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Details

Stereochemistry ACHIRAL
Molecular Formula C14H22O
Molecular Weight 206.3239
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-DI-TERT-BUTYLPHENOL

SMILES

CC(C)(C)C1=CC=CC(=C1O)C(C)(C)C

InChI

InChIKey=DKCPKDPYUFEZCP-UHFFFAOYSA-N
InChI=1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3

HIDE SMILES / InChI

Molecular Formula C14H22O
Molecular Weight 206.3239
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
General anesthetic potencies of a series of propofol analogs correlate with potency for potentiation of gamma-aminobutyric acid (GABA) current at the GABA(A) receptor but not with lipid solubility.
2001 Apr
[Determination of 2,4,6-tri-tert-butylphenol and related compounds in foods].
2001 Dec
Estrogenic activity of phenolic additives determined by an in vitro yeast bioassay.
2001 Feb
[Partially hydrogenated aryl-1,2/1,4-anthraquinone derivatives, 5-lipoxygenase inhibitors with arotinoid structure].
2001 Jul
Autoxidation of substituted phenols catalyzed by cobalt Schiff base complexes in supercritical carbon dioxide.
2001 Jul 2
Three-coordinate copper(II)-phenolate complexes.
2001 Nov 19
Structural evidence that propofol stabilizes different GABA(A) receptor states at potentiating and activating concentrations.
2002 Sep 1
[Methylated 2-aryl-1,4-naphtoquinone derivatives with diminished antioxidative activity].
2003 Aug
Percutaneous absorption of 2,6-di-tert-butyl-4-nitrophenol (DBNP) in isolated perfused porcine skin.
2003 Jun
High-affinity block of voltage-operated rat IIA neuronal sodium channels by 2,6 di-tert-butylphenol, a propofol analogue.
2003 Mar
[Studies on the new antiarthritic drug candidate S-2474].
2003 May
Improving the performance of methylalumoxane: a facile and efficient method to trap "free" trimethylaluminum.
2003 Oct 15
QSAR study of dual cyclooxygenase and 5-lipoxygenase inhibitors 2,6-di-tert-butylphenol derivatives.
2003 Sep 15
Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate.
2004 Feb 7
2,6 di-tert-butylphenol, a nonanesthetic propofol analog, modulates alpha1beta glycine receptor function in a manner distinct from propofol.
2004 Jul
Evaluation of the antioxidant properties of propofol and its nitrosoderivative. comparison with homologue substituted phenols.
2004 Mar
[The degradation characteristics of degrading bacterium of 2,6-di-tert-butylphenol].
2004 May
Parallel kinetic resolution of tert-butyl (RS)-3-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 3-alkyl-cispentacin derivatives.
2004 Nov 21
Degradation of 2,6-di-tert-butylphenol by an isolated high-efficiency bacterium strain.
2005
Antioxidant activity of propofol and related monomeric and dimeric compounds.
2005 Mar
2,6-di-tert-butylphenol revisited at 110 K.
2005 Nov
Synthesis and biological evaluation of acyclic triaryl (Z)-olefins possessing a 3,5-di-tert-butyl-4-hydroxyphenyl pharmacophore: dual inhibitors of cyclooxygenases and lipoxygenases.
2006 Aug 1
New analogues of butylated hydroxytoluene as anti-inflammatory and antioxidant agents.
2006 Aug 15
Determination of chlorine dioxide in water by gas chromatography-mass spectrometry.
2006 Aug 4
Use of SPME-GC-MS in the study of time evolution of the constituents of saffron aroma: modifications of the composition during storage.
2006 Jan
Synthesis and antioxidant activity of [60]fullerene-BHT conjugates.
2006 Jun 2
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
[Effects of two kinds of allelochemicals on photosynthesis and chlorophyll fluorescence parameters of Solanum melongena L. seedlings].
2006 Sep
Synthesis and evaluation of the antiinflammatory activity of N-[2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-oxo-thiazolidin-3-yl]-nicotinamide.
2007
Synthesis, characterization and properties of some divalent metal(II) complexes: their electrochemical, catalytic, thermal and antimicrobial activity studies.
2007 Jul
Substituent effect on g-tensor: multifrequency ESR study and DFT calculation of polycrystalline phenoxyl radicals in diamagnetic crystals.
2007 May 31
Biological stability of polyurethane modified with covalent attachment of di-tert-butyl-phenol.
2007 Sep 15
Hydrogen atom transfer reactions of imido manganese(V) corrole: one reaction with two mechanistic pathways.
2007 Sep 19
Structural characterization and electrochemical properties of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone.
2008 Aug
The non-anaesthetic propofol analogue 2,6-di-tert-butylphenol fails to modulate GABA(A) receptor function.
2009
Iron (III) porphyrin bearing 2,6-di-tert-butylphenol pendants deposited onto gold electrodes for amperometric determination of L-histidine.
2009 Apr 15
Antioxidative activity of ferrocenes bearing 2,6-di-tert-butylphenol moieties.
2010
Determination of antioxidants in new and used lubricant oils by headspace-programmed temperature vaporization-gas chromatography-mass spectrometry.
2010 Dec
Chiral indium alkoxide complexes as initiators for the stereoselective ring-opening polymerization of rac-lactide.
2010 Jan 18
Spike avalanches exhibit universal dynamics across the sleep-wake cycle.
2010 Nov 30
Prevention of polyurethane oxidative degradation with phenolic antioxidants covalently attached to the hard segments: structure-function relationships.
2010 Sep 1
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:40:00 UTC 2023
Edited
by admin
on Fri Dec 15 16:40:00 UTC 2023
Record UNII
21294V58PF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DI-TERT-BUTYLPHENOL
HSDB  
Systematic Name English
DI-TERT-BUTYLPHENOL, 2,6-
Systematic Name English
2,6-DI-TERT-BUTYL-PHENOL
Systematic Name English
2,6-DI-TERT-BUTYLPHENOL [HSDB]
Common Name English
NSC-49175
Code English
Code System Code Type Description
CAS
128-39-2
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
EPA CompTox
DTXSID6027052
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-884-0
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
NSC
49175
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
WIKIPEDIA
2,6-DI-TERT-BUTYLPHENOL
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
HSDB
5616
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
FDA UNII
21294V58PF
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
PUBCHEM
31405
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
MESH
C035407
Created by admin on Fri Dec 15 16:40:00 UTC 2023 , Edited by admin on Fri Dec 15 16:40:00 UTC 2023
PRIMARY
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