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Details

Stereochemistry ACHIRAL
Molecular Formula C14H20O2
Molecular Weight 220.3074
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-BIS(1,1-DIMETHYLETHYL)-2,5-CYCLOHEXADIENE-1,4-DIONE

SMILES

CC(C)(C)C1=CC(=O)C=C(C1=O)C(C)(C)C

InChI

InChIKey=RDQSIADLBQFVMY-UHFFFAOYSA-N
InChI=1S/C14H20O2/c1-13(2,3)10-7-9(15)8-11(12(10)16)14(4,5)6/h7-8H,1-6H3

HIDE SMILES / InChI

Molecular Formula C14H20O2
Molecular Weight 220.3074
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Novel square pyramidal iron(III) complexes of linear tetradentate bis(phenolate) ligands as structural and reactive models for intradiol-cleaving 3,4-PCD enzymes: Quinone formation vs. intradiol cleavage.
2010-10-28
Determination of synthetic phenolic antioxidants and their metabolites in water samples by downscaled solid-phase extraction, silylation and gas chromatography-mass spectrometry.
2010-10-08
Copper (II) complexes of the anti-inflammatory drug naproxen and 3-pyridylmethanol as auxiliary ligand. Characterization, superoxide dismutase and catecholase--mimetic activities.
2010-09
Mono- and dinuclear manganese(III) complexes showing efficient catechol oxidase activity: syntheses, characterization and spectroscopic studies.
2009-10-28
A UV-transparent passive concentrator/spectrum deconvolution method for simultaneous detection of endocrine disrupting chemicals (EDCs) and related contaminants in natural waters.
2009-08
Combining two non-innocent ligands in isomeric complexes [Pt(pap)(m)Q(n)](0) (pap = phenylazopyridine, Q = 3,5-di-tert-butyl-benzoquinone.
2009-06-28
Metal-catalyzed reversible conversion between chemical and electrical energy designed towards a sustainable society.
2009
Catechol oxidase activity of a series of new dinuclear copper(II) complexes with 3,5-DTBC and TCC as substrates: syntheses, X-ray crystal structures, spectroscopic characterization of the adducts and kinetic studies.
2008-08-18
Binuclear copper(II) complexes with N4O3 coordinating heptadentate ligand: synthesis, structure, magnetic properties, density-functional theory study, and catecholase activity.
2008-05-19
Effect of water on the catalytic oxidation of catechols.
2008-04-16
Macromolecular salen catalyst with largely enhanced catalytic activity.
2008-01-17
Structure-catalytic function relationship of SiO2-immobilized mononuclear Cu complexes: an EPR study.
2007-09-25
Migration and sensory properties of plastics-based nets used as food-contacting materials under ambient and high temperature heating conditions.
2006-06
Volatile organic compounds in natural biofilm in polyethylene pipes supplied with lake water and treated water from the distribution network.
2005-10
Dinuclear and mononuclear manganese(IV)-radical complexes and their catalytic catecholase activity.
2004-11-21
Application of quantitative structure-toxicity relationships for the comparison of the cytotoxicity of 14 p-benzoquinone congeners in primary cultured rat hepatocytes versus PC12 cells.
2004-09
Radical-scavenging activity of butylated hydroxytoluene (BHT) and its metabolites.
2004-07
Unique example of flexible phenol coordination in mononuclear manganese compounds.
2004-05-07
Structural identification of extractables from rubber closures used for pre-filled semisolid drug applicator by chromatography, mass spectrometry, and organic synthesis.
2004-03-10
Catalytic oxidation of 3,5-Di-tert-butylcatechol by a series of mononuclear manganese complexes: synthesis, structure, and kinetic investigation.
2003-10-06
Antioxidative properties of probucol estimated by the reactivity with superoxide and by electrochemical oxidation.
2001-08
Autoxidation of substituted phenols catalyzed by cobalt Schiff base complexes in supercritical carbon dioxide.
2001-07-02
Copper(II) complexes of aminocarbohydrate beta-ketoenaminic ligands: efficient catalysts in catechol oxidation.
2001-05-18
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:00:35 GMT 2025
Edited
by admin
on Mon Mar 31 19:00:35 GMT 2025
Record UNII
4C9D8L0Y0T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-BIS(1,1-DIMETHYLETHYL)-2,5-CYCLOHEXADIENE-1,4-DIONE
Systematic Name English
NSC-14448
Preferred Name English
2,6-DI-T-BUTYL-1,4-BENZOQUINONE
Systematic Name English
3,5-DI-TERT-BUTYLQUINONE
Common Name English
2,6-DI-T-BUTYL-P-BENZOQUINONE [HSDB]
Common Name English
BIS(1,1-DIMETHYLETHYL)-2,6-CYCLOHEXADIENE-1,4-DIONE, 2,6-
Common Name English
3,5-DI-TERT-BUTYL-P-BENZOQUINONE
Common Name English
2,6-DI-TERT-BUTYL-1,4-BENZOQUINONE
Systematic Name English
2,5-CYCLOHEXADIENE-1,4-DIONE, 2,6-BIS(1,1-DIMETHYLETHYL)-
Systematic Name English
Code System Code Type Description
NSC
14448
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID7021493
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY
FDA UNII
4C9D8L0Y0T
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY
HSDB
2775
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY
PUBCHEM
12867
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-946-0
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY
CAS
719-22-2
Created by admin on Mon Mar 31 19:00:35 GMT 2025 , Edited by admin on Mon Mar 31 19:00:35 GMT 2025
PRIMARY