19264-68-7

Usage

Uses

Used in Organic Electronic Devices:
9-BENZOYLCARBAZOLE is used as a component in organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs) for its high thermal stability and electron transporting properties, which are crucial for the performance and longevity of these devices.
Used in Medicinal Chemistry:
9-BENZOYLCARBAZOLE is used as a potential therapeutic agent for its antioxidant, anti-inflammatory, and neuroprotective activities. Its potential in medicinal chemistry is further highlighted by its anti-tumor and anti-cancer properties, as demonstrated in certain studies.
Used in Anticancer Research:
In the field of oncology, 9-BENZOYLCARBAZOLE is used as a subject of research for its potential to combat cancer. Its anti-tumor and anti-cancer properties are of particular interest, warranting further investigation into its mechanisms of action and possible clinical applications.
Used in Antioxidant and Anti-inflammatory Applications:
9-BENZOYLCARBAZOLE is utilized for its antioxidant properties, which can help protect cells from oxidative stress and damage. Additionally, its anti-inflammatory activity makes it a candidate for treatments targeting inflammation-related conditions.
Overall, 9-BENZOYLCARBAZOLE is a versatile compound with a wide range of potential applications across various industries, from electronics to medicine, underscoring its significance in contemporary research and development.

InChI:InChI=1/C5H10Br2/c1-4(6)3-5(2)7/h4-5H,3H2,1-2H3

Upstream product

• 86-74-8 9H-carbazole 
• 98-88-4 benzoyl chloride 
• 93-97-0 benzoic acid anhydride 
• 611-74-5 N,N-dimethylbenzamide 
• 769-78-8 vinyl benzoate 
• 82390-31-6 N-(2-biphenylyl)-N-hydroxybenzamide 
• 19402-87-0 9-benzyl-9H-carbazole 
• 21711-71-7 2-phenylnitrosobenzene 
• 7404-97-9 2-(benzoylamino)biphenyl 
• 591-50-4 iodobenzene 
• 13939-06-5 molybdenum hexacarbonyl 
• 15310-02-8 o-iodobenzanilide 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 201230-82-2 carbon monoxide 

Downstream Products

• 872270-18-3 1-(9-benzoyl-carbazol-2-yl)-ethanone 
• 76-84-6 triphenylmethyl alcohol 
• 23592-77-0 2,9-dibenzoylcarbazole 
• 912764-83-1 1-carbazol-2-yl-2-phenyl-ethanone 
• 700863-88-3 1-(9-benzoyl-carbazol-2-yl)-2-phenyl-ethanone 
• 19264-66-5 9H-carbazole-3-yl(phenyl)methanone 
• 17274-71-4 3,6-dichloro-N-benzoylcarbazole 
• 177775-87-0 (3-bromo-9H-carbazol-9-yl)(phenyl)methanone 
• 912850-81-8 9-benzoyl-3,6-dibromo-carbazole 
• 101880-09-5 9-benzoyl-3-nitro-carbazole 
• 86-74-8 9H-carbazole 
• 23592-74-7 2-acetylcarbazole 
• 51094-28-1 9H-carbazole-2-carboxylic acid 
• 92552-42-6 1-(9-methyl-9H-carbazol-2-yl)ethanone 

Relevant academic research and scientific papers

Palladium-catalyzed phosphination and amination through C–H bond functionalization on biphenyl: Amido-substituent as directing group

The formation of N-(2’-(diphenylphosphoryl)-[1,1′-biphenyl]-2-yl)-2,3,4,5,6-pentafluorobenzamide (3_eaaa) has been achieved through the palladium-catalyzed and Ag(I)-assisted C–H functionalization of N-([1,1′-biphenyl]-2-yl)-2,3,4,5,6-pentafluorobenzamide

Visible-light induced synthesis of 8H-indolo[3,2,1-de]phenanthridin-8-ones and related heterocycles using benzothiadiazole as photocatalyst

A simple and mild approach to access polycyclic 8H-indolo[3,2,1-de]phenanthridin-8-ones through a visible-light induced free radical cyclization of (2-bromophenyl)(9H-carbazol-9-yl)methanones using benzothiadiazole-containing photocatalyst is reported. This transition metal free method can be utilized for the synthesis of 7H-thieno[2′,3′:4,5]pyrido[3,2,1-jk]carbazol-7-one, 14H-isoquinolino[4,3,2-kl]phenoxazin-14-one, 14H-isoquinolino[4,3,2-kl]phenothiazin-14-one, and 10,11,12,13-tetrahydro-8H-indolo[3,2,1-de]phenanthridin-8-one. Moreover, some products were found to emit strong blue or green fluorescence.

Electrochemical Palladium-Catalyzed Intramolecular C—H Amination of 2-Amidobiaryls for Synthesis of Carbazoles

The synthesis of carbazoles based on the electrochemical Pd-catalyzed intramolecular C—H amination of 2-amidobiaryls through oxidative cross coupling has been achieved under mild reaction conditions. The reaction can be carried out in undivided cell without the addition of external chemical oxidant. Besides good functional group compatibility, the desired carbazoles can be scaled up and modified easily. Compared with previous methods, this protocol affords a simple and sustainable avenue for the construction of carbazoles.

Method for the synthesis of 1-carbazole-boric acid pinacol ester by amide ortho-orthogonal directing borification

The present invention discloses a method of synthesizing 1-carbazole - boronic acid pinacol ester by orthophoreinization of an amide orthostatic directional boronate, the steps comprising: (1) the carbazole and the amidation reagent under the action of a

Electrochemical Synthesis of Carbazoles by Dehydrogenative Coupling Reaction

A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N-protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.

X-ray excited ultralong room-temperature phosphorescence for organic afterglow scintillators

We present X-ray-excitable organic ultralong room temperature phosphorescence (X-OURTP) for afterglow scintillators through implanting lone-pair electron involved n-π? transitions and efficient charge transfer characters into H-aggregations of organic cry

N-Acylcarbazoles and N-Acylindoles: Electronically Activated Amides for N-C(O) Cross-Coupling by Nlpto Ar Conjugation Switch

The development of new amide precursors for selective, catalytic activation of carbon-nitrogen bonds in amides is a fundamental objective of this emerging reactivity manifold. We report the palladium-catalyzed Suzuki-Miyaura cross-coupling of N-acylcarbazoles and N-acylindoles with arylboronic acids by a highly selective N-C(O) cleavage. The key amide bond ground-state destabilization stems from Nlp to Ar conjugation and enables us for the first time to achieve reactivity similar to that for N-acylsulfonamide and N-acylcarbamate activation in simple anilides.

Acyl-Directed ortho-Borylation of Anilines and C7 Borylation of Indoles using just BBr3

Indoles are privileged heterocycles found in many biologically active pharmaceuticals and natural products. However, the selective functionalization of the benzenoid moiety in indoles in preference to the more reactive pyrrolic unit is a significant challenge. Herein we report that N-acyl directing groups enable the C7-selective C?H borylation of indoles using just BBr3. This transformation shows some functional-group tolerance and notably proceeds with C6 substituted indoles. The directing group can be readily removed in situ and the products isolated as the pinacol boronate esters. Acyl-directed electrophilic borylation can be extended to carbazoles and anilines with excellent ortho selectivity. 4-amino-indoles are amenable to this process, with acyl group installation and directed electrophilic C?H borylation enabling selective formation of C5-BPin-indoles.

TICT (twisted intramolecular charge transfer) triplet-state electroluminescent material and device

The invention provides an electroluminescent material and an electroluminescent device utilizing the same as a luminous layer. The electroluminescent material comprises a compound represented in formula I in the description, wherein R1, R2, R3, R4 and R5

SELECTIVE INHIBITORS OF GENOTOXIC STRESS-INDUCED IKK/NF-kB PATHWAYS

The invention relates to chemical compounds and their use as a medicament in the treatment of a disease associated with genotoxic stress-induced I KK/NF-κΒ (NF-kappaB) activation, preferably in the treatment of a subject suffering from cancer exhibiting g