2,6-XYLENOL

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 Search

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

Title	Date	PubMed
Estimation of glycated hemoglobin by 2,6-dimethylphenol: Sulphuric acid conventional method.	2001 Jan	23105290
Determination of phenols in soil by supercritical fluid extraction-capillary electrochromatography.	2001 Jan 12	11217037
Structural requirements of phenol derivatives for direct activation of chloride currents via GABA(A) receptors.	2001 Jun 8	11399263
Chiral proton donor reagents: tin tetrachloride--coordinated optically active binaphthol derivatives.	2002	12112869
Molybdenum-phosphorus triple bond stabilization by ancillary alkoxide ligation: synthesis and structure of a terminal phosphide tris-1-methylcyclohexanoxide complex.	2003 Aug 6	12889934
Optically active mexiletine analogues as stereoselective blockers of voltage-gated Na(+) channels.	2003 Nov 20	14613326
Depolymerization of poly(2,6-dimethyl-1,4-phenylene oxide) under oxidative conditions.	2003 Sep 5	12953209
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	15139275
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	14662728
Evaluation of the antioxidant properties of propofol and its nitrosoderivative. comparison with homologue substituted phenols.	2004 Mar	15129739
Polymer-based adsorption medium prepared using a fragment imprinting technique for homologues of chlorinated bisphenol A produced in the environment.	2004 Mar 12	15032347
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 Aug	16052268
Selective oxidative para C-C dimerization of 2,6-dimethylphenol.	2005 Dec 14	16307153
[Inhibitory effects of phenolic ecotoxicants on photobacteria at various pH values].	2005 Nov-Dec	16358753
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	16633656
Determination of chlorine dioxide in water by gas chromatography-mass spectrometry.	2006 Aug 4	16716337
High-affinity blockade of voltage-operated skeletal muscle sodium channels by 2,6-dimethyl-4-chlorophenol.	2006 Mar	16430789
Detailed examination of the degradation of phenol derivatives under oxygen delignification conditions.	2007 Feb 21	17300151
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 Jun 21	17844662
Proton-coupled electron-transfer oxidation of phenols by hexachloroiridate(IV).	2008 Dec 15	19006385
[New efficient producers of fungal laccases].	2008 Jan-Feb	18491602
Synthesis of (1-adamantylimido)vanadium(V) complexes containing aryloxo, ketimide ligands: effect of ligand substituents in olefin insertion/metathesis polymerization.	2008 Jul 21	18557610
Selective and stability-indicating methods for the simultaneous determination of mexiletine hydrochloride and/or its related substance: 2,6-dimethylphenol.	2008 Jul-Aug	18727529
[New promising antioxidants based on 2,6-dimethylphenol].	2008 Jul-Aug	18695730
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	18447332
A catalytic enantioselective conjugate addition of cyanide to enones.	2008 May 14	18419119
Engineering and Applications of fungal laccases for organic synthesis.	2008 Nov 20	19019256
trans-4-[(2,6-Dimethyl-phen-oxy)methyl]cyclo-hexa-necarboxylic acid.	2008 Nov 8	21581244
Potential of Penicillium species in the bioremediation field.	2009 Apr	19440525
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.	2009 Apr 15	19231207
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals.	2009 Dec 30	19692169
Two methods for catalytic generation of reactive enolates promoted by a chiral poly gd complex: application to catalytic enantioselective protonation reactions.	2009 Mar 25	19249830
Novel multiwalled carbon nanotubes-polyaniline composite film coated platinum wire for headspace solid-phase microextraction and gas chromatographic determination of phenolic compounds.	2009 May 1	19306999
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.	2010 Apr 15	19963316
9-(2,6-Dimethyl-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate.	2010 Oct 23	21589102
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	20689870

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:14:25 GMT 2023` Edited by `admin` on `Fri Dec 15 19:14:25 GMT 2023`
Record UNII	I8N0RO87OV
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

2,6-XYLENOL

Systematic Name

English

DIMETHYLPHENOL, 2,6-

Systematic Name

English

XYLENOL 2,6-DIMETHYLPHENOL [MI]

Common Name

English

2,6-DIMETHYLPHENOL

Systematic Name

English

XYLENOL 2,6-DIMETHYLPHENOL

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