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Product Details
|
Uses |
9-(2-Bromophenyl)-9H-carbazole is a useful reagent for organic synthesis. |
| XLogP3-AA | 5.7 |
N-(2-Bromophenyl)carbazole can be used as pharmaceutical intermediates; general reagents; OLED material intermediates; OLED intermediates.
Isomeric SMILES: C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=CC=CC=C4Br
InChIKey: KEWDVYIULXXMPP-UHFFFAOYSA-N
InChI: InChI=1S/C18H12BrN/c19-15-9-3-6-12-18(15)20-16-10-4-1-7-13(16)14-8-2-5-11-17(14)20/h1-12H
This work reports a detailed structure–p...
Herein, we report two simple and efficie...
Two rigid spiro-type TADF emitters (CBZA...
The present invention relates to an orga...
The present invention relates to a compo...
The invention belongs to the technical f...
9H-carbazole
2,3-dibromobenzene
9-(2-bromophenyl)-9H-carbazole
| Conditions | Yield |
|---|---|
|
9H-carbazole; 2,3-dibromobenzene; With potassium carbonate; for 0.5h; Inert atmosphere;
With copper(l) iodide; L-lysine; at 163 ℃; for 38h;
|
83% |
|
With copper(I) oxide; potassium phosphate; N,N-dimethylethylenediamine; In toluene; at 120 ℃;
|
58% |
|
With copper(I) oxide; potassium phosphate; N,N`-dimethylethylenediamine; In 5,5-dimethyl-1,3-cyclohexadiene; at 130 ℃; for 48h; Inert atmosphere; Schlenk technique;
|
58% |
|
With copper(I) oxide; potassium phosphate; N,N`-dimethylethylenediamine; In toluene; at 120 ℃; for 72h;
|
55% |
|
With copper; potassium carbonate; In dimethyl sulfoxide; at 20 ℃; for 20.5h; Inert atmosphere; Reflux;
|
55% |
|
With copper; potassium carbonate; In dimethyl sulfoxide; at 20 ℃; for 20.5h; Inert atmosphere; Reflux;
|
55% |
|
With copper; potassium carbonate; In dimethyl sulfoxide; at 20 ℃; for 20.5h; Inert atmosphere; Reflux;
|
55% |
|
With copper; potassium carbonate; In dimethyl sulfoxide; at 20 ℃; for 20.5h; Inert atmosphere; Reflux;
|
55% |
|
With copper; potassium carbonate; In dimethyl sulfoxide; at 20 ℃; for 0.5h; Inert atmosphere;
|
55% |
|
With copper(l) iodide; 18-crown-6 ether; In 1,2-dichloro-benzene; at 100 - 210 ℃; Inert atmosphere; Darkness;
|
53% |
|
With copper(I) oxide; 1,10-Phenanthroline; potassium carbonate; In N,N-dimethyl-formamide; at 155 ℃; for 24h; Inert atmosphere;
|
41% |
|
With copper(l) iodide; 1,10-Phenanthroline; potassium hydroxide; In o-xylene; for 8h; Reflux; Inert atmosphere;
|
39% |
|
With copper(l) iodide; potassium carbonate; In N,N-dimethyl acetamide; at 160 ℃; for 72h; Inert atmosphere; Schlenk technique;
|
38% |
|
With copper(l) iodide; potassium carbonate; In N,N-dimethyl-formamide;
|
|
|
With copper(l) iodide; potassium carbonate; In N,N-dimethyl acetamide; for 24h; Inert atmosphere; Reflux;
|
|
|
With copper(l) iodide; potassium carbonate; In N,N-dimethyl acetamide; for 24h; Inert atmosphere; Reflux;
|
1-Bromo-2-iodobenzene
9H-carbazole
9-(2-bromophenyl)-9H-carbazole
| Conditions | Yield |
|---|---|
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; for 12h; Inert atmosphere; Reflux;
|
85% |
|
With potassium phosphate; copper(l) iodide; N,N`-dimethylethylenediamine; In 5,5-dimethyl-1,3-cyclohexadiene; at 120 ℃; for 48h;
|
65% |
|
With copper; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; for 48h; Inert atmosphere; Reflux;
|
56% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; for 48h; Inert atmosphere; Reflux;
|
56% |
|
With copper(l) iodide; potassium carbonate; In N,N-dimethyl-formamide; at 140 ℃; for 48h;
|
47% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; at 120 ℃; for 12h; Inert atmosphere;
|
45% |
|
With copper(I) oxide; 2,2,6,6-tetramethylheptane-3,5-dione; potassium hydroxide; In N,N-dimethyl-formamide; at 110 ℃; for 24h; Inert atmosphere; Schlenk technique;
|
41% |
|
With tri-tert-butyl phosphine; bis(dibenzylideneacetone)-palladium(0); sodium t-butanolate; In toluene; at 100 ℃; for 20h; Inert atmosphere; Reflux;
|
29% |
|
With potassium carbonate; copper(l) iodide; In xylene; Heating / reflux;
|
25% |
|
With potassium carbonate; copper(l) iodide; In xylene; Reflux; Inert atmosphere;
|
25% |
|
With potassium carbonate; copper(l) iodide; In xylene; Reflux; Inert atmosphere;
|
25% |
|
With copper(l) iodide; potassium carbonate; In N,N-dimethyl acetamide; at 130 ℃; for 48h; Inert atmosphere;
|
25% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; at 120 ℃;
|
25.5% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; Inert atmosphere; Reflux;
|
25% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; Inert atmosphere; Reflux;
|
25% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; Reflux; Inert atmosphere;
|
25% |
|
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; Reflux; Inert atmosphere;
|
|
|
With potassium carbonate; copper(II) sulfate; In 1,2-dichloro-benzene;
|
1-Bromo-2-iodobenzene
9H-carbazole
2,3-dibromobenzene
2-bromoaniline
8,8-diphenyl-8H-indolo[3,2,1-de]acridine
8-(4-bromophenyl)-8-phenyl-8H-indolo-[3,2,1-de]acridine
8,8-bis(4-bromophenyl)-8H-indolo-[3,2,1-de]acridine
9-(2-(diethylphosphino)phenyl)-9H-carbazole
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CAS:15155-41-6
Molecular Formula:C6H2Br2N2S
Molecular Weight:293.97
CAS:1428551-28-3
Molecular Formula:C24H16BrN
Molecular Weight:398.3
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CAS:1028648-22-7
Molecular Formula:C24H18BNO2
Molecular Weight:363.2
