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Merck
CN

648906

1,3,5-Tris(4-bromophenyl)benzene

97%

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About This Item

Empirical Formula (Hill Notation):
C24H15Br3
CAS Number:
7511-49-1
Molecular Weight:
543.09
NACRES:
NA.23
PubChem Substance ID:
329760011
UNSPSC Code:
12352103
MDL number:
MFCD00362911
Assay:
97%
Form:
solid

Key Documents

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InChI

1S/C24H15Br3/c25-22-7-1-16(2-8-22)19-13-20(17-3-9-23(26)10-4-17)15-21(14-19)18-5-11-24(27)12-6-18/h1-15H

SMILES string

Brc1ccc(cc1)-c2cc(cc(c2)-c3ccc(Br)cc3)-c4ccc(Br)cc4

InChI key

HJQRITCAXSBOPC-UHFFFAOYSA-N

assay

97%

form

solid

mp

261-265 °C

Quality Level

200

Related Categories

General description

1,3,5-Tris(4-bromophenyl)benzene (TBB) is a halogenated aromatic monomer that can be used in the formation of covalent aromatic frameworks(COF).

Application

TBB can be used to synthesize porous aromatic frameworks for the development of adsorption membranes to treat organic pollutants. It can also be used in the fabrication of pyridine based high efficiency organic light emitting diodes(OLEDs).

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318,H413

Hazard Classifications

Aquatic Chronic 4 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG9594
BCCC8723
BCBR2155V
BCBL8852V
BCBH9198V

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Star-shaped oligothiophenes for solution-processible organic electronics: flexible aliphatic spacers approach
Ponomarenko SA, et al.
Chemistry of Materials, 18(17), 4101-4108 (2006)
Surface mediated synthesis of 2D covalent organic frameworks: 1, 3, 5-tris (4-bromophenyl) benzene on graphite (001), Cu (111), and Ag (110)
Gutzler R, et al.
Chemical Communications (Cambridge, England), 4456-4458 (2009)
Synthesis of a porous aromatic framework for adsorbing organic pollutants application
Ren H, et al.
Journal of Materials Chemistry, 21(28), 10348-10353 (2011)
Pyridine-containing triphenylbenzene derivatives with high electron mobility for highly efficient phosphorescent OLEDs
Su, Shi-Jian; Chiba, Takayuki; et al.
Advanced Materials, 20(11), 2125-2130 (2008)
Ruiyan Sun et al.
ChemSusChem, 12(14), 3278-3285 (2019-04-30)
Methyl formate was produced in one pot through the hydrogenation of CO2 to formic acid/formate followed by an esterification step. The route offers the possibility to integrate renewable energy into the fossil-based chemical value chain. In this work, a phosphine-polymer-anchored

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