6-Phenyl-1,3,2lambda~6~,4lambda~6~-dioxadithiane-2,2,4,4-tetrone

Base Information

• Chemical Name: 6-Phenyl-1,3,2lambda~6~,4lambda~6~-dioxadithiane-2,2,4,4-tetrone
• CAS No.: 77383-20-1
• Molecular Formula: C₈H₈O₆S₂
• Molecular Weight: 264.28
• DSSTox Substance ID: DTXSID80505700

Synonyms:77383-20-1;DTXSID80505700;6-Phenyl-1,3,2lambda~6~,4lambda~6~-dioxadithiane-2,2,4,4-tetrone

Chemical Property of 6-Phenyl-1,3,2lambda~6~,4lambda~6~-dioxadithiane-2,2,4,4-tetrone

Chemical Property:

• XLogP3: 0.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 263.97623032
• Heavy Atom Count: 16
• Complexity: 434

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(OS(=O)(=O)OS1(=O)=O)C2=CC=CC=C2

Technology Process of 6-Phenyl-1,3,2lambda~6~,4lambda~6~-dioxadithiane-2,2,4,4-tetrone

There total 2 articles about 6-Phenyl-1,3,2lambda~6~,4lambda~6~-dioxadithiane-2,2,4,4-tetrone 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:

styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) → 6-Phenyl-[1,3,2,4]dioxadithiane 2,2,4,4-tetraoxide (77383-20-1)

Guidance literature:

With sulfur trioxide; In 1,4-dioxane; dichloromethane; at -30 ℃;

DOI:10.1002/recl.19921110106

Reference yield:

styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) → (E)-2-phenylethene-1-sulfonic acid (139555-12-7) + 6-Phenyl-[1,3,2,4]dioxadithiane 2,2,4,4-tetraoxide (77383-20-1)

Guidance literature:

With sulfur trioxide; In 1,4-dioxane; dichloromethane; at -30 - 25 ℃; Product distribution; Mechanism;

DOI:10.1002/recl.19921110106

upstream raw materials:

styrene

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