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132071

Sigma-Aldrich

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:
102-25-0
Molecular Weight:
162.27
Beilstein:
2039481
EC Number:
203-017-3
MDL number:
MFCD00009261
UNSPSC Code:
12352100
PubChem Substance ID:
24847545
NACRES:
NA.22

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

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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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H413

Hazard Classifications

Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

168.8 °F - closed cup

Flash Point(C)

76 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBL4695V
1448126V
1448125
1448126
02723BH

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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
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.

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