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Details

Stereochemistry ACHIRAL
Molecular Formula C17H13N
Molecular Weight 231.2918
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-DIPHENYLPYRIDINE

SMILES

C1=CC=C(C=C1)C2=CC=CC(=N2)C3=CC=CC=C3

InChI

InChIKey=PJUOHDQXFNPPRF-UHFFFAOYSA-N
InChI=1S/C17H13N/c1-3-8-14(9-4-1)16-12-7-13-17(18-16)15-10-5-2-6-11-15/h1-13H

HIDE SMILES / InChI

Molecular Formula C17H13N
Molecular Weight 231.2918
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Iridium cyclometalated complexes with axial symmetry. Synthesis and photophysical properties of a trans-biscyclometalated complex containing the terdentate ligand 2,6-diphenylpyridine.
2004 Mar 22
Synthesis and luminescence of a charge-neutral, cyclometalated iridium(III) complex containing N--C--N- and C--N--C-coordinating terdentate ligands.
2004 Oct 18
Proton transfer reactions of methylanthracene radical cations with nitrogen-centered bases under non-steady-state conditions. a search for the possible effect of reactant impurities upon the kinetic data.
2005 Feb 18
Iridium cyclometalated complexes with axial symmetry: time-dependent density functional theory investigation of trans-bis-cyclometalated complexes containing the tridentate ligand 2,6-diphenylpyridine.
2005 Mar 7
Influence of aggregates and solvent aromaticity on the emission of conjugated polymers.
2006 Dec 14
Anticancer cyclometalated [Au(III)m(C(wedge)N(wedge)C)mL]n+ compounds: Synthesis and cytotoxic properties.
2006 Jul 5
Luminescent complexes of iridium(III) containing N/\C/\N-coordinating terdentate ligands.
2006 Oct 16
A class of luminescent cyclometalated alkynylgold(III) complexes: synthesis, characterization, and electrochemical, photophysical, and computational studies of [Au(C=N=C)(C triple bond C-R)] (C=N=C = kappa(3)C,N,C bis-cyclometalated 2,6-diphenylpyridyl).
2007 Apr 11
Ditopic N-Crowned 4-(p-Aminophenyl)-2,6-diphenylpyridines: implications of macrocycle topology on the spectroscopic properties, cation complexation, and differential anion responses.
2007 Apr 16
(μ-Diphenyl-phosphanido-κP:P')bis-[2,2'-(pyridine-2,6-diyl)diphenyl-κC,N,C)gold(III)] perchlorate acetonitrile solvate.
2008 Aug 6
2,9-Dimethyl-4,7-diphenyl-1,10-phenanthrolin-1-ium tetra-chloridoaurate(III).
2009 Apr 2
2-[3-(2-Pyrid-yl)pyrazin-2-yl]pyridinium tetra-chloridoaurate(III).
2009 Apr 8
Theoretical studies on structures and spectroscopic properties of cyclometalated gold(III) complexes.
2009 Aug 20
Direct ortho-arylation of N-phenacylpyridinium bromide by palladium-catalyzed C-H-bond activation.
2009 Dec 7
From classical adducts to frustrated Lewis pairs: steric effects in the interactions of pyridines and B(C6F5)3.
2009 Nov 2
Energetic and structural study of diphenylpyridine isomers.
2009 Oct 15
Hand-held mass spectrometer for environmentally relevant analytes using a variety of sampling and ionization methods.
2010
Control of enantioselectivity with flexible biaryl axes: terpene-based alkylzinc catalysts in enantioselective dialkylzinc additions.
2010 Dec 3
3-Phenyl-pyridinium tetra-chlorido-aurate(III).
2010 Feb 27
Bis(tribenzyl-ammonium) tetra-chloridoaurate(III) chloride.
2010 Jan 30
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:03:11 GMT 2023
Edited
by admin
on Fri Dec 15 18:03:11 GMT 2023
Record UNII
ZI75V15Y1T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DIPHENYLPYRIDINE
Systematic Name English
PYRIDINE, 2,6-DIPHENYL-
Systematic Name English
NSC-133378
Code English
Code System Code Type Description
NSC
133378
Created by admin on Fri Dec 15 18:03:11 GMT 2023 , Edited by admin on Fri Dec 15 18:03:11 GMT 2023
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CAS
3558-69-8
Created by admin on Fri Dec 15 18:03:11 GMT 2023 , Edited by admin on Fri Dec 15 18:03:11 GMT 2023
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EPA CompTox
DTXSID7022209
Created by admin on Fri Dec 15 18:03:11 GMT 2023 , Edited by admin on Fri Dec 15 18:03:11 GMT 2023
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PUBCHEM
72920
Created by admin on Fri Dec 15 18:03:11 GMT 2023 , Edited by admin on Fri Dec 15 18:03:11 GMT 2023
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FDA UNII
ZI75V15Y1T
Created by admin on Fri Dec 15 18:03:11 GMT 2023 , Edited by admin on Fri Dec 15 18:03:11 GMT 2023
PRIMARY
ECHA (EC/EINECS)
222-620-2
Created by admin on Fri Dec 15 18:03:11 GMT 2023 , Edited by admin on Fri Dec 15 18:03:11 GMT 2023
PRIMARY