Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Imidodisulfurylchloride

Base Information Edit
  • Chemical Name:Imidodisulfurylchloride
  • CAS No.:15873-42-4
  • Molecular Formula:Cl2H N O4 S2
  • Molecular Weight:214.05
  • Hs Code.:
  • European Community (EC) Number:812-732-5
  • Nikkaji Number:J1.249.017H
  • Mol file:15873-42-4.mol
Imidodisulfurylchloride

Synonyms:Bis(chlorosulfonyl)imide;Imidobis(sulfuryl chloride); Iminodisulfuryl chloride

Suppliers and Price of Imidodisulfurylchloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 22 raw suppliers
Chemical Property of Imidodisulfurylchloride Edit
Chemical Property:
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:212.8724052
  • Heavy Atom Count:9
  • Complexity:231
Purity/Quality:

99.9% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:N(S(=O)(=O)Cl)S(=O)(=O)Cl
Technology Process of Imidodisulfurylchloride

There total 12 articles about Imidodisulfurylchloride 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:
Guidance literature:
In thionyl chloride; amidosulfuric acid placed into a flask and suspended in thionyl dichloride under dry N2; HSO3Cl added, then the flask fitted with a reflux condenser, connected to a CaCl2 drying tube; heated at 130°C for 24 h; reaction mixture fractionally distilled under vacuum; main fraction collected at 95°C/650 Pa;
DOI:10.1002/zaac.200400325
Guidance literature:
With chlorosulfonic acid; at 130 ℃; for 24h; Inert atmosphere;
Refernces Edit
Post RFQ for Price