13438-50-1

Basic information

• Product Name: 3-BROMOFLUORANTHENE
• Synonyms: 3-BROMOFLUORANTHENE
• CAS NO: 13438-50-1
• Molecular Formula: C₁₆H₉Br
• Molecular Weight: 281.15
• EINECS: 1312995-182-4
• Mol File: 13438-50-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 106.0 to 200.0 °C
• Boiling Point: 207°C/0.2mmHg(lit.)
• Flash Point: 209.4 °C
• Appearance: /
• Density: 1.578 g/cm³
• Refractive Index: 1.858
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: 3-BROMOFLUORANTHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMOFLUORANTHENE(13438-50-1)
• EPA Substance Registry System: 3-BROMOFLUORANTHENE(13438-50-1)

Safety Data

• Hazardous Substances Data: 13438-50-1(Hazardous Substances Data)

Usage

Uses

3-Bromofluoranthene is an intermediate in synthesizing 3-Methylfluoranthene (M305315), an environmental pollutant that is an active tumor initiator.

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 
• 64-19-7 acetic acid 
• 1351407-87-8 9-(3-bromoprop-2-ynyl)-9H-fluorene 
• 2768-94-7 9-(prop-2-ynyl)-9H-fluorene 
• 13823-55-7 2-Acetamidofluoranthene 
• 13823-61-5 3-Brom-2-acetamino-fluoranthen 
• 75-15-0 carbon disulfide 
• 7726-95-6 bromine 
• 7789-60-8 phosphorus tribromide 
• 13823-62-6 3-Brom-2-amino-fluoranthen 

Downstream Products

• 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 
• 744255-53-6 2-fluoranthen-3-yl-aniline 

Relevant articles and documents

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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 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.

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