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Cas:1564-64-3
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inquiry1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; ...... Appearance:Yellow crystalline powder Storage:0-6°C Package:1kg/foil bag;
Cas:1564-64-3
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9-Bromoanthracene CAS No.:1564-64-3 Name: 9-Bromoanthracene Molecular Structure Molecular Formula: C14H9Br Molecular Weight: 257.13 CAS Registry N
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Cas:1564-64-3
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inquiryProduct Description Product website: http://www.finerchem.com/pro01en/id/1413.html Product Name 9-Bromoanthracene
Cas:1564-64-3
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Cas:1564-64-3
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inquiryProduct name 9-Bromoanthracene Product category Anthracene series CAS NO. 1564-64-3 Structural formula Appearance:White powder Storage:Store in cool and dry place, away from sun light. Package:25
Cas:1564-64-3
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Cas:1564-64-3
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inquiryProduct Name: 9-Bromoanthracene BROMOANTHRACENE CAS: 1564-64-3 MF: C14H9Br MW: 257.13 EINECS: 216-359-3 Mol File: 1564-64-3.mol 9-Bromoanthracene Structure 9-Bromoanthracene Chemical Properties Melting point 97-100 °C (lit.
About Product Details Items Specifications Test Results Appearance White to white crystalline powde
Cas:1564-64-3
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Cas:1564-64-3
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inquiry1.Appearance: White acicular crystalline powder 2.CAS No. 1564-64-3 3.MF: C14H9Br 4.Assay:99.0%min ISO9001 Appearance:White acicular crystalline powder Storage:Store in dry and cool place with good seal Package: 25kg/drum, or as per your reque
Product Detail Minimum Order Qty. 10 Gram
Cas:1564-64-3
Min.Order:10 Gram
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Type:Trading Company
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Cas:1564-64-3
Min.Order:100 Gram
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Cas:1564-64-3
Min.Order:1 Gram
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inquiryConditions | Yield |
---|---|
With bis(trifluoroacetoxy)iodobencene; trimethylsilyl bromide In dichloromethane at 20℃; Inert atmosphere; | 100% |
With N,N,N’,N’-tetrabromobenzene-1,3-disulfonamide In dichloromethane at 25℃; for 0.583333h; | 98% |
With copper(ll) bromide In chloroform Reflux; | 94% |
(10-bromo-9-anthracenyl)boronic acid
9-Bromoanthracene
Conditions | Yield |
---|---|
With [Pd(N-phenylbenzaldimine)(OAc)(PPh3)] In tetrahydrofuran at 20℃; for 24h; Schlenk technique; chemoselective reaction; | 99% |
1-(anthracen-10-yl)-2-bromoethanone
A
9-acetylanthracene
B
9-Bromoanthracene
Conditions | Yield |
---|---|
With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; acetic acid for 0.7h; Irradiation; Inert atmosphere; | A 94% B 2% |
9-iodoanthracene
9-Bromoanthracene
Conditions | Yield |
---|---|
In tetrahydrofuran at 25℃; for 3h; Reagent/catalyst; Time; Temperature; | 92% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; 2,4,6-trimethylaniline In dichloromethane at 0℃; for 8h; Inert atmosphere; regioselective reaction; | A 84% B 7% |
With N-Bromosuccinimide; C5H13NO3S In n-heptane at 60℃; for 4.5h; Darkness; | A 81% B 8% |
With N-Bromosuccinimide; iodine In tetrachloromethane Bromination; Heating; |
9,10-Dibromoanthracene
A
9-Bromoanthracene
B
9-<4-(N,N-dimethylamino)phenyl>-9,10-dihydroanthracene
C
4,4'-methylene-bis(N,N-dimethylaniline)
Conditions | Yield |
---|---|
With N,N-dimethyl-aniline In acetonitrile Irradiation; Further byproducts given; | A 70% B 7.2% C 13.4% D 8.2% |
9,10-Dibromoanthracene
N,N-dimethyl-aniline
A
9-Bromoanthracene
B
9-<4-(N,N-dimethylamino)phenyl>-9,10-dihydroanthracene
C
crystal violet bromide
D
4,4'-methylene-bis(N,N-dimethylaniline)
Conditions | Yield |
---|---|
In acetonitrile Product distribution; Irradiation; photolysis; | A 70% B 7.2% C 1.2% D 13.4% E 8.2% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide In chloroform at 60℃; for 2h; Inert atmosphere; | 61.2% |
9,10-Dibromoanthracene
potassium phenolate
A
9-Bromoanthracene
B
bromo-9 phenoxy-10 anthracene
C
9,10-phenanthrenequinone
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 153℃; for 3h; | A 3% B 35% C 2% |
Conditions | Yield |
---|---|
Kinetics; |
9,19-Dibromo-9,10-dihydroanthracene
9-Bromoanthracene
Conditions | Yield |
---|---|
With toluene; copper(I) bromide |
anthracene
2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one
9-Bromoanthracene
Conditions | Yield |
---|---|
Kinetics; |
9,19-Dibromo-9,10-dihydroanthracene
chloroform
diethylamine
A
9-Bromoanthracene
B
anthracene
chloro-trimethyl-silane
9,10-Dibromoanthracene
A
9-Bromoanthracene
B
9-Brom-10-(trimethylsilyl)anthracen
Conditions | Yield |
---|---|
With n-butyllithium 1.) ether, pentane, 20 deg C, 45 min, 2.) ether, THF, 20 deg C, 20 h; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; |
anthracene
A
9-chloroanthracene
B
9-Bromoanthracene
C
9-iodoanthracene
Conditions | Yield |
---|---|
With aluminium trichloride; cyanogen iodide; tetrabutylammomium bromide In diethyl ether; nitromethane at 25℃; for 20h; | A 6 % Chromat. B 88 % Chromat. C 1 % Chromat. |
9,19-Dibromo-9,10-dihydroanthracene
hydrogen sulfide
acetic acid
A
9-Bromoanthracene
B
anthracene
Conditions | Yield |
---|---|
at 50℃; |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; biphenyl In benzene at 20℃; for 2h; Irradiation; | A 88.9 % Chromat. B 11.1 % Chromat. |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; N,N-dimethyl-formamide; palladium dichloride at 120℃; for 18h; |
1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione
anthracene
A
9-Bromoanthracene
B
9,10-Dibromoanthracene
Conditions | Yield |
---|---|
Stage #1: 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; anthracene In ethyl acetate for 2.5h; Refluxing; Stage #2: In tetrahydrofuran |
Conditions | Yield |
---|---|
With dihydrogen peroxide; acetic acid; potassium bromide In water at 60℃; for 6h; regioselective reaction; | A 85 %Spectr. B 15 %Spectr. |
anthracene
A
9-Bromoanthracene
B
9,10-Dibromoanthracene
C
9,10-phenanthrenequinone
Conditions | Yield |
---|---|
With Oxone; quartz; sodium bromide In n-heptane for 0.333333h; Milling; chemoselective reaction; |
9-Bromoanthracene
trimethylsilylacetylene
[2-(anthracen-9-yl)ethynyl]trimethylsilane
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine In tetrahydrofuran for 15h; Heating; | 100% |
With piperidine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide In triethylamine at 110℃; Sonogashira Cross-Coupling; | 99% |
Stage #1: 9-Bromoanthracene; trimethylsilylacetylene With triethylamine for 0.0833333h; Sonogashira coupling; Inert atmosphere; Stage #2: With copper(l) iodide at 50 - 65℃; Sonogashira coupling; Inert atmosphere; | 98% |
9-Bromoanthracene
2-Methoxyphenylboronic acid
9-(2'-methoxyphenyl)anthracene
Conditions | Yield |
---|---|
With potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); C31H27FeOP In toluene at 70℃; for 24h; Reagent/catalyst; Time; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere; Sealed tube; | 100% |
With tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate monohydrate; C30H25FeP In toluene at 100℃; for 24h; Suzuki-Miyaura Coupling; Sealed tube; | 95% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; toluene for 20h; Heating; | 90% |
bis(diethylamino)chlorophosphine
9-Bromoanthracene
9-anthryl-bis(diethylamino)phosphine
Conditions | Yield |
---|---|
With n-butyllithium In diethyl ether; hexane at -78 - 20℃; for 16h; | 100% |
Stage #1: 9-Bromoanthracene With n-butyllithium In diethyl ether; hexane at -78 - 0℃; for 1h; Inert atmosphere; Stage #2: bis(diethylamino)chlorophosphine In diethyl ether; hexane at -78 - 20℃; Inert atmosphere; |
9-Bromoanthracene
2-Biphenylboronic acid
9‐([1,1'‐biphenyl]‐2‐yl)anthracene
Conditions | Yield |
---|---|
With potassium phosphate monohydrate; R-Phos; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane at 100℃; for 0.5h; Suzuki coupling; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane at -78 - 20℃; for 1h; Inert atmosphere; | 99.4% |
Stage #1: 9-Bromoanthracene With n-butyllithium In tetrahydrofuran at -78℃; for 1h; Stage #2: dimethylmonochlorosilane In tetrahydrofuran at -78 - 20℃; for 8h; | 59% |
With n-butyllithium In diethyl ether; hexane at 25℃; for 72h; | 54% |
With n-butyllithium In diethyl ether at -40 - 20℃; for 17.5h; Inert atmosphere; | 43% |
Conditions | Yield |
---|---|
With 2-H-1,3-di-tert-butyl-1,3,2-diazaphosphorinane; 2,2'-azobis(isobutyronitrile) In toluene at 90℃; for 5h; | 99% |
With 1,3-bis(2,6-diisopropylphenyl)-2,4-diphenylimidazole In N,N-dimethyl-formamide at 20℃; for 36h; Glovebox; | 98% |
With N1,N1,N12,N12-tetramethyl-7,8-dihydro-6H-dipyrido[1,2-a:2,1'-c][1,4]diazepine-2,12-diamine In N,N-dimethyl-formamide at 20℃; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With potassium phosphate; d(4)-methanol; palladium diacetate; catacxium A In toluene at 80℃; for 16h; | 99% |
With dimethylsulfoxide-d6; 9-N-methylamino-1-oxophenalene; potassium tert-butylate; potassium at 25 - 30℃; for 24h; Inert atmosphere; Glovebox; | 74% |
With n-butyllithium; water-d2 In diethyl ether at 0℃; | 57% |
Conditions | Yield |
---|---|
With potassium phosphate; rac-2,8-bis(diphenylphosphanyl)-4,10-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocine; palladium diacetate In toluene at 90℃; Suzuki Coupling; Schlenk technique; Inert atmosphere; | 99% |
With potassium carbonate In (2)H8-toluene at 100℃; for 24h; Reagent/catalyst; Suzuki-Miyaura Coupling; | 99% |
With {2,6-bis[(di-1-piperidinylphosphino)amino]phenyl}palladium(II) chloride; potassium carbonate In 1,4-dioxane; water; butan-1-ol at 100℃; for 0.5h; Suzuki-Miyaura reaction; | 98% |
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate; triphenylphosphine In 1,2-dimethoxyethane; water at 80℃; for 17h; Inert atmosphere; | 99% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; toluene for 24h; Inert atmosphere; Reflux; Sealed tube; | 90% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 90℃; for 16h; Inert atmosphere; | 90% |
9-Bromoanthracene
2-bromo-6-[2-(diphenylphosphinoyl)ethyl]pyridine
2-(9-anthracyl)-6-[2-(diphenylphosphinoyl)ethyl]pyridine
Conditions | Yield |
---|---|
Stage #1: 9-Bromoanthracene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: With zinc(II) chloride In tetrahydrofuran; hexane at 20℃; for 1h; Stage #3: 2-bromo-6-[2-(diphenylphosphinoyl)ethyl]pyridine With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran; hexane at 60℃; for 24h; Negishi-Takahashi coupling; | 99% |
9-Bromoanthracene
2-Methylphenylboronic acid
9-(2-methylphenyl)anthracene
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate monohydrate; C30H25FeP In toluene at 100℃; for 24h; Suzuki-Miyaura Coupling; Sealed tube; | 99% |
With potassium phosphate; C29H37O2P; palladium diacetate In toluene at 110℃; for 3h; Suzuki-Miyaura Coupling; Inert atmosphere; Schlenk technique; | 94% |
With potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); 1′-triethylsilyl-1-(2-(E)-phenylvinyl)-2-(diphenylphosphino)ferrocene In toluene at 70℃; for 24h; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere; Sealed tube; | 89% |
Conditions | Yield |
---|---|
With palladium; triphenylphosphine In tetrahydrofuran at 70℃; for 24h; Catalytic behavior; Negishi Coupling; Inert atmosphere; Green chemistry; | 99% |
9-Bromoanthracene
p-tolylboronic pinacol ester
9-(4-methylphenyl)anthracene
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride; potassium hydroxide In neat (no solvent) at 110℃; for 24h; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere; | 99% |
9-Bromoanthracene
tributyl(p-tolyl)stannane
9-(4-methylphenyl)anthracene
Conditions | Yield |
---|---|
With palladium diacetate; cesium fluoride; tricyclohexylphosphine In neat (no solvent) at 110℃; under 760.051 Torr; for 24h; Stille Cross Coupling; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With manganese(II) chloride dihydrate; lithium In tetrahydrofuran at 25℃; for 0.5h; Birch reaction; Inert atmosphere; | 98% |
With potassium hydroxide semihydrate; phosphorus; water In dimethyl sulfoxide at 100℃; for 3h; Inert atmosphere; | 90% |
With Dicalcium Nitride Electride In tetrahydrofuran; isopropyl alcohol at 65℃; for 24h; Birch Reduction; Inert atmosphere; | 84% |
With tetraethylammonium perchlorate; triethylamine In dimethyl sulfoxide at 20℃; for 4h; Electrolysis; Green chemistry; | 65% |
9-Bromoanthracene
4-methoxyphenylboronic acid
9-(p-methoxyphenyl)anthracene
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene for 24h; Suzuki Coupling; Reflux; Inert atmosphere; | 98% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 105℃; for 18h; Temperature; Inert atmosphere; | 90% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; toluene at 110℃; for 20h; Temperature; Inert atmosphere; | 90% |
9-Bromoanthracene
1-Naphthylboronic acid
10-(naphthalen-1-yl)anthracene
Conditions | Yield |
---|---|
With potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); C31H27FeOP In toluene at 70℃; for 24h; Reagent/catalyst; Time; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere; Sealed tube; | 98% |
With C70H40Cl2F68N2O6Pd2; tetrabutylammomium bromide; potassium carbonate In water at 140℃; for 0.2h; Suzuki-Miyaura reaction; Microwave irradiation; | 97% |
With tetrabutylammomium bromide; potassium carbonate In ethanol; water; toluene at 70 - 75℃; for 2h; Inert atmosphere; | 97.46% |
9-Bromoanthracene
7H-Dibenzofluorenone
Conditions | Yield |
---|---|
Stage #1: 9-Bromoanthracene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: 7H-Dibenzofluorenone In tetrahydrofuran; hexane at -78 - 20℃; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With palladium diacetate; caesium carbonate; XPhos In tetrahydrofuran-d8 for 20h; Sonogashira Cross-Coupling; Glovebox; Schlenk technique; Inert atmosphere; Heating; | 98% |
9-Bromoanthracene
naphthalene-2-boronic acid
9-(naphthyl-2-yl)anthracene
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); sodium hydroxide In tetrahydrofuran at 50 - 90℃; for 13h; Inert atmosphere; | 97.4% |
With potassium carbonate; triphenylphosphine; palladium diacetate In 1,2-dimethoxyethane; water for 8h; Suzuki cross-coupling; Heating; | 92% |
With potassium carbonate; palladium diacetate; tris-(o-tolyl)phosphine In 1,2-dimethoxyethane; water at 80℃; for 3h; Suzuki-Miyaura coupling; | 92% |
Conditions | Yield |
---|---|
With C70H40Cl2F68N2O6Pd2; tetrabutylammomium bromide; potassium carbonate In water at 140℃; for 0.2h; Suzuki-Miyaura reaction; Microwave irradiation; | 97% |
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene In toluene at 20℃; for 1h; | 97% |
With tris-(dibenzylideneacetone)dipalladium(0); DavePhos In toluene at 20℃; for 1h; Reagent/catalyst; |
9-Bromoanthracene
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate; XPhos In water; toluene at 80℃; for 18h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With C30H43O2P*C13H12N(1-)*CH3O3S(1-)*Pd(2+); lithium hexamethyldisilazane In 1,4-dioxane at 100℃; for 16h; Inert atmosphere; | 97% |
9-Bromoanthracene
Conditions | Yield |
---|---|
Stage #1: N-tert-butoxycarbonyl-N,N-bis[4-(di-tert-butylphenylamino)phenyl]amine With trifluoroacetic acid at 20℃; for 0.166667h; Stage #2: 9-Bromoanthracene With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate In toluene Inert atmosphere; Reflux; | 97% |
Conditions | Yield |
---|---|
Stage #1: 9-Bromoanthracene With bis(tri-t-butylphosphine)palladium(0); oxygen In toluene at 20℃; for 0.0166667h; Schlenk technique; Stage #2: methyllithium In toluene at 20℃; for 0.0333333h; Schlenk technique; | 97% |
9-Bromoanthracene
2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)quinoline
Conditions | Yield |
---|---|
Stage #1: 9-Bromoanthracene; 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)quinoline With potassium carbonate In ethanol; toluene for 0.333333h; Inert atmosphere; Stage #2: With tetrakis(triphenylphosphine) palladium(0) In ethanol; toluene Reflux; | 97% |
Conditions | Yield |
---|---|
With bis[chloro(1,2,3-trihapto-allylbenzene)palladium(II)]; C30H42N2; sodium t-butanolate In tetrahydrofuran at 80℃; for 1h; Kinetics; Buchwald-Hartwig Coupling; Glovebox; Inert atmosphere; Molecular sieve; Sealed tube; | 97% |
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