13438-50-1

Usage

Uses

Used in Chemical Synthesis:
3-Bromofluoranthene is used as an intermediate in the synthesis of 3-Methylfluoranthene (M305315), an environmental pollutant that acts as an active tumor initiator. This synthesis process is crucial for understanding the formation and impact of such pollutants on human health and the environment.
Used in Environmental Research:
3-Bromofluoranthene plays a significant role in environmental research, particularly in studying the effects of 3-Methylfluoranthene on ecosystems and human health. By understanding the synthesis and properties of 3-Bromofluoranthene, researchers can better evaluate the risks associated with exposure to 3-Methylfluoranthene and develop strategies for mitigating its impact.
Used in Pharmaceutical Development:
Although not explicitly mentioned in the provided materials, 3-Bromofluoranthene may also have potential applications in the development of pharmaceuticals, given its role as a synthetic intermediate. Its unique chemical structure could be utilized in the creation of new drugs or drug delivery systems, contributing to advancements in medicine and healthcare.

InChI:InChI=1/C16H9Br/c17-15-9-8-13-11-5-2-1-4-10(11)12-6-3-7-14(15)16(12)13/h1-9H

Upstream product

• 206-44-0 fluoranthene 
• 417710-46-4 4-bromo-1,2,3,10b-tetrahydro-fluoranthene 
• 118-75-2 chloranil 
• 108-38-3 m-xylene 
• 75-15-0 carbon disulfide 
• 7726-95-6 bromine 
• 7789-60-8 phosphorus tribromide 
• 64-19-7 acetic acid 
• 13823-61-5 3-Brom-2-acetamino-fluoranthen 
• 2768-94-7 9-(prop-2-ynyl)-9H-fluorene 
• 1351407-87-8 9-(3-bromoprop-2-ynyl)-9H-fluorene 
• 13823-55-7 2-Acetamidofluoranthene 
• 13823-62-6 3-Brom-2-amino-fluoranthen 

Downstream Products

• 851767-73-2 C₅₆H₃₆N₂ 
• 359012-63-8 7,12-diphenylbenzo[k]fluoranthene-3-boronic acid 
• 1426401-64-0 C₂₈H₁₇Br 
• 1426401-43-5 C₅₈H₃₆N₂ 
• 667940-21-8 3-(4-bromophenyl)fluoranthene 
• 1426401-35-5 C₅₂H₃₂N₂ 
• 1392844-39-1 C₄₆H₂₈N₂ 

Relevant academic research and scientific papers

Phosphoryl substituted Fluoranthene derivatives and organic electroluminescent device including the same

Provided are phosphoryl group bonded fluoranthene derivatives represented by chemical formula 1. In chemical formula 1, the definition of each substituent group is the same as described in the specification. The fluoranthene derivatives have excellent current density and durability in comparison to a conventional material, and can be used to an organic electroluminescent device, thereby lowering the driving voltage and improving luminous efficiency while extending the lifespan.

NOVEL ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

The present invention relates to a novel compound and an organic electroluminescent device containing the same. Since the compounds according to the present invention have high efficiency in transporting electrons, crystallization could be prevented when manufacturing the device, and since they are adaptable in the formation of the layers, the current characteristic of the device is improved, and finally they can manufacture an organic electroluminescent device having lowered driving voltage, advanced power efficiency, and improved light emitting efficiency and lifetime characteristic compared with devices comprising the conventional materials.

NOVEL COMPOUNDS FOR ORGANIC ELECTRONIC MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

Provided are novel compounds for organic electronic material and an organic electroluminescent device using the same. Because the compounds for organic electronic material according to the present invention are highly efficient at transporting electrons, crystallization is prevented when manufacturing a device and current properties of the device are improved due to favorably formed layers. Accordingly, OLED devices having improved power efficiency as well as reduced operating voltage can be manufactured.

Metal- and chemical-oxidant-free c-h/c-h cross-coupling of aromatic compounds: The use of radical-cation pools

Pool and couple: A method for oxidative C-H/C-H cross-coupling has been developed using "radical-cation pools". Aromatic compounds react with aryl radical cations, which are generated and accumulated by low-temperature electrolysis (see scheme). This method avoids both the nonselective oxidation of substrates and oxidation of products and effects the C-H/C-H cross-coupling of aromatic compounds without metal complexes and chemical oxidants. Copyright

ORGANIC ELECTROLUMINESCENCE DEVICE AND ANTHRACENE DERIVATIVE

An anthracene derivative having a specific asymmetric structure is provided. The asymmetric anthracenes are useful in an organic electroluminescence device and exhibit efficient light emission and a long performance lifetime.

Synthesis of fluoranthenes by hydroarylation of alkynes catalyzed by gold(I) or gallium trichloride

Electrophilic gold(I) catalyst 6 competes with GaCl3 as the catalyst of choice in the synthesis of fluoranthenes by intramolecular hydroarylation of alkynes. The potential of this catalyst for the preparation of polyarenes is illustrated by a s