
In water aluminium shot is added; heating to 110°C for 10h; Cl(1-) is removed by Ag2O; distg. with H2SO4; anhyd. acid is obtained;;
calcium perchlorate

calcium perchlorate

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In water byproducts: Ca(OH)2, H2O; thermal decompn.;;
chloride
16887-00-6

chloride

perchloric acid
7601-90-3

perchloric acid

Conditions
ConditionsYield
In not given Electrolysis; in accumulator;;

A

perchloric acid
7601-90-3

perchloric acid

B

chloric acid
7790-93-4

chloric acid

Conditions
ConditionsYield
With water In not given Electrolysis;
With H2O In not given Electrolysis;
perchloric acid
7601-90-3

perchloric acid

pentetrazole
54-95-5

pentetrazole

1-ferrocenylmethanol
1273-86-5

1-ferrocenylmethanol

3(4)-(ferrocenylmethylene)-1,5-pentamethylenetetrazolium perchlorate

3(4)-(ferrocenylmethylene)-1,5-pentamethylenetetrazolium perchlorate

Conditions
ConditionsYield
In dichloromethane; water aq. HClO4 was added to mixt. of corazol and Fe-complex in CH2Cl2, 12 min, Et2O was added; filtered, washed with ether, dried; elem. anal.;100%
perchloric acid
7601-90-3

perchloric acid

oxygen
80937-33-3

oxygen

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

Conditions
ConditionsYield
With C57H42CoFe3N4 at 20℃; Catalytic behavior; Reagent/catalyst; Electrochemical reaction;100%
With catalyst: Ba/carbon In perchloric acid aq. HClO4; Electrochem. Process; electroreduced on Ba/carbon in 0.1 M HClO4 (1 bar, 21+/-0.5°C, 1.2 V vs. RHE);
With catalyst: Ce/carbon In perchloric acid aq. HClO4; Electrochem. Process; electroreduced on Ce/carbon in 0.1 M HClO4 (1 bar, 21+/-0.5°C, 1.2 V vs. RHE);
perchloric acid
7601-90-3

perchloric acid

[CoIII(1,4,8,12-tetramethyl-1,4,8,12-tetraazacyclopentadecane)(O2)]+

[CoIII(1,4,8,12-tetramethyl-1,4,8,12-tetraazacyclopentadecane)(O2)]+

acetonitrile
75-05-8

acetonitrile

[CoIII(1,4,8,12-tetramethyl-1,4,8,12-tetraazacyclopentadecane)(O2H)(CH3CN)]2+

[CoIII(1,4,8,12-tetramethyl-1,4,8,12-tetraazacyclopentadecane)(O2H)(CH3CN)]2+

Conditions
ConditionsYield
at 0℃;100%
2,6-Diacetylpyridine
1129-30-2

2,6-Diacetylpyridine

perchloric acid
7601-90-3

perchloric acid

palladium diacetate
3375-31-3

palladium diacetate

[Pd(O1,N1,C1-pyridine-2-acetyl-6-(C(O)CH2))(acetonitrile)]ClO4
1372169-85-1

[Pd(O1,N1,C1-pyridine-2-acetyl-6-(C(O)CH2))(acetonitrile)]ClO4

Conditions
ConditionsYield
Stage #1: 2,6-Diacetylpyridine; perchloric acid In diethyl ether; water for 2h; Inert atmosphere;
Stage #2: palladium diacetate In diethyl ether; water; acetonitrile for 2h; Inert atmosphere;
100%
perchloric acid
7601-90-3

perchloric acid

N,N'-dimethyl-N,N'-ethylenebis(2-aminomethyl-4-bromo-6-formylphenolato)copper(II)
181575-42-8

N,N'-dimethyl-N,N'-ethylenebis(2-aminomethyl-4-bromo-6-formylphenolato)copper(II)

ethylenediamine
107-15-3

ethylenediamine

(Cu(H(CH2N(CH3)CH2C6H2OBrCHNCH2)2))2(2+)*2ClO4(1-)=((Cu(H(CH2N(CH3)CH2C6H2OBrCHNCH2)2))2)(ClO4)2

(Cu(H(CH2N(CH3)CH2C6H2OBrCHNCH2)2))2(2+)*2ClO4(1-)=((Cu(H(CH2N(CH3)CH2C6H2OBrCHNCH2)2))2)(ClO4)2

Conditions
ConditionsYield
In water; N,N-dimethyl-formamide to soln. ethylenediamine in DMF Cu complex was added and stirred at roomtemp. for 2 h, suspn. was acidified with aq. HClO4; ppt. was collected, washed with Et2O and dried in vacuo; elem. anal.;99%
perchloric acid
7601-90-3

perchloric acid

[Cr2(tris(2-pyridylmethyl)amine)2(μ-O)(μ-C2H5NO)](ClO4)4

[Cr2(tris(2-pyridylmethyl)amine)2(μ-O)(μ-C2H5NO)](ClO4)4

[Cr2(tris(2-pyridylmethyl)amine)2(μ-OH)(μ-C2H5NO)](ClO4)5

[Cr2(tris(2-pyridylmethyl)amine)2(μ-OH)(μ-C2H5NO)](ClO4)5

Conditions
ConditionsYield
In acetonitrile addn. of one drop concd. HClO4 to soln. of Cr-complex; pptn. on ether addn., washing (ether), drying in air; elem. anal.;99%
hydrogenchloride
7647-01-0

hydrogenchloride

perchloric acid
7601-90-3

perchloric acid

α-antiβ-[Co(3,6,9-triazaundecane-1,11-diamine)OH2]Cl3 * H2O

α-antiβ-[Co(3,6,9-triazaundecane-1,11-diamine)OH2]Cl3 * H2O

α-antiβ-[Co(3,6,9-triazaundecane-1,11-diamine)OH2]Cl2 * ClO4 * 0.5H2O

α-antiβ-[Co(3,6,9-triazaundecane-1,11-diamine)OH2]Cl2 * ClO4 * 0.5H2O

Conditions
ConditionsYield
In water crystn. on cooling, collection, washing (EtOH, ether), drying (air);99%
perchloric acid
7601-90-3

perchloric acid

[CH2(CH2NHCH2CH2NHCH2)2NC3N3(NH2)2Cu(OClO3)2]*H2O
449146-32-1

[CH2(CH2NHCH2CH2NHCH2)2NC3N3(NH2)2Cu(OClO3)2]*H2O

Cu(CH2(CH2NHCH2CH2NHCH2)2NC3N3H(NH2)2)(ClO4)2(1+)*ClO4(1-)*H2O=[CH2(CH2NHCH2CH2NHCH2)2NC3N3H(NH2)2Cu(OClO3)2]ClO4*H2O
449728-76-1

Cu(CH2(CH2NHCH2CH2NHCH2)2NC3N3H(NH2)2)(ClO4)2(1+)*ClO4(1-)*H2O=[CH2(CH2NHCH2CH2NHCH2)2NC3N3H(NH2)2Cu(OClO3)2]ClO4*H2O

Conditions
ConditionsYield
In perchloric acid aq. HClO4; 0.1 M HClO4; recrystn., elem. anal.;99%
perchloric acid
7601-90-3

perchloric acid

trans-[Mo(O)2(1,2-bis(diphenylphosphino)ethane)2] * 2 CH3OH

trans-[Mo(O)2(1,2-bis(diphenylphosphino)ethane)2] * 2 CH3OH

trans-[Mo(O)(OH)(1,2-bis(diphenylphosphino)ethane)2](ClO4)

trans-[Mo(O)(OH)(1,2-bis(diphenylphosphino)ethane)2](ClO4)

Conditions
ConditionsYield
In methanol slow addn. of excess 1 M HClO4 to Mo-complex; crystn.; elem. anal.;99%
perchloric acid
7601-90-3

perchloric acid

1-methyl-5-phenyltetrazole
20743-50-4

1-methyl-5-phenyltetrazole

1-ferrocenylmethanol
1273-86-5

1-ferrocenylmethanol

C5H5FeC5H4CH2N4CCH3C6H5(1+)*ClO4(1-)=C5H5FeC5H4CH2N4CCH3C6H5ClO4

C5H5FeC5H4CH2N4CCH3C6H5(1+)*ClO4(1-)=C5H5FeC5H4CH2N4CCH3C6H5ClO4

Conditions
ConditionsYield
In dichloromethane; water aq. HClO4 was added to mixt. of corazol and Fe-complex in CH2Cl2, 15 min, Et2O was added; filtered, washed with ether, dried; elem. anal.;99%
perchloric acid
7601-90-3

perchloric acid

1-ferrocenylmethanol
1273-86-5

1-ferrocenylmethanol

1,5-diphenyltetrazole
7477-73-8

1,5-diphenyltetrazole

C5H5FeC5H4CH2N4C(C6H5)2(1+)*ClO4(1-)=C5H5FeC5H4CH2N4C(C6H5)2ClO4

C5H5FeC5H4CH2N4C(C6H5)2(1+)*ClO4(1-)=C5H5FeC5H4CH2N4C(C6H5)2ClO4

Conditions
ConditionsYield
In dichloromethane; water aq. HClO4 was added to mixt. of corazol and Fe-complex in CH2Cl2, 20 min, Et2O was added; filtered, washed with ether, dried; elem. anal.;99%
perchloric acid
7601-90-3

perchloric acid

Mn4O4(O2P(C6H4OCH3)2)6

Mn4O4(O2P(C6H4OCH3)2)6

Mn4O4(O2P(C6H4OCH3)2)6(1+)*ClO4(1-)=(Mn4O4(O2P(C6H4OCH3)2)6)ClO4

Mn4O4(O2P(C6H4OCH3)2)6(1+)*ClO4(1-)=(Mn4O4(O2P(C6H4OCH3)2)6)ClO4

Conditions
ConditionsYield
With air In not given Mn complex oxidized by air in presence of HClO4;99%
copper (II) carbonate hydroxide

copper (II) carbonate hydroxide

perchloric acid
7601-90-3

perchloric acid

1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

{Cu(H2O)phan2}(ClO4)2

{Cu(H2O)phan2}(ClO4)2

Conditions
ConditionsYield
Stage #1: copper (II) carbonate hydroxide; perchloric acid In isopropyl alcohol for 0.166667h; Heating;
Stage #2: 1,10-Phenanthroline In isopropyl alcohol at 20℃;
99%
perchloric acid
7601-90-3

perchloric acid

chloro(2,3,7,8,12,13,17,18-octaethylporphyrinato-N,N',N'',N''')iron(III) complex
28755-93-3

chloro(2,3,7,8,12,13,17,18-octaethylporphyrinato-N,N',N'',N''')iron(III) complex

bis(methanol-O)(2,3,7,8,12,13,17,18-octaethylporphyrinato-N,N',N'',N''')iron(III) perchlorate bis(methanol) solvate

bis(methanol-O)(2,3,7,8,12,13,17,18-octaethylporphyrinato-N,N',N'',N''')iron(III) perchlorate bis(methanol) solvate

Conditions
ConditionsYield
In methanol treating with 5% HClO4 for 2 d, stay for 2 d to crystn.;98%
perchloric acid
7601-90-3

perchloric acid

di-μ-chloro-bis[chloro(η5-pentamethylcyclopentadienyl)cobalt]
82595-77-5

di-μ-chloro-bis[chloro(η5-pentamethylcyclopentadienyl)cobalt]

Triaqua(pentamethylcyclopentadienyl)cobalt-diperchlorat

Triaqua(pentamethylcyclopentadienyl)cobalt-diperchlorat

Conditions
ConditionsYield
evapn. at 0 °C in high vac.;98%
perchloric acid
7601-90-3

perchloric acid

ferrocenyl(2,4,6-trimethoxyphenyl)methanol
223139-66-0

ferrocenyl(2,4,6-trimethoxyphenyl)methanol

Ferrocenyl(2,4,6-trimethoxyphenyl)carbenium perchlorate
223139-82-0

Ferrocenyl(2,4,6-trimethoxyphenyl)carbenium perchlorate

Conditions
ConditionsYield
In perchloric acid; ethanol aq. HClO4; stirring Fe-complex suspn. (in EtOH) with 1.1 equiv. of 60% aq. HClO4 (0°C, 15 min); crystn. (-30°C);98%
In perchloric acid; diethyl ether aq. HClO4; stirring Fe-complex with slight excess of 60% HClO4 (0°C, 15 min); elem. anal.;94%
In methanol; perchloric acid aq. HClO4; stirring Fe-complex suspn. (in MeOH) with 1.1 equiv. of 60% aq. HClO4 (0°C, 15 min); crystn. (-30°C);86%
perchloric acid
7601-90-3

perchloric acid

trans-[PtCl{(E)-HNC(Me)OMe}2(PPh3)]Cl*2H2O

trans-[PtCl{(E)-HNC(Me)OMe}2(PPh3)]Cl*2H2O

trans-[PtCl{(E)-HN=C(Me)OMe}2(PPh3)](ClO4)

trans-[PtCl{(E)-HN=C(Me)OMe}2(PPh3)](ClO4)

Conditions
ConditionsYield
In water pH=3;98%
perchloric acid
7601-90-3

perchloric acid

C48H54N3O6P3Pd3

C48H54N3O6P3Pd3

acetonitrile
75-05-8

acetonitrile

C48H54N6P3Pd3(3+)*3ClO4(1-)

C48H54N6P3Pd3(3+)*3ClO4(1-)

Conditions
ConditionsYield
Stage #1: perchloric acid; C48H54N3O6P3Pd3 In tetrahydrofuran; water at 20℃; for 12h; Inert atmosphere;
Stage #2: acetonitrile Inert atmosphere;
98%
copper (II) carbonate hydroxide

copper (II) carbonate hydroxide

perchloric acid
7601-90-3

perchloric acid

1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

Cu(1,10-phenanthroline)(OH2)2(OClO3)2

Cu(1,10-phenanthroline)(OH2)2(OClO3)2

Conditions
ConditionsYield
Stage #1: copper (II) carbonate hydroxide; perchloric acid In isopropyl alcohol for 0.166667h; Heating;
Stage #2: 1,10-Phenanthroline In isopropyl alcohol at 20℃; for 3h;
98%
perchloric acid
7601-90-3

perchloric acid

bis[3-(dimethylamino)propyl]tin dichloride
133957-42-3

bis[3-(dimethylamino)propyl]tin dichloride

C10H26Cl3N2O4Sn(1+)*ClO4(1-)

C10H26Cl3N2O4Sn(1+)*ClO4(1-)

Conditions
ConditionsYield
In water for 5h;98%
perchloric acid
7601-90-3

perchloric acid

bis(3-(dimethylamino)propyl)difluorodistannane dihydrate

bis(3-(dimethylamino)propyl)difluorodistannane dihydrate

C10H26F2N2Sn(2+)*2ClO4(1-)

C10H26F2N2Sn(2+)*2ClO4(1-)

Conditions
ConditionsYield
In water for 1h;98%
methanol
67-56-1

methanol

perchloric acid
7601-90-3

perchloric acid

[ReH2(nitrosyl)(triphenylphosphine)3]
58694-74-9

[ReH2(nitrosyl)(triphenylphosphine)3]

{ReH(CH3OH)(NO)(P(C6H5)3)3}(1+)*ClO4(1-)={ReH(CH3OH)(NO)(P(C6H5)3)3}ClO4

{ReH(CH3OH)(NO)(P(C6H5)3)3}(1+)*ClO4(1-)={ReH(CH3OH)(NO)(P(C6H5)3)3}ClO4

Conditions
ConditionsYield
In dichloromethane Re-compd. and HClO4 suspended in MeOH at 0°C, addn. of CH2Cl2 until reaction had begun, addn. of diethyl ether, stirred for 5 min at 0°C; filtered (vac., N2), washed (diethyl ether);97%
perchloric acid
7601-90-3

perchloric acid

ferrocenyl(2,6-dimethoxyphenyl)methanol
223139-72-8

ferrocenyl(2,6-dimethoxyphenyl)methanol

Ferrocenyl(2,6-dimethoxyphenyl)carbenium perchlorate
223139-96-6

Ferrocenyl(2,6-dimethoxyphenyl)carbenium perchlorate

Conditions
ConditionsYield
In perchloric acid; diethyl ether aq. HClO4; stirring Fe-complex with slight excess of 60% HClO4 (0°C, 15 min); elem. anal.;97%
perchloric acid
7601-90-3

perchloric acid

silver(l) oxide
20667-12-3

silver(l) oxide

[Ag(cyanogunidine)2]ClO4
573987-19-6

[Ag(cyanogunidine)2]ClO4

Conditions
ConditionsYield
In water Ag2O was dissolved in aq. HClO4 in a polypropylene beaker, 4 equiv. of N-compd. was added in H2O; standing for 20 min at room temp., crystals were filtered, washed with small vol. of ice-cold H2O, dried in a desiccator; filtrate waskept at 0 °C for 24 h, further amt. of compd. could be isolated, elem. anal.;97%
perchloric acid
7601-90-3

perchloric acid

1-phenyl-1,2-butanedione
3457-55-4

1-phenyl-1,2-butanedione

2-amino-5-trifluoromethyl-1,3,4-thiadiazole
10444-89-0

2-amino-5-trifluoromethyl-1,3,4-thiadiazole

A

C5HN3SCH3CF3C6H5(1+)*ClO4(1-)

C5HN3SCH3CF3C6H5(1+)*ClO4(1-)

B

7-methyl-5-phenyl-2-trifluoromethyl-[1,3,4]thiadiazolo[3,2-a]pyrimidinylium; perchlorate

7-methyl-5-phenyl-2-trifluoromethyl-[1,3,4]thiadiazolo[3,2-a]pyrimidinylium; perchlorate

Conditions
ConditionsYield
In ethanol in boiling ethanol ( 0.2 h ), with 20 % 1-phenylbutane-1,2-dione excess;A 4%
B 96%
In ethanol in boiling ethanol ( 0.2 h ), with 20 % 1-phenylbutane-1,2-dione excess;A 4%
B 96%
formaldehyd
50-00-0

formaldehyd

formic acid
64-18-6

formic acid

perchloric acid
7601-90-3

perchloric acid

(1,8-diammonio-3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosane) copper(II) nitrate

(1,8-diammonio-3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosane) copper(II) nitrate

(1,8-bis(dimethylammonio)-3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosane) copper(II) perchlorate trihydrate

(1,8-bis(dimethylammonio)-3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosane) copper(II) perchlorate trihydrate

Conditions
ConditionsYield
In formic acid aq. formic acid; refluxing soln. of Cu-complex and HCHO (48 h), evapn. (reduced pressure), dissolving in hot H2O, pptn. on HClO4 addn.; filtration, washing (EtOH, Et2O), drying (vac. desiccator); elem. anal.;96%
perchloric acid
7601-90-3

perchloric acid

10-methyl-9, 10-dihydro-9-acridinone
719-54-0

10-methyl-9, 10-dihydro-9-acridinone

2,4,6-trimethylphenyl bromide
576-83-0

2,4,6-trimethylphenyl bromide

9-(2-mesityl)-10-methylacridinium perchlorate

9-(2-mesityl)-10-methylacridinium perchlorate

Conditions
ConditionsYield
Stage #1: 2,4,6-trimethylphenyl bromide With tert.-butyl lithium In diethyl ether; pentane at -78℃; for 0.5h; Cooling with acetone-dry ice;
Stage #2: 10-methyl-9, 10-dihydro-9-acridinone In diethyl ether; pentane at -78 - 25℃; for 72h; Cooling with acetone-dry ice;
Stage #3: perchloric acid In ethyl acetate
96%
perchloric acid
7601-90-3

perchloric acid

C13H11N2O2S(1-)*Cu(2+)*NO3(1-)

C13H11N2O2S(1-)*Cu(2+)*NO3(1-)

acetonitrile
75-05-8

acetonitrile

C13H11N2O2S(1-)*Cu(2+)*C2H3N*ClO4(1-)

C13H11N2O2S(1-)*Cu(2+)*C2H3N*ClO4(1-)

Conditions
ConditionsYield
Stage #1: perchloric acid; C13H11N2O2S(1-)*Cu(2+)*NO3(1-) In methanol; water for 4h;
Stage #2: acetonitrile In methanol; dichloromethane
96%

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