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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O
Molecular Weight 122.1644
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-XYLENOL

SMILES

CC1=CC=CC(C)=C1O

InChI

InChIKey=NXXYKOUNUYWIHA-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Estimation of glycated hemoglobin by 2,6-dimethylphenol: Sulphuric acid conventional method.
2001 Jan
Determination of phenols in soil by supercritical fluid extraction-capillary electrochromatography.
2001 Jan 12
Structural requirements of phenol derivatives for direct activation of chloride currents via GABA(A) receptors.
2001 Jun 8
Chiral proton donor reagents: tin tetrachloride--coordinated optically active binaphthol derivatives.
2002
Block of voltage-operated sodium channels by 2,6-dimethylphenol, a structural analogue of lidocaine's aromatic tail.
2002 Sep
Depolymerization of poly(2,6-dimethyl-1,4-phenylene oxide) under oxidative conditions.
2003 Sep 5
Phenol and lactone receptors in the distal sensilla of the Haller's organ in Ixodes ricinus ticks and their possible role in host perception.
2004
Luminescence quenching of tris(2,2'-bipyridine)ruthenium(II) by 2,6-dimethylphenol and 4-bromo-2,6-dimethylphenol in sol-gel-processed silicate thin films.
2004 Feb 15
An improved model for the binding of lidocaine and structurally related local anaesthetics to fast-inactivated voltage-operated sodium channels, showing evidence of cooperativity.
2004 Jan
Oxidative polymerization of 2,6-dimethylphenol to form poly(2,6-dimethyl-1,4-phenyleneoxide) in water.
2004 Jan 30
Effects of speciation on partitioning of iodine in aqueous biphasic systems and onto ABEC resins.
2004 Jul 25
Evaluation of the antioxidant properties of propofol and its nitrosoderivative. comparison with homologue substituted phenols.
2004 Mar
Polymer-based adsorption medium prepared using a fragment imprinting technique for homologues of chlorinated bisphenol A produced in the environment.
2004 Mar 12
Structural features of phenol derivatives determining potency for activation of chloride currents via alpha(1) homomeric and alpha(1)beta heteromeric glycine receptors.
2005 Aug
Antioxidant activity of propofol and related monomeric and dimeric compounds.
2005 Mar
[Inhibitory effects of phenolic ecotoxicants on photobacteria at various pH values].
2005 Nov-Dec
Tropospheric multiphase chemistry of 2,5- and 2,6-dimethylphenols: determination of the mass accommodation coefficients and the Henry's law constants.
2006 Apr 14
Determination of chlorine dioxide in water by gas chromatography-mass spectrometry.
2006 Aug 4
High-affinity blockade of voltage-operated skeletal muscle sodium channels by 2,6-dimethyl-4-chlorophenol.
2006 Mar
Proton-coupled electron-transfer oxidation of phenols by hexachloroiridate(IV).
2008 Dec 15
[New efficient producers of fungal laccases].
2008 Jan-Feb
Synthesis of (1-adamantylimido)vanadium(V) complexes containing aryloxo, ketimide ligands: effect of ligand substituents in olefin insertion/metathesis polymerization.
2008 Jul 21
Selective and stability-indicating methods for the simultaneous determination of mexiletine hydrochloride and/or its related substance: 2,6-dimethylphenol.
2008 Jul-Aug
Versatile scorpionates and new developments in the denticity changes of NNCp hybrid scorpionate/cyclopentadienyl ligands in Sc and Y compounds: from kappa1-Neta5-Cp to kappa2-NNeta5-Cp.
2008 Jun 2
A catalytic enantioselective conjugate addition of cyanide to enones.
2008 May 14
Engineering and Applications of fungal laccases for organic synthesis.
2008 Nov 20
trans-4-[(2,6-Dimethyl-phen-oxy)methyl]cyclo-hexa-necarboxylic acid.
2008 Nov 8
Potential of Penicillium species in the bioremediation field.
2009 Apr
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.
2009 Apr 15
Two methods for catalytic generation of reactive enolates promoted by a chiral poly gd complex: application to catalytic enantioselective protonation reactions.
2009 Mar 25
Chemical oxidation of 2,6-dimethylaniline in the fenton process.
2009 Nov 15
Controlled synthesis of mononuclear or binuclear aryloxo ytterbium complexes supported by beta-diketiminate ligand and their activity for polymerization of epsilon-caprolactone and L-lactide.
2010 Aug 7
Catalytic carbon-carbon bond-forming reactions of aminoalkane derivatives with imines.
2010 Mar 17
9-(2,6-Dimethyl-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.
2010 Oct 23
Gas-phase phenol methylation over Mg/Me/O (Me = Al, Cr, Fe) catalysts: mechanistic implications due to different acid-base and dehydrogenating properties.
2010 Sep 28
Patents
Name Type Language
2,6-XYLENOL
FHFI  
Systematic Name English
DIMETHYLPHENOL, 2,6-
Systematic Name English
XYLENOL 2,6-DIMETHYLPHENOL [MI]
Common Name English
2,6-DIMETHYLPHENOL
HSDB  
Systematic Name English
XYLENOL 2,6-DIMETHYLPHENOL
MI  
Systematic Name English
2,6-XYLENOL [FHFI]
Common Name English
NSC-2123
Code English
2,6-DIMETHYLPHENOL [HSDB]
Common Name English
FEMA NO. 3249
Code English
1-HYDROXY-2,6-DIMETHYLBENZENE
Systematic Name English
MEXILETINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
Common Name English
METACRESOL IMPURITY D [EP IMPURITY]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION 2,6-XYLENOL
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
Code System Code Type Description
MESH
C036531
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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WIKIPEDIA
2,6-XYLENOL
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
PRIMARY
HSDB
5697
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
PRIMARY
NSC
2123
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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MERCK INDEX
m11549
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
PRIMARY Merck Index
CAS
576-26-1
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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JECFA MONOGRAPH
586
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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EPA CompTox
DTXSID9024063
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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ECHA (EC/EINECS)
209-400-1
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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FDA UNII
I8N0RO87OV
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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PUBCHEM
11335
Created by admin on Fri Dec 15 19:14:25 GMT 2023 , Edited by admin on Fri Dec 15 19:14:25 GMT 2023
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