6286-72-2

Usage

Uses

Used in Organic Synthesis:
9-(2-nitrophenyl)carbazole is used as a building block for the synthesis of organic compounds, contributing to the development of new materials and molecules with potential applications in various industries.
Used in Dye and Pigment Production:
As a starting material, 9-(2-nitrophenyl)carbazole is utilized in the production of dyes and pigments, which are essential for coloring various products in industries such as textiles, plastics, and paints.
Used in Pharmaceutical Industry:
9-(2-nitrophenyl)carbazole serves as a starting material for the production of pharmaceuticals, potentially leading to the development of new drugs and therapeutic agents.
Used in Organic Electronic Devices:
9-(2-nitrophenyl)carbazole has been studied for its potential use in organic electronic devices, suggesting its role in advancing technology in areas such as organic light-emitting diodes (OLEDs) and organic solar cells.
Used as a Fluorescence Probe in Biological Imaging:
9-(2-nitrophenyl)carbazole has been explored for its use as a fluorescence probe in biological imaging, which could enhance the visualization and understanding of biological processes and structures.
It is crucial to handle 9-(2-nitrophenyl)carbazole with care due to its potential health and environmental hazards, ensuring safe practices in its application across industries.

InChI:InChI=1/C18H12N2O2/c21-20(22)18-12-6-5-11-17(18)19-15-9-3-1-7-13(15)14-8-2-4-10-16(14)19/h1-12H

Upstream product

• 86-74-8 9H-carbazole 
• 88-73-3 2-Chloronitrobenzene 
• 1493-27-2 ortho-nitrofluorobenzene 
• 577-19-5 2-nitrophenyl bromide 
• 609-73-4 o-nitroiodobenzene 

Downstream Products

• 101716-43-2 2-(9H-carbazol-9-yl)aniline 
• 205-95-8 indolo<3,2,1-jk>carbazole 
• 1174032-81-5 2-bromoindolo[3,2,1-jk]carbazole 
• 102749-79-1 2-(2-carbazol-9-yl-anilino)-cyclohexanone 
• 1213715-86-6 C₃₆H₂₅NSi 
• 1421701-40-7 C₃₀H₁₈BrN 
• 1421701-41-8 C₅₄H₃₆N₂ 
• 1421701-42-9 C₂₄H₁₄BrN 
• 1421701-44-1 C₆₀H₄₀N₂ 
• 1421701-39-4 C₅₄H₃₆N₂ 

Relevant academic research and scientific papers

Metal-organic frameworks derived CuONPs@C nanocatalysts for synthesizing optoelectronic triarylamine molecules

Carbon encapsulated copper oxide nanoparticles (CuONPs@C) fabricated using copper metal organic frameworks (Cu-MOFs) used as reusable nanocatalysts in Ullmann C[sbnd]N coupling reactions for synthesizing optoelectronic triphenylamine (TPA) and carbazole (CBZ) derivatives. The formation of CuONPs in carbon matrix was confirmed by powder X-ray diffraction (PXRD), X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HR-TEM). The catalytic activity of CuONPs@C was performed with diphenylamine/carbazole with substituted aryl halides in presence of mild K2CO3 base that produced triarylamines with 63–83% yields. Carbazole triarylamines exhibited strong solid state fluorescence (Φf = 14.54–36.32%) with λmax between 370 and 420 nm.

Deep blue fluorescent material with a narrow FWHM based on indolo[3,2,1-jk]carbazol/pyrimidine hybrids

A series of blue fluorescent materials containing electron accepting pyrimidine and electron donating bis(biphenyl)amine, diphenylcarbazole, and diphenylindolo[3,2,1-jk]carbazole moieties were synthesized in moderate yields, and their optical and electroc

Novel indolo[3,2,1-jk]carbazole-based bipolar host material for highly efficient thermally activated delayed-fluorescence organic light-emitting diodes

A novel bipolar material (ICzPyr) composed of electron-donating indolo[3,2,1-jk]carbazole and electron-withdrawing pyridmidine was developed and its use as a host material in thermally activated delayed-fluorescence (TADF) organic light-emitting diode (OL

Organic electroluminescent compound, preparation method thereof and organic electroluminescent device

The invention discloses an organic electroluminescent compound, a preparation method thereof and an organic electroluminescent device. The structural general formula of the organic electroluminescentcompound is shown in the specification, the compound provided by the invention has good thermal stability, and the organic electroluminescent device containing the compound has high luminous efficiency and long service life, and is an organic electroluminescent compound with excellent performance.

Through-space charge transfer in luminophore based on phenyl-linked carbazole- and phthalimide moieties utilized in cyan-emitting OLEDs

Two new carbazole-containing aromatic imides were synthesized by three-step synthetic pathway with the moderate yields up to 76%. The compounds were investigated theoretically. TD-DFT computational studies revealed low singlet-triplet energy differences. The compounds were found to have relatively high thermal stability with 5% mass loss temperatures in the range of 280–310 °C. Phthalimide-based compound exhibited aggregation-induced emission enhancement and thermally activated delayed fluorescence with photoluminescence quantum efficiency of 20% in the solid state. Structure-properties relationship of this compound was investigated and it was found that charge-transfer through space mechanism is responsible for the emission. Series of green-emitting doped and non-doped electroluminescent devices were fabricated based on the carbazole-phthalimide derivative were fabricated to reveal best-performing mCP-doped device demonstrating maximum external quantum efficiency of 2.4% with current efficiency of 6.6 cd/A and power efficiency of 4.0 lm/W with maximum brightness of 8300 cd/m2.

Triphenylamine based reactive coloro/fluorimetric chemosensors: Structural isomerism and solvent dependent sensitivity and selectivity

Triphenyl amine based chemosensors, (2-(((2-(9H-carbazol-9-yl)phenyl)imino)methyl)-5-(diphenylamino)phenol (ortho-CPDP) and 2-(((4-(9H–carbazol-9-yl)phenyl)imino)methyl)-5-(diphenylamino)phenol (para-CPDP), showed solvent and isomerism dependent selective

Delay fluorescent compound and using the same and display device having the organic light-emitting diode (by machine translation)

The present invention relates to delay fluorescent compound and the use of the compound of the organic light-emitting diode and the display device. Fluorescent compounds of the present invention is shown as delay 1 is shown, wherein n is 1 or 0, A is selected from the following formula 2, D is selected from the following formula 3, L 1 and L 2 each independently is selected from the following formula 4, wherein type 2 of in R 1 is selected from hydrogen or phenyl, X, Y and Z each independently selected from the group consisting of carbon and nitrogen, and the X, Y and Z for at least two of the nitrogen, type 4 of in R 2 is selected from hydrogen or C1-C10 alkyl. (by machine translation)

DELAYED FLUORESCENCE COMPOUND, AND ORGANIC LIGHT EMITTING DIODE AND DISPLAY DEVICE USING THE SAME

Discussed is a delayed fluorescence compound including a first electron donor moiety of indolo-[3,2,1-j,k]carbazole; a second electron donor moiety selected from indolo-[3,2,1-j,k]carbazole, carbazole or triphenylamine; and an electron acceptor moiety selected from dibenzothiophene sulfone or diphenyl sulfone, wherein the first and second electron donor moieties are combined to the electron acceptor moiety, and the electron acceptor moiety is combined to a first position or a para-position of the first electron donor moiety.

Condensed cyclic compound and organic light emitting device including the same

Disclosed are a condensed-ring compound and an organic light emitting device comprising the same. The condensed-ring compound is represented by chemical formula 1A or 1C. The organic light emitting device comprising the condensed-ring compound can have a

Indolocarbazol [3, 2, 1-jk] Hydroxycarbazole compound and an organic light emitting element having the same

There is provided an indolo[3,2,1-jk]carbazole compound having an excellent membrane property, a high T1 energy, and a deep HOMO level. There is also provided an organic light-emitting device that contains the indolo[3,2,1-jk]carbazole compound. There is