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657336 Sigma-Aldrich

1,3,5-Tris(bromomethyl)benzene

97%

Synonym: 2,4,6-Tri(bromomethyl)benzene, Tribromomesitylene

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Properties

Related Categories Materials Science, Organic and Printed Electronics, Synthetic Intermediates, Synthetic Tools and Reagents
Quality Level   100
assay   97%
mp   94-99 °C
SMILES string   BrCc1cc(CBr)cc(CBr)c1
InChI   1S/C9H9Br3/c10-4-7-1-8(5-11)3-9(2-7)6-12/h1-3H,4-6H2
InChI key   GHITVUOBZBZMND-UHFFFAOYSA-N

Description

General description

1,3,5-Tris(bromomethyl)benzene has three bromo substituents around an aromatic ring that can be used as a cross-linker. It is mainly utilized in the synthesis of ligands and dendrimeric monomers.

Application

1,3,5-Tris(bromomethyl)benzene can be crosslinked with triptycene monomers by using Friedel-Crafts alkylation reaction to form microporous polymers for selective adsorption of CO2 and H2. Proton exchange membranes (PEMs) can be fabricated by covalently linking polybenzimidazole (PBI) and 1,3,5-tris(bromomethyl)benzene as part of the tri-functional bromomethyls for fuel cell applications. It is also used in the synthesis of trifluoroacetamide derivative triaza[33]cyclophane.

A monomer for synthesizing dendrimers and light emitting oligomers.

Packaging

5, 10 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS05  GHS05
Signal word 
Danger
Hazard statements 
RIDADR 
UN 3261 8 / PGII
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles

Articles

Progress for High Performance Tandem Organic Solar Cells

The Centre of Nanoscale Science and Technology and Key Laboratory of Functional Polymer Materials, Institute of Polymer Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China State...
Keywords: Absorption, Nucleic acid annealing, Polymer science, Recombination, Renewable energy, Semiconductor, Separation, Solar cells

Peer-Reviewed Papers
15

References

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