657336
1,3,5-Tris(bromomethyl)benzene
97%
Synonym(s):
2,4,6-Tri(bromomethyl)benzene, Tribromomesitylene
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About This Item
Linear Formula:
C9H9Br3
CAS Number:
Molecular Weight:
356.88
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Product Name
1,3,5-Tris(bromomethyl)benzene, 97%
InChI
1S/C9H9Br3/c10-4-7-1-8(5-11)3-9(2-7)6-12/h1-3H,4-6H2
SMILES string
BrCc1cc(CBr)cc(CBr)c1
InChI key
GHITVUOBZBZMND-UHFFFAOYSA-N
assay
97%
form
solid
mp
94-99 °C
Quality Level
Related Categories
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.
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.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Triptycene based microporous polymers (TMPs): Efficient small gas (H2 and CO2) storage and high CO2/N2 selectivity
Bera R, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 257(6), 253-261 (2018)
Fabrication of crosslinked polybenzimidazole membranes by trifunctional crosslinkers for high temperature proton exchange membrane fuel cells
Yang J, et al.
International Journal of Hydrogen Energy, 43(6), 3299-3307 (2018)
Synthesis, 39-39 (2008)
1, 3, 5-Tris (bromomethyl) benzene
Fernandes J, et al.
Acta Crystallographica Section C, Structural Chemistry, 67(6), o198-o200 (2011)
Papri Sutar et al.
Inorganic chemistry, 56(16), 9417-9425 (2017-08-10)
The recent upsurge in research on coordination polymer gels (CPGs) stems from their synthetic modularity, nanoscale processability, and versatile functionalities. Here we report self-assembly of an amphiphilic, tripodal low-molecular weight gelator (L) that consists of 4,4',4-[1,3,5-phenyl-tri(methoxy)]-tris-benzene core and 2,2':6',2″-terpyridyl termini
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