4,5-Bis(2-hydroxyethylsulfanyl)-1,3-dithiol-2-one

Base Information

• Chemical Name: 4,5-Bis(2-hydroxyethylsulfanyl)-1,3-dithiol-2-one
• CAS No.: 128258-72-0
• Molecular Formula: C7H10O3S4
• Molecular Weight: 270.41300
• DSSTox Substance ID: DTXSID80396574
• Wikidata: Q82197352
• Mol file: 128258-72-0.mol

Synonyms:4,5-bis(2-hydroxyethylsulfanyl)-1,3-dithiol-2-one;128258-72-0;4,5-bis[(2-hydroxyethyl)sulfanyl]-1,3-dithiol-2-one;STK368240;4,5-Bis-(2-hydroxy-ethylsulfanyl)-[1,3]dithiol-2-one;SCHEMBL12766022;DTXSID80396574;AKOS005445021;bis[(2-hydroxyethyl)sulfanyl]-2H-1,3-dithiol-2-one

Chemical Property of 4,5-Bis(2-hydroxyethylsulfanyl)-1,3-dithiol-2-one

Chemical Property:

• PSA: 164.61000
• LogP: 1.33860
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 6
• Exact Mass: 269.95127887
• Heavy Atom Count: 14
• Complexity: 219

Purity/Quality:

4,5-BIS-(2-HYDROXY-ETHYLSULFANYL)-[1,3]DITHIOL-2-ONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C(CSC1=C(SC(=O)S1)SCCO)O

Technology Process of 4,5-Bis(2-hydroxyethylsulfanyl)-1,3-dithiol-2-one

There total 2 articles about 4,5-Bis(2-hydroxyethylsulfanyl)-1,3-dithiol-2-one 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: 52.0%

4,5-bis[(2'-hydroxyethyl)thio]1,3-dithiole-2-thione (128258-71-9) → 4,5-bis(β-hydroxyethylthio)-1,3-dithiol-2-one (128258-72-0)

Guidance literature:

With mercury(II) diacetate; acetic acid; In chloroform; for 5h; Heating;

Reference yield:

2,5-diketo-1,3,4,6-tetrathiapentalene (64394-45-2) + 2-bromoethanol (540-51-2) → 4,5-bis(β-hydroxyethylthio)-1,3-dithiol-2-one (128258-72-0)

Guidance literature:

With sodium methylate; Yield given. Multistep reaction; 1.) CH₃OH, 2.) DMF, 15 min;

Reference yield: 97.0%

4,5-bis(β-hydroxyethylthio)-1,3-dithiol-2-one (128258-72-0) + benzoyl chloride (98-88-4) → 4,5-bis(β-benzoyloxyethylthio)-1,3-dithiol-2-one (128258-80-0)

Guidance literature:

With triethylamine; In 1,4-dioxane; at 20 ℃; for 4h;

upstream raw materials:

4,5-bis[(2'-hydroxyethyl)thio]1,3-dithiole-2-thione

2,5-diketo-1,3,4,6-tetrathiapentalene

2-bromoethanol

Downstream raw materials:

4,5-bis(β-benzoyloxyethylthio)-1,3-dithiol-2-one

4,5-bis(β-p-chlorophenylsulfonyloxyethylthio)-1,3-dithiol-2-one

4,5-bis(2-chloroethylthio)-1,3-dithiol-2-one

4,5-bis(β-bromoethylthio)-1,3-dithiol-2-one