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Details

Stereochemistry ACHIRAL
Molecular Formula C12H18
Molecular Weight 162.2713
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3,5-TRIETHYLBENZENE

SMILES

CCC1=CC(CC)=CC(CC)=C1

InChI

InChIKey=WJYMPXJVHNDZHD-UHFFFAOYSA-N
InChI=1S/C12H18/c1-4-10-7-11(5-2)9-12(6-3)8-10/h7-9H,4-6H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C12H18
Molecular Weight 162.2713
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Selective recognition of tetrahedral dianions by a hexaaza cryptand receptor.
2009-11-21
Poly[[{μ(3)-tris-[2-(4-phenyl-1,2,3-triazol-1-yl)eth-yl]amine}silver(I)] hexa-fluorido-phosphate].
2008-09-13
Syntheses of novel di- and trinucleating ligands having a triethylbenzene core with N,N-bidentate tethers: their complexation toward Pd and Rh organometallic fragments.
2008-04-14
A tricatecholic receptor for carbohydrate recognition: synthesis and binding studies.
2007-05-11
Modeling the mononuclear, dinuclear, and trinuclear copper(I) reaction centers of copper proteins using pyridylalkylamine ligands connected to 1,3,5-triethylbenzene spacer.
2006-12-25
New efficient organic activators for highly enantioselective reduction of aromatic ketones by trichlorosilane.
2006-08-17
Formation of tetra(ethylene oxide) terminated Si-C linked monolayers and their derivatization with glycine: an example of a generic strategy for the immobilization of biomolecules on silicon.
2005-11-08
Structure and photoluminescence property of two-dimensional coordination polymer complexes involving Cu(I)(6)X(6)(X = Cl, Br, I) hexagon prism cluster supported by a tripodal tripyridine ligand with 1,3,5-triethylbenzene spacer.
2005-10-07
Adsorption of single-ring organic compounds to wood charcoals prepared under different thermochemical conditions.
2005-06-01
A new tripodal receptor for molecular recognition of monosaccharides. A paradigm for assessing glycoside binding affinities and selectivities by 1H NMR spectroscopy.
2004-12-22
Molecular recognition of carbohydrates with acyclic pyridine-based receptors.
2004-10-29
Supramolecular and coordination polymer complexes supported by a tripodal tripyridine ligand containing a 1,3,5-triethylbenzene spacer.
2004-07-26
Tris(arylmethyl) derivatives of 1,3,5-trimethoxy- and 1,3,5-triethylbenzene.
2003-05-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:51:22 GMT 2025
Edited
by admin
on Mon Mar 31 18:51:22 GMT 2025
Record UNII
02K328WWZQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3,5-TRIETHYLBENZENE
Systematic Name English
NSC-406584
Preferred Name English
BENZENE, 1,3,5-TRIETHYL-
Systematic Name English
Code System Code Type Description
DAILYMED
02K328WWZQ
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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CAS
102-25-0
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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WIKIPEDIA
1,3,5-Triethylbenzene
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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MESH
C516768
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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EPA CompTox
DTXSID30881228
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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ECHA (EC/EINECS)
203-017-3
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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PUBCHEM
7602
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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FDA UNII
02K328WWZQ
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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RXCUI
2475073
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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NSC
406584
Created by admin on Mon Mar 31 18:51:22 GMT 2025 , Edited by admin on Mon Mar 31 18:51:22 GMT 2025
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