[1,1':3',1''-Terphenyl]-2',5'-diol

Base Information

• Chemical Name: [1,1':3',1''-Terphenyl]-2',5'-diol
• CAS No.: 13379-77-6
• Molecular Formula: C18H14O2
• Molecular Weight: 262.308
• DSSTox Substance ID: DTXSID10441829
• Nikkaji Number: J1.254.728E
• Wikidata: Q82258794

Synonyms:[1,1':3',1''-Terphenyl]-2',5'-diol;2,6-diphenylhydroquinone;13379-77-6;2,6-diphenyl hydroquinone;SCHEMBL1535921;DTXSID10441829;SYAHSEYNOYOEQI-UHFFFAOYSA-N

Chemical Property of [1,1':3',1''-Terphenyl]-2',5'-diol

Chemical Property:

• XLogP3: 4.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 262.099379685
• Heavy Atom Count: 20
• Complexity: 264

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC(=CC(=C2O)C3=CC=CC=C3)O

Technology Process of [1,1':3',1''-Terphenyl]-2',5'-diol

There total 3 articles about [1,1':3',1''-Terphenyl]-2',5'-diol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

Tenax TA, containing 2,6-diphenyl-p-phenylene ether units → 2,6-diphenyl-1,4-dihydroquinone (13379-77-6) + 2,6-diphenyl-[1,4]benzoquinone (2887-97-0) + benzaldehyde (100-52-7) + benzoic acid (65-85-0,8013-63-6)

Guidance literature:

With Nitrogen dioxide; at 21 ℃; Further Variations:; Reagents; Product distribution;

DOI:10.1021/es025680f

Reference yield:

benzothiophene-2,3-dicarboxylic anhydride (5732-24-1) + Benzo[b]thiophene (95-15-8,11095-43-5) → 2,6-diphenyl-1,4-dihydroquinone (13379-77-6) + 2,5-diphenyl-1,4-dihydroxybenzene (5422-91-3)

Guidance literature:

With aluminium trichloride; PPA; Raney nickel W₇; Yield given. Multistep reaction. Yields of byproduct given;

DOI:10.1002/jhet.5570340313

Reference yield:

2,6-diphenyl-[1,4]benzoquinone (2887-97-0) → 2,6-diphenyl-1,4-dihydroquinone (13379-77-6) + 2,4b,6,8b-Tetraphenyl-4a,4b,8a,8b-tetrahydro-biphenylene-1,4,5,8-tetraone

Guidance literature:

In benzene; Rate constant; Mechanism; Irradiation; further solvents and pH;

upstream raw materials:

2,6-diphenyl-[1,4]benzoquinone

benzothiophene-2,3-dicarboxylic anhydride

Benzo[b]thiophene

Downstream raw materials:

4-(2,6-diphenyl-4-methoxyphenoxy)-4-methoxy-2,6-diphenylcyclohexa-2,5-dienone

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