{[(Benzylsulfanyl)(phenyl)methyl]sulfanyl}benzene

Base Information

• Chemical Name: {[(Benzylsulfanyl)(phenyl)methyl]sulfanyl}benzene
• CAS No.: 62740-57-2
• Molecular Formula: C₂₀H₁₈S₂
• Molecular Weight: 322.495
• DSSTox Substance ID: DTXSID50566267
• Mol file: 62740-57-2.mol

Synonyms:62740-57-2;{[(Benzylsulfanyl)(phenyl)methyl]sulfanyl}benzene;DTXSID50566267

Chemical Property of {[(Benzylsulfanyl)(phenyl)methyl]sulfanyl}benzene

Chemical Property:

• XLogP3: 6.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 322.08499292
• Heavy Atom Count: 22
• Complexity: 286

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of {[(Benzylsulfanyl)(phenyl)methyl]sulfanyl}benzene

There total 4 articles about {[(Benzylsulfanyl)(phenyl)methyl]sulfanyl}benzene 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: 74.0%

benzaldehyde (100-52-7) + thiophenol (108-98-5) + phenylmethanethiol (100-53-8) → bis(phenylthio)methylbenzene (7695-69-4) + benzaldehyde dibenzyldithioacetal (5418-20-2) + benzyl(phenyl(phenylthio)methyl)sulfane (62740-57-2)

Guidance literature:

With camphor-10-sulfonic acid; In ethyl acetate; at 20 ℃; for 1h; Overall yield = 91 percent; Overall yield = 0.29 g; Schlenk technique;

DOI:10.1002/chem.202004835

Reference yield: 54.0%

benzyltrimethylsilane (770-09-2) + phenyl dithiobenzoate (949-00-8) → benzyl(phenyl(phenylthio)methyl)sulfane (62740-57-2)

Guidance literature:

With molecular sieve; tetrabutyl ammonium fluoride; In N,N-dimethyl-formamide;

DOI:10.1016/0040-4039(94)88190-1

Reference yield:

Dibenzyl sulfoxide (621-08-9) + thiophenol (108-98-5) → benzyl(phenyl(phenylthio)methyl)sulfane (62740-57-2)

Guidance literature:

With ethylmagnesium bromide; diisopropylamine; Yield given. Multistep reaction; 1.) Et₂O, 0 deg C, 20 min, 2.) Et₂O, RT, overnight;

DOI:10.1246/bcsj.69.2645

upstream raw materials:

benzyltrimethylsilane

phenyl dithiobenzoate

dibenzyl sulfide

thiophenol