3,5-DI-TERT-BUTYLCATECHOL

Details

Stereochemistry	ACHIRAL
Molecular Formula	C14H22O2
Molecular Weight	222.3233
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

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

InChI

InChIKey=PJZLSMMERMMQBJ-UHFFFAOYSA-N

InChI=1S/C14H22O2/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8,15-16H,1-6H3

HIDE SMILES / InChI

Approval Year

PubMed

Title	Date	PubMed
Structural correlation of catecholase-like activities of oxy-bridged dinuclear copper(II) complexes.	2001 Apr	11374579
Substrate binding in catechol oxidase activity: biomimetic approach.	2002 Jul 29	12132925
Effects of aminoacids on the autooxidation of 3,5-di-tert-butylcatechol in the presence of surface-active copper(II) complexes.	2002 Nov 15	12505092
Synthesis, structure and catechol-oxidase activity of copper(II) complexes of 17-hydroxy-16-(N-3-oxo-prop-1-enyl)amino steroids.	2002 Sep	12231119
Catalytic oxidation of 3,5-Di-tert-butylcatechol by a series of mononuclear manganese complexes: synthesis, structure, and kinetic investigation.	2003 Oct 6	14514302
Dinuclear and mononuclear manganese(IV)-radical complexes and their catalytic catecholase activity.	2004 Nov 21	15540128
Solution chemical properties and catecholase-like activity of the copper(II)-Ac-His-His-Gly-His-OH system, a relevant functional model for copper containing oxidases.	2005 Oct 7	16172644
New unsymmetric dinuclear Cu(II)Cu(II) complexes and their relevance to copper(II) containing metalloenzymes and DNA cleavage.	2006 May	16563512
Mechanisms of the antispasmodic activity of 3,5-di-t-butyl catechol (DTCAT) on rat vascular smooth muscles.	2007 Apr 30	17292353
Synthesis, characterization and properties of some divalent metal(II) complexes: their electrochemical, catalytic, thermal and antimicrobial activity studies.	2007 Jul	17046317
Cyclometallated iridium and platinum complexes with noninnocent ligands.	2007 May 14	17439204
Iron(III) complexes of tridentate 3N ligands as functional models for catechol dioxygenases: the role of ligand N-alkyl substitution and solvent on reaction rate and product selectivity.	2007 Nov 26	17958355
Oxidative double dehalogenation of tetrachlorocatechol by a bio-inspired CuII complex: formation of chloranilic acid.	2008	18449873
Novel iron(III) complexes of sterically hindered 4N ligands: regioselectivity in biomimetic extradiol cleavage of catechols.	2008 Aug 4	18597419
Oxidative C-H and C-C bond cleavage by a (2,2'-bipyridine)copper(I) chloride complex.	2008 Jul 21	18578492
Structural motifs of diiodine complexes with amides and thioamides.	2008 Oct 14	18813369
New family of ferric spin clusters incorporating redox-active ortho-dioxolene ligands.	2009 Aug 17	19594116
Molecular structure and catechol oxidase activity of a new copper(I) complex with sterically crowded monodentate N-donor ligand.	2009 Mar	19135259
Mono- and dinuclear manganese(III) complexes showing efficient catechol oxidase activity: syntheses, characterization and spectroscopic studies.	2009 Oct 28	19809751
A unique nickel system having versatile catalytic activity of biological significance.	2010 Apr 5	20192227
A functional model of extradiol-cleaving catechol dioxygenases: mimicking the 2-his-1-carboxylate facial triad.	2010 May 17	20392074
Copper (II) complexes of the anti-inflammatory drug naproxen and 3-pyridylmethanol as auxiliary ligand. Characterization, superoxide dismutase and catecholase--mimetic activities.	2010 Sep	20605277

Name

Type

Language

3,5-DI-TERT-BUTYLCATECHOL

Systematic Name

English

NSC-59767

Code

English

DI-TERT-BUTYLCATECHOL, 3,5-

Systematic Name

English

Code System Code Type Description

NSC

59767