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
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
Glucuronidation of propofol and its analogs by human and rat liver microsomes.	2003 Feb	12576683
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
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	14697702
Effects of speciation on partitioning of iodine in aqueous biphasic systems and onto ABEC resins.	2004 Jul 25	15177173
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	15912136
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
Detailed examination of the degradation of phenol derivatives under oxygen delignification conditions.	2007 Feb 21	17300151
Proton-coupled electron-transfer oxidation of phenols by hexachloroiridate(IV).	2008 Dec 15	19006385
[New efficient producers of fungal laccases].	2008 Jan-Feb	18491602
Selective and stability-indicating methods for the simultaneous determination of mexiletine hydrochloride and/or its related substance: 2,6-dimethylphenol.	2008 Jul-Aug	18727529
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
trans-4-[(2,6-Dimethyl-phen-oxy)methyl]cyclo-hexa-necarboxylic acid.	2008 Nov 8	21581244
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.	2009 Apr 15	19231207
Chemical oxidation of 2,6-dimethylaniline in the fenton process.	2009 Nov 15	20028063
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	20571684
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

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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