[2,2-Bis(ethylsulfonyl)-1-phenylsulfanylethenyl]sulfanylbenzene

Base Information

• Chemical Name: [2,2-Bis(ethylsulfonyl)-1-phenylsulfanylethenyl]sulfanylbenzene
• CAS No.: 90127-79-0
• Molecular Formula: C₁₈H₂₀O₄S₄
• Molecular Weight: 428.618
• DSSTox Substance ID: DTXSID50527550
• Wikidata: Q82396759
• Mol file: 90127-79-0.mol

Synonyms:90127-79-0;DTXSID50527550;AKOS003245091;1,1'-{[2,2-Di(ethanesulfonyl)ethene-1,1-diyl]disulfanediyl}dibenzene

Chemical Property of [2,2-Bis(ethylsulfonyl)-1-phenylsulfanylethenyl]sulfanylbenzene

Chemical Property:

• XLogP3: 4.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 428.02444381
• Heavy Atom Count: 26
• Complexity: 614

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCS(=O)(=O)C(=C(SC1=CC=CC=C1)SC2=CC=CC=C2)S(=O)(=O)CC

Technology Process of [2,2-Bis(ethylsulfonyl)-1-phenylsulfanylethenyl]sulfanylbenzene

There total 4 articles about [2,2-Bis(ethylsulfonyl)-1-phenylsulfanylethenyl]sulfanylbenzene 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: 76.0%

1-Chloro-1,2,2-tris-ethanesulfonyl-ethene (123351-62-2) + thiophenol (108-98-5) → bis(ethylsulfonyl)methane (1070-92-4) + (1-Chloro-2,2-bis-ethanesulfonyl-vinylsulfanyl)-benzene (123351-65-5) + C18H20O4S4 (90127-79-0)

Guidance literature:

In acetonitrile; at 50 ℃; for 2h;

DOI:10.1007/BF00958051

Reference yield: 14.0%

1-Chloro-1,2,2-tris-ethanesulfonyl-ethene (123351-62-2) + thiophenol (108-98-5) → (1-Chloro-2,2-bis-ethanesulfonyl-vinylsulfanyl)-benzene (123351-65-5) + 2,2-Bis-ethanesulfonyl-1-phenylsulfanyl-ethenol (90127-82-5) + C18H20O4S4 (90127-79-0) + (Tris-ethanesulfonyl-vinylsulfanyl)-benzene (90127-76-7)

Guidance literature:

In dichloromethane; at 30 - 35 ℃; for 2h; Further byproducts given;

DOI:10.1007/BF00958051

Reference yield: 14.0%

1-Chloro-1,2,2-tris-ethanesulfonyl-ethene (123351-62-2) + thiophenol (108-98-5) → bis(ethylsulfonyl)methane (1070-92-4) + (1-Chloro-2,2-bis-ethanesulfonyl-vinylsulfanyl)-benzene (123351-65-5) + 2,2-Bis-ethanesulfonyl-1-phenylsulfanyl-ethenol (90127-82-5) + C18H20O4S4 (90127-79-0) + (Tris-ethanesulfonyl-vinylsulfanyl)-benzene (90127-76-7)

Guidance literature:

With urea; In dichloromethane; at 30 - 35 ℃; for 2h; Product distribution; Mechanism; also without urea addition, other temperatures, other time (1 h); reactions with further thiols;

DOI:10.1007/BF00958051

upstream raw materials:

tetrakis-ethanesulfonyl-ethene

thiophenol

1-Chloro-1,2,2-tris-ethanesulfonyl-ethene