2-(2-Phenylethyl)benzene-1,3,5-triol

Base Information

• Chemical Name: 2-(2-Phenylethyl)benzene-1,3,5-triol
• CAS No.: 143207-80-1
• Molecular Formula: C14H14O3
• Molecular Weight: 230.263
• DSSTox Substance ID: DTXSID70576525
• Nikkaji Number: J2.199.315H
• Wikidata: Q82466267

Synonyms:2-(2-Phenylethyl)benzene-1,3,5-triol;143207-80-1;SCHEMBL9742762;DTXSID70576525

Chemical Property of 2-(2-Phenylethyl)benzene-1,3,5-triol

Chemical Property:

• XLogP3: 3.1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 230.094294304
• Heavy Atom Count: 17
• Complexity: 214

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CCC2=C(C=C(C=C2O)O)O

Technology Process of 2-(2-Phenylethyl)benzene-1,3,5-triol

There total 9 articles about 2-(2-Phenylethyl)benzene-1,3,5-triol 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: 79.0%

1,3,5-Trimethoxy-2-phenethylbenzene (133350-08-0) → 2,4,6-trihydroxybibenzyl (143207-80-1)

Guidance literature:

With boron tribromide; In dichloromethane; at 0 - 20 ℃;

DOI:10.1248/cpb.40.1130

Reference yield: 46.0%

3,5-dihydroxyphenol (108-73-6) + phenylacetaldehyde (122-78-1) → 2,4,6-trihydroxybibenzyl (143207-80-1)

Guidance literature:

With hydrogen; palladium on activated charcoal; In methanol; for 18h; under 760 Torr;

DOI:10.1016/j.tetlet.2005.05.132

Reference yield:

→ 2,4,6-trihydroxybibenzyl (143207-80-1)

Guidance literature:

With hydrogenchloride; amalgamated zinc;

upstream raw materials:

2-phenyl-2',4',6'-trihydroxyacetophenone

1,3,5-Trimethoxy-2-phenethylbenzene

3,5-dihydroxyphenol

phenylacetaldehyde

Downstream raw materials:

2,4,6-triacetoxy-bibenzyl

4,6-diacetoxy-bibenzyl-2-ol

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