6318-17-8

Basic information

• Product Name: 9,10-dihydro-9,10-diphenylanthracene-9,10-diol
• Synonyms: 9,10-dihydro-9,10-diphenylanthracene-9,10-diol;9,10-Dihydro-9,10-diphenyl-9,10-anthracenediol;9,10-Diphenyl-9,10-dihydroxy-9,10-dihydroanthracene
• CAS NO: 6318-17-8
• Molecular Formula: C₂₆H₂₀O₂
• Molecular Weight: 364.4358
• EINECS: 228-661-2
• Mol File: 6318-17-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 553.6°C at 760 mmHg
• Flash Point: 251.7°C
• Appearance: /
• Density: 1.277g/cm³
• Vapor Pressure: 4.31E-13mmHg at 25°C
• Refractive Index: 1.7
• CAS DataBase Reference: 9,10-dihydro-9,10-diphenylanthracene-9,10-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-dihydro-9,10-diphenylanthracene-9,10-diol(6318-17-8)
• EPA Substance Registry System: 9,10-dihydro-9,10-diphenylanthracene-9,10-diol(6318-17-8)

Safety Data

• Hazardous Substances Data: 6318-17-8(Hazardous Substances Data)

Usage

General Description

9,10-dihydro-9,10-diphenylanthracene-9,10-diol is a chemical compound with the molecular formula C28H20O2. It is a dihydroxyanthracene derivative, consisting of two phenyl rings attached to a central anthracene ring. 9,10-dihydro-9,10-diphenylanthracene-9,10-diol is of interest in the field of organic chemistry and materials science due to its potential applications in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). It has been studied for its unique electronic properties and potential use as a fluorophore in various optoelectronic applications. Additionally, its structural features and functional groups make it a valuable building block for the synthesis of more complex organic molecules.

InChI:InChI=1/C26H20O2/c27-25(19-11-3-1-4-12-19)21-15-7-9-17-23(21)26(28,20-13-5-2-6-14-20)24-18-10-8-16-22(24)25/h1-18,27-28H

Upstream product

• 6486-01-7 9,10-dichloro-9,10-diphenyl-9,10-dihydro-anthracene 
• 108-86-1 bromobenzene 
• 84-65-1 9,10-phenanthrenequinone 
• 1499-10-1 9,10-diphenylanthracene 
• 56-23-5 tetrachloromethane 
• 859332-30-2 9,10-di(thiophen-2-yl)-9,10-dihydroanthracene-9,10-diol 
• 100-58-3 phenylmagnesium bromide 
• 17763-67-6 Phenyl triflate 
• 5471-63-6 1,3-diphenylisobenzofuran 
• 19061-38-2 (9s,10s)-9,10-diphenyl-9,10-dihydro-9,10-epoxyanthracene 
• 84-11-7 9,10-phenanthrenequinone 
• 5146-30-5 10-phenyl-10-hydroxy-9-anthracenone 

Downstream Products

• 1499-10-1 9,10-diphenylanthracene 
• 84-65-1 9,10-phenanthrenequinone 
• 803-58-7 cis,trans-9,10-diphenyl-9,10-dihydroanthracene 

Relevant articles and documents

Synthesis of 9,10-Diarylanthracenes via Mg(TMP) 2 ·2LiCl-Mediated Benzyne Generation/[4+2] Cycloaddition and Deoxygenation of 9,10-Epoxyanthracene Intermediates

A new synthetic route to functionalized 9,10-diarylanthracenes has been developed. 9,10-Epoxyanthracene intermediates were prepared by [4+2] cycloaddition of 1,3-diarylisobenzofuran with a variety of functionalized benzyne intermediates, which were obtained by Mg(TMP) 2 ·2LiCl-mediated benzyne generation. For the cleavage of the resultant 9,10-epoxyanthracene intermediates, we developed mild deoxygenation conditions using a combination of trifluoroacetic acid and Et 3 SiH. The utility of this sequence was demonstrated by application to the synthesis of 5,7,12,14-tetraphenylpentacene.

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