2,6-DI-TERT-BUTYLPHENOL

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 Search

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

Title	Date	PubMed
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	11259561
[Determination of 2,4,6-tri-tert-butylphenol and related compounds in foods].	2001 Dec	11875820
Estrogenic activity of phenolic additives determined by an in vitro yeast bioassay.	2001 Feb	11266322
Three-coordinate copper(II)-phenolate complexes.	2001 Nov 19	11703106
Structural evidence that propofol stabilizes different GABA(A) receptor states at potentiating and activating concentrations.	2002 Sep 1	12196563
Percutaneous absorption of 2,6-di-tert-butyl-4-nitrophenol (DBNP) in isolated perfused porcine skin.	2003 Jun	12781207
High-affinity block of voltage-operated rat IIA neuronal sodium channels by 2,6 di-tert-butylphenol, a propofol analogue.	2003 Mar	12650493
[Studies on the new antiarthritic drug candidate S-2474].	2003 May	12772588
2,6 di-tert-butylphenol, a nonanesthetic propofol analog, modulates alpha1beta glycine receptor function in a manner distinct from propofol.	2004 Jul	15281510
Degradation of 2,6-di-tert-butylphenol by an isolated high-efficiency bacterium strain.	2005	16295904
Antioxidant activity of propofol and related monomeric and dimeric compounds.	2005 Mar	15744114
2,6-di-tert-butylphenol revisited at 110 K.	2005 Nov	16272597
New analogues of butylated hydroxytoluene as anti-inflammatory and antioxidant agents.	2006 Aug 15	16690318
Determination of chlorine dioxide in water by gas chromatography-mass spectrometry.	2006 Aug 4	16716337
Calix[4]arene-linked bisporphyrin hosts for fullerenes: binding strength, solvation effects, and porphyrin-fullerene charge transfer bands.	2006 Dec 13	17147403
Hydrogen atom transfer reactions of imido manganese(V) corrole: one reaction with two mechanistic pathways.	2007 Sep 19	17718564
The non-anaesthetic propofol analogue 2,6-di-tert-butylphenol fails to modulate GABA(A) receptor function.	2009	19065063
Synthesis, structure, and reactivity of low-coordinate 1,1,3,3-tetraethylguanidinate complexes.	2009 Aug 17	19624099
Antioxidative activity of ferrocenes bearing 2,6-di-tert-butylphenol moieties.	2010	20631836
Determination of antioxidants in new and used lubricant oils by headspace-programmed temperature vaporization-gas chromatography-mass spectrometry.	2010 Dec	20938768
Chiral indium alkoxide complexes as initiators for the stereoselective ring-opening polymerization of rac-lactide.	2010 Jan 18	20000658
Spike avalanches exhibit universal dynamics across the sleep-wake cycle.	2010 Nov 30	21152422

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:40:00 GMT 2023` Edited by `admin` on `Fri Dec 15 16:40:00 GMT 2023`
Record UNII	21294V58PF
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

2,6-DI-TERT-BUTYLPHENOL

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