Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-

Base Information

• Chemical Name: Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-
• CAS No.: 3462-50-8
• Molecular Formula: C20H18S2
• Molecular Weight: 322.495
• DSSTox Substance ID: DTXSID80401672
• Nikkaji Number: J1.440.494E
• Wikidata: Q82204885
• Mol file: 3462-50-8.mol

Synonyms:Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-;3462-50-8;(1,1-bisphenylthioethyl)benzene;DTXSID80401672;AKOS024406474;(1,1-BIS(PHENYLTHIO)ETHYL)BENZENE

Chemical Property of Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-

Chemical Property:

• XLogP3: 6.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 322.08499292
• Heavy Atom Count: 22
• Complexity: 290

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C1=CC=CC=C1)(SC2=CC=CC=C2)SC3=CC=CC=C3

Technology Process of Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-

There total 10 articles about Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis- 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: 95.0%

1,1,-diethoxy-1-phenylethane (4316-37-4) + thiophenol (108-98-5) → 1,1-bis(phenylsulfanyl)ethylbenzene (3462-50-8)

Guidance literature:

With copper bis(dodecyl sulfate); In water; at 20 ℃; for 0.25h; Inert atmosphere;

DOI:10.1055/s-0029-1218693

Reference yield: 85.0%

thiophenol (108-98-5) + acetophenone (98-86-2) → 1,1-bis(phenylsulfanyl)ethylbenzene (3462-50-8)

Guidance literature:

With vanadyl trifluoromethanesulfonate; In dichloromethane; acetonitrile; at 20 ℃; for 35h; Inert atmosphere;

DOI:10.1016/j.tet.2009.10.012

Reference yield: 85.0%

2-methyl-2-phenyl-1,3-dioxolane (3674-77-9) + thiophenol (108-98-5) → 1,1-bis(phenylsulfanyl)ethylbenzene (3462-50-8)

Guidance literature:

With diethyl ether; lithium perchlorate; at 28 ℃; for 16h;

DOI:10.1021/jo00095a049

upstream raw materials:

thiophenol

acetophenone

2-methyl-2-phenyl-1,3-dioxolane

phenylthiotrimethylsilane

Downstream raw materials:

1-phenyl-1-phenylthio-1-trimethylsilylethane

C₂₂H₃₀S

[(1-phenylethyl)thio]benzene

acetophenone