[(2-Chloro-2-phenylethyl)sulfanyl]benzene

Base Information

• Chemical Name: [(2-Chloro-2-phenylethyl)sulfanyl]benzene
• CAS No.: 19326-95-5
• Molecular Formula: C14H13ClS
• Molecular Weight: 248.776
• DSSTox Substance ID: DTXSID40549206
• Mol file: 19326-95-5.mol

Synonyms:[(2-Chloro-2-phenylethyl)sulfanyl]benzene;19326-95-5;DTXSID40549206

Chemical Property of [(2-Chloro-2-phenylethyl)sulfanyl]benzene

Chemical Property:

• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 248.0426493
• Heavy Atom Count: 16
• Complexity: 183

Purity/Quality:

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)Cl

Technology Process of [(2-Chloro-2-phenylethyl)sulfanyl]benzene

There total 8 articles about [(2-Chloro-2-phenylethyl)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: 89.0%

styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) + ethyl benzenesulfenate (54815-45-1) → (β-chloro-phenethyl)-phenyl sulfide (19326-95-5)

Guidance literature:

With chloro-trimethyl-silane; at 20 ℃; Inert atmosphere;

DOI:10.1007/s11172-008-0370-7

Reference yield: 70.0%

styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) + benzenesulfenyl chloride (931-59-9) → (β-chloro-phenethyl)-phenyl sulfide (19326-95-5) + C19H18NS(1+)*2C5H5N*AlCl4(1-)

Guidance literature:

With pyridine; In dichloromethane; at 20 ℃; for 0.5h;

Reference yield: 19.0%

styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) + Pyridine; compound with GENERIC INORGANIC NEUTRAL COMPONENT + benzenesulfenyl chloride (931-59-9) → (β-chloro-phenethyl)-phenyl sulfide (19326-95-5) + C19H18NS(1+)*2C5H5N*AlCl4(1-)

Guidance literature:

In dichloromethane; at 20 ℃; for 0.5h;

upstream raw materials:

styrene

benzenesulfenyl chloride

ethyl benzenesulfenate

benzenesulfonyl chloride

Downstream raw materials:

2,2-Dimethyl-3-phenyl-4-phenylsulfanyl-butyric acid ethyl ester

1-(4-chloro-phenylsulfanyl)-1-phenyl-2-phenylsulfanyl-ethane

allyl phenyl thioether

4-phenyl-5-(phenylthio)-1-pentene

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