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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
Supramolecular and coordination polymer complexes supported by a tripodal tripyridine ligand containing a 1,3,5-triethylbenzene spacer.
2004 Jul 26
Molecular recognition of carbohydrates with acyclic pyridine-based receptors.
2004 Oct 29
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 Nov 8
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 Oct 7
New efficient organic activators for highly enantioselective reduction of aromatic ketones by trichlorosilane.
2006 Aug 17
Modeling the mononuclear, dinuclear, and trinuclear copper(I) reaction centers of copper proteins using pyridylalkylamine ligands connected to 1,3,5-triethylbenzene spacer.
2006 Dec 25
A tricatecholic receptor for carbohydrate recognition: synthesis and binding studies.
2007 May 11
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 Apr 14
Poly[[{μ(3)-tris-[2-(4-phenyl-1,2,3-triazol-1-yl)eth-yl]amine}silver(I)] hexa-fluorido-phosphate].
2008 Sep 13
Selective recognition of tetrahedral dianions by a hexaaza cryptand receptor.
2009 Nov 21
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:45:02 GMT 2023
Edited
by admin
on Fri Dec 15 17:45:02 GMT 2023
Record UNII
02K328WWZQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3,5-TRIETHYLBENZENE
Systematic Name English
BENZENE, 1,3,5-TRIETHYL-
Systematic Name English
NSC-406584
Code English
Code System Code Type Description
DAILYMED
02K328WWZQ
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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CAS
102-25-0
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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WIKIPEDIA
1,3,5-Triethylbenzene
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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MESH
C516768
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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EPA CompTox
DTXSID30881228
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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ECHA (EC/EINECS)
203-017-3
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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PUBCHEM
7602
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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FDA UNII
02K328WWZQ
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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RXCUI
2475073
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
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NSC
406584
Created by admin on Fri Dec 15 17:45:02 GMT 2023 , Edited by admin on Fri Dec 15 17:45:02 GMT 2023
PRIMARY