2432-11-3 | 2,6-Diphenylphenol

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$15.00	$10.00
1g	95%	in stock	$16.00	$11.00
10g	95%	in stock	$23.00	$17.00
25g	95%	in stock	$53.00	$38.00

Description

• Catalog Number: AB60724
• Chemical Name: 2,6-Diphenylphenol
• CAS Number: 2432-11-3
• Molecular Formula: C18H14O
• Molecular Weight: 246.30316000000002
• MDL Number: MFCD00238172
• SMILES: Oc1c(cccc1c1ccccc1)c1ccccc1

Computed Properties

• Complexity: 237
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 4.8

Literature

• The vinylogous aldol reaction of unsaturated esters and enolizable aldehydes using the novel Lewis acid aluminum tris(2,6-di-2-naphthylphenoxide).

  Organic letters 20120601

• Experimental and computational studies into an ATPH-promoted exo-selective IMDA reaction: a short total synthesis of Delta9-THC.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20100726

• Stereoselective construction of halogenated quaternary stereogenic centers via catalytic asymmetric Diels-Alder reaction.

  Journal of the American Chemical Society 20100428

• Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization.

  Journal of the American Chemical Society 20100331

• Metal-pi interactions dominate in the solid-state structures of molecular heterobimetallic alkali-metal-europium(II) aryloxo complexes.

  Chemistry, an Asian journal 20090803

• Charge-separated and molecular heterobimetallic rare earth-rare earth and alkaline earth-rare earth aryloxo complexes featuring intramolecular metal-pi-arene interactions.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

• Substrate encapsulation: an efficient strategy for the RCM synthesis of unsaturated epsilon-lactones.

  Organic letters 20081218

• Developments in heterobimetallic s-block systems: synthesis and structural survey of molecular M/Ae (M=Li, Na, K, Cs; Ae=Ca, Sr) aryloxo complexes.

  Inorganic chemistry 20080602

• Clathrate formation from octaazaphthalocyanines possessing bulky phenoxyl substituents: a new cubic crystal containing solvent-filled, nanoscale voids.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

• Synthesis of gamma-hydroxybutenolides applying crossed aldol condensation in the presence of a bulky lewis acid and their anti-tumor activity.

  Chemical & pharmaceutical bulletin 20070901

• Absolute asymmetric synthesis of stereochemically labile aldehyde helicates and subsequent chirality transfer reactions.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20050905

• Chiral molecular recognition by aluminum tris(2,6-diphenylphenoxide) in an asymmetric 1,4-addition.

  Angewandte Chemie (International ed. in English) 20040213

• Synthesis, spectroscopic characterization and redox reactivity of some transition metal complexes with salicylaldimines bearing 2,6-di-phenylphenol.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20040101

• 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.

  Inorganic chemistry 20030922

• 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.

  Journal of the American Chemical Society 20030521

• Diverse heteroleptic ytterbium(III) thiocyanate complexes by oxidation from bis(thiocyanato)ytterbium(II).

  Chemistry (Weinheim an der Bergstrasse, Germany) 20010417