1150-62-5
- Product Name:9-phenylcarbazole
- Molecular Formula:C18H13N
- Purity:99%
- Molecular Weight:243.308
Product Details;
CasNo: 1150-62-5
Molecular Formula: C18H13N
factory and supplier 1150-62-5 9-phenylcarbazole in stock
- Molecular Formula:C18H13N
- Molecular Weight:243.308
- Vapor Pressure:4.16E-07mmHg at 25°C
- Melting Point:95-97 °C(lit.)
- Refractive Index:1.643
- Boiling Point:415.3 °C at 760 mmHg
- Flash Point:205 °C
- PSA:4.93000
- Density:1.11 g/cm3
- LogP:4.78370
N-PHENYLCARBAZOLE HYDROCHLORIDE(Cas 1150-62-5) Usage
|
Synthesis Reference(s) |
Tetrahedron Letters, 29, p. 1115, 1988 DOI: 10.1016/S0040-4039(00)86664-2 |
InChI:InChI=1/C18H13N/c1-2-8-14(9-3-1)19-17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13H
1150-62-5 Relevant articles
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, p. 7081 - 7092 (2016)
We devised and synthesized a series of e...
Multifunctional iridium complexes based on carbazole modules as highly efficient electrophosphors
Wong, Wai-Yeung,Ho, Cheuk-Lam,Gao, Zhi-Qiang,Mi, Bao-Xiu,Chen, Chin-Hsin,Cheah, Kok-Wai,Lin, Zhenyang
, p. 7800 - 7803 (2006)
(Figure Presented) Getting the green lig...
Synthesis of N-Arylcarbazoles by Palladium-Catalyzed Direct C–H Arylation of 2-(Diarylamino)phenyl Triflates
Uwa, Koji,Tseng, Ya-Yi,Kamikawa, Ken
, p. 892 - 895 (2017)
The palladium-catalyzed direct arylation...
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Grellmann et al.
, p. 1881 (1963)
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The interplay of photophysical properties in carbazole fluorescent oligomers
Hsu, Chung-Yi,Hsieh, Mu-Tao,Chen, Yen-Fu,Hsu, Chun-Chia,Hung, Tzu-Lin,Chen, Chun-Shuo,Whang, Thou-Jen
, p. 579 - 589 (2013)
The photophysical properties and the org...
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Steinhoff,Henry
, p. 2808 (1964)
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A simple and versatile strategy for realizing bright multicolor mechanoluminescence
Sun, Qikun,Zhang, Kai,Zhang, Zhenzhen,Tang, Linagliang,Xie, Zongliang,Chi, Zhenguo,Xue, Shanfeng,Zhang, Haichang,Yang, Wenjun
, p. 8206 - 8209 (2018)
Multicolor mechanoluminescence (ML) was ...
The double N-arylation of primary amines: Toward multisubstituted carbazoles with unique optical properties
Nozaki, Kyoko,Takahashi, Keita,Nakano, Koji,Hiyama, Tamejiro,Tang, Hong-Zhi,Fujiki, Michiya,Yamaguchi, Shigehiro,Tamao, Kohei
, p. 2051 - 2053 (2003)
A powerful method: A variety of sterical...
Nickel-Catalyzed N-Arylation Using N -Trimethylsilyl-carbazole
Minami, Yasunori,Komiyama, Takeshi,Shimizu, Kenta,Uno, Shu-Ichi,Hiyama, Tamejiro,Goto, Osamu,Ikehira, Hideyuki
, p. 2407 - 2410 (2017)
Nickel-catalyzed N-arylation reaction of...
Metal-organic frameworks derived CuONPs@C nanocatalysts for synthesizing optoelectronic triarylamine molecules
Kundu, Anu,Kumar, Vadivel Vinod,Anthony, Savarimuthu Philip
, (2021)
Carbon encapsulated copper oxide nanopar...
Ternary donor-acceptor phosphine oxide hosts with peculiar high energy gap for efficient blue electroluminescence
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, p. 9469 - 9478 (2015)
Ternary donor (D)-acceptor (A)-acceptor ...
Transition Metal-Free Carbazole Synthesis from Arylureas and Cyclohexanones
Wu, Jun,Xie, Yanjun,Chen, Xiangui,Deng, Guo-Jun
, p. 3206 - 3211 (2016)
An efficient strategy for carbazole synt...
Spectroscopic observation of the dimerization reactions of the 9-phenylcarbazole cation radical in acetonitrile
Oyama, Munetaka,Matsui, Jun
, p. 953 - 957 (2004)
The dimerization reaction processes of t...
Palladium- and copper-catalyzed synthesis of triarylamines in an aqueous-organic emulsion
Davydov, D. V.,Beletskaya, I. P.
, p. 1141 (1995)
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Rh(III)-Catalyzed C-H Activation of Boronic Acid with Aryl Azide
Xu, Shiyang,Huang, Baoliang,Qiao, Guanyu,Huang, Ziyue,Zhang, Zhen,Li, Zongyang,Wang, Peng,Zhang, Zhenhua
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A Rh(III)-catalyzed C-H activation of bo...
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[Figure not available: see fulltext.] Ne...
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The syntheses of novel well-defined star...
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A continuous flow UV light reactor has b...
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In the present work, we have developed a...
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, p. 1602 - 1609 (2019)
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Touch-sensitive mechanoluminescence crystals comprising a simple purely organic molecule emit bright blue fluorescence regardless of crystallization methods
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, p. 5225 - 5228 (2018)
Simple N-phenylcarbazole (NPC) could rea...
Synthesis and characterization of nano-cellulose immobilized phenanthroline-copper (I) complex as a recyclable and efficient catalyst for preparation of diaryl ethers, N-aryl amides and N-aryl heterocycles
Aghili, Nora,Hosseinzadeh, Rahman,Mavvaji, Mohammad
, (2022/01/03)
Functionalized nanocellulose was prepare...
Photochemistry of triphenylamine (TPA) in homogeneous solution and the role of transient N -phenyl-4 a,4 b -dihydrocarbazole. A steady-state and time-resolved investigation
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The photoreactivity of triphenylamine in...
Preparation method of N-arylcarbazole-3-boric acid
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Paragraph 0026-0028; 0040-0042, (2021/02/06)
The invention discloses a preparation me...
Amine-based compound and organic light emitting diode comprising the same
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Paragraph 0223; 0227-0228, (2021/03/16)
Disclosed are an amine-based compound an...
1150-62-5 Process route
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-
86-74-8,105184-46-1,97960-57-1
9H-carbazole
-
-
583-53-9
2,3-dibromobenzene
-
-
1150-62-5
N-phenylcarbazole
-
-
902518-11-0
9-(2-bromophenyl)-9H-carbazole
| Conditions | Yield |
|---|---|
|
With
copper(I) oxide; potassium phosphate; N,N`-dimethylethylenediamine;
In
5,5-dimethyl-1,3-cyclohexadiene;
at 170 ℃;
for 24h;
Inert atmosphere;
|
60% 13.8% |
-
-
86-74-8,105184-46-1,97960-57-1
9H-carbazole
-
-
583-53-9
2,3-dibromobenzene
-
-
1150-62-5
N-phenylcarbazole
-
-
902518-11-0
9-(2-bromophenyl)-9H-carbazole
-
-
9-(2-iodophenyl)-9H-carbazole
| Conditions | Yield |
|---|---|
|
With
copper(l) iodide; potassium carbonate;
In
5,5-dimethyl-1,3-cyclohexadiene;
for 168h;
Reagent/catalyst;
Inert atmosphere;
Reflux;
|
60% 10% Ca. 15 %Chromat. |
1150-62-5 Upstream products
-
86844-02-2
9-phenyl-6,7,8,9-tetrahydro-5H-carbazole
-
591-50-4
iodobenzene
-
86-74-8
9H-carbazole
-
75-09-2
dichloromethane
1150-62-5 Downstream products
-
6286-88-0
2-(9H-carbazol-9-yl)benzoic acid
-
66131-43-9
2-carbazol-9-yl-isophthalic acid
-
73087-83-9
3,6-dibromo-9-(4-bromophenyl)-9H-carbazole
-
127464-87-3
dihydro-1,4 phenyl-9 carbazole
Relevant Products
-
2,5-Dimethoxy-Beta-Nitrostyrene
CAS:40276-11-7
-
3-Iodo-N-phenylcarbazole
CAS:502161-03-7
-
3-bromo-9-phenyl-9H-carbazole
CAS:1153-85-1

