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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

Molecular Formula C8H10O
Molecular Weight 122.1644
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
9-(2,6-Dimethyl-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.
2010-10-23
Gas-phase phenol methylation over Mg/Me/O (Me = Al, Cr, Fe) catalysts: mechanistic implications due to different acid-base and dehydrogenating properties.
2010-09-28
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.
2010-08-07
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.
2010-04-15
Catalytic carbon-carbon bond-forming reactions of aminoalkane derivatives with imines.
2010-03-17
Mitochondrial biotransformation of omega-(phenoxy)alkanoic acids, 3-(phenoxy)acrylic acids, and omega-(1-methyl-1H-imidazol-2-ylthio)alkanoic acids: a prodrug strategy for targeting cytoprotective antioxidants to mitochondria.
2010-02-15
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals.
2009-12-30
Chemical oxidation of 2,6-dimethylaniline in the fenton process.
2009-11-15
Coupling poly-(methacrylic acid-co-ethylene glycol dimethacrylate) monolith microextraction to capillary electrophoresis for the determination of phenols in water samples.
2009-06-15
Substituted isoxazole analogs of farnesoid X receptor (FXR) agonist GW4064.
2009-06-01
Reaction of an oxaruthenacycle with DMAD. Stoichiometric transformations of 2,6-xylenol to allylic phenols and benzopyrans via sp(3) C-H bond cleavage reaction.
2009-05-07
Novel multiwalled carbon nanotubes-polyaniline composite film coated platinum wire for headspace solid-phase microextraction and gas chromatographic determination of phenolic compounds.
2009-05-01
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.
2009-04-15
Potential of Penicillium species in the bioremediation field.
2009-04
Two methods for catalytic generation of reactive enolates promoted by a chiral poly gd complex: application to catalytic enantioselective protonation reactions.
2009-03-25
Proton-coupled electron-transfer oxidation of phenols by hexachloroiridate(IV).
2008-12-15
Engineering and Applications of fungal laccases for organic synthesis.
2008-11-20
trans-4-[(2,6-Dimethyl-phen-oxy)methyl]cyclo-hexa-necarboxylic acid.
2008-11-08
Selective and stability-indicating methods for the simultaneous determination of mexiletine hydrochloride and/or its related substance: 2,6-dimethylphenol.
2008-08-30
[New promising antioxidants based on 2,6-dimethylphenol].
2008-08-13
Synthesis of (1-adamantylimido)vanadium(V) complexes containing aryloxo, ketimide ligands: effect of ligand substituents in olefin insertion/metathesis polymerization.
2008-07-21
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.
2008-06-02
[New efficient producers of fungal laccases].
2008-05-22
A catalytic enantioselective conjugate addition of cyanide to enones.
2008-05-14
Synthesis, magnetic behaviour, and X-ray structures of dinuclear copper complexes with multiple bridges. Efficient and selective catalysts for polymerization of 2,6-dimethylphenol.
2007-06-21
Detailed examination of the degradation of phenol derivatives under oxygen delignification conditions.
2007-02-21
Determination of chlorine dioxide in water by gas chromatography-mass spectrometry.
2006-08-04
Tropospheric multiphase chemistry of 2,5- and 2,6-dimethylphenols: determination of the mass accommodation coefficients and the Henry's law constants.
2006-04-14
High-affinity blockade of voltage-operated skeletal muscle sodium channels by 2,6-dimethyl-4-chlorophenol.
2006-03
[Inhibitory effects of phenolic ecotoxicants on photobacteria at various pH values].
2005-12-20
Selective oxidative para C-C dimerization of 2,6-dimethylphenol.
2005-12-14
A comparative study of water soluble 5,10,15,20-tetrakis(2,6-dichloro-3-sulfophenyl)porphyrin and its metal complexes as efficient sensitizers for photodegradation of phenols.
2005-08
Structural features of phenol derivatives determining potency for activation of chloride currents via alpha(1) homomeric and alpha(1)beta heteromeric glycine receptors.
2005-08
Antioxidant activity of propofol and related monomeric and dimeric compounds.
2005-03
Effects of speciation on partitioning of iodine in aqueous biphasic systems and onto ABEC resins.
2004-07-25
Polymer-based adsorption medium prepared using a fragment imprinting technique for homologues of chlorinated bisphenol A produced in the environment.
2004-03-12
Evaluation of the antioxidant properties of propofol and its nitrosoderivative. comparison with homologue substituted phenols.
2004-03
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.
2004-02-15
Oxidative polymerization of 2,6-dimethylphenol to form poly(2,6-dimethyl-1,4-phenyleneoxide) in water.
2004-01-30
An improved model for the binding of lidocaine and structurally related local anaesthetics to fast-inactivated voltage-operated sodium channels, showing evidence of cooperativity.
2004-01
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
Optically active mexiletine analogues as stereoselective blockers of voltage-gated Na(+) channels.
2003-11-20
Depolymerization of poly(2,6-dimethyl-1,4-phenylene oxide) under oxidative conditions.
2003-09-05
Molybdenum-phosphorus triple bond stabilization by ancillary alkoxide ligation: synthesis and structure of a terminal phosphide tris-1-methylcyclohexanoxide complex.
2003-08-06
Glucuronidation of propofol and its analogs by human and rat liver microsomes.
2003-02
Vibrational analysis of substituted phenols: part II. Transferability of valence force constants.
2002-12
Block of voltage-operated sodium channels by 2,6-dimethylphenol, a structural analogue of lidocaine's aromatic tail.
2002-09
Chiral proton donor reagents: tin tetrachloride--coordinated optically active binaphthol derivatives.
2002
Structural requirements of phenol derivatives for direct activation of chloride currents via GABA(A) receptors.
2001-06-08
Estimation of glycated hemoglobin by 2,6-dimethylphenol: Sulphuric acid conventional method.
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:39:36 GMT 2025
Edited
by admin
on Mon Mar 31 19:39:36 GMT 2025
Record UNII
I8N0RO87OV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-Xylenol
FHFI  
Systematic Name English
2,6-DIMETHYLPHENOL
HSDB  
Preferred Name English
DIMETHYLPHENOL, 2,6-
Systematic Name English
XYLENOL 2,6-DIMETHYLPHENOL [MI]
Common 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 Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
Code System Code Type Description
MESH
C036531
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
WIKIPEDIA
2,6-XYLENOL
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
HSDB
5697
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
NSC
2123
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
MERCK INDEX
m11549
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY Merck Index
SMS_ID
300000052973
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
CAS
576-26-1
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
JECFA MONOGRAPH
586
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID9024063
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-400-1
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
FDA UNII
I8N0RO87OV
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
PUBCHEM
11335
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (GC)
EP