132071
1,3,5-Triethylbenzene
≥97%
Synonym(s):
1,3,5-Triethylbenzene
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About This Item
Linear Formula:
C6H3(C2H5)3
CAS Number:
Molecular Weight:
162.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-017-3
Beilstein/REAXYS Number:
2039481
MDL number:
Assay:
≥97%
Form:
liquid
Quality Level
assay
≥97%
form
liquid
refractive index
n20/D 1.495 (lit.)
bp
215 °C (lit.)
density
0.862 g/mL at 25 °C (lit.)
SMILES string
CCc1cc(CC)cc(CC)c1
InChI
1S/C12H18/c1-4-10-7-11(5-2)9-12(6-3)8-10/h7-9H,4-6H2,1-3H3
InChI key
WJYMPXJVHNDZHD-UHFFFAOYSA-N
Application
1,3,5-Triethylbenzene was used as a supramoelcular template to organize molecular-recognition elements. It was also used to synthesize a series of di- and trinucleating ligands.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
168.8 °F - closed cup
flash_point_c
76 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Xing Wang et al.
Beilstein journal of organic chemistry, 8, 1-10 (2012-03-17)
1,3,5-triethylbenzenes have been widely used as supramolecular templates to organize molecular-recognition elements. It is believed that the steric-gearing effect of the 1,3,5-triethylbenzene template directs the binding elements toward the same face of the central ring, hence increasing the binding affinity.
Gou Higashihara et al.
Dalton transactions (Cambridge, England : 2003), (14)(14), 1888-1898 (2008-03-29)
A series of di- and trinucleating ligands with a 1,3,5-triethylbenzene core connected to N,N-bidentate tethers was synthesized. The ligands readily reacted with monuclear Rh and Pd precursors to give the corresponding di- and trinuclear complexes, which were characterized by using
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 132071-25G | 04061838728777 |
| 132071-5G | 04061838728784 |