103012-26-6

  • Product Name3-Phenyl-9h-carbazole
  • Molecular FormulaC18H13N
  • Molecular Weight243.3
  • Purity99%
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Product Details

Quick Details

  • CasNo: 103012-26-6
  • Molecular Formula: C18H13N
  • Purity: 99%

>99% Purity 3-phenyl-9H-carbazole 103012-26-6 with Cheap Price

  • Molecular Formula:C18H13N
  • Molecular Weight:243.308
  • Melting Point:222.8-224.1℃ 
  • Boiling Point:474.3±14.0 °C(Predicted) 
  • PKA:16.97±0.30(Predicted) 
  • PSA:15.79000 
  • Density:1.208±0.06 g/cm3(Predicted) 
  • LogP:4.98810 

3-phenyl-9H-carbazole(Cas 103012-26-6) Usage

Uses

3-Phenyl-9H-carbazole is a useful research chemical.

Chemical Properties

off-white powder

 

103012-26-6 Relevant articles

Rh(I)-catalyzed decarbonylation synthesis of carbazoles via C-N cleavage

Fan, Weizheng,Jiang, Shan,Feng, Bainian

, p. 4035 - 4038 (2015)

A one-pot Rh(I)-catalyzed synthesis of 9...

A strategy to construct multifunctional TADF materials for deep blue and high efficiency yellow fluorescent devices

Guo, Runda,Liu, Wei,Lv, Xialei,Sun, Shuaiqiang,Wang, Lei,Wang, Yaxiong,Ye, Shaofeng,Zhang, Qing

, p. 4818 - 4826 (2020)

Three deep blue thermally activated dela...

Carbazole synthesis by platinum-catalyzed C-H functionalizing reaction using water as reoxidizing reagent

Yamamoto, Mitsuru,Matsubara, Seijiro

, p. 172 - 173 (2007)

Treatment of 1-aminobiphenyl and dipheny...

One-pot synthesis of carbazoles from cyclohexanones and arylhydrazine hydrochlorides under metal-free conditions

Xiao, Fuhong,Liao, Yunfeng,Wu, Mingyue,Deng, Guo-Jun

, p. 3277 - 3280 (2012)

One-pot synthesis of carbazoles from cyc...

A novel bipolar host material based on carbazole and 1,3,5-triazine with an extremely low efficiency roll-off for green PhOLEDs

Fan, Xiaxia,Gao, Zhixiang,Huang, Jinhai,Li, Wei,Miao, Yanqin,Qu, Wenshan,Shi, Yunlong,Wang, Hua,Yu, Guichen,Zhou, Haitao

, (2021/10/04)

In this contribution, a novel bipolar ho...

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE

-

Paragraph 0219; 0220-0221, (2021/09/03)

The present invention relates to a compo...

Synthesis of Carbazoles by a Diverted Bischler-Napieralski Cascade Reaction

Faltracco, Matteo,Ortega-Rosales, Said,Janssen, Elwin,Cioc, Rǎzvan C.,Vande Velde, Christophe M. L.,Ruijter, Eelco

, p. 3100 - 3104 (2021/05/05)

An unforeseen twist in a seemingly trivi...

An electroluminescent compound and an electroluminescent device comprising the same

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Paragraph 0266; 0279-0282; 0594-0598, (2020/09/26)

The present invention relates to an orga...

103012-26-6 Process route

4-phenyldiphenylamine
32228-99-2

4-phenyldiphenylamine

3-phenyl-9H-carbazole
103012-26-6

3-phenyl-9H-carbazole

Conditions
Conditions Yield
With water; platinum on activated charcoal; at 250 ℃; for 12h;
38%
With oxygen; In acetic acid; toluene; at 80 ℃; under 760.051 Torr;
 
With oxygen; palladium diacetate; acetic acid; In toluene; at 120 ℃; for 9h;
 
With oxygen; acetic acid; In toluene; Inert atmosphere;
 
3-bromo-9H-carbazole
1592-95-6

3-bromo-9H-carbazole

phenylboronic acid
98-80-6

phenylboronic acid

3-phenyl-9H-carbazole
103012-26-6

3-phenyl-9H-carbazole

Conditions
Conditions Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; for 4h; Reflux; Inert atmosphere;
96%
With palladium diacetate; potassium carbonate; tris-(o-tolyl)phosphine; In ethanol; water; toluene; for 4h; Inert atmosphere; Reflux;
91%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In water; N,N-dimethyl-formamide; at 80 ℃; for 4h; Inert atmosphere;
90%
With tetrakis(triphenylphosphine) palladium(0); sodium hydroxide; In tetrahydrofuran; water; at 80 ℃;
89%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; toluene; at 100 ℃; for 12h; Inert atmosphere;
89%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; at 60 ℃; for 12h;
83%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 60 ℃; for 8h;
80%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In 1,4-dioxane; toluene; at 100 ℃; for 12h;
66.9%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 12h; Reflux;
64%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In 1,4-dioxane; water; toluene; for 12h; Reflux;
62.1%
With potassium carbonate; tris-(o-tolyl)phosphine; palladium diacetate; In ethanol; water; toluene; at 80 ℃; for 2h;
47%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; for 6h; Reflux;
 
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃;
7.1 g
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃;
7.1 g
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃;
7.1 g
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 12h;
22 g
With cesium fluoride; bis(dibenzylideneacetone)-palladium(0); tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; at 120 ℃; for 4h; Inert atmosphere; Schlenk technique;
 
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 12h;
22.0 g

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