Skip to Content
Merck
All Photos(1)

Key Documents

648906

Sigma-Aldrich

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

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C24H15Br3
CAS Number:
Molecular Weight:
543.09
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

97%

form

solid

mp

261-265 °C

SMILES string

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

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

InChI key

HJQRITCAXSBOPC-UHFFFAOYSA-N

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

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 4 - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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)
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)
Synthesis of a porous aromatic framework for adsorbing organic pollutants application
Ren H, et al.
Journal of Materials Chemistry, 21(28), 10348-10353 (2011)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service