1,1-Diphenyl-2-phenylsulfanylethanol

Base Information

• Chemical Name: 1,1-Diphenyl-2-phenylsulfanylethanol
• CAS No.: 13307-77-2
• Molecular Formula: C20H18 O S
• Molecular Weight: 306.4213
• NSC Number: 170766
• DSSTox Substance ID: DTXSID30305434
• Nikkaji Number: J2.072.933C
• Wikidata: Q82052074

Synonyms:13307-77-2;1,1-diphenyl-2-phenylsulfanylethanol;NSC170766;DTXSID30305434;NSC-170766

Chemical Property of 1,1-Diphenyl-2-phenylsulfanylethanol

Chemical Property:

• Vapor Pressure: 2.98E-10mmHg at 25°C
• Boiling Point: 485.9°C at 760 mmHg
• Flash Point: 235.6°C
• Density: 1.2g/cm³
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 306.10783637
• Heavy Atom Count: 22
• Complexity: 294

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(CSC2=CC=CC=C2)(C3=CC=CC=C3)O

Technology Process of 1,1-Diphenyl-2-phenylsulfanylethanol

There total 10 articles about 1,1-Diphenyl-2-phenylsulfanylethanol 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: 96.0%

benzophenone (119-61-9) + (phenylsulfanylmethyl)trimethylsilane (17873-08-4) → 1,1-diphenyl-2-(phenylthio)ethan-1-ol (13307-77-2)

Guidance literature:

With tetrabutyl ammonium fluoride; fluoride; In tetrahydrofuran; 1.) 5 deg C, 30 min; 2.) r.t, 1.5 h;

DOI:10.1016/0040-4039(88)85151-7

Reference yield: 82.0%

2-benzenesulfinyl-1,1-diphenylethanol (23975-23-7) → 1,1-diphenyl-2-(phenylthio)ethan-1-ol (13307-77-2)

Guidance literature:

With triphenyl phosphite; [MoO₂Cl₂(dmf)₂]; In acetonitrile; Heating;

DOI:10.1055/s-2004-829104

Reference yield: 78.0%

1,1-Diphenylethylene (530-48-3) + thiophenol (108-98-5) → 1,1-diphenyl-2-(phenylthio)ethan-1-ol (13307-77-2)

Guidance literature:

With tert.-butylhydroperoxide; In water; N,N-dimethyl-formamide; at 25 ℃; for 96h; Time;

DOI:10.1021/acs.joc.5b00123

upstream raw materials:

benzophenone

phenylthiomethyl chloride

(phenylsulfanylmethyl)trimethylsilane

(phenylthio)methyllithium

Downstream raw materials:

2,2-diphenyl-1-phenylthioethene

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