2,6-DIPHENYLPHENOL

Details

Stereochemistry	ACHIRAL
Molecular Formula	C18H14O
Molecular Weight	246.3032
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC1=C(C=CC=C1C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=ATGFTMUSEPZNJD-UHFFFAOYSA-N

InChI=1S/C18H14O/c19-18-16(14-8-3-1-4-9-14)12-7-13-17(18)15-10-5-2-6-11-15/h1-13,19H

HIDE SMILES / InChI

Molecular Formula	C18H14O
Molecular Weight	246.3032
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
Diverse heteroleptic ytterbium(III) thiocyanate complexes by oxidation from bis(thiocyanato)ytterbium(II).	2001 Apr 17	11349921
Molecular recognition of alpha,beta-unsaturated carbonyl compounds using aluminum tris(2,6-diphenylphenoxide) (ATPH): structural and conformational analysis of ATPH complexes and application to the selective vinylogous aldol reaction.	2003 May 21	12785852
Synthesis of group 1 metal 2,6-diphenylphenoxide complexes [M(OC6H3Ph2-2,6)] (M = Li, Na, K, Rb, Cs) and structures of the solvent-free complexes [Rb(OC6H3Ph2-2,6)]x and [Cs(OC6H3Ph2-2,6)x: one-dimensional extended arrays of metal aryloxides.	2003 Sep 22	12971781
Chiral molecular recognition by aluminum tris(2,6-diphenylphenoxide) in an asymmetric 1,4-addition.	2004 Feb 13	14966889
Synthesis, spectroscopic characterization and redox reactivity of some transition metal complexes with salicylaldimines bearing 2,6-di-phenylphenol.	2004 Jan	14670459
Absolute asymmetric synthesis of stereochemically labile aldehyde helicates and subsequent chirality transfer reactions.	2005 Sep 5	15984037
Synthesis of gamma-hydroxybutenolides applying crossed aldol condensation in the presence of a bulky lewis acid and their anti-tumor activity.	2007 Sep	17827763
Clathrate formation from octaazaphthalocyanines possessing bulky phenoxyl substituents: a new cubic crystal containing solvent-filled, nanoscale voids.	2008	18446911
Substrate encapsulation: an efficient strategy for the RCM synthesis of unsaturated epsilon-lactones.	2008 Dec 18	19053741
Developments in heterobimetallic s-block systems: synthesis and structural survey of molecular M/Ae (M=Li, Na, K, Cs; Ae=Ca, Sr) aryloxo complexes.	2008 Jun 2	18459769
Charge-separated and molecular heterobimetallic rare earth-rare earth and alkaline earth-rare earth aryloxo complexes featuring intramolecular metal-pi-arene interactions.	2009	19360834
Metal-pi interactions dominate in the solid-state structures of molecular heterobimetallic alkali-metal-europium(II) aryloxo complexes.	2009 Aug 3	19585640
Stereoselective construction of halogenated quaternary stereogenic centers via catalytic asymmetric Diels-Alder reaction.	2010 Apr 28	20373752
Experimental and computational studies into an ATPH-promoted exo-selective IMDA reaction: a short total synthesis of Delta9-THC.	2010 Jul 26	20589855
Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization.	2010 Mar 31	20205478

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 20:01:17 GMT 2023` Edited by `admin` on `Fri Dec 15 20:01:17 GMT 2023`
Record UNII	LA93W35M96
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

2,6-DIPHENYLPHENOL

Systematic Name

English

(M-TERPHENYL)-2'-OL

Systematic Name

English

(1,1':3',1''-TERPHENYL)-2'-OL

Systematic Name

English

2'-HYDROXY-M-TERPHENYL

Systematic Name

English

M-TERPHENYL-2'-OL

Systematic Name

English

PHENOL, 2,6-DIPHENYL-

Systematic Name

English

Code System Code Type Description

FDA UNII

LA93W35M96